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Recent Concepts in Minimal Access Surgery: Deborshi Sharma Priya Hazrah
Recent Concepts in Minimal Access Surgery: Deborshi Sharma Priya Hazrah
Recent Concepts in Minimal Access Surgery: Deborshi Sharma Priya Hazrah
in Minimal
Access Surgery
Volume 1
Deborshi Sharma
Priya Hazrah
Editors
Recent Concepts in Minimal Access Surgery
Deborshi Sharma • Priya Hazrah
Editors
Recent Concepts in
Minimal Access Surgery
Volume 1
Editors
Deborshi Sharma Priya Hazrah
Department of Surgery Department of Surgery
Lady Hardinge Medical College Lady Hardinge Medical College
New Delhi, India New Delhi, India
© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapore
Pte Ltd. 2022
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Foreword
It gives me great pleasure to write a foreword for the first volume of ‘Recent
Concepts in Minimal Access Surgery’ edited by Dr. Deborshi Sharma, Co-editor Dr.
Priya Hazrah and published by Springer Nature which has expressed a few impor-
tant recent concepts of minimally invasive laparoscopic, robotic, and endoscopic
surgical procedures that have evolved in the past decade. The book is a compilation
of contributions from various renowned authors and experts in the field of minimal
access surgery and is arranged into 21 chapters.
The topics in this first edition of recent concept series encompass a variety of
subjects from basic concepts of ergonomics and meshes to advanced techniques
such as robotic and laparoscopic oncological resections, advanced bariatric surgery,
organ transplantation and retroperitoneal adrenalectomy. Endoscopic interventions
in arenas of surgical practice such as third space endoscopy and endoscopic man-
agement of pancreatic fluid collections are also notable attractions of the edition.
Catering to this evolving era of cooperative laparoscopic, robotic and endoscopic
surgery, written in a simple language with more than 250 illustrations and operative
pictures demonstrating the different techniques followed by compilation of recent
meta-analysis in the respective subjects. This publication can be of immense aid to
students and budding surgeons as also to surgeons/physicians in the field of minimal
access surgery.
I congratulate everyone associated with the compilation, edition and publication
of the book and extend my best wishes for its successful publication.
v
Preface
The above proverb holds true in the field of minimal access surgery which is in
the process of constant rapid metamorphosis.
“Recent Concepts in Minimal Access Surgery” (RCMAS) is an annual publication
which aims to highlight the newer evolving concepts and ideas with their current results,
in arenas of laparoscopic, robotic and endoscopic surgery. The chapters of this publica-
tion are a concise assimilation of knowledge with their concepts and techniques as prac-
ticed by experts in the respective arenas. The publication also intends to bring forth the
evolving techniques and technological advances to help keep abreast in knowledge and
provides a common platform to students, surgeons, and physicians, both trainees and
trainers alike, interested in the field of minimal access surgery. With 21 recent topic
chapters written by renowned faculty, more than 250 operative photographs and sche-
matic illustrations along with the latest results of relevant meta-analysis on the particular
topics tabulated in the “editors note” section of the book can serve as an easy reference
guide. It provides step-by-step descriptions accompanied by numerous helpful photo-
graphs and anatomical drawings. It also includes the controversies and gives a cumula-
tive opinion on the changes developing in minimal access surgery (MAS). It includes
system wise topics and separate chapters on the different topics within the system.
RCMAS is conceptualized as an annual publication with intend to bring forth a
yearly update on newer topics in every and subsequent volumes, as also about
changes and latest developments on earlier addressed issues.
Editors (RCMAS)
vii
viii Preface
The very first volume of RCMAS would not have been impossible to complete
without the expertise, dedication and hard work of each of our expert authors. I
would like to thank each of the authors for their vision, expertise and enormous
dedication in bringing work to this project. I am deeply indebted to them for sharing
their knowledge and enthusiasm about their topic, concluding in an outstanding
overall product. My thanks to our senior faculty for teaching laparoscopic surgery
and their motivation towards this work.
Late (Dr.) U C Biswal, Ex HOD, PGIMER and Dr. RMLH
Dr. V K Ramteke, Ex HOD MAMC and Ex Faculty LHMC
Dr. P K Ganguly, Ex Faculty PGIMER and Dr. RMLH
Dr. K N Srivastava, Ex Faculty PGIMER and Dr. RMLH
Dr. Ajay Kumar, Ex HOD, LHMC
Dr. C K Durga, Ex HOD, PGIMER and Dr. RMLH
Dr O P Pathania Ex HOD, LHMC
Dr. Romesh Lal, HOD, LHMC
Dr. Rana A K Singh, Director, PGIMER and Dr. RMLH
Dr. Chintamani, Faculty, HOD, VMMC and Safdarjung Hospital
Dr. Sanjeev Kumar Tudu, Faculty, LHMC
Dr. Ashok Kumar, Faculty, LHMC
Dr. Munish Guleria, Faculty, PGIMER and Dr. RMLH
and all other faculty and colleagues in LHMC and RMLH.
I must also thank our residents Dr. Akshay Kumar, Dr. Ankit Raj, Dr. Parikshith
Manjunatha, Dr. Ashutosh Nagpal and Mr. S. Gupta for their help in proofreading
the chapters, arranging references, designing the images and tables.
I would also like to thank the publishing team at Springer, who again has been
instrumental in making this volume a reality.
ix
x Acknowledgements
Laparoscopic Nissen’s Fundoplication for GERD:
Current Perspective ������������������������������������������������������������������������������������������ 1
Rajinder Parshad and Aditya Kumar
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer
with Special Reference to D2 Lymphadenectomy������������������������������������������ 33
Rakesh Shivhare, Manish Khasgiwale, Mohit Gangwal, and
Akshat Dhanuka
Laparoscopic Subtotal Cholecystectomy �������������������������������������������������������� 63
Kalpesh Jani and Samir Contractor
Prediction and Grading Methods of a Difficult
Laparoscopic Cholecystectomy������������������������������������������������������������������������ 83
Nikhil Gupta, Priya Hazrah, and Gautam Anand
Robotic Assisted Pancreaticoduodenectomy �������������������������������������������������� 111
Brij B. Agarwal and Neeraj Dhamija
Laparoscopic Surgery for Rectal Prolapse������������������������������������������������������ 133
Manash Ranjan Sahoo, Suyash Bajoria, and Ankit Sahoo
Laparoscopic Lymphadenectomy for Colorectal Cancers:
Concepts and Current Results�������������������������������������������������������������������������� 155
Saumitra Rawat, Chelliah Selvasekar, and Saurabh Bansal
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence���������������� 193
Priya Hazrah, Deborshi Sharma, Gautam Anand, and
Kayenaat Puran Singh Jassi
Surgical Meshes Used in Laparoscopic Procedures���������������������������������������� 219
Anubhav Vindal, Yashika Gupta, and Piyush Kumar Agrawal
Staging Laparoscopy in Intra-Abdominal Cancers���������������������������������������� 247
Sudhir Kumar Singh, Farhanul Huda,
Rajkumar Kottayasamy Seenivasagam, and Somprakas Basu
xi
xii Contents
Role of ICG Fluoroscence Imaging in Laparoscopic
Bowel Anastomosis�������������������������������������������������������������������������������������������� 267
Deborshi Sharma, Sanjay Meena, Amanjeet Singh, and Priya Hazrah
Minimizing Pain in Laparoscopic Hernia Surgery ���������������������������������������� 283
Naveen Sharma, Deborshi Sharma, and Sanjay Meena
Extended-View Totally Extraperitoneal Approach (eTEP)
for Inguinal Hernia Repair ������������������������������������������������������������������������������ 293
Deborshi Sharma, Gautam Anand, and Priya Hazrah
Mini Gastric Bypass������������������������������������������������������������������������������������������ 305
Anshuman Poddar, Om Tantia, and Tamonas Chaudhuri
Robotic Roux-en-Y Gastric Bypass������������������������������������������������������������������ 331
Vivek Bindal
Third Space Endoscopy������������������������������������������������������������������������������������ 351
Ashok Dalal, Ujjwal Sonika, and Amol S. Dahale
Endoscopic Management of Pancreatic Fluid Collection������������������������������ 371
Vaishali Bhardwaj and Vikram Bhatia
Management of Solitary Pulmonary Nodule�������������������������������������������������� 401
Kamran Ali and Sabyasachi Bal
Minimally Invasive Thymectomy���������������������������������������������������������������������� 419
Aloy J. Mukherjee, Mohsin Khan, and Charu Gauba
Retroperitoneoscopic Minimally Invasive Adrenalectomy���������������������������� 443
Sameer Rege
Laparoscopic Donor Nephrectomy������������������������������������������������������������������ 469
Umesh Sharma and Hemant Goel
About the Editor
xiii
Laparoscopic Nissen’s Fundoplication
for GERD: Current Perspective
Rajinder Parshad and Aditya Kumar
Introduction
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 1
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_1
2 R. Parshad and A. Kumar
Clinical Presentation
The patients with GERD, classically present with heartburn and regurgitation. Other
symptoms include chest pain, dysphagia, waterbrash, globus sensation and odyno-
phagia. Another spectrum of symptoms includes the extraesophageal symptoms
such as cough, wheeze and hoarseness. A summary of symptoms associated with
GERD is included in Table 1.
For the successful outcome of fundoplication, it is important to establish GERD
as the cause of patient’s symptoms. It is common to find a small hiatus hernia and
to operate on such patients without establishing the symptom correlation, is bound
to result in a disgruntled patient.
The following investigations help in establishing the diagnosis, correlation with
symptoms and planning the surgery.
Apart from GERD, they are helpful in locating GEJ in relation to the hiatus
and help in estimating the size and reducibility of hiatus hernias. It is recom-
mended as a key investigation in the diagnosis of Hiatus Hernia’s [7].
2. CT Scans: A CT Scan may be useful in hiatus hernia to demonstrate cephalad
migration of the GEJ and fundus especially on oral contrast films [7]. They are
also useful in emergency cases of paraesophageal volvulus.
3. Upper Gastrointestinal Endoscopy (UGIE): It is used to evaluate symptom-
atic patients and especially those with alarm symptoms or suspected associ-
ated esophageal syndromes (peptic strictures, Barrett’s esophagus and
esophageal adenocarcinoma). Biopsies can be taken in presence of any abnor-
mal mucosa or mass. Grading of esophagitis according to Los Angeles
Classification is done. LA-C/D are considered indications for surgery in GERD
[10]. UGIE also is useful to visualize hiatal hernias and remains the mainstay
in its diagnosis [7].
4. Ambulatory pH monitoring: It provides confirmatory evidence of GERD. It is
especially useful in patients with normal UGIE findings and in patients with
atypical symptoms. This test provides the number of reflux episodes and acid
exposure times (AET) of the esophagus. Increased yield is seen with the wireless
capsule study which may be used for 48–96 h. Esophageal reflux is defined as a
pH value<4 and a composite pH score or deMeester score >14.72.
Reflux monitoring is possible in both ‘off PPI (proton pump inhibitor)’ and
‘on PPI’. The Lyon Consensus states that testing always be performed off ther-
apy to demonstrate baseline AET in ‘unproven GERD’, which includes no (or
low-grade) oesophagitis at endoscopy, and no prior positive pH testing. ‘On PPI’
testing is recommended in patients with ‘proven GERD’ (prior LA grade C or D
oesophagitis, long segment Barrett’s oesophagus or prior abnormal pH-metry)
and should be evaluated on double-dose PPI therapy to establish correlation
between refractory symptoms and reflux episodes and/or to exclude inadequate
acid suppression or poor compliance as the mechanism of persisting symp-
toms [11].
5. High Resolution Manometry (HRM): It is usually performed to place leads for
impedance pH monitoring. Other uses include, diagnosing additional motor dis-
orders or when symptoms don’t improve with PPI.
Recent interest has arisen on the use of HRM in GERD due to understanding
of the complex anatomical and pathophysiological aberrations leading to
GERD. Assessment of transient LES relaxation, GEJ location and morphology,
esophageal motor function and contraction reserve have been evaluated through
HRM in patients who don’t respond to empiric medical therapy and have normal
UGI Endoscopy [12].
Various therapeutic modules have been described in managing these patients
which starts from lifestyle modification (raise head end of bed, avoid bedtime meals,
weight loss) to medical therapy (proton pump inhibitors, H2 receptor antagonists,
antacids and prokinetics), surgical techniques (laparoscopic fundoplication, mag-
netic ring implants) and endoluminal techniques (transoral incisionless fundoplica-
tion and radiofrequency ablation).
4 R. Parshad and A. Kumar
Use of proton pump inhibitors is the backbone of medical therapy for GERD [13]
but its use is limited by long term use, patient compliance, costs, relapse of symp-
toms on discontinuation and side effects of long term use. Two metanalysis have
been published comparing medical therapy with surgical management. The first
metanalysis by Rickenbacher et al included 11 publications, 7 trials concluded that
patients under the surgical arm had a better quality of life, improved symptoms and
were more satisfied as compared to the medical arm. However, a considerable pro-
portion (16–62%) of patients needed medical therapy post-surgery. They concluded
that surgery is an equivalent alternative to medical therapy [14]. This study however
did not include a subgroup analysis based on follow up time. Another metanalysis
published a year later found similar findings to the previous study and also con-
ducted a subgroup analysis on follow up. They observed that surgery had signifi-
cantly better results in the short-term period (<3 year) but did not find statistically
significant improvement on long term over medical management. De-Meester
scores were lower in patients in the surgery arm. This metanalysis also favoured
surgical therapy over medical therapy, especially in a follow up of three years [15].
Fundoplication
Introduction
The first fundoplication was described by Rudolf Nissen in 1955 and included a
360° wrap of the fundus of the stomach around the esophagus by plication of both
the anterior and posterior walls of the gastric fundus around the lesser curvature.
Several modifications to his original technique have been described and the modi-
fied Nissen’s Fundoplication (NF) is the most widely performed surgical procedure
for GERD [16].
Laparoscopic Nissen’s Fundoplication (LNF) was first described in 1991 by
Dallemagne, following which, it has gained popularity and largely replaced the open
techniques [1]. LNF is commonly performed in patients of GERD and Hiatus Hernia’s.
An intricate valve mechanism is present at the level of the GEJ that counteracts the
positive gastric pressure and the negative thoracic pressures. A lack of balance in
this natural antireflux mechanism is thought to be the primary cause of
GERD. Components of this barrier mechanism is postulated to include [17]:
(a) Lower Esophageal Sphincter (LES) tone, length and intra-abdominal length.
These may be defective in GERD and hiatus hernias.
(b) Pinchcock action of the crural diaphragm on the GEJ.
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 5
The aim of fundoplication is to correct the defective hiatal anatomy in the hope
of restoring anti reflux barrier.
Indications of Surgery
After objective confirmation for GERD and evaluation for associated problems, sur-
gical therapy is recommended in patients with [6]:
Laparoscopic Nissen’s fundoplication (LNF) was first described following the suc-
cess of laparoscopic cholecystectomy. Following which several studies were per-
formed to evaluate its advantages over open surgery. Two metanalysis including 12
RCT’s (randomized controlled trials) with over 500 procedures have clearly favoured
the laparoscopic approach over open technique. Advantages of the technique included
6 R. Parshad and A. Kumar
short hospital stay, early return to work, reduced risk of complications and higher
patient satisfaction rates. The drawbacks seen included longer operating time and
higher long-term reoperation rates. Similar outcomes were noted with both tech-
niques in terms of safety, efficacy and dysphagia rates [20, 21]. The laparoscopic
approach is hence preferred and is recommended as approach of choice [6].
Obesity has been seen to be associated with increase in GERD, erosive esophagitis
and esophageal adenocarcinoma. It has been seen to increase with increasing weight
(BMI >30 kg/m2) [25, 26]. The safety and long term of effectiveness of fundoplication
in this population is controversial. A recent metanalysis published on the outcomes of
fundoplication in non-obese patients (n = 6246) compared to obese patients (n = 1753)
included 13 studies and found no difference in rates of operative morbidity, redo sur-
gery, need for endoscopic dilation, conversion to open surgery or return to theatre.
However, recurrence of reflux was higher in the obese group (11.4%) compared to
non-obese group (3.4%). This led them to conclude that laparoscopic fundoplication
is safe in obese patients but risk of recurrence of GERD is higher, making it important
to counsel the patients regarding the possibility of poor outcomes [27]. They were
unable to perform a subgroup analysis on the best technique of fundoplication due to
heterogeneity and absence of technique reporting in some studies.
LF (laparoscopic fundoplication) has been thought to improve GERD in morbidly
obese patients (BMI >35 kg/m2), however, it does not help treat the underlying dis-
ease i.e. obesity. Hence, studies have compared laparoscopic gastric bypass (LGB) with
laparoscopic fundoplication (LF). It has been seen that both these techniques have simi-
lar safety and efficacy in reducing symptoms of GERD but LGB provides additional
health benefits by acting as a bariatric procedure for weight loss [28–30]. SAGES (Society
of American Gastrointestinal and Endoscopic Surgeons) too recommends use of LGB
in morbidly obese patients while suggesting further study in the obese group [6].
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 7
• Opening the phreno-esophageal ligament to approach the hiatus and the distal
esophagus from the left to the right with preservation of the hepatic branch of the
anterior vagus nerve where possible.
• Complete dissection of both crura.
• Generous transhiatal mobilization of the esophagus to allow approximately 3 cm
of intra- abdominal length of the distal esophagus.
• Division of short gastric vessels to allow a tension-free wrap.
• Posterior crural repair using nonabsorbable sutures. In case of a very large hiatal
defect, a few anterior crural sutures may be placed.
• Creation of short (1.5–2 cm) and floppy wrap with the most distal suture (nonab-
sorbable) incorporating the anterior wall musculature of the esophagus.
• At the time of the construction of the wrap, introduction of a large bougie through
the esophagus is recommended but not defined as essential
providing patient satisfaction, but there is a higher risk of reoperation for recurrent
symptoms with anterior wrap [34].
Fig. 5 Crural
Approximation
Fig. 7 Creation of
Floppy Wrap
Crural Closure
Closure vs non-closure of crura is a controversial topic with some reporting benefits
while others showing no benefit. No Metanalysis or RCT’s are available and recom-
mendations made are based on case series. General recommendation is to close
crural when hiatal opening is large and mesh reinforcement may benefit in decreas-
ing wrap migration [6].
One RCT comparing anterior (n = 47) vs posterior closure (n = 55) did not show
any difference in dysphagia with soft solids/liquids, need for medication and overall
satisfaction at 10 years follow up [45]. They concluded that anterior repair was at
least as good as posterior repair.
Redo Fundoplication
Although laparoscopic fundoplication has satisfactory outcomes postoperatively,
some patients have persistent or recurrence of symptoms. Another problem noted
with the procedure is development of dysphagia. Apart from these there is a heter-
ogenous cause of complications associated with the procedure needing reoperation.
Several systematic reviews have been performed on the best method of treating
these and outcomes associated. Recurrent reflux and dysphagia were found to be the
most common reason for redo fundoplication. The most common causes of failure
were seen to be wrap migration, wrap disruption and tight wrap accounting to nearly
half the patients. Most of the patients were dealt with redo fundoplication and lapa-
roscopy was the commonly used approach. Morbidity, mortality, longer operative
times and conversion to open was higher in redo fundoplication when compared to
index surgery. Most commonly witnessed complications were esophago-gastric
perforations and bleeding. Symptomatic outcomes of redo fundoplication were
good to excellent. Technically this surgery is more complex and should be per-
formed by experienced surgeons [51–53].
Therefore laparoscopic redo fundoplication is safe, feasible and effective with
higher complication rates than index surgery and due to its complexity should be
performed by experienced surgeons [6].
Newer Modalities
Robotic Fundoplication
With the advent of robotics in late 1990s and identification of its distinct advantages
of improved 3D vision, precise movements, added dexterity and improved
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 13
The LINX magnetic implant system was approved for use in GERD in 2012 by the
FDA. This device works through a ring of magnets implanted laparoscopically
around the LES. They augment LES pressure upto 15–25 mm of Hg to prevent
reflux but at same time allow passage of food through it. This device was found to
be safe in patients for GERD and the changes it brought were evaluated via manom-
etry and published in a study of 121 patients. Results have been tabulated in Table 2
[55] (Fig. 8).
Apart from this, the study also showed that patients with a manometrically
defective LES were restored 67% of the time to a normal sphincter and those with
a structurally defective or severely defective LES improved to a normal LES in
77% and 56% of patients, respectively. Only 18% of patients with a normal preop-
erative manometric LES deteriorated to a lower category. The results of this study
were very promising with significant improvement in LES tone without deleterious
effects on the body and it managed to restore a manometrically defective LES to
normal sphincter and leaving a normal sphincter stable.
The excitement following this procedure led to comparisons with the traditional
surgical method of fundoplication.
Two metanalysis and systemic review comparing early outcomes of LINX vs
LNF were published with the latter including 7 observational studies including
1211 patients [56, 57]. In both the metanalysis LINX and LNF were both seen to be
safe and effective at 1 year follow-up. PPI suspension, need for endoscopic dilata-
tion and QOL rates were similar for both groups with LINX procedure associated
with less gas/bloat symptoms and increased ability to vomit and belch. LNF was
found to take longer operative times and was technically challenging needing skilled
surgeons. The findings need to be assessed with caution as these included only
observational studies and no RCT’s were available. Long term safety, efficacy and
durability are yet to be ascertained for the LINX procedure.
Conclusion
Although newer modalities such as robotics, magnetic sphincter implants and also the
advent of endoscopic fundoplication bring excitement to the field of antireflux sur-
gery, the definite role, safety and reliability are yet to be ascertained on long term
follow up studies. Laparoscopic Nissen’s Fundoplication remains a tested modality
for over four decades and can be considered to be the gold standard surgical approach.
LNF remains the alternate therapy of choice for long term/refractory medical
management.
Editor’s Note1
References: Main chapter references are included after the “References Editor’s Note” section.
1
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 17
Fig. EN1 Schematic
diagram of Laparoscopic
sleeve fundoplication
Fig. EN2 Schematic
diagram showing the end
result of Endoscopic
Fundoplication/Transoral
incisionless fundoplication
18 R. Parshad and A. Kumar
esophagus and secured with fasteners above the Z line (Figure EN2). Though it
appears to be promising in PPI refractory GERD in the short term, its long-term
efficacy is yet to be evaluated and when compared with LNF currently TIF appears
to have an inferior outcome [5–8].
Stretta Procedure
Quality of Life
Table EN4 (continued)
Study, first author, year Result/ conclusion
A Meta-Analysis of Randomized No difference between the procedures in the following:
Controlled Trials to Compare • Operative time,
Long-Term Outcomes of Nissen • Perioperative complications,
and Toupet Fundoplication for • Postoperative satisfaction,
Gastroesophageal Reflux • Recurrence,
Disease. Tian ZC 2015 [26] • Rates of medication adoption
• Re-operation due to recurrence
Significantly higher following parameters after LNF:
• Dysphagia,
• Gas-bloat syndrome,
• Inability to belch
• Re-operation due to severe dysphagia
Laparoscopic anterior 180-degree 180° LAF vs LNF 1 and 5 years:
versus Nissen fundoplication for Dysphagia and gas-related symptoms are lower after LAF
gastroesophageal reflux disease: No difference in:
systematic review and meta- • Esophageal acid exposure
analysis of randomized clinical • Esophagitis
trials. Broeders JA 2013 [27] • Heartburn scores,
• Patient satisfaction,
• Dilatations
• Reoperation rate
A meta-analysis comparing LPF:
laparoscopic partial versus • Less post-operative dysphagia (OR = 0.44, P < 0.0001) and
Nissen fundoplication. Ma S • Less inability to belch (OR = 0.41, P < 0.005)
2012 [28] LNF:
• Significant reduction of post-operative heartburn
(OR = 1.94, P < 0.01).
• Patient satisfaction comparable between the two groups.
Laparoscopic anterior versus LAF vs LPF short term (6−12 months)
posterior fundoplication for Higher after LAF
gastroesophageal reflux disease: • Esophageal acid exposure time (3.3% vs. 0.8%: wmd
systematic review and meta- 2.04; 95% confidence interval [ci] [0.84–3.24]; p < 0.001),
analysis of randomized clinical • Heartburn (21% vs. 8%; rr 2.71; 95%ci [1.72–4.26];
trials. Broeders JA 2011 [29] p < 0.001)
• Reoperation rate (8% vs. 4%; RR 1.94; 95%CI [0.97–
3.87]; P = 0.06)
Lower after LAF:
• Dakkak dysphagia score (2.5 vs. 5.7; WMD −2.87;
95%CI [−3.88 to −1.87]; P < 0.001).
No short-term differences in prevalence of
• Esophagitis,
• Regurgitation
• Perioperative outcomes.
LAF vs LPF long term (2−10 years)
Higher after LAF
• Heartburn (31% vs. 14%; RR 2.15; 95% CI [1.49–3.09];
p < 0.001)
• More PPI use (25% vs. 10%; RR 2.53; 95% CI [1.40–
4.45]; p = 0.002).
• Reoperation rate (10% vs. 5%; RR 2.12; 95% CI
[1.07–4.21]; p = 0.03).
No long term difference
Long-term Dakkak dysphagia scores, inability to belch, gas
bloating and satisfaction were not different.
(continued)
24 R. Parshad and A. Kumar
Table EN4 (continued)
Study, first author, year Result/ conclusion
Meta-analysis of laparoscopic LNF versus LTF:
total (Nissen) versus posterior • Control of reflux was good
(Toupet) fundoplication for • Occurrence of heartburn similar
gastro-oesophageal reflux disease • Lower early and late post-operative dysphagia ltf group.
based on randomized clinical • Patient’s satisfaction similar
trials.Tan G 2011 [30]
Systematic review and meta- LNF vs LTF higher prevalence in LNF of:
analysis of laparoscopic Nissen • Postoperative dysphagia (RR 1.61 (95 per cent confidence
(posterior total) versus Toupet interval 1.06 to 2.44); P = 0.02)
(posterior partial) fundoplication • Dilatation for dysphagia (RR 2.45 (1.06 to 5.68);
for gastro-oesophageal reflux P = 0.04).
disease. Broeders JA 2010 [31] • Surgical reinterventions (RR 2.19 (1.09 to 4.40);
P = 0.03),
• Inability to belch (RR 2.04 (1.19 to 3.49); P = 0.009)
• Gas bloating (RR 1.58 (1.21 to 2.05); P < 0.001
No differences regarding:
• Recurrent pathological acid exposure (RR 1.26 (0.82 to
1.95); P = 0.29),
• Oesophagitis (RR 1.20 (0.78 to 1.85); P = 0.40),
• Subjective reflux recurrence,
• Patient satisfaction,
• Operating time
• In-hospital complications
LNF Laparoscopic Nissen Fundoplication, LAF Laparoscopic anterior fundoplication, LPF
Laparoscopic posterior fundoplication, LTF Laparoscopic Toupet fundoplication, OR Odds ratio,
RR Relative risk, LES Lower esophageal Sphincter, WMD Weighted Mean difference, PPI Proton
Pump Inhibitors
Table EN5 Meta-analysis comparing short gastric division versus non division in laparoscopic
fundoplication
Study, first author, year Result/ conclusion
Laparoscopic Nissen fundoplication with or SGVD had longer:
without short gastric vessel division: a meta- • Operative time
analysis. Khatri K 2012 [32] • Hospital stay.
No difference in terms of functional
outcomes for 1- and 10-year follow-up
Systematic review and meta-analysis of No statistically significant effect on rates of:
laparoscopic Nissen fundoplication with or • Reoperation,
without division of the short gastric vessels. • Postoperative dysphagia
Markar SR 2011 [33] • Reflux.
• Length of hospital stay,
• Postoperative complications,
• Postoperative gas bloat syndrome
• Demeester score.
SGV division was associated with:
• Longer duration of operation
• Reduced postoperative lower oesophageal
sphincter pressure.
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 25
Table EN5 (continued)
Study, first author, year Result/ conclusion
Meta-analysis of two randomized controlled No significant differences in:
trials to identify long-term symptoms after • Heartburn
division of the short gastric vessels during • Dysphagia,
Nissen fundoplication. Engström C 2011 [34] • Ability to belch or vomit,
• Use of antisecretory medications.
Division of the short gastric vessels was
associated with a higher rate of bloating
symptoms (72 versus 48 per cent;
P = 0.002) at 10-12 years follow up
SGV/SGVD short gastric vessel division
26 R. Parshad and A. Kumar
1. Patterson EJ, Herron DM, Hansen PD, Ramzi N, Standage BA, Swanström
LL. Effect of an esophageal bougie on the incidence of dysphagia following
Nissen fundoplication: a prospective, blinded, randomized clinical trial. Arch
Surg. 2000 Sep; 135(9):1055–61; discussion 1061–2.
2. Omar A. Jarral, Thanos Athanasiou, George B. Hanna and Emmanouil
Zacharakis. Is an intra-oesophageal bougie of use during Nissen fundoplica-
tion? Interactive CardioVascular and Thoracic Surgery 14 (2012) 828–833.
3. Rebecchi F, Allaix ME, Cinti L, Nestorović M, Morino M. Comparison of the
outcome of laparoscopic procedures for GERD. Updates Surg. 2018
Sep;70(3):315–21.
4. Aiolfi A, Micheletto G, Marin J, Rausa E, Bonitta G, Bona D. Laparoscopic
Sleeve-Fundoplication for Morbidly Obese Patients with Gastroesophageal
Reflux: Systematic Review and Meta-analysis. Obes Surg. 2021
Apr;31(4):1714–21. https://doi.org/10.1007/s11695-020-05189-6. Epub 2021
Jan 3. PMID: 33389630; PMCID: PMC8012327.
5. Gerson L, Stouch B, Lobonţiu A. Transoral Incisionless Fundoplication (TIF
2.0): A Meta-Analysis of Three Randomized, Controlled Clinical Trials.
Chirurgia (Bucur). 2018 Mar-Apr;113(2):173–84. https://doi.org/10.21614/
chirurgia.113.2.173. PMID: 29733015.
6. Richter JE, Kumar A, Lipka S, Miladinovic B, Velanovich V. Efficacy of
Laparoscopic Nissen Fundoplication vs Transoral Incisionless Fundoplication
or Proton Pump Inhibitors in Patients With Gastroesophageal Reflux Disease: A
Systematic Review and Network Meta-analysis. Gastroenterology. 2018
Apr;154(5):1298–308.e7. https://doi.org/10.1053/j.gastro.2017.12.021. Epub
2018 Jan 3. PMID: 29305934.
7. McCarty TR, Itidiare M, Njei B, Rustagi T. Efficacy of transoral incisionless
fundoplication for refractory gastroesophageal reflux disease: a systematic
review and meta-analysis. Endoscopy. 2018 Jul;50(7):708–25. https://doi.
org/10.1055/a-0576-6589. Epub 2018 Apr 6. PMID: 29625507.
8. Huang X, Chen S, Zhao H, Zeng X, Lian J, Tseng Y, Chen J. Efficacy of tran-
soral incisionless fundoplication (TIF) for the treatment of GERD: a systematic
review with meta-analysis. Surg Endosc. 2017 Mar;31(3):1032–44. https://doi.
org/10.1007/s00464-016-5111-7. Epub 2016 Aug 5. PMID: 27495332.
9. Fass R, Cahn F, Scotti DJ, Gregory DA. Systematic review and meta-analysis
of controlled and prospective cohort efficacy studies of endoscopic radiofre-
quency for treatment of gastroesophageal reflux disease. Surg Endosc. 2017
Dec;31(12):4865–82. https://doi.org/10.1007/s00464-017-5431-2. Epub 2017
Feb 23. PMID: 28233093.
10. Lipka S, Kumar A, Richter JE. No evidence for efficacy of radiofrequency abla-
tion for treatment of gastroesophageal reflux disease: a systematic review and
meta-analysis. Clin Gastroenterol Hepatol. 2015 Jun;13(6):1058–67.e1. https://
doi.org/10.1016/j.cgh.2014.10.013. Epub 2014 Oct 18. PMID: 25459556.
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 27
11. Kumar A, Raja K, Kumar S, et al. (September 26, 2020) Quality of Life in
Gastroesophageal Reflux Disease Three Months After Laparoscopic Nissen’s
Fundoplication. Cureus 2020 Sep 26;12(9)
12. Sanberg Ljungdalh J, Rubin KH, Durup J, et al. Long-term patient satisfaction
and durability of laparoscopic anti-reflux surgery in a large Danish cohort:
study protocol for a retrospective cohort study with development of a novel
scoring system for patient selection. BMJ Open 2020 Mar 16;10(3).
13. Salminen P: The laparoscopic Nissen fundoplication--a better operation?
Surgeon. 2009, 7:224–7.
14. Guidozzi N, Wiggins T, Ahmed AR, Hanna GB, Markar SR. Laparoscopic
magnetic sphincter augmentation versus fundoplication for gastroesophageal
reflux disease: systematic review and pooled analysis. Dis Esophagus. 2019
Nov 13;32(9):doz031. https://doi.org/10.1093/dote/doz031. PMID: 31069388.
15. Aiolfi A, Asti E, Bernardi D, Bonitta G, Rausa E, Siboni S, Bonavina L. Early
results of magnetic sphincter augmentation versus fundoplication for gastro-
esophageal reflux disease: Systematic review and meta-analysis. Int J Surg.
2018 Apr;52:82–8. https://doi.org/10.1016/j.ijsu.2018.02.041. Epub 2018 Feb
20. PMID: 29471155
16. Skubleny D, Switzer NJ, Dang J, Gill RS, Shi X, de Gara C, Birch DW, Wong
C, Hutter MM, Karmali S. LINX® magnetic esophageal sphincter augmenta-
tion versus Nissen fundoplication for gastroesophageal reflux disease: a sys-
tematic review and meta-analysis. Surg Endosc. 2017 Aug;31(8):3078–84.
https://doi.org/10.1007/s00464-016-5370-3. Epub 2016 Dec 15. PMID:
27981382
17. Chen MY, Huang DY, Wu A, Zhu YB, Zhu HP, Lin LM, Cai XJ. Efficacy of
Magnetic Sphincter Augmentation versus Nissen Fundoplication for
Gastroesophageal Reflux Disease in Short Term: A Meta-Analysis. Can J
Gastroenterol Hepatol. 2017;2017:9596342. https://doi.
org/10.1155/2017/9596342. Epub 2017 Mar 30. PMID: 28466002; PMCID:
PMC5390656.
18. Wang Z, Zheng Q, Jin Z. Meta-analysis of robot-assisted versus conventional
laparoscopic Nissen fundoplication for gastro-oesophageal reflux disease. ANZ J
Surg. 2012 Mar;82(3):112–7. https://doi.org/10.1111/j.1445-2197.2011.05964.x.
Epub 2012 Jan 17. PMID: 22510118.
19. Markar SR, Karthikesalingam AP, Hagen ME, Talamini M, Horgan S, Wagner
OJ. Robotic vs. laparoscopic Nissen fundoplication for gastro-oesophageal
reflux disease: systematic review and meta-analysis. Int J Med Robot. 2010
Jun;6(2):125–31. https://doi.org/10.1002/rcs.309. PMID: 20506440.
20. Mi J, Kang Y, Chen X, Wang B, Wang Z. Whether robot-assisted laparoscopic
fundoplication is better for gastroesophageal reflux disease in adults: a sys-
tematic review and meta-analysis. Surg Endosc. 2010 Aug;24(8):1803–14.
https://doi.org/10.1007/s00464-009-0873-9. Epub 2010 Jan 29. PMID:
20112116.
28 R. Parshad and A. Kumar
21. Zhang P, Tian JH, Yang KH, Li J, Jia WQ, Sun SL, Ma B, Liu YL. Robot-
assisted laparoscope fundoplication for gastroesophageal reflux disease: a sys-
tematic review of randomized controlled trials. Digestion. 2010;81(1):1–9.
https://doi.org/10.1159/000235920. Epub 2009 Dec 22. PMID: 20029202.
22. Andreou A, Watson DI, Mavridis D, Francis NK, Antoniou SA. Assessing the
efficacy and safety of laparoscopic antireflux procedures for the management of
gastroesophageal reflux disease: a systematic review with network meta-
analysis. Surg Endosc. 2020 Feb;34(2):510–20. https://doi.org/10.1007/
s00464-019-07208-9. Epub 2019 Oct 18. PMID: 31628621.
23. Du X, Wu JM, Hu ZW, Wang F, Wang ZG, Zhang C, Yan C, Chen
MP. Laparoscopic Nissen (total) versus anterior 180° fundoplication for gastro-
esophageal reflux disease: A meta-analysis and systematic review. Medicine
(Baltimore). 2017 Sep;96(37):e8085. https://doi.org/10.1097/
MD.0000000000008085. PMID: 28906412; PMCID: PMC5604681.
24. Du X, Hu Z, Yan C, Zhang C, Wang Z, Wu J. A meta-analysis of long follow-up
outcomes of laparoscopic Nissen (total) versus Toupet (270°) fundoplication
for gastro-esophageal reflux disease based on randomized controlled trials in
adults. BMC Gastroenterol. 2016 Aug 2;16(1):88. https://doi.org/10.1186/
s12876-016-0502-8. PMID: 27484006; PMCID: PMC4969978.
25. Memon MA, Subramanya MS, Hossain MB, Yunus RM, Khan S, Memon
B. Laparoscopic anterior versus posterior fundoplication for gastro-esophageal
reflux disease: a meta-analysis and systematic review. World J Surg. 2015
Apr;39(4):981–96. https://doi.org/10.1007/s00268-014-2889-0. PMID: 25446479.
26. Tian ZC, Wang B, Shan CX, Zhang W, Jiang DZ, Qiu M. A Meta-Analysis of
Randomized Controlled Trials to Compare Long-Term Outcomes of Nissen and
Toupet Fundoplication for Gastroesophageal Reflux Disease. PLoS One. 2015
Jun 29;10(6):e0127627. https://doi.org/10.1371/journal.pone.0127627. PMID:
26121646; PMCID: PMC4484805.
27. Broeders JA, Roks DJ, Ahmed Ali U, Watson DI, Baigrie RJ, Cao Z, Hartmann
J, Maddern GJ. Laparoscopic anterior 180-degree versus nissen fundoplication
for gastroesophageal reflux disease: systematic review and meta-analysis of
randomized clinical trials. Ann Surg. 2013 May;257(5):850–9. https://doi.
org/10.1097/SLA.0b013e31828604dd. PMID: 23470572.
28. Ma S, Qian B, Shang L, Shi R, Zhang G. A meta-analysis comparing laparo-
scopic partial versus Nissen fundoplication. ANZ J Surg. 2012
Jan-Feb;82(1–2):17–22. https://doi.org/10.1111/j.1445-2197.2010.05637.x.
Epub 2011 Jan 20. PMID: 22507490.
29. Broeders JA, Roks DJ, Ahmed Ali U, Draaisma WA, Smout AJ, Hazebroek
EJ. Laparoscopic anterior versus posterior fundoplication for gastroesophageal
reflux disease: systematic review and meta-analysis of randomized clinical tri-
als. Ann Surg. 2011 Jul;254(1):39–47. https://doi.org/10.1097/
SLA.0b013e31821d4ba0. PMID: 21543968.
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 29
References
1. Dallemagne B, Weerts JM, Jehaes C, Markiewicz S, Lombard R. Laparoscopic Nissen fundo-
plication: preliminary report. Surg Laparosc Endosc. 1991 Sep;1(3):138–43.
2. Vakil N, van Zanten SV, Kahrilas P, Dent J, Jones R, The Global Consensus Group. The
Montreal definition and classification of gastroesophageal reflux disease: a global evidence-
based consensus. Am J Gastroenterol. 2006 Aug;101(8):1900–20.
3. Gaddam S, Sharma P. Shedding light on the epidemiology of gastroesophageal reflux disease
in India—a big step forward. Indian J Gastroenterol. 2011 May;30(3):105–7.
4. Franzén T, Tibbling L. Is the severity of gastroesophageal reflux dependent on hiatus hernia
size? World J Gastroenterol WJG. 2014 Feb 14;20(6):1582–4.
5. Barrett NR. Hiatus hernia: a review of some controversial points. Br J Surg. 1954
Nov;42(173):231–43.
6. Stefanidis D, Hope WW, Kohn GP, Reardon PR, Richardson WS, Fanelli RD, et al.
Guidelines for surgical treatment of gastroesophageal reflux disease. Surg Endosc. 2010
Nov;24(11):2647–69.
7. Kohn GP, Price RR, DeMeester SR, Zehetner J, Muensterer OJ, Awad Z, et al. Guidelines for
the management of hiatal hernia. Surg Endosc. 2013 Dec;27(12):4409–28.
8. Siegal SR, Dolan JP, Hunter JG. Modern diagnosis and treatment of hiatal hernias. Langenbecks
Arch Surg. 2017 Dec;402(8):1145–51.
9. Badillo R. Diagnosis and treatment of gastroesophageal reflux disease. World J Gastrointest
Pharmacol Ther. 2014;5(3):105.
10. Lundell L, Dent J, Bennett J, Blum A, Armstrong D, Galmiche J, et al. Endoscopic assessment
of oesophagitis: clinical and functional correlates and further validation of the Los Angeles
classification. Gut. 1999 Aug;45(2):172–80.
11. Gyawali CP, Kahrilas PJ, Savarino E, Zerbib F, Mion F, Smout AJPM, et al. Modern diagnosis
of GERD: the Lyon Consensus. Gut. 2018 Jul;67(7):1351–62.
12. Gyawali CP, Roman S, Bredenoord AJ, Fox M, Keller J, Pandolfino JE, et al. Classification
of esophageal motor findings in gastro-esophageal reflux disease: Conclusions from an inter-
national consensus group. Neurogastroenterol Motil Off J Eur Gastrointest Motil Soc. 2017
Dec;29(12)
13. Katz PO, Gerson LB, Vela MF. Guidelines for the diagnosis and management of gastroesopha-
geal reflux disease. Am J Gastroenterol. 2013 Mar;108(3):308–28; quiz 329.
14. Rickenbacher N, Kötter T, Kochen MM, Scherer M, Blozik E. Fundoplication versus medical
management of gastroesophageal reflux disease: systematic review and meta-analysis. Surg
Endosc. 2014 Jan;28(1):143–55.
15. Jiang Y, Cui W-X, Wang Y, Heng D, Tan J-C, Lin L. Antireflux surgery vs medical treat-
ment for gastroesophageal reflux disease: A meta-analysis. World J Meta-Anal. 2015 Dec
26;3(6):284–94.
16. Salminen P. The laparoscopic Nissen fundoplication--a better operation? Surg J R Coll Surg
Edinb Irel. 2009 Aug;7(4):224–7.
17. Herbella FAM, Schlottmann F, Patti MG. Pathophysiology of gastroesophageal reflux disease:
how an antireflux procedure works (or does not work). Updat Surg. 2018 Sep;70(3):343–7.
18. Lundell L. Borderline indications and selection of gastroesophageal reflux disease patients: “Is
surgery better than medical therapy”? Dig Dis Basel Switz. 2014;32(1–2):152–5.
19. Beck PE, Watson DI, Devitt PG, Game PA, Jamieson GG. Impact of gender and age on the
long-term outcome of laparoscopic fundoplication. World J Surg. 2009 Dec;33(12):2620–6.
20. Siddiqui MRS, Abdulaal Y, Nisar A, Ali H, Hasan F. A meta-analysis of outcomes after open
and laparoscopic Nissen’s fundoplication in the treatment for gastro-oesophageal reflux dis-
ease. Eur Surg. 2012 Jun 1;44(3):138–49.
21. Peters MJ, Mukhtar A, Yunus RM, Khan S, Pappalardo J, Memon B, et al. Meta-analysis
of randomized clinical trials comparing open and laparoscopic anti-reflux surgery. Am J
Gastroenterol. 2009 Jun;104(6):1548–61.
Laparoscopic Nissen’s Fundoplication for GERD: Current Perspective 31
22. Dean BB, Gano AD, Knight K, Ofman JJ, Fass R. Effectiveness of proton pump inhibitors
in nonerosive reflux disease. Clin Gastroenterol Hepatol Off Clin Pract J Am Gastroenterol
Assoc. 2004 Aug;2(8):656–64.
23. Park J-M, Chi K-C. Antireflux surgery is equally beneficial in nonerosive and erosive gastro-
esophageal reflux disease. Ann Surg Treat Res. 2018 Aug;95(2):94–9.
24. Broeders JA, Draaisma WA, Bredenoord AJ, Smout AJ, Broeders IA, Gooszen HG. Long-
term outcome of Nissen fundoplication in non-erosive and erosive gastro-oesophageal reflux
disease. Br J Surg. 2010 Jun;97(6):845–52.
25. Hampel H, Abraham NS, El-Serag HB. Meta-analysis: obesity and the risk for gastroesopha-
geal reflux disease and its complications. Ann Int Med. 2005 Aug 2;143(3):199–211.
26. El-Serag H. The association between obesity and GERD: a review of the epidemiological
evidence. Dig Dis Sci. 2008 Sep;53(9):2307–12.
27. Abdelrahman T, Latif A, Chan DS, Jones H, Farag M, Lewis WG, et al. Outcomes after laparo-
scopic anti-reflux surgery related to obesity: A systematic review and meta-analysis. Int J Surg
Lond Engl. 2018 Mar;51:76–82.
28. Varela JE, Hinojosa MW, Nguyen NT. Laparoscopic fundoplication compared with laparo-
scopic gastric bypass in morbidly obese patients with gastroesophageal reflux disease. Surg
Obes Relat Dis Off J Am Soc Bariatr Surg. 2009 Apr;5(2):139–43.
29. Patterson EJ, Davis DG, Khajanchee Y, Swanström LL. Comparison of objective outcomes
following laparoscopic Nissen fundoplication versus laparoscopic gastric bypass in the mor-
bidly obese with heartburn. Surg Endosc. 2003 Oct;17(10):1561–5.
30. Sise A, Friedenberg FK. A comprehensive review of gastroesophageal reflux disease and obe-
sity. Obes Rev Off J Int Assoc Study Obes. 2008 May;9(3):194–203.
31. Attwood SEA, Lundell L, Ell C, Galmiche J-P, Hatlebakk J, Fiocca R, et al. Standardization
of surgical technique in antireflux surgery: the LOTUS trial experience. World J Surg. 2008
Jun;32(6):995–8.
32. Ramos RF, Lustosa SAS, de Almeida CAP, da Silva CP, Matos D. Surgical treatment of gas-
troesophageal reflux disease: total or partial fundoplication? Systematic review and meta-
analysis. Arq Gastroenterol. 2011 Dec;48(4):252–60.
33. Du X, Hu Z, Yan C, Zhang C, Wang Z, Wu J. A meta-analysis of long follow-up outcomes
of laparoscopic Nissen (total) versus Toupet (270°) fundoplication for gastro-esophageal
reflux disease based on randomized controlled trials in adults. BMC Gastroenterol. 2016 Aug
2;16(1):88.
34. Du X, Wu J-M, Hu Z-W, Wang F, Wang Z-G, Zhang C, et al. Laparoscopic Nissen (total) ver-
sus anterior 180° fundoplication for gastro-esophageal reflux disease. Medicine (Baltimore)
[Internet]. 2017 Sep;96(37)
35. Donahue PE, Samelson S, Nyhus LM, Bombeck CT. The floppy Nissen fundoplication.
Effective long-term control of pathologic reflux. Arch Surg Chic Ill 1960. 1985 June;120(6):
663–8.
36. DeMeester TR, Bonavina L, Albertucci M. Nissen fundoplication for gastroesophageal
reflux disease. Evaluation of primary repair in 100 consecutive patients. Ann Surg. 1986
Jul;204(1):9–20.
37. Watson DI, Pike GK, Balgrie RJ, Mathew G, Devitt PG, Britten-Jones R, Jamieson
GG. Prospective double-blind randomized trial of laparoscopic Nissen fundoplication
with division and without division of short gastric vessels. Ann Surg. 1997 Nov;226(5):
642–52.
38. Kinsey-Trotman SP, Devitt PG, Bright T, Thompson SK, Jamieson GG, Watson DI. Randomized
trial of division versus nondivision of short gastric vessels during Nissen fundoplication:
20-year outcomes. Ann Surg. 2018 Aug;268(2):228–32.
39. Mardani J, Lundell L, Lönroth H, Dalenbäck J, Engström C. Ten-year results of a randomized
clinical trial of laparoscopic total fundoplication with or without division of the short gastric
vessels. Br J Surg. 2009 Jan;96(1):61–5.
32 R. Parshad and A. Kumar
40. Luostarinen ME, Koskinen MO, Isolauri JO. Effect of fundal mobilisation in Nissen-Rossetti
fundoplication on oesophageal transit and dysphagia. A prospective, randomised trial. Eur J
Surg Acta Chir. 1996 Jan;162(1):37–42.
41. de Farah JFM, Grande JCD, Goldenberg A, Martinez JC, Lupinacci RA, Matone J. Randomized
trial of total fundoplication and fundal mobilization with or without division of short gastric
vessels: a short-term clinical evaluation. Acta Cir Bras. 2007 Dec;22(6):422–9.
42. Kösek V, Wykypiel H, Weiss H, Höller E, Wetscher G, Margreiter R, et al. Division of the
short gastric vessels during laparoscopic Nissen fundoplication: clinical and functional out-
come during long-term follow-up in a prospectively randomized trial. Surg Endosc. 2009
Oct;23(10):2208–13.
43. O’Boyle CJ, Watson DI, Jamieson GG, Myers JC, Game PA, Devitt PG. Division of short
gastric vessels at laparoscopic Nissen fundoplication: a prospective double-blind randomized
trial with 5-year follow-up. Ann Surg. 2002 Feb;235(2):165–70.
44. Wyman JB, Dent J, Heddle R, Dodds WJ, Toouli J, Downton J. Control of belching by the
lower oesophageal sphincter. Gut. 1990 Jun;31(6):639–46.
45. Chew CR, Jamieson GG, Devitt PG, Watson DI. Prospective randomized trial of laparoscopic
Nissen fundoplication with anterior versus posterior hiatal repair: late outcomes. World J Surg.
2011 Sep;35(9):2038–44.
46. Zhang C, Liu D, Li F, Watson DI, Gao X, Koetje JH, et al. Systematic review and meta-
analysis of laparoscopic mesh versus suture repair of hiatus hernia: objective and subjective
outcomes. Surg Endosc. 2017;31(12):4913–22.
47. Castelijns PSS, Ponten JEH, van de Poll MCG, Nienhuijs SW, Smulders JF. A collective
review of biological versus synthetic mesh-reinforced cruroplasty during laparoscopic Nissen
fundoplication. J Minimal Access Surg. 2018;14(2):87–94.
48. Bülbüller N, Oner OZ. Esophageal calibration with soft orogastric tube during laparoscopic
Nissen fundoplication may reduce postoperative transient dysphagia. Indian J Surg. 2015
Dec;77(Suppl 3):759–63.
49. Patterson EJ, Herron DM, Hansen PD, Ramzi N, Standage BA, Swanström LL. Effect of an
esophageal bougie on the incidence of dysphagia following Nissen fundoplication: a prospec-
tive, blinded, randomized clinical trial. Arch Surg Chic Ill 1960. 2000 Sep;135(9):1055–61;
discussion 1061–1062.
50. Novitsky YW, Kercher KW, Callery MP, Czerniach DR, Kelly JJ, Litwin DEM. Is the use of
a bougie necessary for laparoscopic Nissen fundoplication? Arch Surg Chic Ill 1960. 2002
Apr;137(4):402–6.
51. van Beek DB, Auyang ED, Soper NJ. A comprehensive review of laparoscopic redo fundopli-
cation. Surg Endosc. 2011 Mar;25(3):706–12.
52. Furnée EJB, Draaisma WA, Broeders IAMJ, Gooszen HG. Surgical reintervention after
failed antireflux surgery: a systematic review of the literature. J Gastrointest Surg. 2009
Aug;13(8):1539–49.
53. Symons NRA, Purkayastha S, Dillemans B, Athanasiou T, Hanna GB, Darzi A, et al.
Laparoscopic revision of failed antireflux surgery: a systematic review. Am J Surg. 2011
Sep;202(3):336–43.
54. Markar SR, Karthikesalingam AP, Hagen ME, Talamini M, Horgan S, Wagner OJ. Robotic vs.
laparoscopic Nissen fundoplication for gastro-oesophageal reflux disease: systematic review
and meta-analysis. Int J Med Robot Comput Assist Surg MRCAS. 2010 Jun;6(2):125–31.
55. Warren HF, Louie BE, Farivar AS, Wilshire C, Aye RW. Manometric changes to the lower
esophageal sphincter after magnetic sphincter augmentation in patients with chronic gastro-
esophageal reflux disease. Ann Surg. 2017;266(1):99–104.
56. Skubleny D, Switzer NJ, Dang J, Gill RS, Shi X, de Gara C, et al. LINX® magnetic esophageal
sphincter augmentation versus Nissen fundoplication for gastroesophageal reflux disease: a
systematic review and meta-analysis. Surg Endosc. 2017;31(8):3078–84.
57. Aiolfi A, Asti E, Bernardi D, Bonitta G, Rausa E, Siboni S, et al. Early results of magnetic
sphincter augmentation versus fundoplication for gastroesophageal reflux disease: Systematic
review and meta-analysis. Int J Surg Lond Engl. 2018 Apr;52:82–8.
Recent Advances in Laparoscopic
Gastrectomy for Gastric Cancer
with Special Reference to D2
Lymphadenectomy
Introduction
R. Shivhare (*)
Department of Surgical Gastroenterology, Minimal Access Surgery & Renal & Liver
Transplant Unit, Eminent Hospital, Indore, India
M. Khasgiwale
GI Surgery & Transplant Unit, Apollo Hospitals, Indore, India
M. Gangwal
GEM Hospital, Coimbatore, India
A. Dhanuka
Index Medical College, Indore, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 33
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_2
34 R. Shivhare et al.
Table 1 enumerates the different types of gastric resection based on the extent of
excision of the stomach. Table 2 enlists the various minimally invasive approaches
of gastrectomy reported in literature.
In HALG one of the hands of the surgeon (commonly the non-dominant hand)
is inserted, into the abdominal cavity, through a small abdominal incision across
a special sleeve appliance or hand port system, designed to maintain the pneu-
moperitoneum during the process. The other components of the surgery are per-
formed like a laparoscopic procedure viz.: creation of pneumoperitoneum for
workspace, visualization through laparoscopic camera system and insertion of
other ports.
An early report of HALG with double stapling and quadruple stapling technique
for anastomosis demonstrated equivalent curative results to that of open surgery and
was found to be less invasive [2]. Other reports on hand assisted distal gastrectomy
in early distal gastric cancers found it to be not as beneficial and has been proposed
to be a steppingstone in the learning curve during transition to totally laparoscopic
gastrectomy [3].
The advantages of hand assisted laparoscopic techniques are that the inserted
hand improves tactile sensation, has a greater degree of freedom of movements as
compared to laparoscopic instruments inserted through fixed trocars and can
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 35
somewhat aid in depth perception. It can help in gentle blunt dissection as well as
retraction and apply immediate haemostasis [4].
However, there are some disadvantages of HALG, pertinent amongst which are:
(1) the hand inserted in the abdomen can compromise the intra-abdominal working
space (2) there can be hand shoulder and forearm muscle fatigue (3) The need for
an incision of 7–8 cm which can offset the advantages of minimal access techniques
(4) added cost of hand port system [2–4].
Table 3 Commonly used anastomotic techniques for restoration of bowel continuity after totally
laparoscopic gastrectomy
Anastomosis after distal Billroth I/Delta anastomosis/Overlap Method
gastrectomy Billroth II
Roux en Y/Beta shaped Roux En Y reconstruction
Uncut Roux En Y
Anastomosis after proximal Esophagogastrostomy
gastrectomy/Total Esophagogastrostomy with antireflux procedure
gastrectomy Esophagojejunostomy can be performed with linear or circular
stapler: (functional end to end anastomosis/overlap method/
inverted T shaped anastomosis)
Jejunal interposition with pouch or without pouch
Double tract reconstruction
36 R. Shivhare et al.
SIDG needs advanced techniques and there is sparse evidence of oncological safety
and therefore has not been generalized. Thereby safety and oncologic outcomes of
SIDG needs validation in large scale studies.
38 R. Shivhare et al.
Robotic Gastrectomy
Peri gastric nodes that are located closest to primary are designated as N1, whereas
distant peri gastric nodes as also nodes situated along major arterial supply of the
stomach are denoted as N2. En bloc removal of the stomach along with N1 level
nodes is termed as gastrectomy with D1 lymphadenectomy whereas D2 lymphade-
nectomy entails enbloc removal of N1 and N2 nodes along with gastrectomy. The
Japanese classification of nodes assigns numbers according to various stations.
Figure 1 depicts common lymph node stations around the stomach.
The Japanese view of a survival benefit with D2 lymphadenectomy stems from
the fact that the initial spread of gastric cancer is largely localized to lymphnodes
around the stomach. Proponents of the western non-radical view believe that more
radical lymphadenectomy increases accuracy of pathologic staging, rather than con-
ferring an improved survival. Most east Asian (Japanese, Chinese and Korean) stud-
ies report a better outcome of gastric cancer surgery when compared to their Western
counterparts and project a beneficial role of D2 dissection however they are largely
nonrandomized trials because the already accepted benefits of D2 dissection raises
ethical concerns in conducting comparative analysis of D1 versus D2. The Dutch
and the MRC studies failed to demonstrate a survival advantage and conversely
noted increased morbidity with D2 dissection as opposed to D1 dissection. A recent
Italian trial has projected a trend towards improved disease-free survival with D2
dissection for node positive T2-T4 tumors [24]. Earlier pancreatico-splenectomy
was routinely added to D2 gastrectomy to ensure a full nodal clearance along the
splenic artery however it was associated with increased morbidity which called for
modification to spleen preserving D2 gastrectomy. Moreover, contamination and
non-compliance to the standards of D1 and D2 lymphadenectomy often confounds
comparisons between reported trials [29]. A recent review on various trials on extent
of lymphadenectomy for gastric cancer observed benefits of pancreas and spleen
preserving D2 lymphadenectomy as compared to D1 lymphadenectomy particu-
larly in node positive advanced gastric cancers [30]. Conversely the AJCC (American
Joint Committee on cancer) eighth edition classification grades prognosis based
upon the number of nodes involved rather than the station/location and recommends
removal of ≥16 regional nodes for reliable prognostic staging, albeit a greater
lymph node yield is expected in D2 lymphadenectomy [30]. A metanalysis of ran-
domized controlled trials noted a benefit regarding disease specific survival with D2
lymphadenectomy and though there was no noted survival benefit regarding overall
survival or disease-free survival, subgroup analysis by country did show a benefit
[31]. The current western consensus is that D2 lymphadenectomy should be per-
formed in high volume centres where the expertise is available [24]. Extended D3
lymphadenectomy entails a more radical en bloc resection including N3 nodes
which are considered to be situated outside normal lymphatic pathways from stom-
ach but may be involved due to retrograde lymphatic flow resultant to blockage of
normal routes in advanced malignancies and may prove beneficial if N2 nodes are
positive however its benefits over D2 is not proven [32].
Laparoscopic surgery has been advocated in early gastric cancer and merits on
aspects related to safety, feasibility, oncologic parameters and better short-term out-
comes than those of open gastrectomy. A metanalysis comparing laparoscopic and
open surgery for early gastric cancer observed that laparoscopic gastrectomy rever-
berated the benefits of laparoscopic surgery viz.: less blood loss, smaller incision
length, reduced postoperative pain and shorter hospital stay besides fewer serious
complications. However, it displayed relative demerits of longer operative time and
fewer harvested nodes [33]. A concurrent metanalysis on laparoscopic gastrectomy
40 R. Shivhare et al.
for advanced gastric cancer suggests an equivalent survival outcome both in arenas
of overall and disease-free survival as compared to open surgery [34]. The crux of
performing a laparoscopic D2 gastrectomy lies in performance of an adequate
lymphadenectomy. Several randomized clinical trials with multicentre participation
and a few systematic review and meta-analysis are being conducted to study the
safety and efficacy of laparoscopic D2 gastrectomy in the context of early as well as
long-term outcome. One must highlight the fact that as laparoscopic experience has
been accumulated between surgeons of the eastern countries, the indications for
laparoscopic approaches have included also more ‘difficult’ and demanding cases
with advanced gastric cancer patients.
Surgical Technique
The patient is placed in a supine reverse Trendelenburg position with legs apart,
under general anaesthesia. The surgeon has two assistants: one assistant stands on
the right side of the patient and holds the laparoscope, and other stands on the left
side of the patient. Carbon dioxide is used for insufflation. Pneumoperitoneum is
established through Hassan technique. An initial 10-mm port is inserted around the
umbilicus. Staging laparoscopy is performed and adequacy to continue further
established. Subsequently four other trocars are inserted a 12 mm port in left upper
flank, a 5 mm port near the xiphisternum and two 5 mm working ports in either flank.
Lesser sac entry: The initial step constitutes of gaining entry into the lesser sac by
dissecting the greater omentum along the border of the transverse colon with the
dissection being continued towards the left exposing the tail of pancreas and
splenic hilum.
Division of left gastroepiploic vessels and dissection of 4sb nodes: The left
gastroepiploic vessels are identified, dissected and divided in between ligatures or
clips. The 4sb nodes are also taken down at the same time.
Dissection of gastrocolic omentum, ligation of right gastroepiploic vessels
and dissection of nodal stations 4d & 6: Gastrocolic omentum/ligament is contin-
ued to be divided proximally beyond the level of gastric dissection. In case of proxi-
mal gastrectomy or total gastrectomy the short gastric vessels are also taken down.
Further dissection of gastrocolic omentum is continued to the right side in the same
plane. Stomach is flipped up at the same time and lymph nodes (No. 4d,6) are also
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 41
dissected along the greater curvature (Fig. 2). The superior leaf of the mesocolon
and the anterior leaf of the pancreas are dissected towards the pylorus along with the
gastric specimen.
In classic D2 dissection the lymph nodes in front of the superior mesenteric vein
(No. 14v) are not included routinely however in D2 plus dissection for advanced
cancer or if they appear to be involved, they may be included. Dissecting along the
right colic vein/Henle’s trunk helps in identification of the superior mesenteric vein
at the neck of pancreas. Further upward dissection, close to the upper border of
pancreatic head leads to identification of the right gastroepiploic artery which is
identified clipped and ligated at its origin from the gastroduodenal artery, along with
dissection of station 6 nodes (infrapyloric group).
Duodenal mobilization and transection: The dissection is continued further
towards the right until the duodenum is visualized. The duodenum is pulled inferi-
orly so that the hepatoduodenal ligament gets tense, where a window is created and
a communication between the dissection planes is established behind the duode-
num. The first part of the duodenum is mobilized by clearing off tissue of its wall
and after properly creating the window a linear stapler is inserted and duodenum is
divided just distal to the pylorus.
Dissection of the hepatoduodenal ligament, ligation of right gastric artery &
vein and dissection of lymph node stations 12a, 8a and 9: The dissection in the
hepatoduodenal ligament proceeds sequentially in right to left fashion. The right
gastric artery is identified divided and cut at its origin. The proper hepatic artery is
laid bare along with dissection of lymph node station 12a. Hepatoduodenal ligament
structures are dissected with removal of lymph nodal stations 8a (along common
hepatic artery) and 9 (coeliac group) as shown in (Fig. 3). In the process the lym-
phnode stations 5 (suprapyloric group) and station 3 are included in the specimen.
Dissection of posterior gastric attachments and station 7, 11p nodes:
Subsequently the stomach is dissected from anterior surface of pancreas, the lymph
nodes near the left gastric artery (station 7), and the splenic artery (No. 11p; Fig. 4)
are dissected.
42 R. Shivhare et al.
Fig. 3 Dissection of
hepatoduodenal ligament
(12 a), common hepatic
artery (No 8a) and celiac
(No 9) lymph nodes
Fig. 4 Clearance of
proximal splenic artery
lymph node (No 11p)
The periumbilical incision is sutured back after retrieval of the specimen and the
pneumoperitoneum re-established.
Billroth II reconstruction: A stapled antecolic Bilroth II side to side gastrojeju-
nostomy is constructed as described below. An access opening is created in the
antimesenteric border of an efferent jejunal loop (at 15–20 cm from duodenojejunal
flexure) and the other in the posterior wall of the gastric stump 2 cm proximal to
transection staple line. An endoscopic linear stapler is inserted with one limb in the
jejunum and the other in the stomach lumen (Fig. 7) and an ante colic Billroth II
side-to-side gastrojejunostomy is created. Some surgeons prefer to fix the jejunum
and gastric stump with stay sutures before applying endoscopic linear staplers, how-
ever it can angulate the jejunum and restrict its mobility thereby hampering proper
placement of staplers. Experienced surgeons prefer placing one arm of the
44 R. Shivhare et al.
endoscopic linear stapler into the jejunal opening then clamping the two arms with-
out stapling thus drawing the jejunum close to the rear of the gastric stump, and
stapling after proper opposition is confirmed. The common opening can be closed
by intracorporeal suturing (Fig. 8) or staplers.
A Laparoscopic Roux-en-Y reconstruction is also preferred by some surgeons,
its advantages being less reflux gastritis and esophagitis as also decreased probabil-
ity of gastric cancer recurrence. Nevertheless, the procedure is complex, time-con-
suming, and requires a greater number of anastomosis thus a higher cost is incurred
consequent to use of endoscopic linear staplers.
Billroth I reconstruction: The main advantage of Billroth I reconstruction
method is its technical simplicity of maintaining physiological intestinal continuity
involving only one anastomotic site. Main disadvantage of the anastomosis is its
sequelae of gastroesophageal and duodeno-gastric reflux and its complications
thereof. Moreover, the procedure may be difficult to perform in obese patients or in
patients with large tumours in the distal or mid stomach where large portions of the
stomach is resected making Billroth I reconstruction not possible.
Sutured anastomosis: As regards the anastomotic methodology, intracorporeal
suturing is relatively difficult and time consuming to perform laparoscopically
despite its low cost.
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 45
An abdominal drain is placed preferably from the right side and port sites are closed.
Perioperative Management
Complications
Enlisted below are some of the specific quoted postoperative complications after D2
gastrectomy (both initial and late).
Conclusion
Editor’s Note1
Open gastrectomy with D2 lymphadenectomy for gastric cancer has been a standard
of practice in east Asian countries however due to increased morbidity particularly
when associated with pancreatico-splenectomy it had failed to gain a similar
approval amongst surgeons in the west. Noncompliance and contamination with the
D2 lymphadenectomy extent and difference in disease biology amongst western as
compared to eastern population were thought to have been the reasons for poor
outcome especially in patients from the west. Lately long-term results emerging
from the Italian trial has shown a trend towards improved survival benefit with D2
over D1 lymphadenectomy for gastric cancer.
With the advent of laparoscopic surgery, the safety and efficacy of laparoscopic D2
gastrectomy as compared with open procedure is being investigated. Several clini-
cal trials randomized clinical trials with multicentre participation and a few system-
atic review and meta-analysis have been studying on safety and efficacy of
laparoscopic gastrectomy. Prominent results of a few RCT and metaanalysis com-
paring laparoscopic and open D2 gastrectomy is tabulated below (Table EN1).
Most trials conclude a non-inferiority of laparoscopic D2 gastrectomy over open
D2 gastrectomy as regards the number of nodes harvested, morbidity mortality and
short-term survival benefits. A recent meta-analysis shows an increase trend for
positive proximal resection margin in laparoscopic as compared to open gastrec-
tomy [8]. Laparoscopic D2 gastrectomy has been stated to be safe with low rates of
complications and demonstrate the benefits of minimally invasive surgery viz.: a
lower blood loss and enhanced postoperative recovery albeit a relative disadvantage
of increased operative time [1–11].
References: Main chapter references are included after the “References Editor’s Note” section.
1
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 49
Table EN1 (continued)
Name of Study Results
Short-term Outcomes of a Multicenter LDG better than ODG in following
Randomized Controlled Trial Comparing parameters:
Laparoscopic Distal Gastrectomy With D2 • Early morbidity
Lymphadenectomy to Open Distal Gastrectomy (LDG 16.6%, ODG 24.1%; P = 0.003).
for Locally Advanced Gastric Cancer (KLASS- • Day of flatus passage:
02-RCT) [2] (LDG 3.5 days, ODG 3.7 days
P = 0.025).
• Pain score and postoperative analgesic
requirement significantly lower after
LDG group:
• Postoperative hospital stay
(LDG vs ODG 8.1 vs 9.3 days
respectively P = 0.005).
No difference LDG vs ODG in:
• 90 days’ mortality rate
(LDG = 0.4%, ODG = 0.6%,
p = 0.682).
• Mean retrieved lymph nodes
(LDG = 46.6, ODG = 47.4, p = 0.451)
Effect of Laparoscopic vs Open Distal No difference in:
Gastrectomy on 3-Year Disease-Free Survival in • 3 year DFS
Patients With Locally Advanced Gastric Cancer: LDG = 76.5%, ODG = 77.8%
The CLASS-01 Randomized Clinical Trial [3] • Three-year OS,
LDG = 83.1%,ODG = 85.2%;
• Cumulative 3-year recurrence rate
LDG = 18.8%, ODG = 16.5%
Morbidity and Mortality of Laparoscopic Versus No difference in:
Open D2 Distal Gastrectomy for Advanced • D2 lymphadenectomy compliance:
Gastric Cancer: A Randomized Controlled LG = 99.4%, OG = 99.6%; P = 0.845.
Trial [4] • Postoperative morbidity
LG = 15.2% OG = 12.9%, 2.3%; 95%
P = .285.
• Mortality rate
LG = 0.4% OG = zero P = .249).
Laparoscopic Versus Open Gastrectomy With D2 LGD2 vs OGD2, Following parameters
Lymph Node Dissection for Advanced Gastric were significant lower in LGD2:
Cancer: A Systematic Review [5] • Intraoperative blood loss,
• Duration of analgesic administration,
• Times to first ambulation
• Time to first flatus
• Time to oral intake,
• Length of postoperative stay,
• Incidence of nonsurgical complications.
LGD2 vs OGD2, no significant differences
were observed between:
• Postoperative in-hospital mortality,
• Retrieved nodes,
• Tumor recurrence,
• 5-year DFS
• Five and three-year OS.
LGD2 had longer operative time.
(continued)
50 R. Shivhare et al.
Table EN1 (continued)
Name of Study Results
Laparoscopic Versus Open Gastrectomy for LG vs OG:
Locally Advanced Gastric Cancer: A Systematic • Operative time more in LG,
Review and Meta-Analysis of Randomized • Estimated intraoperative blood loss
Controlled Studies [6] lower in LG
LG vs OG similar outcome in:
• Length of hospital stay
• Time to flatus passage
• Number of retrieved nodes
Long-term Oncologic Outcomes of a No difference in:
Randomized Controlled Trial Comparing • Survival in Kaplan Meier
Laparoscopic Versus Open Gastrectomy With D2 • 5-year OS:
Lymph Node Dissection for Advanced Gastric (LG = 49.0%, OG = 50.7%)
Cancer [7] • 5-year DFS
(LG = 47.2% OG =49.6%)
• 5-year tumor recurrence rate no
difference
Long-term and short-term outcomes after In RCTs, LG were better than OG in terms
laparoscopic versus open surgery for advanced of:
gastric cancer: An updated meta-analysis [8] • Estimated blood loss,
• First oral intake day
• First day to pass flatus
LG fared worse than OG as regards:
• Operation time
• Proximal margin positivity
• Overall survival
• Disease-free survival (DFS)
LGD2,LGD,LG Laparoscopic D2 gastrectomy, OGD2,OGD,OG Open D2 gastrectomy, RCT
Randomized Controlled Trials
Gastrectomy
Various function preserving partial gastrectomy reported in literature are: distal gas-
trectomy, proximal gastrectomy, pylorus preserving gastrectomy, middle segment
gastrectomy, segmentectomy and local resection which provide good oncological
outcome in early gastric cancer
Lymphadenectomy
Variations in extent of lymphadenectomy described has been D1, D1 + alpha, D1 + Beta,
D2, D2 plus dissections and D3. The definitions of D1, D1 plus and D2 gastrectomy
varies according to the site of tumor and gastrectomy viz.: total gastrectomy, distal gas-
trectomy, pylorus preserving gastrectomy and proximal gastrectomy.
D1 and D1 + alpha, D1 + beta lymphadenectomy: In classic D1 gastrectomy
perigastric lymph nodes station 1–6 nodes are removed. In D1 alpha additional
groups removed are level 7 (left gastric) or 8a (common hepatic). In D1 beta dissec-
tion additional 7, 8a and 9 (coeliac) are removed.
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 51
Total gastrectomy
• D0: Lymphadenectomy less than D1.
• D1: 1–7.
• D1+: D1 + 8a, 9, 11p.
• D2: D1 + 8a, 9, 11p, 11d, 12a.
Distal gastrectomy
• D0: Lymphadenectomy less than D1.
• D1: 1, 3, 4sb, 4d, 5, 6, 7.
• D1+: D1 + 8a, 9.
• D2: D1 + 8a, 9, 11p, 12a.
Pylorus-preserving gastrectomy
• D0: Lymphadenectomy less than D1.
• D1: 1, 3, 4sb, 4d, 6, 7.
• D1+: D1 + 8a, 9.
Proximal gastrectomy
• D0: Lymphadenectomy less than D1.
• D1: 1, 2, 3a, 4sa, 4sb, 7
• D1+: D1 + 8a, 9, 11p
Techniques in Anastomosis
Fig. EN2 Schematic
diagram showing the Delta
anastomosis
Stomach
Stapler
Duodenum
• Esophagogastrostomy (EG)
• Esophagogastrostomy plus fundoplication
• Esophagogastrostomy plus angle of his repair
• Esophagogastrostomy plus double flap technique (DFT)
• Double tract reconstruction (DTR) (Fig. EN3)
• Jejunal pouch interposition (JPI)
• Jejunal interposition (JI)
The “non touch lesion lifting method” is a new emerging concept in this regard
for small early gastric cancers. Intraperitoneal spillage being a concern especially in
non touch technique and further modifications are proposed to overcome it [32].
1. Park YK, Yoon HM, Kim YW, et al. Laparoscopy-assisted versus open D2 distal
gastrectomy for advanced gastric cancer: results from a randomized phase II
multicenter clinical trial (COACT 1001). Ann Surg. 2018;267(4):638–45.
https://doi.org/10.1097/SLA.0000000000002168.
2. Lee HJ, Hyung WJ, Yang HK, et al. Short-term outcomes of a multicenter ran-
domized controlled trial comparing laparoscopic distal gastrectomy with D2
lymphadenectomy to open distal gastrectomy for locally advanced gastric can-
cer (KLASS-02-RCT). Ann Surg. 2019;270(6):983–91. https://doi.org/10.1097/
SLA.0000000000003217.
3. Yu J, Huang C, Sun Y, et al. Effect of laparoscopic vs open distal gastrectomy
on 3-year disease-free survival in patients with locally advanced gastric cancer:
the CLASS-01 randomized clinical trial. JAMA. 2019;321(20):1983–92.
https://doi.org/10.1001/jama.2019.5359.
4. Hu Y, Huang C, Sun Y, et al. Morbidity and mortality of laparoscopic versus
open D2 distal gastrectomy for advanced gastric cancer: a randomized con-
trolled trial. J Clin Oncol. 2016;34(12):1350–7. https://doi.org/10.1200/
JCO.2015.63.7215.
5. Mitrousias AS, Makris MC, Zani JR, et al. Laparoscopic versus open gastrec-
tomy with D2 lymph node dissection for advanced gastric cancer: a systematic
review. J BUON. 2019;24(3):872–82.
6. Beyer K, Baukloh AK, Kamphues C, et al. Laparoscopic versus open gastrec-
tomy for locally advanced gastric cancer: a systematic review and meta-analysis
of randomized controlled studies. World J Surg Oncol. 2019;17(1):68. https://
doi.org/10.1186/s12957-019-1600-1.
7. Shi Y, Xu X, Zhao Y, Qian F, Tang B, Hao Y, Luo H, Chen J, Yu P. Long-
term oncologic outcomes of a randomized controlled trial comparing laparo-
scopic versus open gastrectomy with D2 lymph node dissection for advanced
gastric cancer. Surgery. 2019;165(6):1211–6. https://doi.org/10.1016/j.
surg.2019.01.003.
8. Zhang W, Huang Z, Zhang J, Che X. Long-term and short-term outcomes
after laparoscopic versus open surgery for advanced gastric cancer: an updated
meta- analysis. J Minim Access Surg. 2021; https://doi.org/10.4103/jmas.
JMAS_219_20.
9. Inaki N, Etoh T, Ohyama T, et al. A multi-institutional, prospective, phase II
feasibility study of laparoscopy-assisted distal gastrectomy with D2 lymph
node dissection for locally advanced gastric cancer (JLSSG0901). World J
Surg. 2015;39(11):2734–41. https://doi.org/10.1007/s00268-015-3160-z.
10. Eshuis WJ, van Berge Henegouwen MI, Draaisma WA, Gisbertz SS. Compliance
to D2 lymphadenectomy in laparoscopic gastrectomy. Updat Surg.
2018;70(2):197–205. https://doi.org/10.1007/s13304-018-0553-1.
11. Degiuli M, De Manzoni G, Di Leo A, et al. Gastric cancer: current status of
lymph node dissection. World J Gastroenterol. 2016;22(10):2875–93. https://
doi.org/10.3748/wjg.v22.i10.2875.
58 R. Shivhare et al.
References
1. Huh YJ, Lee JH. The advances of laparoscopic gastrectomy for gastric cancer. Gastroenterol
Res Pract. 2017;2017:9278469. https://doi.org/10.1155/2017/9278469.
2. Tanimura S, Higashino M, Fukunaga Y, Osugi H. Hand-assisted laparoscopic distal gastrec-
tomy with regional lymph node dissection for gastric cancer. Surg Laparosc Endosc Percutan
Tech. 2001;11(3):155–60.
3. Kim YW, Bae JM, Lee JH, et al. The role of hand-assisted laparoscopic distal gastrec-
tomy for distal gastric cancer. Surg Endosc. 2005;19(1):29–33. https://doi.org/10.1007/
s00464-004-8119-3.
4. Litwin DE, Darzi A, Jakimowicz J, et al. Hand-assisted laparoscopic surgery (HALS) with the
HandPort system: initial experience with 68 patients. Ann Surg. 2000;231(5):715–23. https://
doi.org/10.1097/00000658-200005000-00012.
5. Kitano S, Shiraishi N. Current status of laparoscopic gastrectomy for cancer in Japan. Surg
Endosc. 2004;18(2):182–5. https://doi.org/10.1007/s00464-003-8820-7.
6. Coburn N, Cosby R, Klein L, et al. Staging and surgical approaches in gastric cancer: a clinical
practice guideline. Curr Oncol. 2017;24(5):324–31. https://doi.org/10.3747/co.24.3736.
7. Kim MG, Kim KC, Kim BS, et al. A totally laparoscopic distal gastrectomy can be an effective
way of performing laparoscopic gastrectomy in obese patients (body mass index≥30). World J
Surg. 2011;35(6):1327–32. https://doi.org/10.1007/s00268-011-1034-6.
8. Kanaya S, Gomi T, Momoi H, et al. Delta-shaped anastomosis in totally laparoscopic Billroth
I gastrectomy: new technique of intraabdominal gastroduodenostomy. J Am Coll Surg.
2002;195(2):284–7. https://doi.org/10.1016/s1072-7515(02)01239-5.
9. Du J, Shuang J, Li J, et al. Totally laparoscopic Billroth II gastrectomy with a novel,
safe, simple, and time-saving anastomosis by only stapling devices. J Gastrointest Surg.
2012;16(4):738–43. https://doi.org/10.1007/s11605-011-1796-z.
10. Motoyama K, Kojima K, Hayashi M, Kato K, Inokuchi M, Sugihara K. β-Shaped intracorpo-
real Roux-en-Y reconstruction after totally laparoscopic distal gastrectomy. Gastric Cancer.
2014;17(3):588–93. https://doi.org/10.1007/s10120-013-0311-5.
11. Okabe H, Obama K, Tanaka E, et al. Intracorporeal esophagojejunal anastomosis after laparo-
scopic total gastrectomy for patients with gastric cancer. Surg Endosc. 2009;23(9):2167–71.
https://doi.org/10.1007/s00464-008-9987-8.
12. Inaba K, Satoh S, Ishida Y, et al. Overlap method: novel intracorporeal esophagojejunos-
tomy after laparoscopic total gastrectomy. J Am Coll Surg. 2010;211(6):e25–9. https://doi.
org/10.1016/j.jamcollsurg.2010.09.005.
13. Nagai E, Ohuchida K, Nakata K, et al. Feasibility and safety of intracorporeal esophagoje-
junostomy after laparoscopic total gastrectomy: inverted T-shaped anastomosis using linear
staplers. Surgery. 2013;153(5):732–8. https://doi.org/10.1016/j.surg.2012.10.012.
14. Shinohara T, Hanyu N, Tanaka Y, Murakami K, Watanabe A, Yanaga K. Totally laparoscopic
complete resection of the remnant stomach for gastric cancer. Langenbeck’s Arch Surg.
2013;398(2):341–5. https://doi.org/10.1007/s00423-012-0979-8.
15. Suh YS, Han DS, Kong SH, et al. Laparoscopy-assisted pylorus-preserving gastrectomy is
better than laparoscopy-assisted distal gastrectomy for middle-third early gastric cancer. Ann
Surg. 2014;259(3):485–93. https://doi.org/10.1097/SLA.0b013e318294d142.
16. Khalayleh H, Kim YW, Yoon HM, Ryu KW. Assessment of lymph node metastasis in patients
with gastric cancer to identify those suitable for middle segmental gastrectomy. JAMA Netw
Open. 2021;4(3):e211840. https://doi.org/10.1001/jamanetworkopen.2021.1840.
17. Kim SM, Cho J, Kang D, et al. A randomized controlled trial of vagus nerve-preserving dis-
tal gastrectomy versus conventional distal gastrectomy for postoperative quality of life in
early-stage gastric cancer patients. Ann Surg. 2016;263(6):1079–84. https://doi.org/10.1097/
SLA.0000000000001565.
18. Ahn SH, Lee JH, Park DJ, Kim HH. Comparative study of clinical outcomes between
laparoscopy-assisted proximal gastrectomy (LAPG) and laparoscopy-assisted total gastrec-
Recent Advances in Laparoscopic Gastrectomy for Gastric Cancer with Special… 61
tomy (LATG) for proximal gastric cancer. Gastric Cancer. 2013;16(3):282–9. https://doi.
org/10.1007/s10120-012-0178-x.
19. An JY, Youn HG, Choi MG, Noh JH, Sohn TS, Kim S. The difficult choice between total
and proximal gastrectomy in proximal early gastric cancer. Am J Surg. 2008;196(4):587–91.
https://doi.org/10.1016/j.amjsurg.2007.09.040.
20. Yoo CH, Sohn BH, Han WK, Pae WK. Long-term results of proximal and total gastrectomy
for adenocarcinoma of the upper third of the stomach. Cancer Res Treat. 2004;36(1):50–5.
https://doi.org/10.4143/crt.2004.36.1.50.
21. Uyama I, Sugioka A, Fujita J, Komori Y, Matsui H, Hasumi A. Completely laparoscopic
proximal gastrectomy with jejunal interposition and lymphadenectomy. J Am Coll Surg.
2000;191(1):114–9. https://doi.org/10.1016/s1072-7515(00)00283-0.
22. Kinoshita T, Gotohda N, Kato Y, Takahashi S, Konishi M, Kinoshita T. Laparoscopic proximal
gastrectomy with jejunal interposition for gastric cancer in the proximal third of the stomach:
a retrospective comparison with open surgery. Surg Endosc. 2013;27(1):146–53. https://doi.
org/10.1007/s00464-012-2401-6.
23. Ahn SH, Jung DH, Son SY, Lee CM, Park DJ, Kim HH. Laparoscopic double-tract proximal
gastrectomy for proximal early gastric cancer. Gastric Cancer. 2014;17(3):562–70. https://doi.
org/10.1007/s10120-013-0303-5.
24. Smyth EC, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D, ESMO Guidelines
Committee. Gastric cancer: ESMO clinical practice guidelines for diagnosis, treatment and
follow-up. Ann Oncol. 2016;27(suppl 5):v38–49. https://doi.org/10.1093/annonc/mdw350.
25. Kim SG, Eom BW, Yoon HM, Kim CG, Kook MC, Kim YW, Ryu KW. Recent updates and
current issues of sentinel node navigation surgery for early gastric cancer. Chin J Cancer Res.
2021;33(2):142–9. https://doi.org/10.21147/j.issn.1000-9604.2021.02.02.
26. Coratti A, Annecchiarico M, Di Marino M, Gentile E, Coratti F, Giulianotti PC. Robot-assisted
gastrectomy for gastric cancer: current status and technical considerations. World J Surg.
2013;37(12):2771–81. https://doi.org/10.1007/s00268-013-2100-z.
27. Kim HI, Park MS, Song KJ, Woo Y, Hyung WJ. Rapid and safe learning of robotic gastrectomy
for gastric cancer: multidimensional analysis in a comparison with laparoscopic gastrectomy.
Eur J Surg Oncol. 2014;40(10):1346–54. https://doi.org/10.1016/j.ejso.2013.09.011.
28. Park JY, Jo MJ, Nam BH, et al. Surgical stress after robot-assisted distal gastrectomy and its
economic implications. Br J Surg. 2012;99(11):1554–61. https://doi.org/10.1002/bjs.8887.
29. Tewari M, Hazra P, Dixit A, Shukla HS. Conservative surgery in cancer of the stomach and the
current status of lymph node dissections. Indian J Surg. 2003;65:336–43.
30. Mogal H, Fields R, Maithel SK, Votanopoulos K. In patients with localized and resectable
gastric cancer, what is the optimal extent of lymph node dissection-D1 versus D2 versus D3?
Ann Surg Oncol. 2019 Sep;26(9):2912–32. https://doi.org/10.1245/s10434-019-07417-5.
31. Mocellin S, McCulloch P, Kazi H, Gama-Rodrigues JJ, Yuan Y, Nitti D. Extent of lymph
node dissection for adenocarcinoma of the stomach. Cochrane Database Syst Rev.
2015;2015(8):CD001964. https://doi.org/10.1002/14651858.CD001964.pub4.
32. Douridas GN, Pierrakakis SK. Is there any role for D3 lymphadenectomy in gastric cancer?
Front Surg. 2018;5:27. https://doi.org/10.3389/fsurg.2018.00027.
33. Zhang CD, Chen SC, Feng ZF, Zhao ZM, Wang JN, Dai DQ. Laparoscopic versus open gas-
trectomy for early gastric cancer in Asia: a meta-analysis. Surg Laparosc Endosc Percutan
Tech. 2013;23(4):365–77. https://doi.org/10.1097/SLE.0b013e31828e3e6e.
34. Choi YY, Bae JM, An JY, Hyung WJ, Noh SH. Laparoscopic gastrectomy for advanced gas-
tric cancer: are the long-term results comparable with conventional open gastrectomy? A sys-
tematic review and meta-analysis. J Surg Oncol. 2013;108(8):550–6. https://doi.org/10.1002/
jso.23438.
35. Lian B, Chen J, Li Z, Ji G, Wang S, Zhao Q, Li M. Risk factors and Clavien-Dindo clas-
sification of postoperative complications after laparoscopic and open gastrectomies for gas-
tric cancer: a single-center, large sample, retrospective cohort study. Cancer Manag Res.
2020;12:12029–39. https://doi.org/10.2147/CMAR.S275621.
62 R. Shivhare et al.
Kalpesh Jani and Samir Contractor
Introduction
In the Western world, 10–15% of the population suffers from gallstone disease in
their lifetime, affecting nearly 1–4% of the people annually [1]. While a majority
are managed conservatively or by straight forward cholecystectomy, in about 6%,
the operative procedure is rendered difficult due to ongoing inflammatory process
that makes the dissection and delineation of local anatomy difficult, e.g., acute
cholecystitis, gangrenous gallbladder, empyema of the gallbladder, perforation
of the gallbladder and Mirizzi’s syndrome or cirrhotic liver with portal hyperten-
sion, that increases the risk of hemorrhage during dissection [2, 3]. The term ‘dif-
ficult gallbladder’ has been coined to describe procedures in such pathologies
[2]. Depending on the inflammation of the gallbladder, the ease of dissection of
the cystic pedicle and the amount of adhesions, Nassar et al have developed an
ascending scale to grade the difficulty of the gallbladder surgery [4]. Various
techniques have been promulgated for carrying out safe surgery in such difficult
situations, including the fundus-first approach, cholecystostomy and subtotal
cholecystectomy [5, 6]. Subtotal cholecystectomy (SC) removes the gallbladder
partially, leaving some portion of the gallbladder in situ, usually, when dissection
of the hepato-cystic triangle or separating the gallbladder from the liver bed is
likely to be dangerous [7]. Table 1 enumerates the various bailout procedures in
difficult laparoscopic cholecystectomy.
As Strasberg points out in his review, a lot of confusion is created by using
both the terms subtotal and partial cholecystectomy interchangeably, and both
the terms often describe the same operation as well as the same term is being
used to describe operations with variable portions of gallbladder left behind [8].
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 63
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_3
64 K. Jani and S. Contractor
History
Subsequent, published literature shows that the terms subtotal and partial cholecys-
tectomy were used interchangeably to describe three types of resections, firstly
where only a strip of gallbladder was left behind, secondly where a portion of the
gallbladder adjacent to the cystic duct was left behind but none on the liver bed and
thirdly, where part of the gallbladder was left behind on the liver bed as well as
adjacent to the cystic duct. Also, the size of gallbladder remnant adjacent to the
cystic duct was variable, ranging in size from millimeters from the internal opening
of the cystic duct to one where only the fundus was excised, leaving a major portion
of the gallbladder intact [1, 7, 15, 17–26].
Palanivelu et al., in 2006, described three variants of laparoscopic subtotal cho-
lecystectomy (LSC) in a paper describing their experience in patients with cirrhosis
and portal hypertension [27]. When the cystic duct and artery were ligated and
divided outside the gallbladder and the organ was removed leaving a strip of it on
the liver bed, it was termed as LSC I (Fig. 1). The mucosa was either stripped off or
destroyed using electrosurgery. This was typically needed where the hepato-cystic
triangle was non-inflamed, but the liver was cirrhotic and there was a danger of
bleeding from the liver bed. However, when the primary danger was of bleeding
during dissection in the hepato-cystic triangle, due to neovascularity and caverno-
matous transformation of the portal vein, the gallbladder was divided at the neck,
just to the right of the cystic duct insertion into it and the stump closed. The distal
organ was removed in its entirety. This was termed as LSC II (Fig. 2). A combina-
tion of the above two, i.e., leaving a stump of gallbladder attached to the cystic duct
as well as a strip of its posterior wall on the liver bed, was defined as LSC III
(Fig. 3). Eventually, they extended the same terminology to these modifications
when performed for other indications like acute inflammation, empyema, etc.
[Personal communication]. Table 2−4 enlists the various nomenclatures and classi-
fications used in subtotal cholecystectomy.
In a 2016 paper, Strasberg et al. suggested a different nomenclature. Removal of
less than half of the distal gallbladder should be termed as fundectomy while the
Laparoscopic Subtotal Cholecystectomy 67
term partial cholecystectomy should be abandoned, the rest being called SC [8].
These were further sub-classified into the ‘fenestrating’ variety, when the proximal
stump of gallbladder is left open and not sutured closed to produce a remnant cystic
structure, and a ‘reconstituting’ variety, in which a cystic remnant is closed (Figs. 2
and 4). Combining both the proposed classification or types of LSC, Type II & Type
III can be of fenestrating and reconstituting types (Tables 2, 3 and 4).
Table 3 Types of Type I A strip of posterior wall of gallbladder left on the liver
Laparoscopic Subtotal bed
Cholecystectomy Type II A residual stump of gall bladder left in situ
[Palanivelu et al]
Type III combination of I and II
Incidence
The incidence of LSC varies in different series depending on the expertise and lapa-
roscopic skills of the surgeon. While many surgeons would opt to convert to an open
cholecystectomy on encountering difficult situations, data from centers performing
a large volume of laparoscopic cholecystectomies report adopting the LSC tech-
nique in 5.6–10.6% of cases, thus reducing the conversion to open in these number
of cases [23, 28, 29]
Indications
The various indications for performing subtotal cholecystectomy, both open as well
as laparoscopic, were summarized in a review which studied literature from 1954 to
2013 [1]. These are as follows:
Technical Variations
Fig. 5 Subtotal
cholecystectomy with
suturing of gall bladder
stump (Arrow) with
continuous sutures. [Image
courtesy: Dr. Deborshi
Sharma]
Fig. 6 Subtotal
cholecystectomy with
inside out suturing of gall
bladder stump (Arrow)
(Palanivelu LSC Type II,
Strasberg’s Reconstitution
type) [Image courtesy: Dr.
Deborshi Sharma]
Table 6 Management options Intracorporeal suturing from within the mucosal side
for gallbladder stump remnant Intracorporeal sutured closure of the stump
after LSC Stapling
Use of endo loop
Impact of LSC
Remnant Cholecystectomy
When stones do recur in the remnant, their symptoms are often clubbed under the
umbrella tag of ‘post-cholecystectomy syndrome’. Very often, the primary surgeon
would not have mentioned that SC has been done and so the subsequent treating
72 K. Jani and S. Contractor
physicians are not aware that the gallbladder remnant exists with its propensity to
cause post-operative problems [45, 46]. Once the remnant becomes symptomatic,
surgery is required. The median time interval between the primary procedure and
re-do procedure varies from 24 to 60 months. Due to low index of suspicion, owing
to some extent to absence of proper information regarding the primary procedure
done, the patients get investigated unnecessarily for other probable causes of their
symptoms and even undergo invasive procedures before the correct diagnosis is
reached.
Ultrasound may fail to detect the condition in up to 11% of the patients. The
condition is readily diagnosed by a CT scan or MRI/MRCP, which clearly delin-
eates the biliary anatomy as well as the size of the remnant and the presence and
number of stones in it. Re-do cholecystectomy is difficult due to the extensive
adhesions and distorted anatomy and should be attempted only by experienced
surgeons. In Concors’ series of 14 patients, 2 cases were attempted laparoscopi-
cally but both needed conversion to open while the remaining 12 were approached
through the open technique [45]. One patient [7.1%] suffered a major bile duct
injury during the process, requiring hepaticojejunostomy. In the largest series
reported till date, open approach was adopted for nearly half [48.4%] of the 93
patients, while laparoscopic approach was attempted in the remaining 51.6% of
which 20.4% required conversion to open [46]. Nearly one-fourth of the patients
had associated CBD stones and around 11% had Mirizzi syndrome, requiring
additional procedures like choledocho-duodenostomy, CBD exploration and
hepaticojejunostomy.
Though difficult, laparoscopic management of the remnant gall bladder has been
reported from high volume centers with experienced laparoscopic surgeons, with
excellent results and low conversion rates [27, 47, 48] (Fig. 8). The size of the gall-
bladder stump should be kept small during laparoscopic subtotal cholecystectomy
and can be ascertained with MRCP (Table 9).
A major concern while performing LSC is the presence of occult gallbladder cancer
[23]. Opening up the gallbladder with spillage of contents when there is an occult
malignancy in the wall of the organ is a recipe for disaster, with poor subsequent
prognosis [28, 49]. If there are any suspicious findings on pre-operative imaging to
suspect malignancy, like irregular thickening of the wall, it is better to convert to
open approach and perform a complete cholecystectomy [23, 28]. Some authorities
also recommend taking biopsies from the mucosa of the remnant for histopathologi-
cal examination to rule out the possibility of malignancy as well as dysplasia in the
remnant [24].
Conclusion
well as the same term is often used to describe operations with variable portions
of gallbladder left behind.
3. In Type I LSC, the mucosa on the strip of gallbladder wall left on the liver bed
may be stripped or may be destroyed using electrocautery, argon beam or radio-
frequency ablation. In Type II a remnant gallbladder stump is left insitu,
whereas Type III is a combination of both.
4. Combining both the proposed classification or types of LSC by Dr. Palanivelu
and Dr. Strasberg, Type II & Type III can be of fenestrating or reconstituting
types based upon no closure or closure of the remnant gall bladder stump.
5. Closure of the gallbladder remnant seems to cause lower incidence of bile fis-
tula. Bile leak after subtotal cholecystectomy is expected and it occurs with a
higher frequency with the fenestrating type (42%) than with the reconstituting
type (16.5%).
6. Subtotal cholecystectomy may be more approachable with laparoscopic tech-
niques rather than open due to the magnification afforded and the proper angle
of view that can be obtained with a 30-degree telescope.
7. No difference in the morbidity, mortality or re-admission rates are seen between
LSC and laparoscopic total cholecystectomy though the total direct costs are
higher in the LSC group.
8. Closed GB remnant may lead to formation of gallstones with subsequent pass-
ing of these stones into the common bile duct and its complications.
Ablation of mucosa of stump may be helpful in preventing stone formation.
9. It is of paramount importance to clearly mention the possible amount of GB
remnant left behind in the primary surgery.
10. Ultrasound may fail to detect the remnant gall bladder with stones in up to 11%
of the patients. It is readily diagnosed by a CT scan or MRI/MRCP, which
clearly delineates the biliary anatomy as well as the size of the remnant and the
presence and number of stones in it.
11. Remnant cholecystectomy by laparoscopy in symptomatic case by experienced
laparoscopic surgeons is feasible with excellent results and low conversion rates.
12. Biopsies from the mucosa of the remnant for histopathological examination
should always be done to rule out the possibility of leaving malignancy as well
as dysplasia in the remnant.
Laparoscopic Subtotal Cholecystectomy 75
Editor’s Note1
References: Main chapter references are included after the “References Editor’s Note” section.
1
76 K. Jani and S. Contractor
in an unsafe cystohepatic triangle anatomy albeit an increased bile leak which can
often be managed with drainage and endoscopic stenting [3]. Figures 5, 6, 7 shows
subtotal cholecystectomy with suturing of gall bladder stump.
Endovesical Approach
Simply known as the inside out approach for management of difficult gallbladder
when Calots triangle dissection is unsafe, was shown to be helpful before perform-
ing a subtotal cholecystectomy [11].
Spyglass Cholangioscopy
Spyglass cholangioscopy is a recently evolving technique which helps visualization
of biliary tract anatomy and is considered useful particularly in altered biliary anat-
omy. The technique may aid detection and treatment of retained or recurrent stones
in the gallbladder remnant after subtotal cholecystectomy.
Laparoscopic Subtotal Cholecystectomy 77
11. Hubert C, Annet L, van Beers BE, Gigot JF. The “inside approach of the gall-
bladder” is an alternative to the classic Calot’s triangle dissection for a safe
operation in severe cholecystitis. Surg Endosc. 2010 Oct;24(10):2626–32.
https://doi.org/10.1007/s00464-010-0966-5. Epub 2010 Mar 25. PMID:
20336321.
12. Kohga A, Suzuki K, Okumura T, et al. Calculus left in remnant gallbladder
cause long-term complications in patients undergoing subtotal cholecystec-
tomy. HPB [Oxford]. 2019;21[4]:508–14. doi:https://doi.org/10.1016/j.
hpb.2018.09.007
13. Chaudery M, Hunjan T, Beggs A, Nehra D. Pitfalls in the use of laparoscopic
staplers to perform subtotal cholecystectomy. BMJ Case Rep. 2013 Apr
16;2013:bcr2013009047. https://doi.org/10.1136/bcr-2013-009047. PMID:
23595185; PMCID: PMC3645125.
14. Chowbey P, Sharma A, Goswami A, et al. Residual gallbladder stones after
cholecystectomy: A literature review. J Minim Access Surg. 2015;11[4]:223–30.
https://doi.org/10.4103/0972-9941.158156
Laparoscopic Subtotal Cholecystectomy 79
References
1. Elshaer M, Gravante G, Thomas K, Sorge R, Al-Hamali S, Ebdewi H. Subtotal cholecys-
tectomy for “difficult gallbladders”: systematic review and meta-analysis. JAMA Surg.
2015;150(2):159–68. https://doi.org/10.1001/jamasurg.2014.1219.
2. Salky BA, Edye MB. The difficult cholecystectomy: problems related to concomitant diseases.
Semin Laparosc Surg. 1998;5(2):107–14. https://doi.org/10.1177/155335069800500205.
3. Laws HL. The difficult cholecystectomy: problems during dissection and extraction. Semin
Laparosc Surg. 1998;5(2):81–91. https://doi.org/10.1177/155335069800500203.
4. Nassar A, Ashkar K, Mohamed A, Hafiz A. Is laparoscopic cholecystectomy possible
without video technology? Min Invas Ther Allied Technol. 2009;4:63–5. https://doi.
org/10.3109/13645709509152757.
5. Lee J, Miller P, Kermani R, Dao H, O'Donnell K. Gallbladder damage control: compro-
mised procedure for compromised patients. Surg Endosc. 2012;26(10):2779–83. https://doi.
org/10.1007/s00464-012-2278-4.
6. Eikermann M, Siegel R, Broeders I, et al. Prevention and treatment of bile duct injuries during
laparoscopic cholecystectomy: the clinical practice guidelines of the European Association
for Endoscopic Surgery [EAES]. Surg Endosc. 2012;26(11):3003–39. https://doi.org/10.1007/
s00464-012-2511-1.
7. Henneman D, da Costa DW, Vrouenraets BC, van Wagensveld BA, Lagarde SM. Laparoscopic
partial cholecystectomy for the difficult gallbladder: a systematic review. Surg Endosc.
2013;27(2):351–8. https://doi.org/10.1007/s00464-012-2458-2.
8. Strasberg SM, Pucci MJ, Brunt LM, Deziel DJ. Subtotal cholecystectomy-“fenestrating” vs
“reconstituting” subtypes and the prevention of bile duct injury: definition of the optimal
procedure in difficult operative conditions. J Am Coll Surg. 2016;222(1):89–96. https://doi.
org/10.1016/j.jamcollsurg.2015.09.019.
9. Bodvall B, Overgaard B. Cystic duct remnant after cholecystectomy: incidence studied by cho-
legraphy in 500 cases, and significance in 103 reoperations. Ann Surg. 1966;163(3):382–90.
https://doi.org/10.1097/00000658-196603000-00009.
10. Kehr H. Introduction to the differential diagnosis of the separate forms of gallstone disease:
based upon his own experience gained from 433 laparotomies for gallstones. Philedelphia: P
Blakiston’s Son and Co; 1901.
11. Pribram BOC. The electrosurgical operation in gall-bladder diseases: results of 13 years’ expe-
rience. Lancet. 1939;234(6061):927–9. https://doi.org/10.1016/S0140-6736[00]71636-9.
12. Bailey H, McNeill Love RJ. Electrosurgical obliteration of the gallbladder without drainage:
Thoreks’ operation. Brit Med J. 1939;2:682. https://doi.org/10.1136/bmj.2.4108.682.
13. Love RJ. Diathermy dissection of the gall-bladder. Br Med J. 1947;2(4513):11–3. https://doi.
org/10.1136/bmj.2.4513.11.
14. Estes WL. Acute gangrenous cholecystitis and the use of partial cholecystectomy in its treat-
ment. Am J Surg. 1938;40:197–204. https://doi.org/10.1016/S0002-9610[38]90607-5.
15. Lerner AI. Partial cholecystectomy. Can Med Assoc J. 1950;63(1):54–6.
16. Mc Elmoyle WA. Cholecystectomy: a method for the difficult gall-bladder. Lancet.
1954;266(6826):1320–3. https://doi.org/10.1016/s0140-6736[54]92210-2.
17. Bornman PC, Terblanche J. Subtotal cholecystectomy: for the difficult gallbladder in portal
hypertension and cholecystitis. Surgery. 1985;98(1):1–6.
18. Gray Turner G. Injuries to the main bile-ducts. Lancet. 1944;243(6298):621–2. https://doi.
org/10.1016/S0140-6736[00]74841-0.
19. Schein M. Partial cholecystectomy in the emergency treatment of acute cholecystitis in the
compromised patient. J R Coll Surg Edinb. 1991;36(5):295–7.
80 K. Jani and S. Contractor
40. Visser BC, Parks RW, Garden OJ. Open cholecystectomy in the laparoendoscopic era. Am J
Surg. 2008;195(1):108–14. https://doi.org/10.1016/j.amjsurg.2007.04.008.
41. Coccolini F, Catena F, Pisano M, et al. Open versus laparoscopic cholecystectomy in acute
cholecystitis. Systematic review and meta-analysis [published correction appears in Int
J Surg. 2015 Dec;24[Pt a]:107]. Int J Surg. 2015;18:196–204. https://doi.org/10.1016/j.
ijsu.2015.04.083.
42. Ros A, Gustafsson L, Krook H, et al. Laparoscopic cholecystectomy versus mini-laparotomy
cholecystectomy: a prospective, randomized, single-blind study. Ann Surg. 2001;234(6):741–9.
https://doi.org/10.1097/00000658-200112000-00005.
43. Lidsky ME, Speicher PJ, Ezekian B, et al. Subtotal cholecystectomy for the hostile gall-
bladder: failure to control the cystic duct results in significant morbidity. HPB (Oxford).
2017;19(6):547–56. https://doi.org/10.1016/j.hpb.2017.02.441.
44. Philips JA, Lawes DA, Cook AJ, et al. The use of laparoscopic subtotal cholecystectomy
for complicated cholelithiasis. Surg Endosc. 2008;22(7):1697–700. https://doi.org/10.1007/
s00464-007-9699-5.
45. Concors SJ, Kirkland ML, Schuricht AL, et al. Resection of gallbladder remnants after sub-
total cholecystectomy: presentation and management. HPB (Oxford). 2018;20(11):1062–6.
https://doi.org/10.1016/j.hpb.2018.05.005.
46. Singh A, Kapoor A, Singh RK, et al. Management of residual gall bladder: A 15-year experi-
ence from a north Indian tertiary care centre. Ann Hepatobiliary Pancreat Surg.
2018;22[1]:36–41. https://doi.org/10.14701/ahbps.2018.22.1.36.
47. Chowbey P, Soni V, Sharma A, Khullar R, Baijal M. Residual gallstone disease - laparoscopic
management. Indian J Surg. 2010;72(3):220–5. https://doi.org/10.1007/s12262-010-0058-8.
48. Tantia O, Jain M, Khanna S, Sen B. Post cholecystectomy syndrome: role of cystic duct stump
and re-intervention by laparoscopic surgery. J Minim Access Surg. 2008;4(3):71–5. https://doi.
org/10.4103/0972-9941.43090.
49. Ouchi K, Mikuni J, Kakugawa Y. Organizing committee, the 30th annual congress of the
Japanese Society of Biliary Surgery. Laparoscopic cholecystectomy for gallbladder carci-
noma: results of a Japanese survey of 498 patients. J Hepato-Biliary-Pancreat Surg.
2002;9(2):256–60. https://doi.org/10.1007/s005340200028.
Prediction and Grading Methods
of a Difficult Laparoscopic
Cholecystectomy
Introduction
N. Gupta
Department of Surgery, ABVIMS and Dr RML Hospital, New Delhi, India
P. Hazrah (*) · G. Anand
Department of Surgery, Lady Hardinge Medical College, New Delhi, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 83
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_4
84 N. Gupta et al.
Grading/scoring systems with intraoperative variables are more objective and have
less bias because they are largely independent of operative skills of the surgeon. The
earliest attempt to define an objective scoring system to measure intraoperative dif-
ficulty was proposed by Cuscheri et al. in 1992 [5] followed by Nassar in 1995 with
modification in 1996. The modified Nassar scale has an addition of grade 5 to the
original 4 categories (Table 1) [12], based on clinico-radiologic and operative
parameters. Randhawa et al. in their attempt to develop a preoperative predictive
system stratified difficulty based upon limited intraoperative parameters viz.: time
taken, bile spillage, injury to duct/ artery and conversion (Table 2) [7]. In a study
using the Delphi technique to define operative difficulty, an elaborate set of intraop-
erative parameters with precise grading was proposed which were broadly catego-
rized as factors related to inflammation of the gallbladder and intra-abdominal
factors unrelated to inflammation. Factors related to inflammation of the gall blad-
der was further subcategorized into: appearance around the gallbladder, appearance
of the Calot’s triangle area, appearance of the gallbladder bed, additional findings of
the gallbladder and its surroundings (Table 3) [13].
Sugrue et al. graded operative difficulty based on a few intraoperative parameters
along with BMI and time taken to identify cystic artery and duct (Table 4) [6]. The
cholecystitis severity/difficulty grading of Parkland et al. incorporates an array of
intraoperative variables as shown in Table 5) [14]. Classifications based on
Prediction and Grading Methods of a Difficult Laparoscopic Cholecystectomy 85
Table 1 Difficulty grading by operative parameters of gallbladder cystic pedicle and adhesions as
proposed by Nassar et al. [12] (Modified Nassar Scale)
Grade description
I Gallbladder—floppy, non-adherent
Cystic pedicle—thin and clear
Adhesions—simple up to the neck/Hartmann’s pouch
II Gallbladder—mucocele, packed with stones
Cystic pedicle—fat laden
Adhesions—simple up to the body
III Gallbladder—deep fossa, acute cholecystitis, contracted, fibrosis, Hartmann’s adherent to
CBD, impaction
Cystic pedicle—abnormal anatomy or cystic duct—short, dilated or obscured
Adhesions—dense up to fundus; involving hepatic flexure or duodenum
IV Gallbladder—completely obscured, empyema, gangrene, mass
Cystic pedicle—impossible to clarify
Adhesions—dense, fibrosis, wrapping the gallbladder, duodenum or hepatic flexure
difficult to separate
V Mirizzi Syndrome type 2 or higher, cholecysto-cutaneous, cholecysto-duodenal or
cholecysto-colic fistula
Please also refer to Table 9, preoperative parameters for grading severity by Nassar et al.
(Published with permission)
Table 3 Intraoperative findings that were considered to potentially contribute to surgical diffi-
culty score in mulitinational collaborative study on surgeons using Delphi technique (2017) [13]
A. Factors related to inflammation of the gallbladder Score
[a] Appearance around the gallbladder
1. Fibrotic adhesions around the gallbladder due to inflammation 2
2. Partial scarring adhesions around the gallbladder 2
3. Diffuse scarring adhesions around the gallbladder 4
[b] Appearance of the Calot’s triangle area
4. Sparse fibrotic change in the Calot’s triangle area 2
5. Dense fibrotic change but no scarring in the Calot’s triangle area 3
6. Partial scarring in the Calot’s triangle area 4
7. Diffuse scarring in the Calot’s triangle area 5
[c] Appearance of the gallbladder bed
8. Sparse fibrotic change in the gallbladder bed 1
9. Dense fibrotic change but no scarring in the gallbladder bed 2
10. Partial scarring in the gallbladder bed 3
11. Diffuse scarring in the gallbladder bed [includes atrophic gallbladder with no 4
lumen due to severe contraction]
[d] Additional findings of the gallbladder and its surroundings
12. Edematous change around the gallbladder/in the Calot’s triangle area/in the 1
gallbladder bed
13. Easy bleeding at dissection around the gallbladder/in the Calot’s triangle area/in the 3
gallbladder bed
14. Necrotic changes around the gallbladder/in the Calot’s triangle area/in the 4
gallbladder bed
15. Non-iatrogenic, perforated gallbladder wall and/or abscess formation towards the 3
abdominal cavity noted during adhesiolysis around the gallbladder
16. Abscess formation towards the liver parenchyma 4
17. Cholecysto-enteric fistula 5
18. Cholecysto-choledochal fistula [included in the expanded classification of Mirizzi 6
syndrome]
19. Impacted gallstone in the confluence of the cystic, common hepatic, and common 5
bile duct [included in the expanded classification of Mirizzi syndrome]
B. Intra-abdominal factors unrelated to inflammation
20. Excessive visceral fat 2
21. Inversion of the gallbladder in the gallbladder bed due to liver cirrhosis 4
22. Collateral vein formation due to liver cirrhosis 4
23. Non-inflammatory [physiological] adhesion around the gallbladder 1
24. Anomalous bile duct 4
25. Gallbladder neck mounting on the common bile duct 3
(Published with permission)
I. Access related
II. Dissection related i.e. dissection of calots/dissection from liver bed
III. Extraction related.
Prediction and Grading Methods of a Difficult Laparoscopic Cholecystectomy 87
Table 4 Operative grading system for cholecystitis severity by Sugrue et al. [6]
Gallbladder appearance
Adhesions <50% of GB 1
Adhesions burying GB 3
Max score 3
Distension/contraction
Distended GB (or contracted shrivelled GB) 1
Unable to grasp with atraumatic laparoscopic forceps 1
Stone ≥1 cm impacted in Hartman’s pouch 1
Access
BMI >30 1
Adhesions from previous surgery limiting access 1
Severe sepsis/complications
Bile or pus outside GB 1
Time to identify cystic artery and duct > 90 min 1
Total max 10
Degree of difficulty
A mild < 2, B moderate 2–4, C severe 5–7, D extreme 8–10
(Published with permission)
Table 6 Tokyo Guidelines 2018 severity grade for acute cholecystitis [15]
Grade III (severe) acute cholecystitis
“Grade III” acute cholecystitis is associated with dysfunction of any one of the following
organs/systems:
1. Cardiovascular dysfunction: Hypotension requiring treatment with dopamine ≥5 lg/kg per
min, or any dose of norepinephrine
2. Neurological dysfunction: Decreased level of consciousness
3. Respiratory dysfunction: PaO2/FiO2 ratio < 300
4. Renal dysfunction: Oliguria, creatinine >2.0 mg/dl
5. Hepatic dysfunction: PT-INR >1.5
6. Hematological dysfunction: Platelet count <100,000/mm3
Grade II (moderate) acute cholecystitis
“Grade II” acute cholecystitis is associated with any one of the following conditions:
1. Elevated WBC count (>18,000/mm3)
2. Palpable tender mass in the right upper abdominal quadrant
3. Duration of complaints >72 ha
4. Marked local inflammation (gangrenous cholecystitis, pericholecystic abscess, hepatic
abscess, biliary peritonitis, emphysematous
Cholecystitis)
Grade I (mild) acute cholecystitis “grade I” acute cholecystitis does not meet the criteria of
“grade III” or “grade II” acute cholecystitis. It can also be defined as acute cholecystitis in a
healthy patient with no organ dysfunction and mild inflammatory changes in the gallbladder,
making cholecystectomy a safe and low-risk operative procedure
(Published with permission)
Table 7 (continued)
Imaging Criteria
AAST Clinical (CT/US/HIDA Operative Pathologic
Grade Description Criteria findings) Criteria Criteria
III GB perforation Localized HIDA with focal Perforated GB Necrosis with
with local peritonitis in transmural wall (non- perforation of
contamination RUQ defect, iatrogenic) with the GB wall
extraluminal bile outside the (non-
fluid collection GB but limited iatrogenic)
or radiotracer to RUQ
but limited to
RUQ
IV GB perforation Localized Abscess in RUQ Pericholecystic Necrosis with
with perichole- peritonitis at outside GB; abscess; perforation of
cystic abscess ormultiple bilio-enteric bilio-enteric the GB wall
gastrointestinal locations; fistula; gallstone fistula; (non-
fistula abdominal ileus gallstone ileus iatrogenic)
distention
with
symptoms of
bowel
obstruction
V GB perforation Above, with Free intra- Above, plus Necrosis with
with generalized generalized peritoneal bile generalized perforation of
peritonitis peritonitis peritonitis the GB wall
(non-
iatrogenic)
(Published with permission)
Table 10 Scoring system proposed to predict intraoperative difficulty based on preoperative
clinico-radiological parameters proposed by Randhawa and Pujahari [7]
Max. score
History
Age <50 yrs (0) >50 yrs (1) 1
Sex Female (0) Male (1) 1
H/o hospitalization N (0) Y (4) 4
Clinical
BMI wt (kg)/ht. (mt2) <25 (0) 25–27.5 (1) >27.5 (2) 2
Abdominal scar N (0) Infra-umbilical (1) supra-umbilical (2) 2
Palpable gallbladder N (0) Y (1) 1
Sonography
Wall thickness Thin (0) Thick >4 mm (2) 2
Pericholecystic N (0) Y (1) 1
collection
Impacted stone N (0) Y (1) 1
Maximum Score 15, Y YES, N NO (Published with permission)
Fig. 1 Abdominal
ultrasound showing
pericholecystic fluid
Fig. 2 Abdominal
ultrasound showing thick
gallbladder wall
acute cholecystitis as proposed by the 2018 Tokyo guidelines [15]. The guidelines
incorporate comorbidity, organ system involvement, features suggestive of local-
ized infection and other operative/non operative parameters. Any of the following
organ involvement is classified as grade 3: cardiovascular, respiratory, neurological,
renal, hepatic and haematological.
The other widely used classification system to stratify management of cholecys-
tectomy in the emergency setting is the AAST EGS (American Association for the
Surgery of Trauma emergency general surgery) grading which incorporates radio-
logic imaging (CT/US/HIDA), intraoperative and pathology variables (Table 7)
[16]. Table 8 enlists risk factors associated with postoperative complications after
cholecystectomy in non-elective settings [17].
Magnetic resonance Cholangiopancreatography (MRCP): MRCP findings
like thickness of GB around the neck, and disruption of common hepatic duct are
94 N. Gupta et al.
There are many risk factors which make laparoscopic cholecystectomy difficult like
old age, male sex, obesity, BMI, attacks of acute cholecystitis, number of previous
attacks of acute cholecystitis, cholangitis, previous interventions like ERCP stent-
ing, fever, leukocytosis, previous abdominal surgery, clinical signs of acute chole-
cystitis, and certain ultrasonographic findings i.e. thickened gall bladder wall,
distended gallbladder, contracted gallbladder, pericholecystic fluid collection, stone
impacted at neck, fixed stones >2 cm, CBD stones and abnormal anatomy.
Challenging intraoperative pathologic encounters like dense adhesions at calot’s
triangle, fibrotic and contracted gallbladder, acutely inflammed edematous or gan-
grenous gall bladder and cholecystoenteric and cholecystocholedochal fistula etc.
are wary premonitions of a difficult laparoscopic cholecystectomy [6, 9, 12,
13, 22–24].
Prediction and Grading Methods of a Difficult Laparoscopic Cholecystectomy 95
Age: Few studies have reported age >50 years as a significant risk factor. Conversion
rates are also higher in elderly population. It may be attributed to long duration of
symptoms and multiple attacks [18, 25, 26].
Gender: Male Sex is also considered as a risk factor for difficult cholecystec-
tomy. Incidence of conversion to open and mortality is higher in male gender than
their female counterparts. Omental and other organ adhesions are more commonly
seen in male patients. It may be due to their late presentation; they generally seek
medical help after multiple attacks of inflammation. It results in chronic changes
which makes surgery more challenging [18, 26–30].
History of hospitalization for acute attacks: Patients who require hospitaliza-
tion for acute attacks generally carry more chances of difficult laparoscopic chole-
cystectomy and conversions. They are found to be having dense adhesions at Calot’s
triangle and GB fossa. Number of previous attacks, cholangitis and ERCP stenting
has significant association with probability of difficult LC [6, 9, 22, 23]. Pain lasting
for more than 4 h has been mentioned as a predictive factor of difficult LC [31].
Diabetes Mellitus: DM has been found to be useful predictor of difficult LC in
multivariate analysis [31, 32].
laparoscopic approach in scarred abdomen due to these reasons [3, 26, 27]. Open
trocar placement at umbilicus to achieve pneumoperitoneum avoids bowel injury in
such cases and allows adhesiolysis. Surgeon should resist eliminating adhesions
excessively. Only those adhesions that prevent placement of canulas or interfere
with visualization of organ of interest should be lysed [36].
Palpable GB: It is a clinical sign seen in patients having mucocele or empyema.
It is difficult to catch hold of the fundus of GB in these cases and aspiration of the
contents is often required; it is time consuming and carries risk of spillage. Randhawa
et al. has found a significant correlation between palpable GB and difficult LC
[7, 37].
Blood parameter: In a study evaluating an array of clinical and biochemical
parameters in predicting difficulty of cholecystectomy, elevated CRP and neutrophil
lymphocyte ratio were considered as independent predictors of complicated acute
cholecystitis in multivariate analysis [38]. A higher WBC count and fibrinogen lev-
els have also been found to be predictors of difficult gallbladders [31, 39]. Bilirubin
>2 mg/dl was found to be an important risk predictor in multivariate analysis in a
study [32]. However alkaline phosphatase level or liver enzymes have not found to
be corroborative in a study [39].
ASA Class: Patients with higher ASA class implying greater comorbidities was
a risk factor for anticipated intraoperative difficulty [18]. ASA >3 has been pro-
posed as a predictor of intraoperative difficulty [20].
Fig. 3 Abdominal
ultrasonography depicting
large gall bladder calculus
with posterior acoustic
shadowing:Impacted stone
at neck
Fig. 4 Abdominal
ultrasonography showing
dilated CBD
Distended GB: Various studies have shown that distension of gallbladder [trans-
verse diameter more than 5 cm] is associated with technical difficulty [43].
Small shrunken gallbladder: A small shrunken gallbladder consequent to
chronic inflammation can result in hard fibrotic adhesions in region of the cystic
artery and duct which are difficult to dissect and can make grasping difficult [31].
Gallbladder wall flow: In a study evaluating sonographic parameters as pointers
of difficulty, gallbladder wall flow emerged as a significant factor [8].
Air in gallbladder lumen, wall or biliary tree: Presence of air in gallbladder
lumen, wall or biliary tree can be resultant to cholecystoenteric fistula or emphyse-
matous cholecystitis both of which are predicaments of difficulty in AAST EGS
classification (Table 7) [16].
CBD stone and CBD diameter: Presence of CBD stones and CBD dilatation
>6 mm were found to be independent risk factors predictive of intraoperative diffi-
culty (Fig. 4) [18, 32].
98 N. Gupta et al.
Certain parameters in CT-Scan have also been reported to be associated with diffi-
cult cholecystectomy viz.: irregular or absent walls, hyperdensity, pericholecystic
fluid, hydrops, wall thickening >4 mm [39].
Parameters in MRCP
Signal intensity variations in MRI have been suggested to predict gallbladder wall
fibrosis or necrosis. In a study using MRI to evaluate signal intensity in patients
with acute cholecystitis it was noted that lower signal intensities were associated
with higher rates of conversion to open, prolonged operating time and need for sub-
total cholecystectomy in patients of acute cholecystitis [44]. Obscuration near the
gallbladder neck, thickness of GB around the neck and disruption of common
hepatic duct on MRCP may also be significant predictors of conversion to open or
subtotal cholecystectomy [20] (Fig. 5).
Preoperative Interventions
Fig. 6 Intraoperative
picture of gall bladder with
calculus impacted at
Hartman’s Pouch (yellow
arrow) and adhesions in
the region of Calots
triangle. [Image Courtesy:
Dr. Deborshi Sharma]
100 N. Gupta et al.
Fig. 8 Intraoperative
picture: gall bladder
obscured due to adhesions
between bowel
omentumand liver. [Image
Courtesy: Dr. Deborshi
Sharma]
Fig. 9 Intraoperative
picture showing inflammed
gall bladder with adhesions
around the gallbladder.
[Image Courtesy: Dr.
Deborshi Sharma]
Fig. 10 Intraoperative
picture of dense adhesions
of gall bladder with colon
and duodenum. [Image
Courtesy: Dr. Deborshi
Sharma]
gallbladder with flimsy adhesions and Fig. 10 shows dense adhesions between gall-
bladder and adjacent duodenum and colon.
Empyema/necrosis/gangrene/perforation of gallbladder: Empyema, perfora-
tion, necrotic or gangrenous gallbladder has been allotted maximum grades/scores
in most scoring systems [5, 12–16].
Fistula of the gallbladder: The presence of a cholecystoenteric or cholecysto-
choledochal fistula was graded with highest points regarding difficulty in one of the
scoring systems grading intraoperative parameters [12–14, 16]. Figure 11 is an
intraoperative picture depicting a shrunken fibrotic gallbladder with cholecystoduo-
denal fistula.
Abscess formation/non iatrogenic perforation/pericholecystic collection/
peritonitis: Pus or biliary collection can be intrahepatic or extrahepatic and may be
associated with localized or generalized peritonitis. Pus or biliary collection with
localized peritonitis is classified in moderate to severe grades of difficulty in most
classification [5, 6, 12–16, 43]. Presence of generalized peritonitis is graded as cat-
egory 5 (highest category) in AAST EGS Classification (Table 7) [16].
102 N. Gupta et al.
Fig. 11 Intraoperative
picture of shrunken
gallbladder with
cholecystoduodenal fistula
(Yellow Arrow). [Image
Courtesy: Dr. Deborshi
Sharma]
Intraoperative parameters which have been proposed to grade difficulty but maybe
dependent on surgeon’s ability include time taken for operation, injury to biliary
duct or vessels, bile or stone spillage and conversion [5–7].
Tables 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 enumerates the various preoperative and
intraoperative parameters that can point out to a difficulty in laparoscopic
cholecystectomy.
Nassar et al. devised a preoperative risk scoring systems from extrapolation of data
from two large databases (Table 9) [18]. The preoperative scoring system was devel-
oped based on intraoperative grading system of difficult laparoscopic cholecystec-
tomy earlier proposed, as enlisted in Table 1 and validated. Increasing age, ASA
Prediction and Grading Methods of a Difficult Laparoscopic Cholecystectomy 103
Different scoring methodologies have been suggested from time to time using over-
lapping criteria, further adding to the controversy. One of the earliest classification
of intraoperative difficulty during cholecystectomy was proposed by Cuscheri in
1992, [5]. Nassar et al. proposed grading of operative difficulty by assessment of
gallbladder, cystic duct pedicle and adhesions, Table 1 [12, 18]. A prospective mul-
ticenter cohort CholeS study using the above grading system observed that with
increase in grades from 1 to 5, the median hospital stay increased from 0 to 4 days,
and the 30-day complication rate increased from 7.6 to 24.4% respectively the find-
ings being significant. The Nassar grading scale emerged as an independent predic-
tor of operative time, conversion to open and 30 days complication and reintervention
rates. Use of this difficulty scale helps standardization of operative findings and thus
is proposed to facilitate audit, training assessment and research across multiple
grades of surgeons [47]. In a multinational collaborative study on surgeons using
Delphi technique, a consensus was reached on multiple intraoperative parameters as
predictors of difficulty. The factors were primarily classified as those related to
inflammation in region of gallbladder, calots and gallbladder bed as well as other
non-inflammatory intraoperative variables (Table 3). Sugrue M et al. have proposed
a G10 operative scoring system to provide simple grading of operative cholecystec-
tomy and predictive need to convert to open cholecystectomy Gallbladder surgery
was considered easy if the G10 score <2, moderate (2–4), difficult (5–7) and extreme
(8–10) (Table 4). In a study comparing Parkland intraoperative grading scale and
AAST EGS scale to assess difficult LC (Table 5), authors observed that the Parkland
scale was a superior predictor of operative difficulty, conversion, complication and
104 N. Gupta et al.
operative time whereas the Parkland and AAST grades had similar predictive value
as regards rates of partial cholecystectomy, readmission, bile leak, and hospital stay
[48]. Higher the Parkland grading scale (particularly for grade 4 and above) the
greater is the chance of acute cholecystitis and gangrenous cholecystitis. A strong
correlation has been noted between Parklands intraoperative grading scale and
Tokyo classification for acute cholecystitis. Increasing Parkland grades has been
associated with increased CRP levels and higher incidence of acute and gangrenous
cholecystitis [49]. An independent validation of AAST EGS system of classification
observed good inter-rater reliability for anatomic grading. With increasing AAST
EGS grade there was increased incidence of complications, prolonged hospital stay,
higher ICU admissions and adverse events. As the above adverse events were noted
even in grade 3 patients of the classification, the authors called for a refinement of
the classification system [50]. In a comparative validation between Tokyo system
and AAST EGS classification the latter was found to outperform the former with
respect to disease severity discrimination [51]. In a multicenter validation of
Parkland scale, Tokyo guideline classification and the AAST EGS stratification sys-
tem, Parkland scale was proposed to be better than AAST EGS system and Tokyo
classification, with the latter two having similar discriminatory power [52].
Table 11 outlines the various treatment options advised classified as per the grades
of disease in Parkland scale, Tokyo guidelines and AAST EGS classification [53].
Scoring systems can identify patients having high risk for LC and thus help in inti-
mation of patients about the anticipated difficulty that may be encountered, the
chances of conversion and further such cases may be scheduled appropriately. These
scoring systems may aid in the decision of early conversion to open or opt to bailout
options like cholecystostomy or subtotal cholecystectomy when difficulty is encoun-
tered. The other probable use of these scoring systems is to select patients more
appropriate for trainee surgeons as opposed to more experienced surgeons.
Conclusion
Table 11 Treatment options for various grades of Parkland, Tokyo and AAST EGS classifica-
tions [53]
Classification Grade Treatment recommendation
Parkland Grade 1 LC can be done with standard operative time and minimal
classification complications/conversion
Grade 2 LC can be done with standard operative time and minimal
complications/conversion
Grade 3 LC feasible but increased difficulty as compared to grade 1 and
grade 2 unpredictable operative time, complications and
conversion rates
Grade 4 LC feasible but increased difficulty as compared to grade 1,
grade 2 and grade 3 unpredictable operative time, complications
and conversion rates
Grade 5 Increased operative time high rates of complications/ conversion
Tokyo guidelines Grade 1 Low risk of complications and conversion as compared to grade
1 and 2, early cholecystectomy can be done in most cases
Grade 2 Moderate rates of complications and conversion
Early cholecystectomy challenging, drainage procedure should
be preferred as an initial option and delayed cholecystectomy
advisable
Grade 3 High complications conversion and 30-day mortality,
preoperative drainage procedure advised
AAST EGS Grade 1 LC can be performed with low risk of conversion
classification Grade 2 LC can be performed with low risk of conversion
Grade 3 LC carries risk of conversion, consider percutaneous
cholecystostomy
Grade 4 LC has high probability of conversion consider OC/percutaneous
drainage
Grade 5 LC has high probability of conversion consider OC/percutaneous
drainage
LC laparoscopic cholecystectomy, OC open cholecystectomy
Summary of different scoring systems for difficult gallbladder tabulated in this chapter
Table 1: proposed by Nassar (1995) and modified (1996)
- intraoperative factors to classify difficulty in LC [12]
Table 2: proposed by Randhawa et al. 2009
- intraoperative factors for difficulty grading in LC [7]
Table 3: a multinational collaborative study on surgeons using Delphi technique 2017
- elaborate and detailed grading of intraoperative factors [13]
Table 4: proposed by Sugrue et al. 2019
- intraoperative factors & few preoperative clinical factors [6]
Table 5: Parkland scale
- Intraoperative factors for grading difficulty of LC [14]
Table 6: 2018 Tokyo guidelines
- severity grading scale for acute cholecystitis: predominantly preoperative factors [15]
Table 7: AAST EGS grading system
- descriptions of acute cholecystitis severity grading: preoperative, intraoperative factors and
pathologic correlation [16]
Table 8: Proposed by Burke J et al. 2021
- preoperative risk scoring system in LC as predictor of complications [17]
106 N. Gupta et al.
References
1. Le VH, Smith DE, Johnson BL. Conversion of laparoscopic to open cholecystectomy in the
current era of laparoscopic surgery. Am Surg. 2012 Dec;78(12):1392–5.
2. Gadacz TR. Update on laparoscopic cholecystectomy, including a clinical pathway. Surg Clin
North Am. 2000;80:1127–45.
3. Khan IA, El-Tinay OE. Laparoscopic cholecystectomy for acute cholecystitis: can preopera-
tive factors predict conversion? Saudi Med J. 2004;25(3):299–302.
4. Elshaer M, Gravante G, Thomas K, Sorge R, Al-Hamali S, Ebdewi H. Subtotal cholecys-
tectomy for “difficult gallbladders”: systematic review and meta-analysis. JAMA Surg.
2015;150(2):159–68. https://doi.org/10.1001/jamasurg.2014.1219.
5. Cuschieri A, Berci G. Laparoscopic biliary surgery. Edinburgh: Blackwell Scientific
Publication; 1992.
6. Sugrue M, Coccolini F, Bucholc M, Johnston A. Contributors from WSES.Intra-operative gall-
bladder scoring predicts conversion of laparoscopic to open cholecystectomy: a WSES pro-
spective collaborative study. World J Emerg Surg. 2019 Mar 14;14:12. https://doi.org/10.1186/
s13017-019-0230-9.
7. Randhawa JS, Pujahari AK. Preoperative prediction of difficult laparoscopic cholecystectomy:
a scoring method. Indian J Surg. 2009;71:198–201.
8. Jalil T, Adibi A, Mahmoudieh M, Keleidari B. Could preoperative sonographic criteria predict
the difficulty of laparoscopic cholecystectomy? J Res Med Sci. 2020 Jun 30;25:57. https://doi.
org/10.4103/jrms.JRMS_345_19. PMID: 33088294; PMCID: PMC7554442.
9. Kania D. Ultrasound measurement of the gallbladder wall thickness in the assessment of the
risk of conversion from elective laparoscopic cholecystectomy to open surgery - Olkusz county
experience. PolPrzeglChir. 2016 Dec 1;88(6):334–45. https://doi.org/10.1515/pjs-2016-0073.
10. Kohga A, Okumura T, Yamashita K, Isogaki J, Kawabe A, Kimura T. Does early surgery
imply a critical risk for patients with grade III acute cholecystitis? Asian J Endosc Surg 2021
Jan;14[1]:7–13. https://doi.org/10.1111/ases.12799. Epub 2020 Mar 23. PMID: 32207215.
11. Miura F, Takada T, Strasberg SM, Solomkin JS, Pitt HA, Gouma DJ, Garden OJ, Büchler MW,
Yoshida M, Mayumi T, Okamoto K, Gomi H, Kusachi S, Kiriyama S, Yokoe M, Kimura Y,
Higuchi R, Yamashita Y, Windsor JA, Tsuyuguchi T, Gabata T, Itoi T, Hata J, Liau KH, Tokyo
Guidelines Revision Committee. TG13 flowchart for the management of acute cholangitis
and cholecystitis. J Hepatobiliary Pancreat Sci. 2013 Jan;20(1):47–54. https://doi.org/10.1007/
s00534-012-0563-1. PMID: 23307003.
12. Nassar AHM, Ng HJ, Wysocki AP, Khan KS, Gil IC. Achieving the critical view of safety
in the difficult laparoscopic cholecystectomy: a prospective study of predictors of failure.
Surg Endosc. 2020 Oct 16. https://doi.org/10.1007/s00464-020-08093-3. Epub ahead of print.
PMID: 33067645.
13. Iwashita Y, Hibi T, Ohyama T, Honda G, Yoshida M, Miura F, et al. An opportunity in diffi-
culty: Japan–Korea–Taiwan expert Delphi consensus on surgical difficulty during laparoscopic
cholecystectomy. J Hepatobiliary Pancreat Sci. 2017;24:191–8.
14. Madni TD, Nakonezny PA, Barrios E, Imran JB, Clark AT, Taveras L, Cunningham HB,
Christie A, Eastman AL, Minshall CT, Luk S, Minei JP, Phelan HA, Cripps MW. Prospective
validation of the parkland grading scale for cholecystitis. Am J Surg. 2019 Jan;217(1):90–97.
https://doi.org/10.1016/j.amjsurg.2018.08.005. Epub 2018 Aug 21. PMID: 30190078.
15. Yokoe M, Hata J, Takada T, Strasberg SM, Asbun HJ, Wakabayashi G, Kozaka K, Endo I,
Deziel DJ, Miura F, Okamoto K, Hwang TL, Huang WS, Ker CG, Chen MF, Han HS, Yoon
YS, Choi IS, Yoon DS, Noguchi Y, Shikata S, Ukai T, Higuchi R, Gabata T, Mori Y, Iwashita
Y, Hibi T, Jagannath P, Jonas E, Liau KH, Dervenis C, Gouma DJ, Cherqui D, Belli G, Garden
OJ, Giménez ME, de Santibañes E, Suzuki K, Umezawa A, Supe AN, Pitt HA, Singh H,
Chan ACW, Lau WY, Teoh AYB, Honda G, Sugioka A, Asai K, Gomi H, Itoi T, Kiriyama S,
Yoshida M, Mayumi T, Matsumura N, Tokumura H, Kitano S, Hirata K, Inui K, Sumiyama
Y, Yamamoto M. Tokyo Guidelines 2018: diagnostic criteria and severity grading of acute
108 N. Gupta et al.
tions after early laparoscopic cholecystectomy for acute cholecystitis: the chole-risk score. J
Gastrointest Surg. 2021 Feb 24. https://doi.org/10.1007/s11605-021-04956-9. Epub ahead of
print. PMID: 33629230.
33. Rosen M, Brody F, Ponsky J. Predictive factors for conversion of laparoscopic cholecystec-
tomy. Am J Surg. 2002;184(3):254–8.
34. Simopoulos C, Polychronidis A, Botaitis S, Perente S, Pitiakoudis M. Laparoscopic cholecys-
tectomy in obese patients. Obes Surg. 2005 Feb;15(2):243–6.
35. Hussien M, Appadurai IR, Delicata RJ, Carey PD. Laparoscopic cholecystectomy in the
grossly obese: 4 years experience and review of literature. HPB. 2002;4(4):157–61.
36. Akyurek N, Salman B, Irkorucu O, Tascilar O, Yuksel O, Sare M, Tatlicioglu E. Laparoscopic
cholecystectomy in patients with previous abdominal surgery. JSLS 2005;9:178–83.
37. Gupta N, Ranjan G, Arora MP, Goswami B, Chaudhary P, Kapur A, et al. Validation of a scor-
ing system to predict difficult laparoscopic cholecystectomy. Int J Surg. 2013;11(9):1002–6.
https://doi.org/10.1016/j.ijsu.2013.05.037.
38. Mahmood F, Akingboye A, Malam Y, Thakkar M, Jambulingam P. Complicated acute chole-
cystitis: the role of C-reactive protein and neutrophil-lymphocyte ratio as predictive markers
of severity. Cureus. 2021 Feb 27;13(2):e13592. https://doi.org/10.7759/cureus.13592. PMID:
33796428; PMCID: PMC8006862.
39. Di Buono G, Romano G, Galia M, Amato G, Maienza E, Vernuccio F, Bonventre G, Gulotta L,
Buscemi S, Agrusa A. Difficult laparoscopic cholecystectomy and preoperative predictive fac-
tors. Sci Rep. 2021 Jan 28;11(1):2559. https://doi.org/10.1038/s41598-021-81938-6. PMID:
33510220; PMCID: PMC7844234.
40. Daradkeh SS, Suwan Z, Abu-Khalaf M. Preoperative ultrasonography and prediction of dif-
ficulties in laparoscopic cholecystectomy. World J Surg. 1998;22:75–7.
41. Majeski J. Significance of preoperative ultrasound measurement of gallbladder wall thickness.
Am Surg. 2007;73(9):926–9.
42. Khan KS, Sajid MA, McMahon RK, Mahmud S, Nassar AHM. Hartmann’s pouch stones
and laparoscopic cholecystectomy: the challenges and the solutions. JSLS. 2020 Jul-
Sep;24(3):e2020.00043. https://doi.org/10.4293/JSLS.2020.00043. PMID: 32831544;
PMCID: PMC7434399.
43. Siddiqui MA, Rizvi SMA, Sartaj S, Ahmad I, Rizvi SWA. A standardized ultrasound scor-
ing system for preoperative prediction of difficult laparoscopic cholecystectomy. J Med
Ultrasound. 2017;25:227–31.
44. Omiya K, Hiramatsu K, Shibata Y, Fukaya M, Fujii M, Aoba T, Arimoto A, Yamaguchi T, Kato
T. Preoperative magnetic resonance cholangiopancreatography for detecting difficult laparo-
scopic cholecystectomy in acute cholecystitis. Diagnostics [Basel]. 2021 Feb 24;11[3]:383.
https://doi.org/10.3390/diagnostics11030383. PMID: 33668281.
45. Jameel SM, Bahaddin MM, Mohammed AA. Grading operative findings at laparoscopic cho-
lecystectomy following the new scoring system in Duhok governorate: cross sectional study.
Ann Med Surg (Lond). 2020 Oct 23;60:266–70. https://doi.org/10.1016/j.amsu.2020.10.035.
PMID: 33204417; PMCID: PMC7649370.
46. Tongyoo A, Chotiyasilp P, Sriussadaporn E, Limpavitayaporn P, Mingmalairak C. The pre-
operative predictive model for difficult elective laparoscopic cholecystectomy: a modifica-
tion. Asian J Surg. 2021 Apr;44(4):656–61. https://doi.org/10.1016/j.asjsur.2020.11.018. Epub
2021 Jan 19. PMID: 33349555.
47. Griffiths EA, Hodson J, Vohra RS, Marriott P, Katbeh T, Zino S, Nassar AHM, West
Midlands Research Collaborative. Utilisation of an operative difficulty grading scale for
laparoscopic cholecystectomy. Surg Endosc. 2019 Jan;33(1):110–21. https://doi.org/10.1007/
s00464-018-6281-2. Epub 2018 Jun 28. Erratum in: Surg Endosc. 2018 Aug 22; PMID:
29956029; PMCID: PMC6336748.
48. Madni TD, Nakonezny PA, Imran JB, Taveras L, Cunningham HB, Vela R, Clark AT,
Minshall CT, Eastman AL, Luk S, Phelan HA, Cripps MW. A comparison of cholecystitis
grading scales. J Trauma Acute Care Surg. 2019 Mar;86(3):471–8. https://doi.org/10.1097/
TA.0000000000002125. PMID: 30399131.
110 N. Gupta et al.
49. Lee W, Jang JY, Cho JK, Hong SC, Jeong CY. Does surgical difficulty relate to severity of
acute cholecystitis? Validation of the parkland grading scale based on intraoperative findings.
Am J Surg. 2020 Apr;219(4):637–41. https://doi.org/10.1016/j.amjsurg.2018.12.005. Epub
2018 Dec 8. PMID: 31718816.
50. Vera K, Pei KY, Schuster KM, Davis KA. Validation of a new American Association for the
Surgery of Trauma (AAST) anatomic severity grading system for acute cholecystitis. J Trauma
Acute Care Surg. 2018 Apr;84(4):650–4. https://doi.org/10.1097/TA.0000000000001762.
PMID: 29271871.
51. Hernandez M, Murphy B, Aho JM, Haddad NN, Saleem H, Zeb M, Morris DS, Jenkins
DH, Zielinski M. Validation of the AAST EGS acute cholecystitis grade and comparison
with the Tokyo guidelines. Surgery. 2018 Apr;163(4):739–46. https://doi.org/10.1016/j.
surg.2017.10.041. Epub 2018 Jan 8. PMID: 29325783.
52. Schuster KM, O’Connor R, Cripps M, Kuhlenschmidt K, Taveras L, Kaafarani HM, El Hechi
M, Puri R, Mull J, Schroeppel TJ, Rodriquez J, Cullinane DC, Cullinane LM, Enniss TM,
Sensenig R, Zilberman B, Crandall M. Multicenter validation of the American Association for
the Surgery of Trauma grading scale for acute cholecystitis. J Trauma Acute Care Surg. 2021
Jan 1;90(1):87–96. https://doi.org/10.1097/TA.0000000000002901. PMID: 33332782.
53. Elkbuli A, Meneses E, Kinslow K, Boneva D, McKenney M. Current grading of gall blad-
der cholecystitis and management guidelines: Is it sufficient? Ann Med Surg (Lond). 2020
Oct 28;60:304–7. https://doi.org/10.1016/j.amsu.2020.10.062. PMID: 33204421; PMCID:
PMC7649581.
Robotic Assisted
Pancreaticoduodenectomy
Brij B. Agarwal and Neeraj Dhamija
Introduction
Pancreatic cancer remains one of the deadliest malignancies even after the advance-
ment in the diagnostic, surgical and adjuvant therapy. The first attempt for mini-
mally invasive resection of the pancreatic head malignancy was made by Gagner
and Pomp [1] in the year 1994. They concluded that there is no added benefit in
performing laparoscopic pancreaticoduodenectomy [2]. Since then, there has been
a very gradual increase in number of pancreatico-duodenectomies performed by
minimally invasive route mostly due to improved optics and instruments along with
reconstruction techniques. It was after the introduction and utilisation of Robotic
platform to perform complex abdominal dissection and anastomosis; we have seen
a consistent rise in the Robotic assisted pancreaticoduodenectomy (RAPD) or com-
plete Robotic pancreaticoduodenectomy procedures (RPD).
There is a consistent increase in number of publications of both Robotic Assisted
and Total Robotic pancreaticoduodenectomy procedure over the last decade [3–5].
There are many case series evaluating the advantages of the minimally invasive
pancreaticoduodenectomy over the traditional open approach [3–8]. A recent ran-
domized controlled trial- PORTAL trial is also under way comparing Robotic pan-
creaticoduodenectomy and open procedure [9].
When the Robotic platform is used for all the sub-steps of pancreaticoduode-
nectomy procedure starting from dissection to resection and reconstruction, the
procedure is called as Total Robotic Pancreaticoduodenectomy procedure.
Whereas when the robot is used only to perform specific sub-steps like creation
of pancreatico- enteric anastomosis and bilio-enteric anastomosis after a
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 111
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_5
112 B. B. Agarwal and N. Dhamija
Patient Selection
With experience more complex cases are being done by utilization of the robotic
platform stretching out the limits of above said patient profile to locally advanced
pancreatic neoplasms which require difficult dissection and vascular resection.
In high volume centers with experienced surgeons, post neoadjuvant chemother-
apy cases and those requiring vascular resections are no longer a contraindication
for RPD. Reports are available of known aberrant RHA being managed during
RPD, while definite better outcome is seen in obese patients on using the robotic
platform [8, 11–13].
Diagnostic Laparoscopy
After painting and draping, pneumoperitoneum is created with the palmer’s point
approach. Staging laparoscopy is done with 5 mm, 30-degree telescope. The pari-
etal and visceral surface of the peritoneum is inspected carefully for any nodules
with suspected metastasis. The peritoneal cavity is inspected for the presence of any
free fluid. In the presence of any nodule or free fluid the samples are taken for
assessment by frozen technique to confirm for metastatic disease which will direct
the further course of surgical management. The standard port position for Robotic
Assisted Pancreatico duodenectomy is shown in the Fig. 1.
The next step is to enter the lesser sac by opening of the gastrocolic omentum. This
step is aided by using the ultrasonic shear dissection and can be easily done by dis-
secting the gastrocolic omentum at the midpoint between the greater curvature and
the colonic margin. The window thus created in the gastrocolic omentum is widened
both cranially and to the right so that the entire posterior surface of the stomach is
clearly seen. Pancreas along with the covering off the posterior peritoneal lining can
be seen at the posterior aspect of the lesser sac. The adhesions between the posterior
surface of the stomach and the pancreas are divided.
114 B. B. Agarwal and N. Dhamija
Fig. 1 Port Placement in Robotic Pancreatico duodenectomy Procedure System Used Da Vinci Si;
C = Camera Arm of Robot (2 cm above and lateral to the umbilicus on the right side); R1 = Right
Hand of Operating Surgeon- Working Arm 1 (Left Mid clavicular line 8 cm from the Camera Port);
R2 = Left Hand of Operating Surgeon- Working Arm 2 (Just Lateral to the Right mid clavicular
line, 8cm from the Camera Port); A1 = Assistant Port 10mm (1cm below and lateral to the umbili-
cus on the left side); A2 = Assistant Port 5mm (Anterior axillary line on the left side 5 cm
from the R1)
While dissecting the gastrocolic omentum medially towards the duodenum the gas-
trocolic vessels are encountered which should be carefully dissected and clipped
separately. This usually ensures the complete mobilisation of the whole of the
greater curvature of the stomach all along till the duodenum.
Fig. 2 Cattell-
BraaschManuever:
(Extended Kocher +
Incision of small bowel
mesentery to posterior
peritoneum to reflect the
ascending colon and
duodenum to the left side
of abdomen)
Hilum Exploration
Dissection of the hepatoduodenal fatty tissue is performed next starting at the lesser
curvature of the stomach. The common hepatic artery is identified, and dissection is
done along the adventitial layer of the vessel which is usually avascular. Proper
understanding of the vascular anatomy of individual case by a detailed study of the
CT angiography will help and aid in the dissection. Careful dissection will eventu-
ally dissect all the fatty tissue along with the lymph nodes which should be sent
separately in an endobag or along with the main specimen for proper histopatho-
logical examination (HPE) and oncological evaluation.
Dissection of the lymph nodes will also make the gastroduodenal artery [GDA] vis-
ible making it easy for dissection. GDA should always be double ligated with two
clips on both proximal and distal side to safely secure this vessel [Fig. 3].
116 B. B. Agarwal and N. Dhamija
Just deep to the GDA is the portal vein which should be visible by now and on
the right side is the CBD. We should carefully dissect the gastroduodenal vein
which is usually present on the right side of GDA. When it is of a significant size,
its injury can be a source of troublesome bleeding.
At the lower border of the pancreas the mesopancreatic tissue is dissected to reveal
the superior mesenteric vein (SMV). The site of SMV can be can be traced by fol-
lowing the previously ligated gastroepiploic vein which leads us to the SMV. Careful
blunt dissection is done with the help of atraumatic grasper or the suction tip.
Usually, this plane is not having any major vessels but occasionally one or more
direct venous tributaries may be seen arising from the posterior surface of the pan-
creas and draining into the SMV. These can be easily secured with either harmonic
scalpel or haemolock clips. The space behind the pancreatic neck is further dis-
sected to reach and meet the already created superior space at the level of GDA
vessel and just medial to it.
Vessel First Approach During a suspected locally advanced lesion and possible
involvement of the vital vascular structures at the posterior aspect of the pancreas a
vessel first approach is utilized for dissection. In this approach the feasibility of Step
number 7 is assessed before Step Number 3, i.e. after the dissection of the epiploic
vessels. The feasibility of the creation of the retropancreatic tunnel over the great
veins- SMV and Splenic vein confluence to form Portal veinis ascertained. This
modification of the technique is important as any abnormal adhesions between the
posterior surface of the pancreas and the great veins will unable us to progress with
the pancreatic neck transection and can result in unwanted bleeding which can be a
catastrophe. This may demand conversion of the procedure to open or abandon the
procedure for non-operability.
Robotic Assisted Pancreaticoduodenectomy 117
Transection of Stomach
Stomach is transected with the help of Endo stapler 60 mm green loads. Classical
pancreatico duodenectomy describes transection of the stomach at the junction of
middle and distal third. Usually, one to two cartridges are used for transection of
stomach. Both side of the transected stomach is then opened like a book aiding in
complete visualization of the pancreatic neck.
A successful creation of the space will enable us for the next important step of pan-
creatic neck transection. The transection of the pancreas at the level of the neck-the
region of the pancreatic neck is identified by posteriorly running superior mesen-
teric vein and splenic vein confluence to form portal vein. The line of transection is
usually parallel to the portal vein. Ultrasonic scissors is preferably used for transec-
tion [Fig. 4]. The trick is to take small bites at minimum level of setting. Careful
dissection will help us to identify the pancreatic duct which is also transected by
cold scissors and the dissection is further continued from caudal to cranial fashion
to complete the transection of the pancreas.
Transection of the Jejunum
After pancreatic transection, the omentum and the transverse colon is flipped-up to
reveal the duodeno-jejunal junction [DJ] and the ligament of Trietz. Approximately
15 cm from the DJ, jejunum is transected with the help of a 60 mm white/blue sta-
pler. The mesentery of the transected jejunum is resected close to the jejunal wall to
reach the ligament of Trietz. Careful dissection of the ligament of Trietz makes the
DJ free and this step enables us to deliver the transected jejunum to the right side of
the abdomen through the retroperitoneal tunnel.
Cholecystectomy
The CBD and the Calot’s triangle are dissected, and the cystic artery is secured. The
cystic duct is ligated in continuity but the gall bladder is not detached immediately
from liver as it aids in the dissection of the important structures at the porta. The
CBD is looped with silastic loop for identification and future transection.
After transection of the pancreas, the specimen is attached with the help of the unci-
nate process and the bile duct. The transection of the bile duct is usually done at the
level of the cystic duct and bile duct confluence. The transected margin of the bile
duct can be sent for frozen section if the indication of the resection is a distal chol-
angiocarcinoma. The transection is usually aided by the harmonic scalpel with care
taken to remain away from the portal vein.
At this step the only structure which is holding the specimen is the uncinate process
of the pancreas. The dissection of the uncinate process begins in a caudal-to-cranial
fashion. Traction over the specimen side and counter traction by assistant surgeon
over the portal vein will expose the mesopancreatic tissue in close proximity to the
superior mesentric artery [SMA]. Careful dissection of the venous tributaries to the
portal vein travelling through the uncinate and ligation of the small arteries from
SMA to the uncinate is done with the help of Harmonic Scalpel and Haemolock
clips/Ligaclips wherever necessary [Fig. 5].
Out of all the vessels in the region of the uncinate the “First jejunal vein” is the
most notorious. It runs as a course of a ‘U’ shaped loop of vein traversing through
the uncinate and therefore you have to either dissect it completely or secure it twice
to have proper control of this vessel. This is a common source of bleeding from the
uncinate process while dissection. A step-by step approach is followed, and the ves-
sels secured to reach and meet the cranial edge of the uncinate where it joins the
already formed window of the dissected bile duct. This will complete the resection
of the specimen of Pancreatico-Duodenectomy.
Specimen Extraction
The resected specimen is placed in an Endobag and retrieved from the port-site. The
specimen can also be retrieved from Natural orifice -Vagina in consenting post-
menopausal women undergoing minimally invasive pancreaticoduodenectomy with
acceptable results.
The Robot is docked from the head end. In the robotic arm-1 a needle holder is
equipped and in the robotic arm-2 atraumatic bowel grasper is equipped. The oper-
ating surgeon sits at the robotic console and the reconstruction is started.
–– Pancreatico-Jejunostomy [PJ]
–– Hepatico-Jejunostomy [HJ]
–– Gastro-Jejunostomy [GJ]
Pancreatico-Jejunostomy [PJ]
Before we start doing the PJ, we make sure that there is adequate mobilization of
approximately 3–5 cm of the pancreas in the posterior aspect so that the posterior
surface of the pancreas is exposed. The reconstruction is done in an end-to-side
fashion where the cut end of the pancreas is anastomosed to the side of the jejunum.
Preferred technique is selective duct-to-mucosa suturing with dunking of the rest of
the pancreas. It consists of a four layered anastomosis. The technique used by the
authors is described here below:
120 B. B. Agarwal and N. Dhamija
I. The first layer consists of the interrupted 4-0 PDS (polydioxanone) sutures
from the posterior surface of the pancreas and the sero-muscular layer of the
jejunum. It is started at a distance of approximately 1 cm from the cut edge of
the pancreas at the posterior surface. It usually takes about 6–8 sutures to com-
plete this layer [Fig. 6].
II. The second layer is a selective duct-to-mucosa layer. As the duct of the pan-
creas is eccentrically located and is closer to the posterior aspect of the p ancreas,
selective sutures are taken between the posterior ductal margin and the posterior
lip mucosa of the jejunal enterotomy. About 4 interrupted sutures with 4-0 PDS
are required in this fashion. Rest of the second layer consists of the interrupted
sutures with 4-0 PDS between the full thickness of the jejunum and the pancre-
atic parenchyma at the level of the duct where at least 2–3 sutures are taken both
cranially and caudally to the duct of the pancreas. At this step a stent [silastic
feeding tube of 5 cm and 6-8Fr] can be introduced into the duct of the pancreas
and the intestinal lumen to create a stented anastomosis [Fig. 7].
III. The third layer of the PJ consists of a 6-8 interrupted 4-0 PDS sutures from the
anterior surface of the cut edge of the pancreas and the anterior lip of enterot-
omy of the jejunum. Care must be taken for not tightening the sutures too much
which can cause tear of the pancreatic parenchyma [Fig. 8].
Fig. 9 Hepatico-
Jejunostomy
IV. The fourth layer is between the anterior surface of the pancreatic serosa and the
sero-muscular layer of the anterior surface of the jejunum. It is done by inter-
rupted 4-0 PDS sutures.
This completes the PJ. The jejunum is then anchored near the bile duct with a 4-0
PDS suture to create a HJ at approximately 10 cm from the PJ.
Hepatico-Jejunostomy [HJ]
An enterotomy is made at the anti-mesenteric border of the jejunum for a length less
than the diameter of the bile duct. An interrupted 4-0 PDS sutures are taken starting
from the posterior layer of the bile duct followed by the anterior layer [Fig. 9]. Stent
or a T-Tube is not placed across the HJ. The jejunum is fixed to the mesenteric win-
dow at the transverse colon and the window is closed by 3-0 vicryl sutures.
122 B. B. Agarwal and N. Dhamija
Undocking of the Robot
After PJ and HJ, the robot is undocked and rest of the procedure is performed by
laparoscopic approach.
Gastro-Jejunostomy [GJ]
Approximately 30 cm from the HJ, a GJ is created. It is preferably done with the
help of a stapler using a blue reload and 60 mm cartridge. An enterotomy is created
at the antimesenteric border of the jejunum and posterior surface of the stomach. An
Endo GIA stapler is passed from the enterotomy, one limb in the stomach and
another in the jejunum to create the stapled GJ. The enterotomy site is closed with
the help of 3-0 PDS suture in a single layer continuous fashion.
After reconstruction, haemostasis is ensured and a ‘Stamm type’ of feeding jeju-
nostomy is done with a 12 Fr Ryles tube.
• From left side of the abdomen at the superior surface of the pancreas above the
PJ and close to the GJ.
• From right side of the abdomen near the HJ.
• A dependent drain in the pelvis from the right side of the abdomen.
The skin incisions are closed in layers after careful closure of the ports with vic-
ryl no.1 and skin with staplers. Ryles tube is generally not required and if inserted
is removed in the post-operative recovery room after full recovery from anesthesia.
Complications of Pancreaticoduodenectomy
Recent reports suggest that after Robotic PD, POPF incidence is only around
10% with high risk factors like soft pancreas and narrow duct ≤2 mm [23]. RPD
also shows decreased incidence of delayed gastric emptying (3%) and has better
oncologic outcomes in comparison to open PD [24].
Conclusion
Editor’s Note1
I. Laparoscopic assisted
II. Totally laparoscopic
III. Total laparoscopic robotic assisted
IV. Totally robotic.
Table EN1 Meta analyses published on outcome of robotic/minimally invasive and open pancre-
aticoduodenectomy in past 5 years
Disadvantages
robotic/
Advantages robotic/ minimally
Study, author [first], year No difference minimally invasive invasive
Perioperative and • Overall survival • Disease-free
oncological outcomes • Operative time survival
following minimally • Postoperative • Time to starting
invasive versus open complications adjuvant
pancreaticoduodenectomy • 30-day mortality chemotherapy,
for pancreatic duct • Rate of vein resection • Length of hospital
adenocarcinoma. • Number of harvested stay
Sun R 2021 [1] lymph nodes • rate of negative
• Rate of positive margins
lymph nodes.
Robotic versus open • Positive margin rate • Less blood loss Longer
pancreaticoduodenectomy: • Lymph nodes • Hospital stay operative time
a meta-analysis of harvested • Wound infection
short-term outcomes. • Postoperative
Yan Q 2020 [2] complications
• Reoperation or
readmission mortality
rate
(continued)
References: Main chapter references are included after the “References Editor’s Note” section.
1
126 B. B. Agarwal and N. Dhamija
Table EN1 (continued)
Disadvantages
robotic/
Advantages robotic/ minimally
Study, author [first], year No difference minimally invasive invasive
A systematic review and • Major complications • Less transfusion Operative time
network meta-analysis of • Fistula • Wound infection for total robotic
different surgical • biliary leak • Pulmonary was longer than
approaches for • mortality complication open
pancreaticoduodenectomy. • R0 resections. • Less hospital stay
Kamarajah SK 2020 [3] than open
• Lower conversion
in total robotic
than total
laparoscopic group
• Higher lymph
node yield in total
robotic
Robotic-assisted versus • Mortality morbidity • Less blood loss Longer
open • Pancreatic fistula operative time
pancreaticoduodenectomy • Delayed gastric
for patients with benign emptying hemorrhage
and malignant • Bile leak
periampullary disease: a • Retrieved lymph
systematic review and nodes
meta-analysis of short-term • Positive margin
outcomes. status.
Podda M 2020 [4]
Minimally invasive versus • Reduced blood Longer
open loss operative time
pancreatoduodenectomy- • Delayed gastric
systematic review and emptying
meta-analysis. • Decreased length
Pędziwiatr M2017 [5] of hospital stay
Systematic review and • Number of lymph • Less complication,
meta-analysis of robotic nodes harvested; • Margin positivity,
versus open • Operation time; • Wound infection,
pancreaticoduodenectomy. • Reoperation rate; • Hospital stay.
Peng L 2017 [6] • Delayed gastric
emptying,
• Bile leakage,
• Pancreatic fistula and
mortality.
Robotic Assisted Pancreaticoduodenectomy 127
Table EN1 (continued)
Disadvantages
robotic/
Advantages robotic/ minimally
Study, author [first], year No difference minimally invasive invasive
Systematic review and • Postoperative • Reduced hospital
updated network meta- mortality length-of-stay,
analysis comparing open, • Postoperative • Estimated blood
laparoscopic, and robotic complications loss,
pancreaticoduodenectomy. number of retrieved • Pulmonary &
Aiolfi A 2020 [7] lymph nodes overall
• R0 resection rates. complications
• Postoperative
bleeding
• hospital
readmission.
Minimally Invasive The TLPD technique • Blood loss Operative time
Pancreaticoduodenectomy: was often the worst • Wound infection and
What is the Best “Choice”? approach especially for • Delayed gastric postoperative
A Systematic Review and overall and major emptying bleeding,
Network Meta-analysis of complications, • Length of hospital
Non-randomized postoperative bleeding stay
Comparative Studies. and biliary leak • Harvested lymph
Ricci C 2018 [8] nodes
• Postoperative
morbidity
Safety and efficacy of • Lymph node • Blood loss Operation time
robot-assisted versus open clearance • Infection rate
pancreaticoduodenectomy: • Postoperative • Reoperation rate,
a meta-analysis of multiple • Pancreatic fistula bile • Overall
worldwide centers. leakage complications
Zhang W 2020 [9] • delayed gastric • Clinical
emptying postoperative
• 90-day mortality pancreatic fistula
• Severe complications
Robotic • Less blood loss Operative time
pancreaticoduodenectomy • Less incidence of
provides better resection margin
histopathological outcomes involvement.
as compared to its open • Higher number of
counterpart: a harvested nodes
meta-analysis
Da Dong X 2021 [10]
Safety and efficacy for • Lymph node yield • Less blood loss Longer
robot-assisted versus open • Rate of pancreatic • Less wound operative time
pancreaticoduodenectomy fistula infection
and distal pancreatectomy: • Delayed gastric • Lower positive
A systematic review and emptying margin rate
meta-analysis. • Reoperation, • Lower overall
Zhao W 2018 [11] • Length of hospital complications
stay • Faster
• Mortality between postoperative
the two groups. off-bed activity
128 B. B. Agarwal and N. Dhamija
Increased operative time was the most consistent drawback of robotic as com-
pared to open pancreaticoduodenectomy, whereas the prominent advantages of
robotic approach were less intraoperative blood loss, lower postoperative complica-
tions and wound infection rate, earlier hospital discharge rates and a possible
improved oncological outcome reflected by increased number of harvested nodes
along with a lower margin positivity noted in some of the studies [1–11].
Mesopancreatic resection and approach to superior mesenteric artery: A
newly emerging concept in pancreaticoduodenectomy is the concept of mesopan-
creas [level 3] dissection a term akin to mesorectum and mesocolon in colorectal
cancers. It is a fascial fusion plane embryologically formed during development of
pancreas. It lies posterior to the pancreas and is comprised of pancreaticoduodenal
vessels, lymphatics, nerve plexus and loose areolar tissue. Approach to the area is
complex due to the complicated anatomy. Reports are emerging on mesopancreatic
resection in robotic pancreaticoduodenectomy. A study comparing meso pancreatic
resection in open and robotic pancreaticoduodenectomy concluded that mesopan-
creas/level 3 dissections in robotic pancreaticoduodenectomy had less blood loss,
no delayed gastric emptying, and lower chyle leakage. The lymph node yield was
higher for mesopancreas/level 3 dissection compared with mesopancreas levels 1
and 2 dissections in the robotic pancreaticoduodenectomy groups. Postoperative
complications and mortality were not different due to the additional mesopancreatic
excision. Complications, including postoperative pancreatic fistula, delayed gastric
emptying, postpancreatectomy hemorrhage, chyle leakage, bile leakage, or wound
infection were similar in level 2 vs level 3 dissections of robotic pancreatectomy
[12]. Various surgical approaches have been described for approaching the superior
mesenteric artery during pancreaticoduodenectomy, viz: anterior, posterior, left and
right approach.
Reconstruction after pancreaticoduodenectomy and Pancreaticoeneteric
anastomosis: The mode of reconstruction of pancreatico-enteric anastomosis has
been a context of debate with some authors preferring a pancreatico-jejunostomy
and others opting for a pancreaticogastrostomy. Occlusion of pancreatic duct with-
out anastomosis a method proposed to circumvent the formation of pancreatic fis-
tula has a high morbidity with increased incidence of diabetes noted in such patients
and thus not recommended [13]. In a recent metaanalysis comparing pancreatico-
gastrostomy with pancreatico-jejunostomy it was noted that the pancreaticogastros-
tomy group had significantly lower incidence in rates of postoperative pancreatic
fistulas, intra-abdominal abscesses and length of hospital stay. However, rates of
biliary fistula, mortality, morbidity, delayed gastric emptying, reoperation, and
bleeding was similar in the two groups [14].
One of the inherent deterrents in minimally invasive gastrointestinal/hepatopan-
creaticobiliary surgery is the construction of an intracorporeal anastomosis. Robotic
anastomotic technique has an obvious advantage over laparoscopic approach due to
better articulation and higher degree of freedom of instrument movement. Among
different meta-analysis, one such report comparing robotic laparoscopic and open
anastomosis in an array of surgical procedures concludes that robotic, laparoscopic
Robotic Assisted Pancreaticoduodenectomy 129
and open techniques of anastomosis yielded similar rates of leak and stricture forma-
tion [15]. Published meta-analysis on robotic pancreaticoduodenectomy also exhibit
a consistent equivalent or lower rate of pancreatic or biliary fistula [Table EN1].
References
1. Gagner M, Pomp A. Laparoscopic pylorus-preserving pancreaticoduodenectomy. Surg
Endosc. 1994;8(5):408–10.
2. Gagner M, Pomp A. Laparoscopic pancreatic resection: is it worthwhile? J Gastrointest Surg.
1997;1:20–6.
3. Chalikonda S, Aguilar-Saavedra JR, Walsh RM. Laparoscopic robotic-assisted pancreaticoduo-
denectomy: a case-matched comparison with open resection. Surg Endosc. 2012;26:2397–402.
4. Buchs NC, Addeo P, Bianco FM, et al. Robotic versus open pancreaticoduodenectomy: a com-
parative study at a single institution. World J Surg. 2011;35:2739–46.
5. Zeh HJ, Zureikat AH, Secrest A, et al. Outcomes after robot-assisted pancreaticoduodenec-
tomy for periampullary lesions. Ann Surg Oncol. 2012;19:864–70.
6. Palanivelu C, Jani K, Senthilnathan P, et al. Laparoscopic pancreaticoduodenectomy: tech-
nique and outcomes. J Am Coll Surg. 2007;205:222–30.
7. Kendrick ML, Cusati D. Total laparoscopic pancreaticoduodenectomy: feasibility and out-
come in an early experience. Arch Surg. 2010;145:19–23.
8. Zureikat AH, Beane JD, Zenati MS, et al. 500 minimally invasive robotic pancreatoduodenec-
tomies: one decade of optimizing performance. Ann Surg. 2021;273(5):966–72.
9. Robotic Versus Open Pancreaticoduodenectomy for Pancreatic and Periampullary
Tumors[PORTAL]. ClinicalTrials.gov Identifier: NCT04400357.
10. Girgis MD, Zenati MS, King JC, et al. Oncologic outcomes after robotic pancreatic resections
are not inferior to open surgery [published online ahead of print, 2019 Oct 28]. Ann Surg.
2019; https://doi.org/10.1097/SLA.0000000000003615.
11. Beane JD, Zenati M, Hamad A, et al. Robotic pancreatoduodenectomy with vascular resection:
Outcomes and learning curve. Surgery. 2019;166(1):8–14.
12. Kim JH, Gonzalez-Heredia R, Daskalaki D, et al. Totally replaced right hepatic artery in pan-
creaticoduodenectomy: Is this anatomical condition a contraindication to minimally invasive
surgery? HPB. 2016;18(7):580–5.
13. Girgis MD, Zenati MS, Steve J, et al. Robotic approach mitigates perioperative morbidity in
obese patients following pancreaticoduodenectomy. HPB. 2017;19(2):93–8.
14. Asbun HJ, Moekotte AL, Vissers FL, et al. The Miami international evidence-based guidelines
on minimally invasive pancreas resection. Ann Surg. 2020;271:1–14.
15. Boone BA, Zenati M, Hogg ME, et al. Assessment of quality outcomes for robotic pancreati-
coduodenectomy. JAMA Surg. 2015;150(5):416–22.
16. Adam MA, Thomas S, Youngwirth L, et al. Defining a hospital volume threshold for minimally
invasive pancreaticoduodenectomy in the United States. JAMA Surg. 2017;152(4):336–42.
17. Takahashi C, Shridhar R, Huston J, et al. Outcomes associated with robotic approach to pan-
creatic resections. J Gastrointest Oncol. 2018;9(5):936–41.
18. Chen S, Chen J-Z, Zhan Q, et al. Robot-assisted laparoscopic versus open pancre-
aticoduodenectomy: A prospective, matched, mid-term follow-up study. Surg Endosc.
2015;29(12):3698–711.
19. Napoli N, Kauffmann EF, Palmeri M, et al. The learning curve in robotic pancreaticoduode-
nectomy. Dig Surg. 2016;33(4):299–307.
20. Zhang T, Zhao Z-M, Gao Y-X, et al. The learning curve for a surgeon in robot-assisted lapa-
roscopic pancreaticoduodenectomy: a retrospective study in a high-volume pancreatic center.
Surg Endosc. 2019;33(9):2927–33.
21. Zhang T, Zhao ZM, Gao YX, Lau WY, Liu R. The learning curve for a surgeon in robot-
assisted laparoscopic pancreaticoduodenectomy: a retrospective study in a high-volume pan-
creatic center. Surg Endosc. 2019;33(9):2927–33. https://doi.org/10.1007/s00464-018-6595-0.
Epub 2018 Nov 27. PMID: 30483970.
22. Torphy RJ, Friedman C, Halpern A, et al. Comparing short-term and oncologic outcomes of
minimally invasive versus open pancreaticoduodenectomy across low and high volume cen-
ters. Ann Surg. 2019;270(6):1147–55.
132 B. B. Agarwal and N. Dhamija
23. Lin R, Lin X, Pan M, Lu F, Yang Y, Wang C, Fang H, Chen Y, Huang H. Perioperative out-
comes of robotic pancreaticoduodenectomy: a single surgeon’s experience with 55 consecutive
cases. Gland Surg. 2021;10(1):122–9. https://doi.org/10.21037/gs-20-552. PMID: 33633969;
PMCID: PMC7882343
24. Baimas-George M, Watson M, Murphy KJ, et al. Robotic pancreaticoduodenectomy may
offer improved oncologic outcomes over open surgery: a propensity-matched single-institu-
tion study. Surg Endosc. 2020;34:3644–9.
Laparoscopic Surgery for Rectal
Prolapse
Introduction
Rectal prolapse is a disorder where the entire thickness of rectal wall protrudes out
through the anal sphincter. It is one of the earliest surgical problems recognized by
medical fraternity [1, 2]. However, many controversies still exist regarding the etiol-
ogy and management of this condition [3].
Rectal prolapse are often associated with a gamut of anatomic abnormalities like
diastasis of levator ani, abnormally deep cul-de-sac, redundant sigmoid colon, patu-
lous anal sphincter or loss of rectal sacral attachments [4]. Rectal intussusception or
solitary rectal ulcer have been hypothesized to be associated with rectal prolapse but
have not been clearly proven [5, 6].
Rectal prolapse is overall a rare occurrence, being higher in females and elderly—
women aged 50 years or above who suffer six times more than men [4]. Interestingly,
the age of incidence for the relatively fewer men with prolapse is generally below
40 years [7]. Autism and developmental delay syndromes have been reported to be
associated with rectal prolapse [8].
Patient Selection
Patients with rectal prolapse may present with issues related to the prolapse itself or
due to associated incontinence. Prolapse may be seen either with defecation or in a
more advanced form, with slight exertion such as coughing or sneezing. Early symp-
toms of prolapse include bowel dysregulation, discomfort, sensation of incomplete
evacuation and tenesmus [9]. It can be a very disabling and in its advanced stage
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 133
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_6
134 M. R. Sahoo et al.
Fecal incontinence with rectal prolapse has been reported in 50–75% of patients
[15]. Repeated stretch and trauma to the area and stimulation of the recto-anal
inhibitory reflex damages the anal sphincter [16]. De-nervation atrophy of the exter-
nal anal sphincter possibly because of pudendal neuropathy has also been demon-
strated [17].
Majority of the patients with a continence disturbance experience improvement
once the prolapse is corrected [18, 19]. Pre-existing faecal incontinence due to any
condition other than prolapse, should be evaluated [20]. If testing reveals decreased
pudendal nerve terminal motor latencies, this may have postoperative prognostic
significance, patients with evidence of nerve damage appear to have a higher rate of
incontinence after surgical correction of the prolapse, although more studies are
necessary to confirm the finding [21, 22].
The basic goals to correct rectal prolapse are threefold.
Laparoscopic Surgery for Rectal Prolapse 135
prolapse in the elderly have shown improved benefits and decreased morbidity and
mortality [35, 36]. Laparoscopic surgery for rectal prolapse, has thus made surgeons
to reconsider more durable abdominal procedures in elderly patients [37, 38].
Laparoscopic surgery has proven to be safe in the elderly and is associated with
decreased ileus, less wound infections and a decreased length of post-operative stay
[39, 40]. Acceptable morbidity has been reported in elderly patients who underwent
a laparoscopic mesh rectopexy [41, 42]. Robotic rectopexy has also been shown to
be a safe and effective option in patients older than 75 years [43]. An increasing
number of elderly patients are being considered for minimally invasive approaches
with acceptable success rates [44, 45].
Procedure
Patient position and port placement: The patient should be placed in the dorsal
lithotomy position. Port position varies but in general camera is at the umbilicus
(Fig. 1). Site for exteriorization of bowel for resection if required should be marked
at time of surgery.
Vascular division: After trocar insertion, patient is generally placed in steep
Trendelenburg position particularly to move the small bowel out of the field.
Dissection is usually done from medial to lateral direction. The vascular division is
done above the level of superior haemorrhoidal vessels at the sacral promontory.
The superior rectal artery is spared because preserving the blood supply to upper
part of rectal stump will minimize the risk of an anastomotic leak. Care should be
taken to preserve the hypogastric nerves that course over the sacral promontory.
Important structures—ureters, gonadal vessels and iliac vessels are safeguarded
[48] (Fig. 2).
Mobilization of rectum: The dissection of the rectum is carried out exactly as in
the ‘abdominal phase of the Miles’ abdomino perineal resection technique except
preserving the blood supply to the rectum and preserving the lateral stalks intact.
The rectum is completely mobilized down to the levator muscles and the freed rec-
tum is drawn up into the abdomen, which makes the lateral stalks prominent. The
stalks are then sutured to the periosteum of the sacrum to hold the organ firmly in
this elevated position. Care must be taken not to narrow the bowel by placement of
sutures which may lead to obstruction [49] (Figs. 3 and 4).
Segmental resection of sigmoid with end-to-end anastomoses: The peri-
toneum lateral to the descending colon is incised upto the splenic flexure and
Laparoscopic Surgery for Rectal Prolapse 137
5 mm
12 mm
Camera 5 mm
port
Possible
extraction
site
the entire left colon is mobilized from the retroperitoneal structures. The redun-
dant colon is resected so that anastomosis is established without tension.
Suturing of endopelvic fascia anteriorly to rectum is done to obliterate cul-de-
sac (Figs. 5–7).
138 M. R. Sahoo et al.
a b
Fig. 3 (a) Lateral dissection and mobilization of rectum; (b) Posterior dissection down to the leva-
tor plate (Image Courtesy: Dr Deborshi Sharma)
Fig. 4 Fixation of
mesorectum to sacral
promontory in resection
rectopexy
Descending
Colon
Redundant
Sigmoid
Rectum Colon
Laparoscopic Surgery for Rectal Prolapse 139
Fig. 7 Colorectal
anastomosis after resection
rectopexy
Advantages May reduce constipation in those who report pre-operatively [50, 51]
and prevent new onset of constipation. New prolapse recurrence rates of <2% and
complication rates of 4% are acceptable which greatly improves functional outcome
with minimal increase in morbidity [52, 53].
Types
1. Laparoscopic Suture rectopexy
2. Laparoscopic mesh rectopexy
a. Laparoscopic anterior mesh rectopexy (Ripstein)
b. Laparoscopic posterior mesh rectopexy (Wells)
c. Laparoscopic lateral mesh rectopexy (Orr -Loygue)
d. Laparoscopic ventral mesh rectopexy (D’Hoore)
Procedure The surgical steps are same as laparoscopic resection rectopexy, except
that sigmoid colon is not resected. Rectum is mobilized till the level of levator ani
muscles, following which rectopexy is performed with sutures or mesh [54].
Use of a mesh during rectopexy is very commonly done with the idea that the for-
eign material will induce adhesion and create fibrosis more than suture rectopexy.
Meshes can be placed anteriorly, posteriorly, laterally or encircling the rectum, all
of which have their advantages and disadvantages.
a b
Fig. 11 (a & b) Mesh edges sutured to peri-rectal tissue bilaterally (Image Courtesy—Dr
Deborshi Sharma)
142 M. R. Sahoo et al.
Described originally in 2004, with dissection limited only to the anterior aspect of
rectum, preserving the lateral ligaments while the rectovaginal septum is dissected
up to the pelvic floor. The procedure preserves the hypogastric and parasympathetic
nerves while it obviates mobilization of mesorectum.
Indications: External rectal prolapse (age should not preclude selection), high
grade internal rectal prolapsed with significant symptoms of obstruction-defecation
or fecal incontinence that have failed conservative measures or is associated with
complex rectocoele or enterocoele.
Laparoscopic Surgery for Rectal Prolapse 143
Fig. 14 Sagittal section of abdomen & pelvis after laparoscopic ventral rectopexy
stretched up to the sacral promontory along the right lateral aspect of rectum. The
mesh is fixed on the promontory and is sutured to the anterior borders of the rectum
in two parallel rows of interrupted non-absorbable material. The mesh is ultimately
placed obliquely angled from the midline distally to the right sacral promontory to
which it is secured. The vaginal vault (or cervix) can be fixed to the mesh without
tension by two additional sutures [66] (Fig. 13).
The mesh is covered by suturing the edges of peritoneum which obliterates the
potential space. In female, bites can be taken through different layers including the
posterior vaginal wall, peritoneum, mesh and anterior rectal wall. This reconstitutes
the recto-vaginal septum as a posterior colporrhaphy is performed and a shallow
neo-pouch of Douglas is forms. This continues caudo-cranially until at the site of
first incision over the promontory where the peritoneum is closed (Fig. 14).
Advantages: Morbidity is less along with reduced length of stay after laparoscopy
even in the elderly [67]. Ventral mobilization prevents bleeding from pre-sacral
venous plexus and long term constipation by retaining the autonomic nerve supply
to the rectum [68]. Re-inforcement of rectovaginal septum and treatment of genital
prolapse, rectocoele and enterocoele, as posterior colporrhaphy and vaginal sacro-
colpopexy may be performed at the same time [69]. Notable is the advantage of
performing anterior colporrhaphy along with vaginal sacro-colpopexy with another
mesh, placed on top of first. No mortality has been reported with this procedure and
recurrence ranges from 0 to 8%. Overall improvement of constipation is also seen
which can be due to preservation of autonomic nerves and prevention of recto-anal
intussusception.
Mesh selection: The mesh used can be either biological or synthetic. The overall
consensus on ventral rectopexy is to use of titanium coated lightweight polypropyl-
ene mesh. Standard polypropylene or polyglecaprone meshes may stretch and can
result in recurrence. Polyester meshes are associated with increased risk of
complication.
Robotic rectal surgery has all the advantages related to access in deep pelvic
surgery.
Today we don’t have enough evidence to suggest or argue for posterior rectal pro-
lapse repairs in comparison to anterior rectal prolapse repairs. Retrospective com-
parison of two single center studies performed in 70 and 40 cases comparing ventral
rectopexy and posterior rectopexy have demonstrated similar recurrence rates [81].
Retrospective analyses of laparoscopic resection rectopexy (LRR) with laparo-
scopic ventral rectopexy (LVR) have shown varied results [82, 83]. Constipation
and incontinence were reduced in both cohorts but more complications were seen
after LRR than LVR [84]. Rigorous clinical trials comparing posterior and ventral
rectopexy are at present absent [85, 86].
Current Scenario
longer for RR but RR is associated with significantly lower blood loss, fewer post-
operative complications and has a shorter hospital course [43].
As far as cost is concerned, robotic surgery lags behind laparoscopic surgery
bearing high costs. The experience of surgical team and the learning also has a bear-
ing on the results of robotic colorectal surgeries, as they influence the operative time
and outcomes.
Ventral rectopexy might be particularly suited for robotic surgery. Robotic recto-
pexy has clear advantage in visualization of the deep pelvis and ease of suturing and
dissection along with placement if mesh in the rectovaginal septum [43, 87].
Although modern surgery is progressing towards robotic operations, the debate as
to which of two- robotic rectopexy (RR) or laparoscopic rectopexy (LR) is better,
continues.
Conclusion
Editor’s Note1
Rectal prolapse is highly associated with multiparity but 1/3rd are nulliparous.
Etiology is often undetermined. F:M = 10:1 and peak in 7th decade [1].
Surgery is the definitive treatment and its goals can be achieved with fixation of
the rectum to sacrum and/or resesction or plication of the redundant bowel.
Laparoscopic procedures include [2,3]:
NOTES-TEM Approach
Trans anal endoscopic microsurgery procedures (TEM) have also been investigated
as a modality to treat internal rectal prolapse termed as EndoRectal ProctoPexy
(ERPP), better known as “internal Delorme” [4,5].
It involves
a. Mucosal resection,
b. Plication of the muscle layer and
c. Resuturing of the mucosal defect under endoscopic guidance.
References: Main chapter references are included after the “References Editor’s Note” section.
1
Laparoscopic Surgery for Rectal Prolapse 149
References
1. Ripstein CB, Lanter B. Etiology and surgical therapy of massive prolapse of the rectum. Ann
Surg. 1963;157:259–64.
2. Küpfer CA, Goligher JC. One hundred consecutive cases of complete prolapse of the rectum
treated by operation. Br J Surg. 1970;57:482–7.
3. Madoff RD, Mellgren A. One hundred years of rectal prolapse surgery. Dis Colon Rectum.
1999;42:441–50.
4. Sabiston DC, Townsend CM, editors. Sabiston textbook of surgery: the biological basis of
modern surgical practice. Philadelphia, PA: Elsevier Saunders; 2012.
5. Sun WM, Read NW, Donnelly TC, Bannister JJ, Shorthouse AJ. A common pathophysiology
for full thickness rectal prolapse, anterior mucosal prolapse and solitary rectal ulcer. Br J Surg.
1989;76:290–5.
6. Felt-Bersma RJ, Tiersma ES, Stella MT, Cuesta MA. Rectal prolapse, rectal intussuscep-
tion, rectocele, solitary rectal ulcer syndrome, and enterocele. Gastroenterol Clin North Am.
2008;37:645–68. ix
7. Gourgiotis S, Baratsis S. Rectal prolapse. Int J Colorectal Dis. 2007;22:231–43.
8. Marceau C, Parc Y, Debroux E, Tiret E, Parc R. Complete rectal prolapse in young patients:
psychiatric disease a risk factor of poor outcome. Colorectal Dis. 2005;7:360–5.
9. Kairaluoma MV, Kellokumpu IH. Epidemiologic aspects of complete rectal prolapse. Scand J
Surg. 2005;94:207–10.
10. Yakut M, Kaymakçioğlu N, Simşek A, Tan A, Sen D. Surgical treatment of rectal prolapse: a
retrospective analysis of 94 cases. Int Surg. 1998;83:53–5.
11. Paquette IM, Varma M, Ternent C, et al. The American Society of colon and rectal surgeons’
clinical practice guideline for the evaluation and management of constipation. Dis Colon
Rectum. 2016;59:479–92.
12. Mollen RM, Kuijpers JH, van Hoek F. Effects of rectal mobilization and lateral ligaments divi-
sion on colonic and anorectal function. Dis Colon Rectum. 2000;43:1283–7.
13. Speakman CT, Madden MV, Nicholls RJ, Kamm MA. Lateral ligament division during recto-
pexy causes constipation but prevents recurrence: results of a prospective randomized study.
Br J Surg. 1991;78:1431–3.
14. Deen KI, Grant E, Billingham C, Keighley MR. Abdominal resection rectopexy with pelvic
floor repair versus perineal rectosigmoidectomy and pelvic floor repair for full-thickness rectal
prolapse. Br J Surg. 1994;81:302–4.
15. Wallenhorst T, Bouguen G, Brochard C, et al. Long-term impact of full-thickness rectal pro-
lapse treatment on fecal incontinence. Surgery. 2015;158:104–11.
16. Brodén B, Snellman B. Procidentia of the rectum studied with cineradiography: a contribution
to the discussion of causative mechanism. Dis Colon Rectum. 1968;11:330–47.
17. Collinson R, Cunningham C, D’Costa H, Lindsey I. Rectal intussusception and unexplained
faecal incontinence: findings of a proctographic study. Colorectal Dis. 2009;11:77–83.
18. Cunin D, Siproudhis L, Desfourneaux V, et al. No surgery for full-thickness rectal prolapse:
what happens with continence? World J Surg. 2013;
19. Scaglia M, Fasth S, Hallgren T, Nordgren S, Oresland T, Hultén L. Abdominal rectopexy for
rectal prolapse: influence of surgical technique on functional outcome. Dis Colon Rectum.
1994;37:805–13.
20. Glasgow SC, Birnbaum EH, Kodner IJ, Fleshman JW, Dietz DW. Preoperative anal manom-
etry predicts continence after perinealproctectomy for rectal prolapse. Dis Colon Rectum.
2006;49:1052–8.
21. Snooks SJ, Henry MM, Swash M. Anorectal incontinence and rectal prolapse: differen-
tial assessment of the innervation to puborectalis and external anal sphincter muscles. Gut.
1985;26:470–6.
152 M. R. Sahoo et al.
22. Paquette IM, Varma MG, Kaiser AM, Steele SR, Rafferty JF. The American Society of Colon
and Rectal Surgeons’ clinical practice guideline for the treatment of fecal incontinence. Dis
Colon Rectum. 2015;58:623–36.
23. Senagore AJ. Management of rectal prolapse: the role of laparoscopic approaches. Semin
Laparosc Surg. 2003;10:197–202.
24. Brown AJ, Anderson JH, McKee RF, Finlay IG. Strategy for selection of type of operation for
rectal prolapse based on clinical criteria. Dis Colon Rectum. 2004;47:103–7.
25. Madbouly KM, Senagore AJ, Delaney CP, Duepree HJ, Brady KM, Fazio VW. Clinically
based management of rectal prolapse. Surg Endosc. 2003;17:99–103.
26. Bordeianou L, Hicks CW, Kaiser AM, Alavi K, Sudan R, Wise PE. Rectal prolapse: an over-
view of clinical features, diagnosis, and patient-specific management strategies. J Gastrointest
Surg. 2014;18:1059–69.
27. Varma M, Rafferty J, Buie WD. Standards Practice Task Force of American Society of Colon
and Rectal Surgeons. Practice parameters for the management of rectal prolapse. Dis Colon
Rectum. 2011;54:1339–46.
28. Sagar PM, Thekkinkattil DK, Heath RM, Woodfield J, Gonsalves S, Landon CR. Feasibility
and functional outcome of laparoscopic sacrocolporectopexy for combined vaginal and rectal
prolapse. Dis Colon Rectum. 2008;51:1414–20.
29. Watts JD, Rothenberger DA, Buls JG, Goldberg SM, Nivatvongs S. The management of proci-
dentia: 30 years’ experience. Dis Colon Rectum. 1985;28:96–102.
30. Steele SR, et al., editors. The ASCRS textbook of colon and rectal surgery. 3rd ed. New York:
Springer; 2016.
31. Mellgren A, Johansson C, Dolk A, et al. Enterocele demonstrated by defaecography is associ-
ated with other pelvic floor disorders. Int J Colorectal Dis. 1994;9:121–4.
32. Schultz IMA, Nilsson BY, Dolk A, Holmstrom B. Preoperative electrophysiologic assessment
cannot predict continence after rectopexy. Dis Colon Rectum. 1998:1392–8.
33. Johansen OB, Wexner SD, Daniel N, Nogueras JJ, Jagelman DG. Perinealrectosigmoidectomy
in the elderly. Dis Colon Rectum. 1993;36:767–72.
34. Pescatori M, Zbar AP. Tailored surgery for internal and external rectal prolapse: functional
results of 268 patients operated upon by a single surgeon over a 21-year period. Colorectal Dis.
2009;11:410–9.
35. Kariv Y, Delaney CP, Casillas S, et al. Long-term outcome after laparoscopic and open surgery
for rectal prolapse: a case-control study. Surg Endosc. 2006;20:35–42.
36. Purkayastha S, Tekkis P, Athanasiou T, et al. A comparison of open vs. laparoscopic
abdominal rectopexy for full thickness rectal prolapse: a meta-analysis. Dis Colon Rectum.
2005;48:1930–40.
37. Fang SH, Cromwell JW, Wilkins KB, et al. Is the abdominal repair of rectal prolapse safer
than perineal repair in the highest risk patients? An NSQIP analysis. Dis Colon Rectum.
2012;55:1167–72.
38. Wijffels N, Cunningham C, Dixon A, Greenslade G, Lindsey I. Laparoscopic ventral recto-
pexy for external rectal prolapse is safe and effective in the elderly. Does this make perineal
procedures obsolete? Colorectal Dis. 2011;13(5):561–6.
39. Byrne CM, Smith SR, Solomon MJ, Young JM, Eyers AA, Young CJ. Long-term functional
outcomes after laparoscopic and open rectopexy for the treatment of rectal prolapse. Dis Colon
Rectum. 2008;51:1597–604.
40. Magruder JT, Efron JE, Wick EC, Gearhart SL. Laparoscopic rectopexy for rectal prolapse to
reduce surgical-site infections and length of stay. World J Surg. 2013;37(5):1110–4.
41. Boccasanta P, Venturi M, Reitano MC, et al. Laparotomic vs. laparoscopic rectopexy in com-
plete rectal prolapse. Dig Surg. 1999;16:415–9.
42. Solomon MJ, Young CJ, Eyers AA, Roberts RA. Randomized clinical trial of laparoscopic
versus open abdominal rectopexy for rectal prolapse. Br J Surg. 2002;89:35–9.
43. Germain A, Perrenot C, Scherrer ML, Ayav C, Brunaud L, Ayav A, et al. Long-term outcome
of robotic-assisted laparoscopic rectopexy for full-thickness rectal prolapse in elderly patients.
Colorectal Dis. 2014;16(3):198–202.
Laparoscopic Surgery for Rectal Prolapse 153
44. Madiba TE, Baig MK, Wexner SD. Surgical management of rectal prolapse. Arch Surg.
2005;140:63–73.
45. Aitola PT, Hiltunen KM, Matikainen MJ. Functional results of operative treatment of rectal
prolapse over an 11-year period: emphasis on transabdominal approach. Dis Colon Rectum.
1999;42:655–60.
46. Frykman HM. Abdominal proctopexy and primary sigmoid resection for rectal procidentia.
Am J Surg. 1955;90:780–9.
47. Frykman HM, Goldberg SM. The surgical treatment of rectal procidentia. Surg Gynecol
Obstet. 1969;129:1225–30.
48. Gordon PH, Nivatvongs S. Principles and practice of surgery for the colon, rectum and anus.
3rd ed. New York: Informa Healthcare; 2007.
49. Corman ML, et al., editors. Corman’s colon and rectal surgery. 6th ed. Philadelphia: Wolters
Kluwer; 2013.
50. Solla JA, Rothenberger DA, Goldberg SM. Colonic resection in the treatment of complete
rectal prolapse. Neth J Surg. 1989;41:132–5.
51. Luukkonen P, Mikkonen U, Järvinen H. Abdominal rectopexy with sigmoidectomy vs.
rectopexy alone for rectal prolapse: a prospective, randomized study. Int J Colorectal Dis.
1992;7:219–22.
52. Sayfan J, Pinho M, Alexander-Williams J, Keighley MR. Sutured posterior abdominal rec-
topexy with sigmoidectomy compared with Marlexrectopexy for rectal prolapse. Br J Surg.
1990;77:143–5.
53. McKee RF, Lauder JC, Poon FW, Aitchison MA, Finlay IG. A prospective randomized study
of abdominal rectopexy with and without sigmoidectomy in rectal prolapse. Surg Gynecol
Obstet. 1992;174:145–8.
54. Hsu A, Brand MI, Saclarides TJ. Laparoscopic rectopexy without resection: a worthwhile
treatment for rectal prolapse in patients without prior constipation. Am Surg. 2007;73:858–61.
55. Briel JW, Schouten WR, Boerma MO. Long-term results of suture rectopexy in patients
with fecal incontinence associated with incomplete rectal prolapse. Dis Colon Rectum.
1997;40:1228–32.
56. Cutait D. Sacro-promontory fixation of the rectum for complete rectal prolapse. Proc R Soc
Med. 1959;52:105.
57. Carter AE. Rectosacral suture fixation for complete rectal prolapse in the elderly, the frail and
the demented. Br J Surg. 1983;70:522–3.
58. Coleman M, Cecil T. Laparoscopic colorectal surgery-the lapco manual. Boca Raton, FL: CRC
Press; 2017.
59. Loygue J, Nordlinger B, Cunci O, Malafosse M, Huguet C, Parc R. Rectopexy to the promon-
tory for the treatment of rectal prolapse: report of 257 cases. Dis Colon Rectum. 1984;27:356–9.
60. Graf W, Karlbom U, Påhlman L, Nilsson S, Ejerblad S. Functional results after abdominal
suture rectopexy for rectal prolapse or intussusception. Eur J Surg. 1996;162:905–11.
61. Khanna AK, Misra MK, Kumar K. Simplified sutured sacral rectopexy for complete rectal
prolapse in adults. Eur J Surg. 1996;162:143–6.
62. Schultz I, Mellgren A, Dolk A, Johansson C, Holmström B. Long-term results and functional
outcome after Ripsteinrectopexy. Dis Colon Rectum. 2000;43:35–43.
63. Novell JR, Osborne MJ, Winslet MC, Lewis AA. Prospective randomized trial of Ivalon
sponge versus sutured rectopexy for full-thickness rectal prolapse. Br J Surg. 1994;81:904–6.
64. Wells C. New operation for rectal prolapse. Proc R Soc Med. 1959;52:602–3.
65. Dulucq JL, Wintringer P, Mahajna A. Clinical and functional outcome of laparoscopic pos-
terior rectopexy (Wells) for fullthickness rectal prolapse: a prospective study. Surg Endosc.
2007;21:2226–30.
66. Wexner SD, Fleshman JW, editors. Master techniques in surgery-colon and rectal surgery:
abdominal operations. 2nd ed. China: Wolters Kluwer; 2019.
67. Samaranayake CB, Luo C, Plank AW, Merrie AE, Plank LD, Bissett IP. Systematic review on
ventral rectopexy for rectal prolapse and intussusception. Colorectal Dis. 2010;12:504–12.
154 M. R. Sahoo et al.
68. Boons P, Collinson R, Cunningham C, Lindsey I. Laparoscopic ventral rectopexy for exter-
nal rectal prolapse improves constipation and avoids de novo constipation. Colorectal Dis.
2010;12:526–32.
69. D’Hoore A, Penninckx F. Laparoscopic ventral recto(colpo)pexy for rectal prolapse: surgical
technique and outcome for 109 patients. Surg Endosc. 2006;20:1919–23.
70. D’Hoore A, Cadoni R, Penninckx F. Long-term outcome of laparoscopic ventral rectopexy for
total rectal prolapse. Br J Surg. 2004;91:1500–5.
71. van Iersel JJ, Paulides TJ, Verheijen PM, Lumley JW, Broeders IA, Consten EC. Current status
of laparoscopic and robotic ventral mesh rectopexy for external and internal rectal prolapse.
World J Gastroenterol. 2016;22:4977–87.
72. Mäkelä-Kaikkonen J, Rautio T, Pääkkö E, Biancari F, Ohtonen P, Mäkelä J. Robot-assisted
vs laparoscopic ventral rectopexy for external or internal rectal prolapse and enterocele: a
randomized controlled trial. Colorectal Dis. 2016;18:1010–5.
73. Bordeianou L, et al, eds. Clinical practice guidelines for the treatment of rectal prolapse.
Diseases Colon Rectum. 2017;60:11
74. Bachoo P, Brazzelli M, Grant A. Surgery for complete rectal prolapse in adults. Cochrane
Database Syst Rev. 2000;2:CD001758.
75. Kim DS, Tsang CB, Wong WD, Lowry AC, Goldberg SM, Madoff RD. Complete rectal pro-
lapse: evolution of management and results. Dis Colon Rectum. 1999;42:460–6.
76. Riansuwan W, Hull TL, Bast J, Hammel JP, Church JM. Comparison of perineal operations
with abdominal operations for full-thickness rectal prolapse. World J Surg. 2010;34:1116–22.
77. Senapati A, Gray RG, Middleton LJ, et al. PROSPER Collaborative Group. PROSPER: a ran-
domised comparison of surgical treatments for rectal prolapse. Colorectal Dis. 2013;15:858–68.
78. Gunner CK, Senapati A, Northover JM, Brown SR. Life after PROSPER: what do people do
for external rectal prolapse? Colorectal Dis. 2016;18:811–4.
79. Azimuddin K, Khubchandani IT, Rosen L, Stasik JJ, Riether RD, Reed JF 3rd. Rectal pro-
lapse: a search for the “best” operation. Am Surg. 2001;67:622–7.
80. Hrabe J, Gurland B. Optimizing treatment for rectal prolapse. Clin Colon Rectal Surg.
2016;29:271–6.
81. DiGiuro G, Ignjatovic D, Brogger J, Bergamaschi R, Rectal Prolapse Recurrence Study Group.
How accurate are published recurrence rates after rectal prolapse surgery? A meta-analysis of
individual patient data. Am J Surg. 2006;191:773–8.
82. Fu CW, Stevenson AR. Risk factors for recurrence after laparoscopic ventral rectopexy. Dis
Colon Rectum. 2017;60:178–86.
83. Badrek-Al Amoudi AH, Greenslade GL, Dixon AR. How to deal with complications after
laparoscopic ventral mesh rectopexy: lessons learnt from a tertiary referral centre. Colorectal
Dis. 2013;15(6):707–12.
84. FormijneJonkers HA, Maya A, Draaisma WA, Bemelman WA, Broeders IA, Consten EC, et al.
Laparoscopic resection rectopexy versus laparoscopic ventral rectopexy for complete rectal
prolapse. Technol Coloproctol. 2014;18(7):641–6.
85. Fengler SA, Pearl RK, Prasad ML, et al. Management of recurrent rectal prolapse. Dis Colon
Rectum. 1997;40:832–4.
86. Tou S, Brown SR, Malik AI, Nelson RL. Surgery for complete rectal prolapse in adults.
Cochrane Database Syst Rev. 2008;4(4):CD001758.
87. Ramage L, Georgiou P, Tekkis P, Tan E. Is robotic ventral mesh rectopexy better than laparos-
copy in the treatment of rectal prolapse and obstructed defecation? A meta-analysis. Technol
Coloproctol. 2015;19:381–9.
Laparoscopic Lymphadenectomy
for Colorectal Cancers: Concepts
and Current Results
Introduction
The mainstay management for colon cancer remains surgery. The pathological find-
ings in the specimen are the most important predictor of further treatment and sur-
vival. Cancer staging depends upon the assessment of primary tumor [T], lymph
node metastasis [N], and distant metastasis [M] and these variables are most impor-
tant for pathologists and treating clinicians.
Nodal metastasis plays a crucial role in determining prognosis, management, and
survival of colorectal cancer patients and consists of an important parameter in con-
temporary prognostic staging systems particularly the widely used tumor node
metastasis [TNM] system proposed by the UICC/AJCC. The 5-year survival rates
range between 70% and 80% in node negative disease, with the corresponding val-
ues in node positive disease being 30%–60%. Adjuvant chemotherapy improves the
survival in node positive disease. Occult lymph node disease is present in 20%–30%
S. Rawat (*)
Department of Surgical Gastroenterology and Liver Transplantation, Sir Ganga Ram
Hospital, New Delhi, India
Royal College of Surgeons of England, London, UK
C. Selvasekar
Divisional Medical Director Clinical Services and Specialist Surgery, Christie NHS
Foundation Hospital, Manchester, UK
Vice Chair of Specialty Surgical Board in General Surgery, Royal College of Surgeons of
Edinburgh, Edinburgh, UK
S. Bansal
Department of Surgical Gastroenterology and Liver Transplantation, Sir Ganga Ram
Hospital, New Delhi, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 155
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_7
156 S. Rawat et al.
cases which is apparently present in completely excised disease [1, 2]. Adjuvant
chemotherapy is beneficial in such a subset of cases when identified. Some of the
other prognostic variables over and above TNM which might affect disease spread,
recurrence and eventually benefit from adjuvant chemotherapy in colorectal cancers
are: (a) venous invasion, (b) perineural invasion, (c) tumour perforation, (d) serosal
involvement and (e) incomplete resection [1, 2]. Incomplete resection particularly
refers to both primary tumor and nodal resection. Therefore, to obtain an accurate
staging a conscientiousness effort is required both by surgeons and patholo-
gists alike.
This chapter further discusses the nodal staging and the concept of adequate
lymphadenectomy in right and left sided colonic tumours and rectum with an
emphasis on the techniques of adequate lymphadenectomy.
Nodal Staging
I. Patient age
II. Gender and body habitus
III. Immune response to neo adjuvant treatment
IV. Tumor site and size
V. Length of colon resected
VI. Experience of surgeon
VII. Diligence and experience of a pathologist.
Current Concepts
The concept of complete mesocolic excision (CME) with central vascular liga-
tion (CVL), paralleling the concept of total mesorectal excision (TME) described by
Professor RJ Heald [20], entails dissection of entire mesocolon in the embryonic
planes of fusion. In the intaruterine period, the colon along with its vascular supply
and lymphatics is suspended in a dorsal mesentery, which subsequently fuses with
the retroperitoneum in the region of caecum, ascending and descending colon. Thus,
an avascular plane exists between the mesocolon and the retroperitoneum (Fig. 1).
It is important to note that the peritoneal bilayer covering the mesocolon envelopes
the entire colon and is not merely limited to the pelvis. The aim of CME with CVL
technique is to separate these two planes and excise the tumour along with the
colon, the mesocolon with its accompanying lymphatic and vascular supply in total-
ity, ensuring an intact visceral fascial layer is maintained. It can be achieved by
sharp dissection between the visceral and the parietal peritoneal layers. Appropriate
knowledge of anatomy of the mesocolon as well as adequate surgical expertise is
desirable for the purpose.
158 S. Rawat et al.
Ascending colon
Small
Bowel
Superior
Mesenteric
Anterior aspect artery
Caecum of mesocolon
Small
Posterior
Bowel
aspect
Mesentry Duodenum
of mesocolon
Toldt’s fascia
Fig. 2 Schematic diagram showing blood supply of right and left colon
demanding procedure due to the complex anatomy of the region and explicit knowl-
edge of vascular anatomy (SMV and SMA) is vital to avoid iatrogenic complica-
tions. As regards oncological adequacy, this procedure is almost equivalent to
eastern concept of Japanese D3 lymphadenectomy.
• The main lymph nodes are situated at the source of the main feeding artery.
• Intermediate lymph nodes lie between the initial and terminal branch of the
main artery
• Pericolic lymph nodes are stationed between the terminal branch of the main
feeding artery and the colonic wall [21, 22].
The notion of total mesorectal excision [TME] for rectal cancer has been the most
revolutionary concept that has evolved during the last three decades. Multiple stud-
ies noted a decrease in local recurrence to the tune of 6%–12%, and a 53%–87%
improvement in 5-year survival after incorporation of TME [23–25].
In TME the rectum, along with its surrounding mesorectum comprising of lym-
phovascular fatty tissue (the first area of drainage of tumour cells), is excised using
precise, sharp dissection in an avascular potential space between the visceral meso-
rectal fascia and parietal endopelvic fascia the so called “Holy plane” a term intro-
duced by Heald [26]. TME minimizes the chances of leaving behind residual tumor
and preserves nerve fibres which supply the urinary bladder, prostate, and vagina
(Fig. 3).
The essence of the TME hypothesis is that lymph nodes randomly distributed
within the mesorectum, which are not visible or palpable, are completely removed.
The size of the normal lymph nodes in mesorectum in about 80% of cases is <3 mm.
160 S. Rawat et al.
Most lymph nodes in the mesorectum are located posteriorly, and 90% of the poste-
rior lymph nodes lie within the upper half of the upper 2/3 of the rectum [27].
Rectal cancers very rarely spread in a downward direction intramurally, but the
lymphatic spread in the mesorectum i.e. extramural spread, appears to be bidirec-
tional (both in distal and proximal directions), within the limits of fascia of meso-
rectum, emphasizing the need for a complete mesorectal excision. Whereas TME is
a beneficial procedure to extirpate lymphatic spread in high rectal carcinomas
located >5 cm above the dentate line, the same is not noted in lower rectal neo-
plasms [less than 5 cm from the dentate line] wherein around 15–20% cases there is
lateral nodal involvement which lies outside the confines of TME. A lateral node
dissection as described below may prove beneficial in such patients.
The lymphatic drainage from the rectum below the peritoneal reflection follows two
major pathways [Fig. 4]:
Total Mesorectal Excision [TME] involves removal of the first pathway of lymph
nodes [28]. Management of the lymph node stations in the second route of drainage
(the lateral nodes) has been a topic of interest lately [29]. It needs to be emphasized
that the internal iliac group of nodes is classified as regional disease (Stage III)
whereas the external and common iliac nodes are grouped as metastatic disease
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 161
5
4
6
Nodes along the common iliac vessels
7 Internal iliac nodes
External iliac nodes
8 9
Obturator nodes
Nodes along the inferior mesenteric artery
Fig. 4 Schematic diagram showing the Lateral pelvic lymph nodes. In the diagram marked ves-
sels are 1. Inferior mesenteric artery, 2. Superior rectal artery, 3. Common Iliac artery, 4. External
Iliac artery, 5. Internal Iliac artery, 6. Obturator artery, 7. Middle rectal artery, 8. Internal pudendal
artery, 9. Inferior rectal artery. (Radjindrin A (2018) Does Lateral Pelvic Lymph node matters in
rectal cancer Glob Surg, 2018 doi: https://doi.org/10.15761/GOS.1000196)
Table 1 Differences in the understanding and management of LLNs between the East and
the West
Western concept Japanese concept
Regional Internal iliac nodes Internal, external and common iliac and
nodes obturator nodes
Metastatic Common iliac, external iliac and Not Applicable
nodes obturator nodes
Management nCRT with RT boost to involved LLN dissection
nodes
Radjindrin A (2018) Does Lateral Pelvic Lymph node matters in rectal cancer Glob Surg, 2018 doi:
https://doi.org/10.15761/GOS.1000196)
(Stage IV) in the TNM classification. Despite the classification radiation oncolo-
gists often treat external and common iliac nodes in rectal cancer with curative
intent in concordance with treatment of regional nodes [Table 1] [30]. The lateral
lymph nodes can be treated with either a radiotherapy boost or surgically by lateral
lymph node dissection [30]. The Japanese guidelines for colorectal cancer [2016]
recommends LLND for all rectal tumours situated caudal to the peritoneal reflection
[31]. According to the JSCCR, LLND decreases intrapelvic recurrence by 50% and
162 S. Rawat et al.
In a study assessing feasibility of lateral pelvic lymph node dissection, when com-
pared with the open approach the laparoscopic approach was considered safe,
incurred a less blood loss, had lower hospital stay and had higher mean number of
harvested nodes [35]. An autonomic nerve preserving approach for laparoscopic
LLND based on vesical-hypogastric fascia and uretero-hypogastric nerve fascia has
been proposed [36]. Robotic LLND has similar short-term outcomes and lymph
node harvest, offering advantages in male narrow pelvis where manipulation of
instruments becomes difficult in laparoscopic approach [37, 38].
The concept of sentinel lymph node biopsy [SLNB], which has significantly
impacted the treatment of melanoma and breast cancer, is being investigated in
colorectal cancers to enhance nodal staging accuracy especially in T1 disease. The
sentinel lymph node is considered the lymph node[s] located the closest in the lym-
phatic mapping area. Despite a potential curative resection, 20–30% of node nega-
tive colorectal cancers develop distant metastasis presumably due to occult
undetected nodal disease [39]. It has been noted that small <5 mm nodal deposits
carry similar survival prognostication as >5 mm deposits emphasizing the impor-
tance of thorough examination of nodes [40]. Though yet controversial, micrometa-
static deposits <2 mm may also benefit from postoperative adjuvant therapy.
Identifying patients who have tumor-negative nodes but are at high risk of
regional or distant node metastasis who might benefit from adjuvant chemotherapy
is challenging. The current histopathological evaluation of lymph nodes with stan-
dard Hematoxylin–Eosin [HE] pathological techniques is inadequate as large
regions of the lymph nodes remains unexamined, with the subsequent risk of unde-
tected residual micrometastases. Therefore, SLN mapping in colon cancer can help
identify nodes that carry the higher risk of metastasis and such nodes can be sub-
jected to detailed pathologic scrutiny, including more sections, immunohistochem-
istry and molecular diagnostic techniques thereby enhancing the staging accuracy.
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 163
We prefer the caudo-cranial approach [also called the initial retrocolic endo-
scopic approach IRETA APPROACH]. All procedures are done in the modified
lithotomy position under general anaesthesia, and table position modified in accor-
dance with the area to be mobilized.
Central Vascular Ligation (Figs. 7 and 8) Tenting the ileocolic mesentery by
lifting it up is a useful technique that helps in identifying the ileocolic vessels which
are dissected and traced to their origin from the superior mesenteric vessels and
clipped. The right colic artery is thereafter addressed. It needs to be noted that it is
inconsistently present. Further attention is directed to the middle colic vessels that
can be identified traversing the transverse mesocolon vertically up when the trans-
verse colon is lifted towards the abdominal wall. There are variations in drainage of
Fig. 7 D3 Right
hemicolectomy dissection
166 S. Rawat et al.
Fig. 8 Right
Hemicolectomy D3
Dissection at completion
right colic and middle colic veins which may be encountered in the process. In
conventional right hemicolectomy only the right branch of middle colic artery is
ligated at its origin.
Fig. 10 Intracorporeal
stappled ileocolic
side-to-side anastomosis
The approaches frequently described in literature for the left colon are:
All procedures are done in the modified lithotomy position under general
anaesthesia.
Placement of Trocars The surgeon and the camera assistant are stationed to the
right of the patient. A 10mm camera port is inserted at the umbilicus. The procedure
is performed with 4 or 5 ports: two 5-mm ports are introduced on either side and
168 S. Rawat et al.
another 12-mm port (for stapler) is placed at 2 cm above and medial to the right
anterior superior iliac spine, additional 5-mm port can be inserted for bowel retrac-
tion (Fig. 11). At the commencement of operation, a diagnostic laparoscopy is per-
formed to assess for metastatic disease. The procedure is performed with patient
placed in Trendelenburg position and the table tilted to left up.
Pedicle Ligation: (Fig. 12) The omentum is displaced superiorly over the liver. A
useful manoevure commonly practised for retraction of the uterus anteriorly is
slinging the uterus using a percutaneous suture loop passed directly and tied above
the skin over a piece of gauze. Retraction of the sigmoid colon to the left and ante-
riorly helps in identification of the sigmoid vessels and inferior mesenteric artery.
The peritoneum is incised caudal and to the right of the vascular trunk, at the
level of sacral promontory and further dissection proceeds cranially to the origin of
the vascular trunk (Fig. 13). Care should be taken to make the tunnel anterior to the
ureter and hypogastric nerve plexuses which lie in close proximity. The superior
rectal artery is lifted cranially and all vessels are skeletonized, and ligated sepa-
rately using endoscopic clips (Fig. 14). In high ligation the inferior mesenteric
artery is ligated at its origin whereas in low ligation, inferior mesenteric artery is
ligated distal to its left colic branch (Fig. 12).
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 169
Fig. 12 Blood supply of left colon with site of doing high or low ligation of inferior mesen-
teric artery
Total Mesorectal Excision and Rectal Mobilization The dissection for TME is
initially done posteriorly and laterally then subsequently anteriorly. The lateral peri-
toneal attachments of the rectum are incised down to the level of peritoneal reflec-
tion. The sigmoid colon is retracted ventrally to open the retrorectal space and
170 S. Rawat et al.
Fig. 15 Dissection
showing the pelvic
parasympathetic nerves*
laterally
dissection is carried out in the avascular presacral plane between the parietal and
visceral pelvic fascia. The hypogastric autonomic nerves which lie posteriorly,
comes close to the mesorectum inferiorly and supply branches to the rectum where
they should be carefully dissected by sparing the pelvic branches. Vessels entering
the rectum can be addressed with harmonic or vessel sealing devices. Caudally the
dissection is continued to the rectosacral fascia following which the rectum curves
anteriorly to the pelvic floor (Fig. 15)
Fig. 16 Colo-anal
anastomosis
Division of the Rectum
After ensuring complete circumferential mobilization to the pelvic floor, the meso-
rectum is dissected to the rectal wall and the rectum is divided at least 2 cm below
the lesion using endostaplers.
Laparoscopic resections for colorectal cancer offers the advantage of the improved
visibility due to magnification and angled optics as also good illumination of the
operation field and can aid in better delineation and preservation of the pelvic auto-
nomic nerves.
After completion of TME and rectal transection, the lateral pelvic nodes are
addressed. They are grouped into three regions:
• common iliac region: comprising of the common iliac & external iliac nodes,
• hypogastric region: internal iliac nodes
• obturator region: obturator nodes (Fig. 4).
172 S. Rawat et al.
The procedure begins by dissecting fibrofatty tissue around the aortic bifurcation
at the origin of the common iliac vessels. The common iliac and external iliac nodes
are dissected, thereafter, the hypogastric group is addressed by exposing the hypo-
gastric nerve, external and internal iliac vessels, and ureter which are laid bare on
the lateral pelvic wall up to the iliac bifurcation. The dissection proceeds to address
the lymphatic tissues between the urinary bladder and the pelvic wall which are
cleared. The lymphatic tissue along internal iliac vessels cleared upto the middle
hemorrhoidal vessels. The obturator fossa is cleared of lymphoareolar tissue to lay
bare the obturator nerve and vessels (Fig. 17).
Complications
Bleeding/Vascular Injury
Anastomotic Leak
Anastomotic leak rates are not found to be different following CME CVL as com-
pared to conventional hemicolectomy, though delayed gastric emptying has been
noted [50, 51, 52].
Chyle Leak
Conclusion
Editor’s Note1
Anatomy
References: Main chapter references are included after the “References Editor’s Note” section.
1
176 S. Rawat et al.
Fig. EN1 Laparoscopic
right hemicolectomy image
showing the dissection in
Ileocolic plane (Yellow
arrow: Caecum and
proximal right colon, Red
arrow: Ileocolic vessels)
Four critical view planes have been proposed in the open book model for standard-
ization of CME in right hemicolectomy. They are essentially derived from the
embryological fusion planes of colon and mesocolon and are: (a) retroperitoneal
plane, (b) ileocolic plane (c) transverse mesocolic plane and (d) mesogastric plane [2].
Table EN1 tabulates the crux of the results of various meta-analysis comparing
mesocolic excision versus non mesocolic excision. An advantage regarding onco-
logical outcome parameters viz: recurrences, diseases free and overall survival has
been consistently reported in latest studies. Surrogate pathological parameters of a
better oncological resection such as number of lymphnodes retrieved, length of
bowel excised, area of the mesocolon in specimen, distance to high tie have all been
reported to be higher in the CME group [3–12].
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 177
Table EN1 Meta-analysis showing results complete mesocolic excision versus conventional exci-
sion in colectomy for colonic cancers
Study Result
Comparing complete mesocolic CME/D3 lymphadenectomy group had better
excision versus conventional oncological outcome as cited below:
colectomy for colon cancer: A • 5-year Overall survival
systematic review and meta- OR = 1.29; 95% CI 1.02 to 1.64, p = 0.03
analysis [3] • 5-year Disease-free survival
OR = 1.61; 95% CI 1.14 to 2.28; p = 0.007.
No significant differences in morbidity and mortality
Complete mesocolic excision CME group was associated with significantly better
versus conventional oncological outcome as follows:
hemicolectomy in patients with • Number of lymph nodes harvested;
right colon cancer: a systematic (MD 9.17, CI 4.67–13.68, p < 0.001).
review and meta-analysis [4]. OS- 3-year;
(OR 1.57, 95% CI 1.17–2.11, p = 0.003),
• OS-5-year;
(OR 1.41, 95% CI 1.06–1.89, p = 0.02),
• DFS-5-year
(OR 1.99, 95% CI 1.29–3.07, p = 0.002).
No difference in:
• complications
• stage III colon cancer no significant benefit of CME on
survival
Oncological reasons for CME group was associated with a significantly better
performing a complete oncological outcome as regards:
mesocolic excision: a systematic • Higher number of lymph nodes retrieved
review and meta-analysis [5] • Better pooled 5-year overall survival
• Lower rates of local recurrence
• Lower rates of distant recurrence
Disadvantage of CME:
• Higher incidence of vascular injury
odds ratio 3, P < 0.001.
Complete mesocolic excision CME/ D3 lymphadenectomy had superior oncological
versus conventional surgery for outcome with respect to:
colon cancer: A systematic • OS -3 year
review and meta-analysis [6] RR 0.69 (95% CI 0.51–0.93, P = 0.016
• OS - 5 year
RR 0.78 (95% CI 0.64–0.95, P = 0.011
• DFS - 5 year
RR 0.67, 95% CI 0.52–0.86, P < 0.001
No statistically significant differences in:
• complications
• anastomotic leak
(continued)
178 S. Rawat et al.
Table EN1 (continued)
Study Result
Complete Mesocolic Excision Better oncological outcome and pathological parameters
and D3 Lymphadenectomy in CME group as follows:
versus Conventional Colectomy • Higher number of retrieved lymph nodes
for Colon Cancer: A Systematic • Greater distance to high tie
Review and Meta-Analysis [7] • Resected length of bowel
• Larger area of resected mesentry
• 3-year OS
(RR 1.09, 95% CI 1.04–1.15)
• 5-year OS
(RR 1.05, 95% CI 1.02–1.08)
• 3-year DFS
(RR 1.10, 95% CI 1.04–1.17, i2 = 22%),
• Decreased local recurrence
(RR 0.35, 95% CI 0.24–0.51, i2 = 51%)
• Fewer distant recurrences
(RR 0.71, 95% CI 0.60–0.85, i2 = 34%).
Disadvantage CME group:
• Higher postoperative complications
(relative risk [RR] 1.13, 95% confidence interval [CI]
1.04–1.2)
No differences were observed in:
• Anastomotic leak rates
• Perioperative mortality.
Right hemicolectomy with Superior oncological outcome with CME in the
complete mesocolic excision is following aspects:
safe, leads to an increased • Higher number of lymph nodes retrieved
lymph node yield and to (MD 7.05, 95% CI 4.06–10.04).
increased survival: results of a • Improved 3-year overall survival
systematic review and meta- (RR 0.42, 95% CI 0.27–0.66)
analysis [8]. • Better 5-year disease-free survival
(RR 0.36, 95% CI 0.17–0.560.
No difference in:
• anastomotic leak rates
• blood loss
• postoperative complications
• serious postoperative complications -Clavien-Dindo grade
III-IV
• reoperation rate
Traditional surgery better as regards to:
• less operating time
(MD 16.43, 95% CI 4.27–28.60)
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 179
Table EN1 (continued)
Study Result
Right-side colectomy with Better oncological outcome and pathological parameters
complete mesocolic excision vs in CME group as regards:
conventional right-side • 5-year DFS
colectomy in the treatment of 1.88 (95% CI 1.02–3.45)
colon cancer: a systematic • 5-year OS
review and meta-analysis [9]. 2.77 (95% CI 1.33–5.74)
• Higher number of retrieved lymph nodes
(MD 7.08 lymph nodes 95% CI 4.90–9.27).
No significant difference with respect to:
• morbidity
• mortality
• blood loss
• hospital stay
Advantage conventional surgery:
• longer duration of surgery with CME
(MD 33.69 min, 95% CI 12.79–54.59)
D3-lymphadenectomy enhances Better oncological outcome and pathological parameters
oncological clearance in patients with CME + D3 as noted below:
with right colon cancer. Results • tumour to vascular tie distance greater,
of a meta-analysis [10]. • greater length of colonic resection,
• wider mesentery resection
• greater number of retrieved lymph nodes.
• decrease risk of local recurrence
(HR:0.17)
• better 3-year OS
(HR:0.53)
• better 5-year OS
(HR:0.57)
No differences noted in:
• morbidity related variables
Laparoscopic Complete CME scored better as regards:
Mesocolic Excision Versus • less blood loss
Noncomplete Mesocolic (P < 0.001, (WMD) = −12.01, 95% (CI): −13.56 to
Excision: A Systematic Review −10.45),
and Meta-analysis [11]. • more harvested lymph nodes
(P < 0.001, WMD = 6.50, 95% CI: 3.57–9.42),
• longer resected colon length
(P = 0.004, WMD = 3.57, 95% CI: 1.12–6.03),
• greater distance from tumor to high tie
(P < 0.001, WMD = 1.36, 95% CI: 0.87–1.85),
• greater distance from nearest bowel wall to high tie
(P < 0.001, WMD = 1.36, 95% CI: 0.87–1.85).
No differences were observed in terms of:
• operative time,
• complications,
• wound infection,
• ileus,
• Proximal resected margin
• Distal resection margin
• Disease-free survival
(continued)
180 S. Rawat et al.
Table EN1 (continued)
Study Result
Safety, quality and effect of Advantage of CME in oncological outcome and
complete mesocolic excision vs pathological parameters:
non-complete mesocolic • longer length of resected colon
excision in patients with colon (WMD 47.06, 95% CI: 10.49–83.62),
cancer: a systemic review and • greater tumor to the high tie distance
meta-analysis [12] (WMD 17.51, 95% CI: 15.16–19.87),
• larger area of resected mesentery
(WMD 36.09, 95% CI: 18.06–54.13)
• more harvested lymph nodes
(WMD 6.13, 95% CI: 1.97–10.28).
• better 5-year survival
(HR) 0.33, 95% CI: 0.13–0.81],
• improved 3-year survival
(HR 0.58, 95% CI: 0.39-0.86)
• better 3-year survival for Stage III disease
(HR 0.69, 95% CI: 0.60–0.80)
Disadvantage CME:
• more intra-operative blood loss
[weighted mean difference (WMD) 79.87, 95% CI:
65.88–93.86],
• higher surgical complications
(relative risk 1.23, 95% CI: 1.08–1.40)
CME complete mesocolic excision, OR odds ratio, HR hazard ratio, WMD weighted mean differ-
ence, CI confidence interval, OS overall survival, DFS disease free survival, RR risk ratio, MD
mean difference
Table EN2 enlists the results of metanalysis comparing laparoscopic and open
mesocolic excision. A better postoperative recovery, lower blood loss, less require-
ment for blood transfusion, lower overall postoperative complications, less wound
infections, early recovery of gastrointestinal function and shorter hospital stay are
some of the reported benefits of laparoscopic over open CME for colonic cancers
[13–16].
Table EN2 (continued)
Study Result
Comparing the safety, LC had was superior to OC in terms of:
efficacy, and • less postoperative complications
oncological outcomes (OR 0.64, p = 0.0003),
of laparoscopic and • reduced blood loss
open colectomy in (WMD –86.84, p < 0.00001),
transverse colon • earlier time to first flatus passage
cancer: a meta- (WMD – 0.94, p < 0.00001)
analysis [16] • early onset of oral diet
(WMD – 1.25, p < 0.00001),
• length of stay
(WMD – 2.39, p < 0.00001).
• lower recurrence rate
OC was advantageous in the following aspect:
• lower operation time
(p < 0.00001).
• higher rate of complete mesocolic excision
(p = 0.001).
LC vs OC equivalent in terms of postoperative survival outcomes.
LCME laparoscopic complete mesocolic excision, OCME open complete mesocolic excision, OR
odds ratio, HR hazard ratio, WMD weighted mean difference, CI confidence interval, OS overall
survival, DFS disease free survival, RR risk ratio, MD mean difference, LC laparoscopic colec-
tomy, OC open colectomy
Table EN3 (continued)
Study Result
Meta-analysis of No difference between groups in the following aspects:
survival and functional • overall survival
outcomes after total • 5-year overall survival
mesorectal excision with • disease-free survival
or without lateral pelvic • 5-year disease-free survival
lymph node dissection in • local recurrence
rectal cancer surgery • distant recurrence
[18] • total recurrence
Total mesorectal excision with lateral pelvic lymph node
dissection resulted in
• longer operative time
(MD: 116.02, 95% CI 89.20–142.83, P < 0.00001, I2 = 68%)
• higher complications
(odds ratio: 1.59, 95% CI 1.14–2.24, P = 0.007, I2 = 0%)
• urinary dysfunction
(odds ratio: 6.66, 95% CI 3.31–13.39, P < 0.00001, I2 = 23%)
• sexual dysfunction
(odds ratio: 9.67, 95% CI 2.38–39.26, P = 0.002; I2 = 51%)
Total mesorectal TME + LLND group fared worse as regards:
excision plus lateral • more complications (OR = 1.48, 95% CI [1.07, 2.03], P = 0.02)
lymph node dissection No significant difference was observed in
vs TME on rectal cancer • overall survival
patients: a meta-analysis • disease-free survival
[19] • local recurrence
• urinary dysfunction
What is the role of LLND after nCRT associated with:
lateral lymph node • lower LLR (P = 0.02).
dissection in rectal LLND disadvantageous due to:
cancer patients with • longer operative time (P < 0.01)
clinically suspected • increased risk of urinary dysfunction (P < 0.01).
lateral lymph node
metastasis after
preoperative
chemoradiotherapy? A
meta-analysis and
systematic review [20].
The efficacy and safety No difference in
of lateral lymph node • 5-year disease-free survival rate
dissection for patients • local recurrences
with rectal cancer: A LLND associated with more:
systematic review and • urinary dysfunction
meta-analysis [21] (OR = 2.14, 95%CI = 1.21–3.79, P = 0.009)
• male sexual dysfunction
(OR = 4.19, 95%CI = 1.55–11.33, P = 0.005)
TME total mesorectal excision, LLND lateral lymphnode dissection, nCRT neoadjuvant chemora-
diotherapy, LLNM lateral lymph node metastasis, LLR lateral lymphnode recurrence, OR odds
ratio, HR hazard ratio, WMD weighted mean difference, CI confidence interval, OS overall sur-
vival, DFS disease free survival, RR risk ratio, MD mean difference
184 S. Rawat et al.
Table EN4 depicts the results of recent metaanalyses on sentinel node biopsy in
colorectal cancers. A high identification rate sensitivity and diagnostic accuracy has
been observed especially for early stage lesions. Colonic cancers, use of laparo-
scopic procedures and indocyanine green for performance of sentinel node biopsy
has been noted to have a better yield [22–24].
19. Wang X, Qiu A, Liu X, Shi Y. Total mesorectal excision plus lateral lymph node
dissection vs TME on rectal cancer patients: a meta-analysis. Int J Colorectal
Dis. 2020 Jun;35(6):997–1006. https://doi.org/10.1007/s00384-020-03610-1.
Epub 2020 May 1. PMID: 32356120.
20. Yang X, Yang S, Hu T, Gu C, Wei M, Deng X, Wang Z, Zhou Z. What is the role
of lateral lymph node dissection in rectal cancer patients with clinically sus-
pected lateral lymph node metastasis after preoperative chemoradiotherapy? A
meta-analysis and systematic review. Cancer Med. 2020 Jul;9(13):4477–89.
https://doi.org/10.1002/cam4.2643. Epub 2020 Apr 30. PMID: 32352659;
PMCID: PMC7333827.
21. Ma P, Yuan Y, Yan P, Chen G, Ma S, Niu X, Xu M, Yang K, Cai H. The efficacy
and safety of lateral lymph node dissection for patients with rectal cancer: A
systematic review and meta-analysis. Asian J Surg. 2020 Sep;43(9):891–901.
https://doi.org/10.1016/j.asjsur.2019.11.006. Epub 2020 Jan 9. PMID:
31926817.
22. Burghgraef TA, Zweep AL, Sikkenk DJ, van der Pas MHGM, Verheijen PM,
Consten ECJ. In vivo sentinel lymph node identification using fluorescent tracer
imaging in colon cancer: A systematic review and meta-analysis. Crit Rev
Oncol Hematol. 2021 Feb;158:103149. https://doi.org/10.1016/j.critrev-
onc.2020.103149. Epub 2020 Nov 11. PMID: 33450679.
23. Qiao L. Sentinel lymph node mapping for metastasis detection in colorectal
cancer: a systematic review and meta-analysis. Rev Esp Enferm Dig. 2020
Sep;112(9):722–30. https://doi.org/10.17235/reed.2020.6767/2019. PMID:
32894022.
24. Villegas-Tovar E, Jimenez-Lillo J, Jimenez-Valerio V, Diaz-Giron-Gidi A,
Faes-Petersen R, Otero-Piñeiro A, De Lacy FB, Martinez-Portilla RJ, Lacy
AM. Performance of Indocyanine green for sentinel lymph node mapping and
lymph node metastasis in colorectal cancer: a diagnostic test accuracy meta-
analysis. Surg Endosc. 2020 Mar;34(3):1035–47. https://doi.org/10.1007/
s00464-019-07274-z. Epub 2019 Nov 21. PMID: 31754853.
188 S. Rawat et al.
References
1. Fang SH, Efron JE, Berho ME, Wexner SD. Dilemma of stage II colon cancer and decision
making for adjuvant chemotherapy. J Am Coll Surg. 2014;219:1056–69 [PMID: 25440029.
https://doi.org/10.1016/j.Jamcollsurg.2014.09.010]
2. Dienstmann R, Salazar R, Tabernero J. Personalizing colon cancer adjuvant therapy: selecting
optimal treatments for individual patients. J Clin Oncol. 2015;33:1787–96 [PMID: 25918287:
https://doi.org/10.1200/JCO.2014.60.0213]
3. Nagtegaal ID, Quirke P. Colorectal tumour deposits in the mesorectum and pericolon; a critical
review. Histopathology. 2007;51:141–9 [PMID: 17532768: https://doi.org/10.1111/j.1365-25
59.2007.02720.x]
4. Quirke P, Williams GT, Ectors N, Ensari A, Piard F, Nagtegaal I. The future of the TNM
staging system in colorectal cancer: time for a debate? Lancet Oncol. 2007;8:651–7 [PMID:
17613427: https://doi.org/10.1016/S1470-2045[07]70205-X]
5. Nagtegaal ID, Quirke P, Schmoll HJ. Has the new TNM classification for colorectal can-
cer improved care? Nat Rev Clin Oncol. 2012;9:119–23 [PMID: 22009076: https://doi.
org/10.1038/nrclinonc.2011.157]
6. Esser S, Reilly WT, Riley LB, Eyvazzadeh C, Arcona S. The role of sentinel lymph node map-
ping in staging of colon and rectal cancer. Dis Colon Rectum. 2001;44(6):850–4.; discussion
854–856. https://doi.org/10.1007/BF02234707.
7. Smith J, Hwang H, Wiseman KW, Filipenko D, Phang PT. Ex vivo sentinel lymph node
mapping in colon cancer: improving the accuracy of pathologic staging? Am J Surg.
2006;191(5):665–8. https://doi.org/10.1016/j.amjsurg.2006.01.045.
8. Bonjer HJ, Hop WC, Nelson H, Sargent DJ, Lacy AM, Castells A, Guillou PJ, Thorpe H,
Brown J, Delgado S, Kuhrij E, Haglind E, Påhlman L; Transatlantic Laparoscopically Assisted
vs Open Colectomy Trials Study Group. Laparoscopically assisted vs open colectomy for
colon cancer: a meta-analysis. Arch Surg. 2007 Mar;142(3):298–303. https://doi.org/10.1001/
archsurg.142.3.298. PMID: 17372057.
9. Guillou PJ, Quirke P, Thorpe H, Walker J, Jayne DG, Smith AM, Heath RM, Brown JM; MRC
CLASICC trial group. Short-term endpoints of conventional versus laparoscopic-assisted
surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, randomised
controlled trial. Lancet. 2005 May 14–20;365(9472):1718–26. https://doi.org/10.1016/
S0140-6736(05)66545-2. PMID: 15894098.
10. Clinical Outcomes of Surgical Therapy Study Group, Nelson H, Sargent DJ, Wieand HS,
Fleshman J, Anvari M, Stryker SJ, Beart RW Jr, Hellinger M, Flanagan R Jr, Peters W, Ota
D. A comparison of laparoscopically assisted and open colectomy for colon cancer. N Engl
J Med. 2004 May 13;350(20):2050–59. https://doi.org/10.1056/NEJMoa032651. PMID:
15141043.
11. Bertelsen CA, Bols B, Ingeholm P, Jansen JE, Neuenschwander AU, Vilandt J. Can the qual-
ity of colonic surgery be improved by standardization of surgical technique with complete
mesocolic excision? Colorectal Dis. 2011 Oct;13(10):1123–29. https://doi.org/10.1111/
j.1463-1318.2010.02474.x. PMID: 20969719.
12. Ma Y, Yang Z, Qin H, Wang Y. A meta-analysis of laparoscopy compared with open colorectal
resection for colorectal cancer. Med Oncol. 2011 Dec;28(4):925–33. https://doi.org/10.1007/
s12032-010-9549-5. Epub 2010 May 11. PMID: 20458560.
13. Colon Cancer Laparoscopic or Open Resection Study Group, Buunen M, Veldkamp R, Hop
WC, Kuhry E, Jeekel J, Haglind E, Påhlman L, Cuesta MA, Msika S, Morino M, Lacy A,
Bonjer HJ. Survival after laparoscopic surgery versus open surgery for colon cancer: long-
term outcome of a randomised clinical trial. Lancet Oncol. 2009 Jan;10(1):44–52. https://doi.
org/10.1016/S1470-2045(08)70310-3. Epub 2008 Dec 13. PMID: 19071061.
14. Fleshman J, Sargent DJ, Green E, Anvari M, Stryker SJ, Beart RW Jr, Hellinger M, Flanagan
R Jr, Peters W, Nelson H; Clinical Outcomes of Surgical Therapy Study Group. Laparoscopic
colectomy for cancer is not inferior to open surgery based on 5-year data from the COST Study
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 189
28. Bell S, Sasaki J, Sinclair G, Chapuis PH, Bokey EL. Understanding the anatomy of lymphatic
drainage and the use of blue-dye mapping to determine the extent of lymphadenectomy in
rectal cancer surgery: unresolved issues. Colorectal Dis. 2009 Jun;11(5):443–9. https://doi.
org/10.1111/j.1463-1318.2009.01769.x. Epub 2009 Jan 17. PMID: 19207711.
29. Kundagulwar GK, Pai VD, Saklani AP. Is there a role of lateral pelvic lymph node dissection
in the current era of neoadjuvant chemoradiotherapy for rectal cancer? J Gastrointest Dig Syst.
2016;6:473. https://doi.org/10.4172/2161-069X.1000473.
30. Yahya JB, Herzig DO, Farrell MJ, Degnin CR, Chen Y, Holland J, Brown S, Jaboin J, Tsikitis
VL, Lu K, Thomas CR Jr, Mitin T. Does a fine line exist between regional and metastatic pelvic
lymph nodes in rectal cancer-striking discordance between national guidelines and treatment
recommendations by US radiation oncologists. J Gastrointest Oncol. 2018 June;9(3):441–7.
https://doi.org/10.21037/jgo.2018.02.05. PMID: 29998009; PMCID: PMC6006036.
31. Watanabe T, Muro K, Ajioka Y, Hashiguchi Y, Ito Y, et al. Japanese Society for Cancer of the
Colon and Rectum [JSCCR] guidelines 2016 for the treatment of colorectal cancer. Int J Clin
Oncol. 2018;23:1–34.
32. Ito M, Kobayashi A, Fujita S, Mizusawa J, Kanemitsu Y, Kinugasa Y, Komori K, Ohue M,
Ota M, Akazai Y, Shiozawa M, Yamaguchi T, Akasu T, Moriya Y; Colorectal Cancer Study
Group of Japan Clinical Oncology Group. Urinary dysfunction after rectal cancer surgery:
Results from a randomized trial comparing mesorectal excision with and without lateral
lymph node dissection for clinical stage II or III lower rectal cancer (Japan Clinical Oncology
Group Study, JCOG0212). Eur J Surg Oncol. 2018 Apr;44(4):463–8. https://doi.org/10.1016/j.
ejso.2018.01.015. Epub 2018 Jan 17. PMID: 29428473.
33. Fujita S, Akasu T, Mizusawa J, Saito N, Kinugasa Y, Kanemitsu Y, Ohue M, Fujii S, Shiozawa
M, Yamaguchi T, Moriya Y; Colorectal Cancer Study Group of Japan Clinical Oncology
Group. Postoperative morbidity and mortality after mesorectal excision with and without lat-
eral lymph node dissection for clinical stage II or stage III lower rectal cancer (JCOG0212):
results from a multicentre, randomised controlled, non-inferiority trial. Lancet Oncol. 2012
Jun;13(6):616–21. https://doi.org/10.1016/S1470-2045(12)70158-4. Epub 2012 May 15.
PMID: 22591948.
34. Saito S, Fujita S, Mizusawa J, Kanemitsu Y, Saito N, Kinugasa Y, Akazai Y, Ota M, Ohue
M, Komori K, Shiozawa M, Yamaguchi T, Akasu T, Moriya Y; Colorectal Cancer Study
Group of Japan Clinical Oncology Group. Male sexual dysfunction after rectal cancer sur-
gery: Results of a randomized trial comparing mesorectal excision with and without lateral
lymph node dissection for patients with lower rectal cancer: Japan Clinical Oncology Group
Study JCOG0212. Eur J Surg Oncol. 2016 Dec;42(12):1851–58. https://doi.org/10.1016/j.
ejso.2016.07.010. Epub 2016 Jul 30. PMID: 27519616.
35. Nagayoshi K, Ueki T, Manabe T, Moriyama T, Yanai K, Oda Y, Tanaka M. Laparoscopic lateral
pelvic lymph node dissection is achievable and offers advantages as a minimally invasive sur-
gery over the open approach. Surg Endosc. 2016 May;30(5):1938–47. https://doi.org/10.1007/
s00464-015-4418-0. Epub 2015 Aug 15. PMID: 26275538.
36. Matsumoto A, Arita K. A technique of laparoscopic lateral pelvic lymph node dissection based
on vesicohypogastric fascia and ureterohypogastric nerve fascia for advanced low rectal can-
cer. Surg Endosc. 2017 Feb;31(2):945–8. https://doi.org/10.1007/s00464-016-5014-7. Epub
2016 Jun 20. PMID: 27324330.
37. Kagawa H, Kinugasa Y, Shiomi A, Yamaguchi T, Tsukamoto S, Tomioka H, Yamakawa Y, Sato
S. Robotic-assisted lateral lymph node dissection for lower rectal cancer: short-term outcomes
in 50 consecutive patients. Surg Endosc. 2015 Apr;29(4):995–1000. https://doi.org/10.1007/
s00464-014-3760-y. Epub 2014 Aug 19. PMID: 25135444.
38. Kim HJ, Choi GS, Park JS, Park SY, Lee HJ, Woo IT, Park IK. Selective lateral pelvic lymph
node dissection: a comparative study of the robotic versus laparoscopic approach. Surg
Endosc. 2018 May;32(5):2466–73. https://doi.org/10.1007/s00464-017-5948-4. Epub 2017
Nov 9. PMID: 29124406.
39. Lips DJ, Koebrugge B, Liefers GJ, van de Linden JC, Smit VT, Pruijt HF, Putter H, van de
Velde CJ, Bosscha K. The influence of micrometastases on prognosis and survival in stage I-II
Laparoscopic Lymphadenectomy for Colorectal Cancers: Concepts and Current Results 191
colon cancer patients: the Enroute⊕ Study. BMC Surg. 2011 May 11;11:11. https://doi.org/1
0.1186/1471-2482-11-11. PMID: 21569373; PMCID: PMC3123166
40. Rodriguez-Bigas MA, Maamoun S, Weber TK, Penetrante RB, Blumenson LE, Petrelli
NJ. Clinical significance of colorectal cancer: metastases in lymph nodes < 5 mm in size. Ann
Surg Oncol. 1996 Mar;3(2):124–30. https://doi.org/10.1007/BF02305790. PMID: 8646511.
41. Tuech JJ, Pessaux P, Di Fiore F, Nitu V, Lefebure B, Colson A, Michot F. Sentinel node
mapping in colon carcinoma: in-vivo versus ex-vivo approach. Eur J Surg Oncol. 2006
Mar;32(2):158–61. https://doi.org/10.1016/j.ejso.2005.11.004. Epub 2006 Jan 11. PMID:
16376515.
42. Funahashi K. Current status of sentinel lymph node-based nodal ultrastaging in colorectal
cancer. Nihon Geka Gakkai Zasshi. 2009 Mar;110(2):73–7. Japanese. PMID: 19348197.
43. Ankersmit M, Bonjer HJ, Hannink G, Schoonmade LJ, van der Pas MHGM, Meijerink
WJHJ. Near-infrared fluorescence imaging for sentinel lymph node identification in colon
cancer: a prospective single-center study and systematic review with meta-analysis. Tech
Coloproctol. 2019 Dec;23(12):1113–26. https://doi.org/10.1007/s10151-019-02107-6. Epub
2019 Nov 18. PMID: 31741099; PMCID: PMC6890578.
44. Bilchik AJ, Saha S, Wiese D, Stonecypher JA, Wood TF, Sostrin S, Turner RR, Wang HJ,
Morton DL, Hoon DS. Molecular staging of early colon cancer on the basis of sentinel node
analysis: a multicenter phase II trial. J Clin Oncol. 2001 Feb 15;19(4):1128–36. https://doi.
org/10.1200/JCO.2001.19.4.1128. Erratum in: J Clin Oncol 2001 May 1;19(9):2583. PMID:
11181678
45. Kong JC, Prabhakaran S, Choy KT, Larach JT, Heriot A, Warrier SK. Oncological reasons
for performing a complete mesocolic excision: a systematic review and meta-analysis. ANZ J
Surg. 2021 Jan;91(1–2):124–31. https://doi.org/10.1111/ans.16518. Epub 2021 Jan 5. PMID:
33400369.
46. Wang C, Gao Z, Shen K, Shen Z, Jiang K, Liang B, Yin M, Yang X, Wang S, Ye Y. Safety, quality
and effect of complete mesocolic excision vs non-complete mesocolic excision in patients with
colon cancer: a systemic review and meta-analysis. Colorectal Dis. 2017 Nov;19(11):962–72.
https://doi.org/10.1111/codi.13900. PMID: 28949060.
47. Anania G, Davies RJ, Bagolini F, Vettoretto N, Randolph J, Cirocchi R, Donini A. Right hemi-
colectomy with complete mesocolic excision is safe, leads to an increased lymph node yield
and to increased survival: results of a systematic review and meta-analysis. Tech Coloproctol.
2021 Jun 12. https://doi.org/10.1007/s10151-021-02471-2. Epub ahead of print. PMID:
34120270.
48. Ferri V, Vicente E, Quijano Y, Duran H, Diaz E, Fabra I, Malave L, Agresott R, Isernia R,
Cardinal-Fernandez P, Ruiz P, Nola V, de Nobili G, Ielpo B, Caruso R. Right-side colectomy
with complete mesocolic excision vs conventional right-side colectomy in the treatment of
colon cancer: a systematic review and meta-analysis. Int J Colorectal Dis. 2021 May 13.
https://doi.org/10.1007/s00384-021-03951-5. Epub ahead of print. PMID: 33983451.
49. Gavriilidis P, Davies RJ, Biondi A, Wheeler J, Testini M, Carcano G, Di Saverio S. Laparoscopic
versus open complete mesocolic excision: a systematic review by updated meta-analysis.
Updates Surg. 2020 Sep;72(3):639–48. https://doi.org/10.1007/s13304-020-00819-1. Epub
2020 May 29. PMID: 32472404.
50. Prevost GA, Odermatt M, Furrer M, Villiger P. Postoperative morbidity of complete meso-
colic excision and central vascular ligation in right colectomy: a retrospective compara-
tive cohort study. World J Surg Oncol. 2018 Oct 30;16(1):214. https://doi.org/10.1186/
s12957-018-1514-3. PMID: 30376849; PMCID: PMC6208021.
51. Crane J, Hamed M, Borucki JP, El-Hadi A, Shaikh I, Stearns AT. Complete mesocolic exci-
sion versus conventional surgery for colon cancer: A systematic review and meta-analysis.
Colorectal Dis. 2021 May 2. https://doi.org/10.1111/codi.15644. Epub ahead of print. PMID:
33934455.
52. Díaz-Vico T, Fernández-Hevia M, Suárez-Sánchez A, García-Gutiérrez C, Mihic-Góngora L,
Fernández-Martínez D, Álvarez-Pérez JA, Otero-Díez JL, Granero-Trancón JE, García-Flórez
LJ. Complete mesocolic excision and D3 lymphadenectomy versus conventional colectomy
192 S. Rawat et al.
for colon cancer: a systematic review and meta-analysis. Ann Surg Oncol. 2021 Jun 4. https://
doi.org/10.1245/s10434-021-10186-9. Epub ahead of print. PMID: 34089109.
53. Ng ZQ, Han M, Beh HN, Keelan S. Chylous ascites in colorectal surgery: A systematic
review. World J Gastrointest Surg. 2021 June 27;13(6):585–96. https://doi.org/10.4240/wjgs.
v13.i6.585.
54. Sun YW, Chi P, Lin HM, Lu XR, Huang Y, Xu ZB, Huang SH. [Risk factors of postoperative
chyle leak following complete mesocolic excision for colon cancer]. Zhonghua Wei Chang
Wai Ke Za Zhi. 2012 Apr;15(4):328–31. Chinese. PMID: 22539374.
55. Li MZ, Li KY, Shen J, Xie DH. Clavien-Dindo classification of complications after complete
mesocolic excision in laparoscopic radical resection of right hemicolon cancer and analysis on
its influencing factors. Zhonghua Wei Chang Wai Ke Za Zhi. 2020 Jan 25;23(1):51–5. Chinese.
https://doi.org/10.3760/cma.j.issn.1671-0274.2020.01.009. PMID: 31958931.
56. Furnes B, Storli KE, Forsmo HM, Karliczek A, Eide GE, Pfeffer F. Risk factors for complica-
tions following introduction of radical surgery for colon cancer: a consecutive patient series.
Scand J Surg. 2019 June;108(2):144–151. https://doi.org/10.1177/1457496918798208. Epub
2018 Sep 6. PMID: 30187819
Ergonomics in Laparoscopic Surgery:
An Appraisal of Evidence
Introduction
Ergonomics literally stands for work rules. Ergonomics deals with the fit between
people their work environment and tools. The international society of ergonomics
defines ergonomics as: the scientific discipline concerned with the understanding of
interactions among humans and other elements of a system and the profession that
applies theory, principles, data and methods to design in order to optimize human
well-being and overall system performance. Whereas ergonomic analyses have
appraised its applications in other non-medical arenas, in the field of medical sci-
ence it has been a largely neglected issue. A recent interest has blossomed with
respect to ergonomics in the surgical field particularly after the advent of laparo-
scopic surgery. Ergonomic adjustments can help in decreasing fatigue and injuries
to doctors making surgery safer besides improving efficiency and thus patient
related outcome. This article reviews the available literature on ergonomical prin-
ciples that are commonly encountered in the practice of laparoscopic surgery, the
doctor and patient related consequences of working in ergonomically inefficient
situations and critical ergonomic adjustments in instrument design and operation
theatre methods recommended to correct these ergonomic inaccuracies.
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 193
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_8
194 P. Hazrah et al.
Improper ergonomics in the operation theatre can lead to: unintentional injuries,
increased operative time, errors and increased morbidity. It has been reported that
poor design of surgical equipments lead to unintentional patient related injuries
thus necessitating the need for standardization of instruments by regulatory author-
ities [1]. From the perspective of the surgeon posture related strains, nerve injuries,
fatigue, decreased efficiency, increased psychological and mental stress can all
result from incorrect ergonomics. In a survey of 260 respondents of gynaecological
oncologist performing minimally invasive surgery, physical discomfort related to
MIS was reported in 88% with complaints of persistent pain in 52%. To decrease
pain, surgeons changed positions 78% of the times, limited the number of cases per
day in 14%, spread cases throughout the week in 6%, limited the total number of
cases in 3%. Of the group 29% had received treatment for pain symptoms in the
form of physical therapy (59%), medical management (28%), surgery (13%), and
time off from work (1%) [2]. The dominant upper extremity has been reported to
be the primary site of discomfort in 73% of respondents in a survey on surgeons
performing laparoscopic cholecystectomy [3]. In another respondent based study
evaluating laparoscopic graspers, 98 completed the questionnaire (response rate
35%), 77% reported physical complaints directly attributable to the use of laparo-
scopic instruments [4]. Though the increased physical workload is eminent in lapa-
roscopic surgery, studies have suggested an increased mental workload also
reflected as increased number of errors in laparoscopic surgery [5]. Thus improper
ergonomics can have important bearing on work efficiency and output with resul-
tant economic implications. Poor table height adjustment, bad monitor positioning
and suboptimal design of instrument handles were reported as important causes of
complications [3].
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence 195
The issue of ergonomics has gained an interest lately after the advent of laparo-
scopic surgery. Whereas an increased awareness and a rational approach to address
problems may be the reason for the upsurge in interest related to the subject, need-
less to say the effects have been multiplicated due to the decreased ergonomic ceil-
ing, resultant to increased physical and mental demands as also task complexity.
Performance of laparoscopic surgery is more stressful than open surgery [6]. The
important arenas in laparoscopic surgery which differs from open surgery and needs
consideration are: (1) Laparoscopic vision (2) Altered body postures (3) Longer
operative times (4) Workplace layout i.e. table height, monitor and foot pedal direc-
tions (5) Design and function of laparoscopic surgical equipments (6) Mental work-
load due to requirement of enhanced skills [7, 8].
(a) The Laparoscopic Vision and eye strain: The essential feature of laparoscopic
vision is that it is an indirect view: (1) depends on image transmission, clarity,
focussing, zooming, colour alteration and the efficient assistance of the camera
holding person. (2) the field of view is restricted to the area under vision as
degree of freedom of camera movement is limited (3) view is not under control
of the surgeon (4) the vision is two dimensional posing difficulty in depth per-
ception and spatial resolution. Resultant to these factors there is increased
demand for visual workload and consequential fatigue [9, 10]. Eye strain was
reported as a prominent ergonomic problem especially amongst junior surgeons
involved in laparoscopic surgery [11]
(b) Body Posture Related Problems: back pain, neck pain, shoulder/arm mus-
cle strain and pains/paresthesia in hand and fingers: Uncommon body pos-
tures excessive muscular load due to fatigue and pressure points causing nerve
injuries are the primary ergonomic concerns [9]. Back pain, neck pain fatigue
irritability and hand discomfort are some of the commonly reported symp-
toms [12].
Back pain and neck pain: Back pain is reported to be 15% more common in
laparoscopy and has been attributed to be due to a number of factors: (a) awk-
ward body posture due to far apart port positions, (b) need to look in one direc-
tion whereas instruments and foot pedals are often improperly positioned in a
different direction (c) increased neck rotation duration due to incorrect align-
ment of monitor and work axis [13] Surgeons exhibit decreased mobility of the
head and back and less anteroposterior weight shifting during laparoscopic
manipulations despite a more upright posture. This more restricted posture dur-
ing laparoscopic surgery may induce fatigue by limiting the natural changes in
body posture that occur during open surgery having an important bearing on
outcome [14]. Increased physical and mental workload both at baseline and
thereafter in the operation theatre can lead to fatigue and facilitate error in sur-
gical operations.
196 P. Hazrah et al.
Shoulder and arm muscle strains: The other posture related problems in lapa-
roscopic surgery are shoulder strains and arm muscle strains due to high level
of operating table compounded with pneumo-peritoneum and long working
instruments. Higher upper extremity muscle strength is required in performing
complex manipulative tasks of laparoscopic surgery [15]. Laparoscopic surgery
requires more skills due to altered instrument designs and increased force due
to use of small muscles. Additionally longer operating times especially initially
in learning curve is needed as also increased concentration. Difference in load-
ing between dominant and non dominant shoulders increased use of power
morcellation repeated insertion and removals of laparoscopic instruments
through trocars wherein strain occurs at the shoulder have been identified as
predominant factors which pose risk to surgeons. An advantage of height of
surgeon in this regard has been observed with increase in height resulting in
decrease in time spent in extreme body posture [13]. Extreme displacements of
the arm both vertical and horizontal due to insertion of instruments through
fixed trocars resulted in increased workload especially on upper arm and foream
muscles [16]. Thus mini breaks have been advised for posture readjust-
ments [17].
Wrist pain/hand pain/laparoscopic thumb/finger numbness: An extended
wrist posture is often used for performing most laparoscopic tasks [18]. The
“laparoscopic surgeons thumb” has been reported as a damage to the lateral
digital nerve of the thumb which is a superficial branch of the radial nerve in the
region [19, 20]. Increased paresthesia of fingers has been reported particularly
more amongst junior surgeons in laparoscopic surgery [11]. The use of a ringed
silicon rubber attachment has been proposed to prevent laparoscopic thumb
[21] A questionnaire based survey with The SAGES Task Force on Ergonomics,
respondents reported 8% to 12% frequent pain in the neck and upper extremi-
ties associated with laparoscopic surgery. The peak and total muscle effort of
forearm and thumb muscles were significantly greater when the grasping task
was performed using the laparoscopic instrument as compared with open hemo-
stat [22].
T Table Height: The height of the operating table has an important bearing on
O
shoulder and hand muscle strain. Most operating tables are constructed keeping in
view of open surgical procedures. The important difference between open and lapa-
roscopic surgery is that the effective working height increases in laparoscopic sur-
gery due to pneumo-peritoneum which distends the abdominal wall. Added to this
issue is the long laparoscopic working instrument, wherein a considerable portion
of the instrument protrudes out of the patients abdominal wall which necessitate
increased shoulder elevation, shoulder abduction and elbow flexion thereby causing
strain. In laparoscopic surgery task performance has been found to be best at the
height of operating table wherein the abdominal wall of the patient corresponds to
the thigh height of the operating surgeon which depends on the instrument handle
type (shank, pistol axial and rod type) as also the angle of insertion of the instrument
[25]. Thus substantial lowering of table, to a height of 30-60cmcm from the floor
has been suggested to facilitate ergonomic working. A concern regarding efficient
floor cleaning and hygiene issue has been raised as in open surgery the table height
is usually at the level of belt height however no substantial evidence against it has
been documented [25]. It has been said that the ideal operating table level should be
such that: (1) the angle between lower & upper arm should be between 90° and
120°. (2) after the insertion of instruments they should be roughly at, or slightly
below the level of the surgeon’s elbows (Fig. 1a, b) [17, 26, 27]. In a study on hand
assisted laparoscopy the optimal table height proposed is such that the extracorpo-
real instrument handle is at elbow level or 5 cm above [28]. The use of arm support
has been also been suggested [29]. Women surgeon experience greater difficulty in
laparoscopic surgery and adjustment in OT table height is often required [30].
198 P. Hazrah et al.
a b
Fig. 1 (a) Instrument handles at or below the level of elbow keeps the shoulder relaxed and indi-
cates correct table height. (b) Incorrect table height and long external length of instruments leads
to forearm being flexed
(a) Lack of haptic feedback: Laparoscopic surgery has the inherent disadvantage of
lack of haptic feedback (tactile as well as force sensation) which necessitates
more concentration and greater skill
(b) Use of long instruments: the long instruments designed to be manoeuvrable
into the depth of the abdominal cavity from exterior have an inefficient force
transmission mechanism and form a large external arc thus more force is
required which can result in fatigue of wrist and forearm muscle.
(c) Limited degree of freedom of movement of laparoscopic instrument [9].
(d) Inefficient instrument designs particularly handle designs [40].
technique [46]. In another study comparing pinch force required to grasp objects
with laparoscopic instruments, tweezers used in open surgery and bare hand, it was
observed that using a lap grasper, 14.5 times many practice trials were required,
whereas with tweezers it was 4.5 times more as compared to bare hand. This diffi-
culty was particularly evident in the grasping of stiff objects and in 84% times the
laparoscopic instruments slipped while holding stiff objects [42].
Additionally, the angle of handle with shaft can be inline or angulated configura-
tion. In contrast with open surgery where most instruments are designed primarily
in an in-line configuration, laparoscopic instruments are generally angulated at shaft
and handle junction as the direction of insertion into the abdominal cavity and direc-
tion of target in abdominal cavity differs.The ring and shank are usually placed in at
an angulation to the shaft whereas the pistol grip handle can be in both co axial or
angulated configurations. A point to be noted here is that the use of term pistol grip
has been varyingly used to denote a palm grip as well as an angulated handle shaft
configuration and similarly ring handle is often used to imply an angulated handle
shaft configuration. The ideal laparoscopic instrument should enable the surgeon to
keep both wrists in a neutral (unbent) position, permit the surgeon to keep both arms
at the sides of their body, avoid pressure points on the hands, allow the surgeon to
apply force with a power grip (hammer or gunstyle) hand position and facilitate fine
manipulation with a precision grip (pencil or forceps style) hand position [17].
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence 203
Precision Grasping for Fine Dissection (Fig. 8): The precision grip handles and
finger grip and are advantageous when work with precision like fine grasping or
dissecting is intended [29, 52].
Grasping Tissues for Prolonged Period: While grasping tissue for prolonged time
periods an instrument with a palm grip and locking mechanism is to be preferred
Instrument that incorporates a locking or ratchet mechanism will maintain the force.
“Palming” an instrument (removing the thumb from the ring and placing the palm
against the handle) can reduce the amount of wrist flexion and increase the sur-
geon’s power (Fig. 9) [17].
In a study evaluating pistol grip with pinch grip survey feedback indicated that a
significantly greater number of participants felt that using the pistol grip they expe-
rienced a greater degree of freedom and lesser discomfort nevertheless the authors
refrained from making any substantial conclusions based upon the study [53].
by the surgeon [17]. The ideal ergonomic characteristics of needle holders suggested
is: Grip opening 65–90 mm, Ring Dimension: length 30 mm, width 24 mm, Angle
between grip and tube 14° to 24°, Presence of spring, Opening and closure by flexors
and extensors of the fingers The two innovative ergonomic handles and needle hold-
ers described are the Cuschieri Ball Handle and the Cuschieri Pencil Handle [47]. In
a crossover trial using laparoscopic simulator studying laparoscopic suturing, the
authors found that the pistol grip handle led to more tissue damage and non goal
directed actions as compared with in line needle holder [64]. The pistol type align-
ment causes lesser ulnar deviation as compared to co axial alignment however the
former alignment may be disadvantageous in many surgical attributes precisely in
laparoscopic suturing where an unrestricted rotation at the wrist is desirable but
restricted with the sharply angulated pistol type alignment due to limitations caused
by hyperextension at the wrist [17]. However other authors have found pistol grip
needle drivers to be beneficial [52]. The other point of consideration for an efficient
laparoscopic suturing is needle insertion angle best within a range of 80° to 100° and
grip placed at proximal and middle third shaft of needle [65].
Hand Size: Most laparoscopic instruments are designed for a hand size of 6.5 or
more therefore surgeons with smaller hand sizes are at an inherent ergonomical
disadvantage in use of laparoscopic ring instruments as also in the use of staplers.
Contrarily in larger hand sizes also there is difficulty in handling smaller instru-
ments where power grip is desirable [55, 56, 66]. Designing equipment with provi-
sion for varying hand sizes is thus desirable. In another anonymous survey a similar
observation was noted. In the survey women reported the following devices more
awkward than their male counterparts: laparoscopic stapler, laparoscopic Harmonic
scalpel, and the laparoscopic LigaSure [67].
The Ratio Between Internal and External Length of the Instrument and Haptic
Perception: The ideal length of the instrument that has to be inserted into the
abdominal cavity has an important bearing on haptic perception. In a study evaluat-
ing the impact of differential length ratios (intraabdominal/external length) of lapa-
roscopic instrument on haptic functions, it was observed that a non symmetrical
bias in tissue stiffness was observed in tangential probing as opposed to radial prob-
ing especially in novices due to the fulcrum effect but the same was not observed in
experts handling [69]. The best ergonomics are thus achieved when ratio of intrab-
dominal length equals external length and is 1 [70].
208 P. Hazrah et al.
Azimuth angle: angle between one side instrument & telescope considered as a
horizontal projection (Fig. 11).
Elevation angle: angle between the instrument and patients body (Fig. 12).
Shaft sign: When the Azimuth angle is small the axis of the scope is circumjacent
to the axis of the instrument and can lead to obstructed visualization due to the
intervening shaft of the instrument known as the shaft sign.
Optical Axis Target View Angle and Optical Axis and Instrument Axis
Alignment: The optical axis target view angle is the angle formed between the
scope axis and target operation area for example the inferior liver surface in
Fig. 10 Manipulation
angle: angle between two
working instruments, ideal
45–75 degree
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence 209
cholecystectomy. It varies with the degree of the scope viz 0 degree scope/30 degree
scope and angulation of insertion. The 90° optical axis target view angle is said to
have the best accuracy i.e. optical axis is at 90° to surface of the target to be viewed
[71]. The various types of optical axis alignment with instrument manipulation are
broadly:
(1) In-optical axis manipulation (one instrument on either side of the laparoscope)
(Fig. 13).
(2) Off-optical axis manipulation-dominant type i.e. both instruments on one side
of the laparoscope to the dominant hand of the surgeon,
(3) Off-optical axis manipulation—non dominant type i.e. both instruments on one
side of the laparoscope on the nondominant side) (Fig. 14).
210 P. Hazrah et al.
Fig. 13 Concepts
demonstrated are:
triangulation of
instruments/in optical axis
alignment (camera
between two working
ports)
iii) Camera Ergonomics
The laparoscopic vision is essentially a 2D vision so depth perception and spatial
orientation is altered. Often hand-eye coordination is disrupted by the incongruent
mapping between the orientation of the endoscopic view and the actual operative
field thereby resulting in higher mental and physical load. Any alteration in camera
axis i.e.rotational distortion can significantly decrease performance. Performance is
best when the endoscopic image is perfectly aligned with the actual task space (0°
image rotation), but degraded progressively as a function of deviation from perfect
alignment [74].
The distance of the camera from the target also affects performance, the greater
the distance worse the performance. The recent innovations that are being investi-
gated to overcome these draw backs are: multiple 2D cameras, shadow introduction,
use of a 3D camera, automatic image realignment system, left to right mirror image
correction, inverted mirror image projection head mounted cameras and autostereo-
scopic monitors [75–78]. The 3D stereoscopic vision has been noted to produce less
visual fatigue and cognitive workload in training curriculum of novices [79].
However though some benefit is seen in novices but no difference was noted in
experts using 3D vs 2D vision [59]. The 2D laparoscopic image is noted to produce
more eye strains however refocussing problems is also an observed drawback of the
3D vision in laparoscopy [80]. The direction of view of the endoscope describes the
angle between the centre of the visual field (optical axis) and the physical axis of the
endoscope. Optical axis to target view angle is the angle between the optical axis of
the endoscope and the plane of the target. The best task performance during endo-
scopic work is obtained with an optical axis to target view angle of 90° [81].
Environment chaos and auditory chaos and distractions affects surgical motor per-
formance and learning and increase surgeons psychological burden in simulated
laparoscopic tasks [82]. Decreasing mental distractions by work environment
212 P. Hazrah et al.
modification can improve mental performance. Classical music has been shown to
consolidate memory [83].
A systematic review of music on simulated surgery performance has failed to
demonstrate significant benefit, however in laparoscopic surgery it has been sug-
gested to improve performance related to efficient transferring of instrument and
decreased mental workload [84, 85].
4. Training of Staff
Higher ergonomic risks and muscular exertion was noted in a NOTES as compared
with conventional laparoscopy [88, 89]. SILS also requires greater skills and has
more ergonomic constraints. The difference in ergonomics between conventional
laparoscopic surgery, NOTES, robotic and SILS is beyond the scope of discussion
in the current topic.
Conclusion
mental strain of the operating team. With increasing experience, proper training and
right choice of equipments one can circumvent the ergonomic constraints of laparo-
scopic surgery.
References
1. Burlington DB. Human factors and the FDA’s goals: improved medical device design. Biomed
Instrum Technol. 1996;30(2):107–9.
2. Franasiak J, Ko EM, Kidd J, Secord AA, Bell M, Boggess JF, Gehrig PA. Physical strain
and urgent need for ergonomic training among gynecologic oncologists who perform mini-
mally invasive surgery. Gynecol Oncol. 2012;126(3):437–42. https://doi.org/10.1016/j.
ygyno.2012.05.016.
3. Sari V, Nieboer TE, Vierhout ME, Stegeman DF, Kluivers KB. The operation room as a hostile
environment for surgeons: physical complaints during and after laparoscopy. Minim Invasive
Ther Allied Technol. 2010;19(2):105–9. https://doi.org/10.3109/13645701003643972.
4. Alleblas CC, Vleugels MP, Nieboer TE. Ergonomics of laparoscopic graspers and the impor-
tance of haptic feedback: the surgeons’ perspective. Gynecol Surg. 2016;13(4):379–84.
5. Yurko YY, Scerbo MW, Prabhu AS, Acker CE, Stefanidis D. Higher mental workload is asso-
ciated with poorer laparoscopic performance as measured by the NASA-TLX tool. Simul
Healthc. 2010;5(5):267–71. https://doi.org/10.1097/SIH.0b013e3181e3f329.
6. Berguer R, Forkey DL, Smith WD. The effect of laparoscopic instrument working angle on
surgeons’ upper extremity workload. Surg Endosc. 2001 Sep;15(9):1027–9.
7. Matern U, Rückauer KD, Farthmann EH. Working posture of laparoscopy-practicing sur-
geons: ideal and reality. Zentralbl Chir. 2000;125(8):698–701.
8. Lucas-Hernández M, Pagador JB, Pérez-Duarte FJ, Castelló P, Sánchez-Margallo
FM. Ergonomics problems due to the use and design of dissector and needle holder: a survey in
minimally invasive surgery. Surg Laparosc Endosc Percutan Tech. 2014;24(5):e170–7. https://
doi.org/10.1097/SLE.0b013e3182937fe8.
9. Matern U. Ergonomic deficiencies in the operating room: examples from minimally invasive
surgery. Work. 2009;33(2):165–8. https://doi.org/10.3233/WOR-2009-0862.
10. Supe AN, Kulkarni GV, Supe PA. Ergonomics in laparoscopic surgery. J Minim Access Surg.
2010;6(2):31–6. https://doi.org/10.4103/0972-9941.65161.
11. Hemal AK, Srinivas M, Charles AR. Ergonomic problems associated with laparoscopy. J
Endourol. 2001;15(5):499–503.
12. Shepherd JM, Harilingam MR, Hamade A. Ergonomics in Laparoscopic Surgery--A Survey of
Symptoms and Contributing Factors. Surg Laparosc Endosc Percutan Tech. 2016;26(1):72–7.
https://doi.org/10.1097/SLE.0000000000000231.
13. Aitchison LP, Cui CK, Arnold A, Nesbitt-Hawes E, Abbott J. The ergonomics of laparoscopic
surgery: a quantitative study of the time and motion of laparoscopic surgeons in live surgical
environments. Surg Endosc. 2016;30(11):5068–76.
14. Berguer R, Rab GT, Abu-Ghaida H, Alarcon A, Chung J. A comparison of surgeons’ posture
during laparoscopic and open surgical procedures. Surg Endosc. 1997;11(2):139–42.
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence 215
15. Berguer R, Chen J, Smith WD. A comparison of the physical effort required for laparoscopic
and open surgical techniques. Arch Surg. 2003;138(9):967–70.
16. Berguer R, Smith WD, Chung YH. Performing laparoscopic surgery is significantly more
stressful for the surgeon than open surgery. Surg Endosc. 2001;15(10):1204–7.
17. Whelan RL. Introductory Remarks Concerning Operating RoomSetup, Patient Positioning,
and Port Placement Chapters. In: Whelan RL, Fleshman JW, Fowler DL, editors. The SAGES
Manual of Perioperative Care in Minimally Invasive Surgery. 1st ed. New York: Springer-
Verlag; 2006. p. 41–7.
18. Bartnicka J, Zietkiewicz AA, Kowalski GJ. An ergonomics study on wrist posture when using
laparoscopic tools in four techniques in minimally invasive surgery. Int J Occup Saf Ergon.
2018;24(3):438–49. https://doi.org/10.1080/10803548.2018.1452666.
19. Kano N, Yamakawa T, Ishikawa Y, Miyajima N, Ohtaki S, Kasugai H. Prevention of laparo-
scopic surgeon’s thumb. Surg Endosc. 1995;9(6):738–9.
20. Lee WJ, Chae YS. Superficial nerve damage of thumb of laparoscopic surgeon. Surg Laparosc
Endosc Percutan Tech. 2001;11(3):207–8.
21. Inaki N, Kanehira E, Kinoshita T, Komai K, Omura K, Watanabe G. Ringed silicon rubber
attachment prevents laparoscopic surgeon’s thumb. Surg Endosc. 2007;21(7):1126–30.
22. Berguer R, Forkey DL, Smith WD. Ergonomic problems associated with laparoscopic surgery.
Surg Endosc. 1999;13(5):466–8.
23. Alarcon A, Berguer R. A comparison of operating room crowding between open and laparo-
scopic operations. Surg Endosc. 1996;10(9):916–9.
24. Klein M, Andersen LP, Alamili M, Gögenur I, Rosenberg J. Psychological and physical stress
in surgeons operating in a standard or modern operating room. Surg Laparosc Endosc Percutan
Tech. 2010;20(4):237–42. https://doi.org/10.1097/SLE.0b013e3181ed851d.
25. Matern U, Faist M, Kehl K, Giebmeyer C, Buess G. Monitor position in laparoscopic surgery.
Surg Endosc. 2005;19(3):436–40.
26. Berquer R, Smith WD, Davis S. An ergonomic study of the optimum operating table height for
laparoscopic surgery. Surg Endosc. 2002;16(3):416–21.
27. Kaur G. Role of OT table height on the task performance of minimal access surgery. World J
Laparosc Surg. 2008;1(1):49–55.
28. Manasnayakorn S, Cuschieri A, Hanna GB. Ergonomic assessment of optimum operating
table height for hand-assisted laparoscopic surgery. Surg Endosc. 2009;23(4):783–9. https://
doi.org/10.1007/s00464-008-0068-9.
29. Steinhilber B, Seibt R, Reiff F, Rieger MA, Kraemer B, Rothmund R. Effect of a laparoscopic
instrument with rotatable handle piece on biomechanical stress during laparoscopic proce-
dures. Surg Endosc. 2016;30(1):78–88. https://doi.org/10.1007/s00464-015-4164-3.
30. Sutton E, Irvin M, Zeigler C, Lee G, Park A. The ergonomics of women in surgery. Surg
Endosc. 2014;28(4):1051–5.
31. van Det MJ, Meijerink WJ, Hoff C, Totté ER, Pierie JP. Optimal ergonomics for laparo-
scopic surgery in minimally invasive surgery suites: a review and guidelines. Surg Endosc.
2009;23(6):1279–85. https://doi.org/10.1007/s00464-008-0148-x.
32. Walczak DA, Pawełczak D, Piotrowski P, Trzeciak PW, Jędrzejczyk A, Pasieka Z. Video dis-
play during laparoscopy - where should it be placed? Wideochir Inne Tech Maloinwazyjne.
2015;10(1):87–91. https://doi.org/10.5114/wiitm.2014.47434.
33. Seagull FJ, Sutton E, Lee T, Godinez C, Lee G, Park A. A validated subjective rating of dis-
play quality: the Maryland visual comfort scale. Surg Endosc. 2011;25(2):567–71. https://doi.
org/10.1007/s00464-010-1220-x.
34. Rousek JB, Brown-Clerk B, Lowndes BR, Balogh BJ, Hallbeck MS. Optimizing integration of
electrosurgical hand controls within a laparoscopic surgical tool. Minim Invasive Ther Allied
Technol. 2012;21(3):222–33. https://doi.org/10.3109/13645706.2011.603340.
216 P. Hazrah et al.
35. Kim FJ, Sehrt D, Molina WR, Pompeo A. Clinical use of a cordless laparoscopic ultrasonic
device. JSLS. 2014;18(3):e2014.001153. https://doi.org/10.4293/JSLS.2014.001153.
36. Youssef Y, Lee G, Godinez C, Sutton E, Klein RV, George IM, Seagull FJ, Park
A. Laparoscopic cholecystectomy poses physical injury risk to surgeons: analysis of hand
technique and standing position. Surg Endosc. 2011;25(7):2168–74. https://doi.org/10.1007/
s00464-010-1517-9.
37. Kramp KH, van Det MJ, Totte ER, Hoff C, Pierie JP. Ergonomic assessment of the French
and American position for laparoscopic cholecystectomy in the MIS suite. Surg Endosc.
2014;28(5):1571–8. https://doi.org/10.1007/s00464-013-3353-1.
38. Liu S, Hemming D, Luo RB, Reynolds J, Delong JC, Sandler BJ, Jacobsen GR, Horgan
S. Solving the surgeon ergonomic crisis with surgical exosuit. Surg Endosc. 2018;32(1):236–44.
https://doi.org/10.1007/s00464-017-5667-x.
39. Berguer R. Surgical technology and the ergonomics of laparoscopic instruments. Surg Endosc.
1998;12(5):458–62.
40. van Veelen MDW, Goossens RH, Snijders CJ. New ergonomic design criteria for handles of
laparoscopic dissection forceps. J Laparoendosc Adv Surg Tech A. 2001;11(1):17–26. https://
doi.org/10.1089/10926420150502896.
41. Susmitha WK, Mathew G, Devasahayam SR, Perakath B, Velusamy SK. Factors influenc-
ing forces during laparoscopic pinching: towards the design of virtual simulator. Int J Surg.
2015;18:211–5. https://doi.org/10.1016/j.ijsu.2015.04.078.
42. Westebring-van der Putten EP, Lysen WW, Henssen VD, Koopmans N, Goossens RH, van den
Dobbelsteen JJ, Dankelman J, Jakimowcz J. Tactile feedback exceeds visual feedback to dis-
play tissue slippage in a laparoscopic grasper. Stud Health Technol Inform. 2009;142:420–5.
43. Ulhaq N, Wadi H, Amlee T, Diesen D, Fey AM. Design and evaluation of haptic constraints
for laparoscopic instrument handling. Conf Proc IEEE Eng Med Biol Soc. 2018;2018:961–4.
https://doi.org/10.1109/EMBC.2018.8512421.
44. Cartmill JA, Shakeshaft AJ, Walsh WR, Martin CJ. High pressures are generated at the tip of
laparoscopic graspers. Aust N Z J Surg. 1999;69(2):127–30.
45. van der Putten EP, van den Dobbelsteen JJ, Goossens RH, Jakimowicz JJDankelman J. The
effect of augmented feedback on grasp force in laparoscopic grasp control. IEEE Trans
Haptics. 2010;3(4):280–91.
46. Quick NE, Gillette JC, Shapiro R, Adrales GL, Gerlach D, Park AE. The effect of using lapa-
roscopic instruments on muscle activation patterns during minimally invasive surgical training
procedures. Surg Endosc. 2003;17(3):462–5.
47. Palanivelu C. Chapter 2, Instrumentation and imaging system in laparoscopy. In: Art of lapa-
roscopic surgery, textbook and atlas, vol. vol 1. 1st ed. Coimbatore: Jaya Publications; 2005.
p. 11–33.
48. Ahmed S, Hanna GB, Cuschieri A. Optimal angle between instrument shaft and handle for
laparoscopic bowel suturing. Arch Surg. 2004;139(1):89–92.
49. Matern U, Koneczny S, Tedeus M, Dietz K, Buess G. Ergonomic testing of two different types
of handles via virtual reality simulation. Surg Endosc. 2005;19(8):1147–50.
50. Santos-Carreras L, Hagen M, Gassert R, Bleuler H. Survey on surgical instrument
handle design: ergonomics and acceptance. Surg Innov. 2012;19(1):50–9. https://doi.
org/10.1177/1553350611413611.
51. Landsmeer JMF. Power grip and precision handling. Ann Rheum Dis. 962;21(2):164–70.
https://doi.org/10.1136/ard.21.2.164.
52. Ramani AP, Braasch M, Botnaru A, Lavers A, Herrera S, Nardi Pedro R, Monga M. Evaluation
of efficacy of four laparoscopic needle drivers. JSLS. 2008;12(1):77–80.
53. Tung KD, Shorti RM, Downey EC, Bloswick DS, Merryweather AS. The effect of ergo-
nomic laparoscopic tool handle design on performance and efficiency. Surg Endosc.
2015;29(9):2500–5. https://doi.org/10.1007/s00464-014-4005-9.
54. Berguer R, Gerber S, Kilpatrick G, Remler M, Beckley D. A comparison of forearm and
thumb muscle electromyographic responses to the use of laparoscopic instruments with either
a finger grasp or a palm grasp. Ergonomics. 1999;42(12):1634–45.
Ergonomics in Laparoscopic Surgery: An Appraisal of Evidence 217
55. Rossi J, Berton E, Grélot L, Barla C, Vigouroux L. Characterisation of forces exerted by the entire
hand during the power grip: effect of the handle diameter. Ergonomics. 2012;55(6):682–92.
https://doi.org/10.1080/00140139.2011.652195.
56. Oh S, Radwin RG. Pistol grip power tool handle and trigger size effects on grip exertions and
operator preference. Hum Factors. 1993;35(3):551–69.
57. Hasson HM. Rotational handle for laparoscopic instrumentation. J Reprod Med.
1993;38(7):494–6.
58. Kraemer B, Seibt R, Stoffels AK, Rothmund R, Brucker SY, Rieger MA, Steinhilber B. An
ergonomic field study to evaluate the effects of a rotatable handle piece on muscular stress and
fatigue as well as subjective ratings of usability, wrist posture and precision during laparo-
scopic surgery: an explorative pilot study. Int Arch Occup Environ Health. 2018;91(8):1021–9.
https://doi.org/10.1007/s00420-018-1344-1.
59. Leite M, Carvalho AF, Costa P, Pereira R, Moreira A, Rodrigues N, Laureano S, Correia-Pinto
J, Vilaça JL, Leão P. Assessment of laparoscopic skills performance: 2D versus 3D vision
and classic instrument versus new hand-held robotic device for laparoscopy. Surg Innov.
2016;23(1):52–61. https://doi.org/10.1177/1553350615585638.
60. Shakeshaft AJ, Cartmill JA, Walsh WR, Martin CJ. A curved edge moderates high pressure
generated by a laparoscopic grasper. Surg Endosc. 2001;15(10):1232–4.
61. Mårvik R, Nesbakken R, Langø T, Yavuz Y, Vanhauwaert Bjelland H, Ottermo MV, Stavdahl
O. Ergonomic design criteria for a novel laparoscopic tool handle with tactile feedback.
Minerva Chir. 2006;61(5):435–44.
62. Ly HH, Tanaka Y, Fukuda T, Sano A. Grasper having tactile sensing function using acoustic
reflection for laparoscopic surgery. Int J Comput Assist Radiol Surg. 2017;12(8):1333–43.
https://doi.org/10.1007/s11548-017-1592-7.
63. Uchida K, Haruta N, Okajima M, Matsuda M, Yamamoto M. Multimedia article. The keys to
the new laparoscopic world Thumbs up! knot and Tornado knot. Surg Endosc. 2005;19(6):859.
https://doi.org/10.1007/s00464-004-6007-5.
64. Uchal M, Brogger J, Rukas R, Karlsen B, Bergamaschi R. In-line versus pistol-grip han-
dles in a laparoscopic simulators. A randomized controlled crossover trial. Surg Endosc.
2002;16(12):1771–3. https://doi.org/10.1007/s00464-002-8816-8.
65. Joice P, Hanna GB, Cuschieri A. Ergonomic evaluation of laparoscopic bowel suturing. Am J
Surg. 1998;176(4):373–8.
66. Berguer R, Hreljac A. The relationship between hand size and difficulty using surgical instru-
ments: a survey of 726 laparoscopic surgeons. Surg Endosc. 2004;18(3):508–12.
67. Adams DM, Fenton SJ, Schirmer BD, Mahvi DM, Horvath K, Nichol P. One size does not fit
all: current disposable laparoscopic devices do not fit the needs of female laparoscopic sur-
geons. Surg Endosc. 2008;22(10):2310–3. https://doi.org/10.1007/s00464-008-9986-9.
68. Li Z, Wang G, Tan J, Sun X, Lin H, Zhu S. Building a framework for ergonomic research
on laparoscopic instrument handles. Int J Surg. 2016;30:74–82. https://doi.org/10.1016/j.
ijsu.2016.04.027.
69. Nisky I, Huang F, Milstein A, Pugh CM, Mussa-Ivaldi FA, Karniel A. Perception of stiffness
in laparoscopy - the fulcrum effect. Stud Health Technol Inform. 2012;173:313–9.
70. Emam TA, Hanna GB, Kimber C, Dunkley P, Cuschieri A. Effect of intracorporeal-
extracorporeal instrument length ratio on endoscopic task performance and surgeon move-
ments. Arch Surg. 2000;135(1):62–5; discussion 66.
71. Rhee R, Fernandez G, Bush R, Seymour NE. The effects of viewing axis on laparoscopic
performance: a comparison of non-expert and expert laparoscopic surgeons. Surg Endosc.
2014;28(9):2634–40. https://doi.org/10.1007/s00464-014-3515-9.
72. Holznecht C, Schmidt T, Gould J. The impact of training under different visual-spatial condi-
tions on reverse-alignment laparoscopic skills development. Surg Endosc. 2012;26(1):120–3.
https://doi.org/10.1007/s00464-011-1836-5.
73. Martinec DV, Gatta P, Zheng B, Denk PM, Swanström LL. The trade-off between flexibil-
ity and maneuverability: task performance with articulating laparoscopic instruments. Surg
Endosc. 2009;23(12):2697–701. https://doi.org/10.1007/s00464-009-0462-y.
218 P. Hazrah et al.
74. Zhang L, Cao CG. The effect of image orientation on a dynamic laparoscopic
task. Proc Hum Factors Ergon Soc Annu Meet. 2010;54(11):774–8. https://doi.
org/10.1177/154193121005401108.
75. Honeck P, Wendt-Nordahl G, Rassweiler J, Knoll T. Three-dimensional laparoscopic imag-
ing improves surgical performance on standardized ex-vivo laparoscopic tasks. J Endourol.
2012;26(8):1085–8. https://doi.org/10.1089/end.2011.0670.
76. Zhang L, Cao CG. Effect of automatic image realignment on visuomotor coordination in
simulated laparoscopic surgery. Appl Ergon. 2012;43(6):993–1001. https://doi.org/10.1016/j.
apergo.2012.02.001.
77. Bogdanova R, Boulanger P, Zheng B. Depth perception of surgeons in minimally invasive
surgery. Surg Innov. 2016;23(5):515–24. https://doi.org/10.1177/1553350616639141.
78. Abodeely AA, Cheah YL, Ryder BA, Aidlen JT, Luks F. Eliminating the effects of paradoxic
imaging during laparoscopic surgery. J Laparoendosc Adv Surg Tech A. 2010;20(1):31–4.
https://doi.org/10.1089/lap.2009.0227.
79. Lin CJ, Cheng CF, Chen HJ, Wu KY. Training performance of laparoscopic surgery
in two- and three-dimensional displays. Surg Innov. 2017;24(2):162–70. https://doi.
org/10.1177/1553350617692638.
80. El Boghdady M, Ramakrishnan G, Alijani A. A study of the visual symptoms in two-
dimensional versus three-dimensional laparoscopy. Am J Surg. 2018;216(6):1114–7. https://
doi.org/10.1016/j.amjsurg.2018.07.051.
81. Hanna GB, Cuschieri A. Influence of the optical axis-to-target view angle on endoscopic task
performance. Surg Endosc. 1999;13(4):371–5.
82. Gao J, Liu S, Feng Q, Zhang X, Jiang M, Wang L, Zhang J, Zhang Q. Subjective and objec-
tive quantification of the effect of distraction on physician’s workload and performance during
simulated laparoscopic surgery. Med Sci Monit. 2019;25:3127–32. https://doi.org/10.12659/
MSM.914635.
83. Conrad C, Konuk Y, Werner PD, Cao CG, Warshaw AL, Rattner DW, Stangenberg L, Ott
HC, Jones DB, Miller DL, Gee DW. A quality improvement study on avoidable stress-
ors and countermeasures affecting surgical motor performance and learning. Ann Surg.
2012;255(6):1190–4. https://doi.org/10.1097/SLA.0b013e318250b332.
84. Oomens P, Fu VX, Kleinrensink GJ, Jeekel J. The effect of music on simulated surgical per-
formance: a systematic review. Surg Endosc. 2019;33(9):2774–84. https://doi.org/10.1007/
s00464-019-06868-x.
85. Oomens P, Fu VX, Kleinrensink VEE, Kleinrensink GJ, Jeekel J. The effects of preferred
music on laparoscopic surgical performance: a randomized crossover study. World J Surg.
2020; https://doi.org/10.1007/s00268-020-05523-0.
86. Tse MA, Masters RS, McManus AM, Lo CY, Patil NG. Trunk muscle training, posture fatigue,
and performance in laparoscopic surgery. J Endourol. 2008;22(5):1053–8.
87. Glassman D, Yiasemidou M, Ishii H, Somani BK, Ahmed K, Biyani CS. Effect of play-
ing video games on laparoscopic skills performance: a systematic review. J Endourol.
2016;30(2):146–52. https://doi.org/10.1089/end.2015.0425.
88. Lee G, Sutton E, Clanton T, Park A. Higher physical workload risks with NOTES versus lapa-
roscopy: a quantitative ergonomic assessment. Surg Endosc. 2011;25(5):1585–93. https://doi.
org/10.1007/s00464-010-1443-x.
89. Montero PN, Acker CE, Heniford BT, Stefanidis D. Single incision laparoscopic surgery
(SILS) is associated with poorer performance and increased surgeon workload compared with
standard laparoscopy. Am Surg. 2011;77(1):73–7.
Surgical Meshes Used in Laparoscopic
Procedures
Anubhav Vindal, Yashika Gupta,
and Piyush Kumar Agrawal
Introduction
The term ‘mesh’ refers to prosthetic material, either a net or a flat sheet, which is
used to strengthen a hernia repair. The logic behind use of mesh is that it reinforces
the native tissue with formation of scar tissue by inducing fibrosis [1].
Mesh can be used:
• To bridge a defect: the mesh is simply fixed over the defect as a tension-free patch;
• To plug a defect: a plug of mesh is pushed into the defect;
• To augment a repair: the defect is closed with sutures and the mesh added for
reinforcement [2].
In this chapter we discuss the various types of meshes used in laparoscopic sur-
gery, their indications, advantages and disadvantages.
History
In 1890, Theodor Billroth suggested that the ideal way to repair hernias is to use a
prosthetic material to close the hernia defect [3]. Phelps in 1894 used silver wire
braided meshes for repair of hernia. Later, in 1900, Goepel, Perry and Witzel also
used these silver wire meshes for hernia repair [4–7]. The stiffness due to the metal
used in the prosthesis prompted a modification of the meshes, and these were
replaced with braided meshes made from stainless steel [8–10].
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 219
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_9
220 A. Vindal et al.
With the turn of twentieth century, use of newer materials like nylon mesh, poly-
vinyl sponge, orlon cloth, teflon and silicon mesh was reported in hernia repair. But
these were soon discarded either due to reported complications or due to less than
optimal results. The start of second world war, lead to an increased demand of steel
and tantalum for military equipment, ultimately raising their cost and scarcity.
Together with this, there was a boom in the plastic and polymer industry. Both of
these events forced the surgeons and manufacturers to develop newer prosthesis
based on these newer polymers. In 1955, Usher focused his attention on newer
materials that could solve the problems with the existing biomaterials, and he was
the first to use a woven mesh made from a new polyolefin material (Marlex). This
new material had large pores, which facilitated incorporation of the prosthesis in
presence of infections. Despite the success, Usher continued to develop better mesh
units. He soon found that knitted polypropylene had many additional advantages: it
could be autoclaved, it had firm borders, had two-way stretching, and could be rap-
idly incorporated in the body [11, 12]. In 1958, Usher published his surgical tech-
nique using a polypropylene mesh. Almost 30 years later the Lichtenstein
“tension-free” mesh repair was popularized for hernia repair [12].
A switch from metal-based prosthesis to polymers lead to the development of
materials like polypropylene, polytetrafluoroethylene (ePTFE) and polyester. These
three materials are still the backbone of most meshes and today are most commonly
used in prosthetic meshes around the world [13–17].
The principles of functional tissue engineering [18] were initially developed to help
guiding the design of implants that help in the replacement or repair of body struc-
tures which have important biomechanical functions. The same principles also
apply to the mesh prostheses used for hernia repair.
The most important properties considered in hernia mesh design and manufac-
turing are as follows in Table 1.
Table 1 (continued)
Property Definition Goals/characteristics
Stiffness The extent to which an object Goals stated as measures of
resists deformation in response to elasticity (currently no
an applied force, and is the opposite standardized range of values).
of compliance.
Pore size Macroporous: >75 μm Neovascularization and tissue
integration are frequently
observed.
Microporous: <10 μm Impedes human cellular
penetration and tissue ingrowth.
Weight Lightweight <33 g/m2 Less intense foreign body
Heavyweight >100 g/m2 reaction in light weight meshes.
Degradation Disappearance of mesh biomaterial The mesh should last until scar
or gradual decline in its mass. or regenerative tissue replaces it
and matures to its maximum
strength.
Constitution Monofilament Multifilament meshes are more
Mutifilament pliable, have higher infection
rate and intense foreign body
reaction.
Anisotropy Degree to which mechanical Almost all synthetic meshes
properties differ in response to exhibit various degrees of
applied loads in different axes. anisotropy.
a b
Fig. 1 Difference between the mesh construction (a) Knit (b) Weave
Biocompatibility
Mechanical Properties
Tensile Strength
Elasticity
Elasticity, compliance and stiffness are terms that are frequently used interchange-
ably. Elasticity is the property of a material to return to its original shape after being
deformed. It indicates the amount of displacement in response to a specific amount
Surgical Meshes Used in Laparoscopic Procedures 223
Stiffness
Pore size and weight are important aspects of mesh design [35–38]. Pores <10 μm
do not allow human cellular penetration and tissue in growth [39]. Pore sizes
≤75 μm, may prevent the access of antimicrobial agents and host immune cells to
bacteria (which are smaller in size), thus, predisposing the prosthesis to bacterial
colonization and infection. Such meshes are sometimes referred to as microporous
meshes, as opposed to macroporous meshes with pore sizes >75 μm [40]. The ePT-
FEsheets (eg: Dualmesh {WL Gore and Associates, USA}) are the only micro
porous synthetic meshes in clinical use, and frequently require explantation when
infected [41–43].
Neovascularization and tissue integration are frequently observed as the pore
size increases to the range of 100–300 μm, but granuloma bridging remains a con-
cern [27]. Granuloma bridging is the phenomenon of coalescence of the foreign
body response around mesh fibres. It can clog the pores of the mesh and prevent its
further tissue integration [27]. In polypropylene meshes, when pore sizes are
<1 mm, granulomas can become confluent, encapsulate the mesh and create a stiff
plate with reduced flexibility [40, 44].
Although it was previously believed that a large pore size would delay tissue
incorporation, this has not been observed in practice. In fact, it has been seen that
the large-pore meshes (with lower surface-area-to-volume ratios) though resulting
in a milder foreign-body reaction, the tissue incorporation is adequate and is facili-
tated by the larger poresize. The caveat is that a reduced mesh material results in a
base mesh with reduced strength.
224 A. Vindal et al.
Weight
Mesh weight is partially dependent on the weight of the polymer from which it is
made [1] but is also dependent on its pore size [44]. With greater pore sizes, less
material is used to construct the mesh, and mesh weight is reduced. The lightweight
meshes generally weigh less than 33 g/m2, while heavyweight meshes generally
weigh more than 100 g/m2 [1, 20]. It is expected that lighter weight meshes will
have lesser foreign body burden [45] and a smaller biomaterial surface area [46],
thereby eliciting a less intense foreign body reaction. However, in practice, the
results have been found to be variable [33, 46].
In practice, large-pore lightweight meshes are reported to have a similar clinical
profile to small-pore heavyweight meshes [47, 48]. Infact one study reported higher
rates of shrinkage for large-pore lightweight mesh compared with small-pore heavy-
weight meshes [49]. Some studies have suggested that large-pore lightweight
meshes result in superior tissue integration [50], better elasticity [51] and a lower
incidence of pain [52], while other studies report a higher recurrence rate for large-
pore lightweight mesh especially in larger groin hernias repaired laparoscopi-
cally [53].
Degradation
Degradation means the disappearance of mesh or a gradual decline in its mass, and
it can be desirable or undesirable. In meshes that are degradable (absorbable), the
aim is to have the mesh provide support until the regenerative tissue replaces it and
matures to the maximum strength. Studies with Vicryl® and Dexon® meshes, have
shown that a three-month time frame for absorption is inadequate [54–56]. Other
studies with the Gore Bio-A® mesh suggest that a longer degradation time of
6 months could be successful [54, 57, 58]. However, the long-term recurrence rate
of the Gore Bio-A® mesh has been reported to be high, ranging from 13% to 37.5%.
It has therefore been suggested that 12 months may be a better time frame for mesh
absorption, to ensure full maturation of the scar tissue with adequate strength to
support the repair. Newer synthetic degradable meshes such as Phasix® and TIGR
Matrix®, that have even slower degradation rates, could be more useful in this con-
text. In clinical situations where the mesh is used to bridge the defect, the mesh is
required to remain indefinitely in place to provide structural support. In these situa-
tions, a degradable mesh is contraindicated and will lead to an early 100% recur-
rence rate [59]. However one must remember that even non-degradable meshes may
slowly degrade over time.
Polyester meshes have been known to have the drawback of long-term degrada-
tion, thereby making them unsuitable for long-term support [60]. Recently, similar
behaviour has also been observed with polypropylene, which is one of the most
widely used biomaterials for meshes [61]. It has been postulated that this degrada-
tion is accelerated with exposure of polypropylene to heat during the manufacturing
Surgical Meshes Used in Laparoscopic Procedures 225
process [62]. Degradation of a mesh that is not meant to degrade may contribute to
mechanical failure of the prosthesis and hernia recurrence.
Another important consideration is to understand what replaces the mesh once it
has degraded: scar or regenerated tissue. Regenerated tissue exhibits a greater
degree of cellular infiltration, degradation, deposition of extracellular matrix, neo-
vascularization, lower inflammatory cell response, and less scar encapsulation,
whereas scar tissue has limited host cell and vessel infiltration, more fibrotic matrix,
and aligned collagen deposition. The meshes that are more antigenic are replaced by
scar, whereas those that are less antigenic are replaced by regenerated tissue.
Constitution
Synthetic meshes can be monofilament (mesh fibres are made of single filaments)
or multifilament (mesh fibres consist of multiple filaments). Examples of multifila-
ment meshes include
Multifilament meshes are more pliable than monofilament meshes [63]. Reports
suggest that multifilament meshes have higher infection rates compared to the
monofilament meshes due to the presence of inaccessible crevices between the fila-
ments and a stronger foreign body reaction due to the larger surface areas [64].
Anisotropy
Classification of Meshes
Amid et al. [67], were the first to attempt to classify the meshes according to the
pore size and found pore size was decisive for compatibility. They defined four dif-
ferent types of meshes based on pore size:
226 A. Vindal et al.
A complex interaction of biological and host response is seen during the tissue
reaction to the mesh material. Mesh architecture and mesh design also affect the
response apart from the material used. Weyhe et al. proved in 2006 that lighter
weight mesh does not necessarily mean lesser biological and host response during a
comparison between light weight and heavy weight prosthesis [68]. In fact, some
heavy weight meshes also show a very good tissue biocompatibility due to the large
pores which decreases scar bridging. Reduced bridging of scar is found to be associ-
ated with reduced mesh contraction [69, 70].
On seeing the increasing popularity of intra-abdominal mesh placement during
laparoscopic procedures, Deeken et al. felt the necessity to further sub-classify the
meshes with additional barrier function [71]. Prosthesis were attempted to be clas-
sified on basis of their properties of elasticity and biomechanical stability. This clas-
sification system could not be popularised due to marked anisotropy giving different
values in different axes [21, 65, 72, 73].
An attempt was made by Klinge et al. to overcome the limitations of anisotropy
[44], and to categorize and subclassify meshes into classes, taking the textile data of
the mesh into consideration and suggest the concept of “mesh porosity”. To nullify
the effect of anisotropy, “effective porosity” was suggested to classify meshes as:
The mesh porosity concept lost favour with researchers with advent of various
new materials in the market, changes in mesh designing and fibres as well as diffi-
culties in measuring porosity. Coda et al. proposed a classification taking into con-
sideration the two important factors i.e. mesh density and weight: [74].
While a heavy-weight mesh is produced with heavy materials, small pore size
and high tensile strength, a light-weight is composed of thin filaments with large
pores, generally larger than 1 mm.
Before deciding which mesh to be used in a given clinical situation, an under-
standing of different raw materials is important. Different clinical situations make it
necessary to use different raw materials. Many surgeons consider the ease of mesh
handling as one of the important factors during laparoscopic mesh repair while
choosing a mesh. Characteristics of mesh handling usually have a bearing over both
the operative time and results.
The meshes can also be classified as uncoated, coated or barrier and biologi-
cal meshes.
1. Polypropylene biomaterials
The advantages of this material are that it is flexible, strong, can be cut easily,
resists infection and may be used in contaminated fields. However, it has the
228 A. Vindal et al.
a b
Fig. 2 Uncoated Meshes (a) Polypropylene biomaterial (b) PTFE biomaterial (c) Polyester
biomaterial
a b
c d
Fig. 3 Coated meshes with a permanent barrier (a) DualMesh® (b) Composix E/X® (c) Composix
L/P® (d) Ti mesh®
230 A. Vindal et al.
a b
Fig. 4 Coated meshes with an absorbable barrier (a) Proceed® (b) Parietex Composite® (c)
Ultrapro® (d) Sepramesh® (e) Dynamesh® (f) Parietene DS®
These are based on collagen scaffold derived from a donor source. The tissues are
decellularized to leave only the highly organized collagen architecture with the sur-
rounding extracellular ground tissue. Removal of all live cells and all nuclear tissue
a b
d e
Fig. 5 Biological meshes (a) Strattice® (b) Xenmatrix® (c) Surgisis® (d) Tutopatch® (e) Surgi
Mend® (f) Collamend® (g) Flex HD®
232 A. Vindal et al.
is done to prevent rejection by the host. Cross linking is done between either inter
molecular or intra molecular amino acids along protein structure to resist degrada-
tion and increase longevity.
1. Human dermis
AlloDerm (LifeCell)
AlloMax (Bard/Davol)
FlexHD (MTF/Ethicon)
2. Porcine Dermis
Permacol (TSL/Covidien)
Collamend (Bard/Davol)
Strattice (LifeCell)
XenMatrix (Brennan Medical)
XCM Biologic (Ethicon/DSM Biomedical)
3. Porcine small intestine submucosa
Surgisis (Cook)
4. Foetal bovine dermis
Surgi Mend (TEI Biosciences)
5. Bovine pericardium
Tutopatch (Tutogen Medical)
Veritas (Synovis)
Another way in which the meshes have been classified is based on their deriva-
tion (synthetic/biological) and their absorbability.
6. Biological meshes
These constitute of collagen rich tissues from human or animals, which have
been stripped of all cellular contents and the resultant extracellular protein struc-
ture being stabilized. It is thought to act as a collagen scaffold for the in growth
and deposition of fibroblast and collagen [76, 77].
Yet another classification divides the meshes according to their composition or
type of material as:
b c
Fig. 6 Newer meshes (a) Zenapro® (b) Absomesh® (c) Phasix® (d) Rebound HRD® (e) Ventrio®
(f) Symbotex composite® (g) Progrip® (h) 3D-Max®
Surgical Meshes Used in Laparoscopic Procedures 235
Fig. 6 (continued)
the parietal surface has an abdominal wall clinging effect which helps to keep
the mesh on position while the fixation is being done.
7. Progrip (Medtronic): It is a self-gripping light-weight mesh with large pore
sizes (1.1–1.7 mm) composed of monofilament polyester and polylactic acid
micro-grips. The immediate adherence to tissue is provided by resorbable micro-
grips, and therefore additional fixation is not needed anymore.
8. Preformed mesh-Bard 3D Max: It is a plain, non-absorbable, large pore size
polypropylene mesh, with an anatomical shape, already precut and reinforced on
the margins. Grossly it has a blue marker for the medial orientation, crest for the
axis of inguinal ligament and an inferior notch for alignment with the external
iliac vessels. These features help in proper placement of the mesh, avoid migra-
tion and ultimately reduce hernia recurrence.
The different surgical mesh classes along with their various advantages and dis-
advantages are listed in the Table 2. The meshes that get absorbed or remodel with
time and are ultimately replaced by either scar tissue or regenerative matrix are
termed as ‘degradable’.
236 A. Vindal et al.
Complications
Hernia Recurrence
Pain and bulge are the most common way of presentation of any recurrence, a
small percentage of patients may present with obstruction or strangulation.
Diagnosis is generally made by clinical examination, ultrasound and a CT scan.
Treatment of hernia recurrence is more complex than the primary surgery due to the
fact that there will be adhesions, a larger defect, and an unfavorable patient
Surgical Meshes Used in Laparoscopic Procedures 237
condition like obesity, comorbidity, etc. Choice of surgical repair will depend on
several factors such as previous surgery, mechanism of failure, obesity, size and
complexity of defect.
Mesh Infection
Open ventral incisional hernia repair has reported an infection rate of 6–10% [42]
mostly compounded by flap necrosis. Incidence of infection is rare after laparo-
endoscopic hernioplasty, due to the limited physical contact of the mesh with the
skin or surgical wound during the surgery. Gram positive bacteria (Staphyococcus
aureus, Streptococcus spp) and Gram negative bacteria (Enterobacteriaceae) are the
most common organisms causing mesh infection. Patient co-morbidity and proce-
dure related risk factors such as obesity, abdominal aortic aneurysm repair, chronic
obstructive pulmonary disease, use of the same incision to perform other procedures
at the time of repair, previous surgical site infection, longer operative time, lack of
tissue coverage of the mesh, enterotomy and enterocutaneous fistulas are some
problems associated with a higher incidence of mesh infection [42]. Various mesh-
related risk factors include the utilization of larger mesh sheets, microporous meshes
or ePTFE mesh [42].
Mesh infections are classified as superficial and deep infections and have been
reported to occur 2 weeks to 39 months from the day of mesh implantation [42].
Infections of the mesh generally respond very poorly to antibiotic treatment.
Superficial infection is treated by intravenous antibiotics and drainage of any col-
lected pus and might have a slightly better prognosis. Prolonged antibiotic treatment
with percutaneous or open drainage of abscess is needed for limited deep seated
infection. In case of extensive infection, a biofilm develops which limits antibiotic
penetration in the infected area. Therefore, in cases like these, the mesh needs to be
removed and surgical debridement of the infected tissue has to be done.
Various preventive measures like following strict aseptic protocol including
change of gloves before handling the mesh and using a no- touch technique as far as
possible helps in minimizing the incidence of mesh related wound infection.
Prophylactic antibiotic coverage is often used but guidelines do not recommend use
of antibiotics in laparoendoscopic hernia repair, although protocols vary institu-
tion wise.
The most debilitating unrelenting infection occurs due to atypical mycobacteria
(Mycobacterium cheloneii). The commonest source is improperly sterilized laparo-
scopic instruments using liquid agents like glutaraldehyde which supports the
growth of these organisms [42]. Autoclaving instruments prevent these infections.
Treatment consists of drainage of any collection and use of anti-tubercular therapy,
however invariably mesh removal is also required. A rescue attempt can be made in
cases of macro porous meshes with extended broad-spectrum antibiotics, local
infected tissue debridement, wound irrigation and vacuum assisted drainage [42].
Complex, contaminated, or potentially contaminated fields are potential indica-
tions of the usage of biological prostheses, but whether and how they are safe for
238 A. Vindal et al.
use is still unclear [86]. Controversy lies in the safety of synthetic non-degradable
meshes in an infected field [86–88]. After the seeding of infection on the non-
degradable mesh, the main concern is inability to treat mesh infection and ulti-
mately mesh explantation. A potential alternative to the biological meshes in
complex or infected fields are the synthetic degradable meshes. High costs of bio-
logic meshes compel some authors to believe that there may be a definite place for
non-degradable meshes in infected fields [89–91].
Adhesion
Visceral adhesion to mesh remains a concern for meshes used in bridging repairs or
for meshes placed intraperitoneally. Various studies depict that bi-face [92] and
barrier-coated [93] composite meshes are effective in reduced adhesion formation.
Temporary barrier coated meshes have a potential problem of lack of specific time-
line for adhesion formation [94]; which may happen any time after mesh implanta-
tion. This issue has been partially addressed by stable hydrophilic coatings that do
not degrade with time but this solution is still in its early stages with limited long
term reports in existing animal model data [95]. ePTFE meshes have been found to
have least adhesion rates [96]. Lightweight meshes, due to their properties of less
foreign body reaction and better integration, have also been reported to show lower
adhesion rates [97].
Postoperative Pain
These include mesh: shrinkage, mesh migration and erosion into bladder.
Shrinkage up-to 20% of the original size of the mesh is expected and depends on
the material of the mesh. Primarily shrinkage is of the mesh textile itself, in con-
junction with collagen fiber shortening as part of wound healing. This is of para-
mount importance and has to be always kept in mind when mesh size is decided for
Surgical Meshes Used in Laparoscopic Procedures 239
a given hernia defect. Improper size of the mesh can be a factor responsible for
hernia related morbidity including recurrence.
Mesh migration has been described with all types of inguinal hernia repair and
with all mesh materials. However, the lowest risk is with the use of a large flat mesh
in a tension free setting.
Mesh erosion into the bladder is a rare complication after laparo-endoscopic
inguinal hernia repair. It is mostly due to unrecognized bladder injury during the
hernia repair and is not related to the mesh material used. Patients may present with
recurrent urinary tract infection, bladder stone formation and hematuria.
There is a lifetime risk of mesh migration and erosion which increases with
increasing duration of mesh implantation, and these must be considered as possi-
bilities when a patient presents with relevant symptoms after hernia repair.
1. Chemically inert
2. Non carcinogenic
3. Non inflammatory
4. Non allergic
5. Resistant to mechanical strain
6. Resistant to infection
7. Elastic and flexible
8. Have a good memory
9. Transparent
10. Have minimal shrinkage
11. Easy to handle
12. Minimal adhesion formation
13. Rapid incorporation
14. Inexpensive
Conclusions
It has been proposed that there should be no standardization of mesh within any
institution, allowing surgeons and patients to have options between different types
of available meshes. As on date, there are no long-term clinical or experimental data
240 A. Vindal et al.
to support the use of most mesh products, and the choices are usually dictated by
personal experiences of the surgeons and hospital policies.
Unfortunately, an ideal mesh has not been developed yet. The problems with the
current meshes include infection, recurrence, post-operative seroma and adhesions,
and these continue to torment the hernia surgeons.
12. There is a lifetime risk of mesh migration and erosion which increases with
increasing duration of mesh implantation, and these must be considered as pos-
sibilities when a patient presents with relevant symptoms after hernia repair.
References
1. Brown CN, Finch JG. Which mesh for hernia repair? Ann R Coll Surg Engl. 2010;92(4):272–8.
2. Tulloh B, Nixon SJ. Abdominal wall, hernia and umbilicus. In: Williams N, O’Connell PR,
McCaskie AW, editors. Bailey and Love’s short practice of surgery. 27th ed. Boca Raton, FL:
CRC Press, Taylor & Francis; 2018. p. 1022–46.
3. Billroth T, Banov L Jr, Speed K. The medical sciences in the German universities: a study in
the history of civilization. New York: Macmillan; 1924.
4. Goepel R. Über die Verschliessung von BruchpfortendurchEinheilunggeflochtenerfertigerSil-
berdrahtnetze{About the opening up of hernial portals through the healing of braided, finished
silver wire nets}. ZentralblChir. 1900;17:3.
5. Perry HB. Implantations of silver filigree for cure of large ventral hernia; report of two cases.
Boston Med Surg J. 1904;151:2.
6. Witzel O. Über den Verschluss von Bauchwunden und BruchpfortendurchversenkteSilberdrah
tnetze{About the closure of abdominal wounds and hernial openings with recessed silver wire
nets}. ZetralblChir. 1900;27:3.
7. Phelps A. A new operation for hernia. N Y Med J. 1894;60:291.
8. Preston DJ, Richards CF. Use of wire mesh prostheses in the treatment of hernia. 24 years’
experience. Surg Clin N Am. 1973;53:549–54.
9. Mathieson AJ, James JH. A review of inguinal hernia repair using stainless steel mesh. J R Coll
Surg Edinb. 1975;20:58–62.
10. Thomeret G, Dubost C, Pillot P. The use of inoxydizable steel gauze in the treatment of even-
trations of hernias. Mem Acad Chir (Paris). 1960;86:500–7.
11. Usher FC, Hill JR, Ochsner JL. Hernia repair with Marlex mesh. A comparison of techniques.
Surgery. 1959;46:718–28.
12. Usher FC, Fries JG, Ochsner JL, Tuttle LL. Marlex mesh, a new plastic mesh for replacing
tissue defects. AMA Arch Surg. 1959;78:138–45.
13. Doran FS, Gibbins RE, Whitehead R. A report on 313 inguinal herniae repaired with nylon
nets. Br J Surg. 1961;48:430–4.
14. Usher FC, Wallace SA. Tissue reaction to plastics; a comparison of nylon, orlon, Dacron,
Teflon, and Marlex. AMA Arch Surg. 1958;76:997–9.
15. DeBord JR. The historical development of prosthetics in hernia surgery. Surg Clin N Am.
1998;78:973–1006.
16. Usher FC, Ochsner J, Tuttle LL Jr. Use of marlex mesh in the repair of incisional hernias. Am
Surg. 1958;24:969–74.
17. Adloff M, Arnaud JP. Surgical management of large incisional hernias by an intraperitoneal
Mersilene mesh and an aponeurotic graft. Surg Gynecol Obstet. 1987;165:204–6.
18. Butler DL, Goldstein SA, Guilak F. Functional tissue engineering: the role of biomechanics. J
Biomech Eng. 2000;122:570–5.
19. Pott PP, Schwarz ML, Gundling R, Nowak K, Hohenberger P, Roessner ED. Mechanical
properties of mesh materials used for hernia repair and soft tissue augmentation. PLoS One.
2012;7:e46978.
20. Bilsel Y, Abci I. The search for ideal hernia repair; mesh materials and types. Int J Surg.
2012;10:317–21.
21. Cobb WS, Peindl RM, Zerey M, Carbonell AM, Heniford BT. Mesh terminology 101. Hernia.
2009;13:1–6.
242 A. Vindal et al.
22. Brandt CJ, Kammer D, Fiebeler A, Klinge U. Beneficial effects of hydrocortisone or spirono-
lactone coating on foreign body response to mesh biomaterial in a mouse model. J Biomed
Mater Res A. 2011;99:335–43.
23. Novitsky YW, Orenstein SB, Kreutzer DL. Comparative analysis of histopathologic responses
to implanted porcine biologic meshes. Hernia. 2014;18:713–21.
24. Klosterhalfen B, Klinge U, Rosch R, Junge K. Long-term inertness of meshes. In: Schumpelick
V, Nyhus L, editors. Meshes: benefits and risks. Berlin, Heidelberg: Springer; 2004. p. 170–8.
25. Grainger DW. All charged up about implanted biomaterials. Nat Biotechnol. 2013;31:507–9.
26. Klosterhalfen B, Hermanns B, Rosch R, Junge K. Biological response to mesh. Eur Surg.
2003;35:16–20.
27. Junge K, Binnebosel M, von Trotha KT, et al. Mesh biocompatibility: effects of cellular
inflammation and tissue remodelling. Langenbeck’s Arch Surg. 2012;397:255–70.
28. Krause HG, Galloway SJ, Khoo SK, Lourie R, Goh JT. Biocompatible properties of surgical
mesh using an animal model. Aust N Z J Obstet Gynaecol. 2006;46:42–5.
29. Brown R. Handbook of polymer testing: physical methods. CRC press; 1999.
30. Langer C, Neufang T, Kley C, Liersch T, Becker H. Central mesh recurrence after incisional
hernia repair with Marlex – are the meshes strong enough? Hernia. 2001;5:164–7.
31. Lintin LA, Kingsnorth AN. Mechanical failure of a lightweight polypropylene mesh. Hernia.
2014;18:131–3.
32. Petro CC, Nahabet EH, Criss CN, et al. Central failures of lightweight monofilament polyester
mesh causing hernia recurrence: a cautionary note. Hernia. 2015;19:155–9.
33. Zuvela M, Galun D, Djuric-Stefanovic A, Palibrk I, Petrovic M, Milicevic M. Central rupture
and bulging of low-weight polypropylene mesh following recurrent incisional sublay hernio-
plasty. Hernia. 2014;18:135–40.
34. Junge K, Klinge U, Prescher A, Giboni P, Niewiera M, Schumpelick V. Elasticity of the ante-
rior abdominal wall and impact for reparation of incisional hernias using mesh implants.
Hernia. 2001;5:113–8.
35. Berrevoet F, Maes L, De Baerdemaeker L, Rogiers X, Troisi R, de Hemptinne B. Comparable
results with 3-year follow-up for large-pore versus small-pore meshes in open incisional hernia
repair. Surgery. 2010;148:969–75.
36. Conze J, Rosch R, Klinge U, Weiss C, Anurov M, Titkowa S, et al. Polypropylene in the intra-
abdominal position: influence of pore size and surface area. Hernia. 2004;8:365–72.
37. Ladurner R, Chiapponi C, Linhuber Q, Mussack T. Long term outcome and quality of life after
open incisional hernia repair – light versus heavy weight meshes. BMC Surg. 2011;11:25.
38. Memon MA, Khan S, Osland E. Meta-analyses of lightweight versus conventional (heavy
weight) mesh in inguinal hernia surgery. Hernia. 2012;16:497–502.
39. Martakos P, Karwoski T. Healing characteristics of hybrid and conventional polytetrafluoro-
ethylene vascular grafts. ASAIO J. 1995;41:M735–41.
40. Collage RD, Rosengart MR. Abdominal wall infections with in situ mesh. Surg Infect.
2010;11:311–8.
41. Petersen S, Henke G, Freitag M, Faulhaber A, Ludwig K. Deep prosthesis infection in inci-
sional hernia repair: predictive factors and clinical outcome. Eur J Surg. 2001;167:453–7.
42. Sanchez VM, Abi-Haidar YE, Itani KM. Mesh infection in ventral incisional hernia repair:
incidence, contributing factors, and treatment. Surg Infect. 2011;12:205–10.
43. Klinge U. Experimental comparison of monofile light and heavy polypropylene meshes: less
weight does not mean less biological response. World J Surg. 2007;31:867–8.
44. Klinge U, Klosterhalfen B. Modified classification of surgical meshes for hernia repair based
on the analyses of 1,000 explanted meshes. Hernia. 2012;16:251–8.
45. Orenstein SB, Saberski ER, Kreutzer DL, Novitsky YW. Comparative analysis of histopatho-
logic effects of synthetic meshes based on material, weight, and pore size in mice. J Surg Res.
2012;176:423–9.
46. Chatzimavroudis G, Papaziogas B, Koutelidakis I, Atmatzidis K. Experimental comparison
of monofile light and heavy polypropylene meshes: less weight does not mean less biological
response. World J Surg. 2007;31:865. author reply 6.
Surgical Meshes Used in Laparoscopic Procedures 243
47. Currie A, Andrew H, Tonsi A, Hurley PR, Taribagil S. Lightweight versus heavyweight mesh
in laparoscopic inguinal hernia repair: a meta-analysis. Surg Endosc. 2012;26:2126–33.
48. Pascual G, Hernandez-Gascon B, Rodriguez M, et al. The long-term behavior of lightweight
and heavyweight meshes used to repair abdominal wall defects is determined by the host tissue
repair process provoked by the mesh. Surgery. 2012;152:886–95.
49. Zogbi L, Trindade EN, Trindade MR. Comparative study of shrinkage, inflammatory response
and fibroplasia in heavyweight and lightweight meshes. Hernia. 2013;17:765–72.
50. Klinge U, Klosterhalfen B, Birkenhauer V, Junge K, Conze J, Schumpelick V. Impact of poly-
mer pore size on the interface scar formation in a rat model. J Surg Res. 2002;103:208–14.
51. Bellon JM, Rodriguez M, Garcia-Honduvilla N, Gomez-Gil V, Pascual G, Bujan J. Comparing
the behavior of different polypropylene meshes (heavy and lightweight) in an experimental
model of ventral hernia repair. J Biomed Mater Res B Appl Biomater. 2009;89:448–55.
52. Agarwal BB, Agarwal KA, Mahajan KC. Prospective double-blind randomized controlled
study comparing heavy- and lightweight polypropylene mesh in totally extraperitoneal repair
of inguinal hernia: early results. Surg Endosc. 2009;23:242–7.
53. Chowbey PK, Garg N, Sharma A, Khullar R, Soni V, Baijal M, et al. Prospective randomized
clinical trial comparing lightweight mesh and heavyweight polypropylene mesh in endoscopic
totally extraperitoneal groin hernia repair. Surg Endosc. 2010;24:3073–9.
54. Deeken CR, Matthews BD. Characterization of the mechanical strength, resorption properties,
and histologic characteristics of a fully absorbable material (poly-4-hydroxybutyrate-PHASIX
mesh) in a porcine model of hernia repair. ISRN Surg. 2013;2013:238067.
55. Gadacz TR, Chase JA, Duke S. Technology of prosthetic material. Semin Laparosc Surg.
1994;1:123–7.
56. Nagy KK, Fildes JJ, Mahr C, et al. Experience with three prosthetic materials in temporary
abdominal wall closure. Am Surg. 1996;62:331–5.
57. Symeonidis D, Efthimiou M, Koukoulis G, Athanasiou E, Mamaloudis I, Tzovaras G. Open
inguinal hernia repair with the use of polyglycolic acid/trimethylene carbonate absorbable
mesh: a critical update of the long-term results. Hernia. 2013;17:85–7.
58. Symeonidis D, Efthimiou M, Koukoulis G, Mamaloudis I, Ioannou M, Tzovaras G. Open
inguinal hernia repair with the use of polyglycolic acid/trimethylene carbonate mesh:
gross and pathologic assessment of the inguinal area at reoperation for recurrence. Hernia.
2013;17:791–4.
59. Huang K, Ding X, Lv B, Wei L, Sun J, Xu Z, et al. Reconstruction of large-size abdominal
wall defect using biodegradable poly-p-dioxanone mesh: an experimental canine study. World
J Surg Oncol. 2014;12:57.
60. Klosterhalfen B, Klinge U, Schumpelick V, Tietze L. Polymers in hernia repair – common
polyester vs. polypropylene surgical meshes. J Mater Sci. 2000;35:4769–76.
61. Ostergard DR. Degradation, infection and heat effects on polypropylene mesh for pelvic
implantation: what was known and when it was known. Int Urogynecol J. 2011;22:771–4.
62. Sternschuss G, Ostergard DR, Patel H. Post-implantation alterations of polypropylene in the
human. J Urol. 2012;188:27–32.
63. Robinson TN, Clarke JH, Schoen J, Walsh MD. Major mesh-related complications fol-
lowing hernia repair: events reported to the Food and Drug Administration. Surg Endosc.
2005;19:1556–60.
64. Jezupors A, Mihelsons M. The analysis of infection after polypropylene mesh repair of
abdominal wall hernia. World J Surg. 2006;30:2270–8.
65. Saberski ER, Orenstein SB, Novitsky YW. Anisotropic evaluation of synthetic surgical meshes.
Hernia. 2011;15:47–52.
66. Anurov MV, Titkova SM, Oettinger AP. Biomechanical compatibility of surgical mesh and
fascia being reinforced: dependence of experimental hernia defect repair results on anisotropic
surgical mesh positioning. Hernia. 2012;16:199–210.
67. Amid P. Classification of biomaterials and their related complications in abdominal wall sur-
gery. Hernia. 1997;1:15–21.
244 A. Vindal et al.
68. Weyhe D, Schmitz I, Belyaev O, et al. Experimental comparison of monofile light and heavy
polypropylene meshes: less weight does not mean less biological response. World J Surg.
2006;30:1586–91.
69. Klinge U, Klosterhalfen B, Ottinger AP, Junge K, Schmpelick V. PVDF as a new polymer for
the construction of surgical meshes. Biomaterials. 2002;23:3487–93.
70. Berger D, Bientzle M. Polyvinylidene fluoride: a suitable mesh material for laparoscopic inci-
sional and parastomal hernia repair! Hernia. 2009;13:167–72.
71. Deeken CR, Faucher KM, Matthews BD. A review of the composition, characteristics, and
effectiveness of barrier mesh prostheses utilized for laparoscopic ventral hernia repair. Surg
Endosc. 2012;26:566–75.
72. Deeken CR, Abdo MS, Frisella MM, Matthews BD. Physicomechanical evaluation of poly-
propylene, polyester, and polytetrafluoroethylene meshes for inguinal hernia repair. J Am Coll
Surg. 2011;212:68–79.
73. Anurov MV, Titkova SM, Oettinger AP. Impact of position of light mesh endoprosthesis with
anisotropic structure for the efficiency of anterior abdominal wall reconstruction. Bull Exp
Biol Med. 2010;149:440–4.
74. Coda A, Lamberti R, Martorana S. Classification of prosthetics used in hernia repair based on
weight and biomaterial. Hernia. 2012;16(1):9–20.
75. Earle DB, Mark LA. Prosthetic material in inguinal hernia repair: how do I choose? Surg Clin
N Am. 2008;88:179–201.
76. Elango S, Perumalsamy S, Ramachandran K, Vadodaria K. Mesh materials and hernia repair.
Biomedicine (Taipei). 2017;7(3):16.
77. Baldwin HS. Early embryonic vascular development. Cardiovasc Res. 1996;31:E34–45.
78. Peralta R, Latifi R. Long-term outcomes of abdominal wall reconstruction. What are the real
numbers? World J Surg. 2012;36:534–8.
79. Ahonen-Siirtola M, Vironen J, Makela J, Paajanen H. Surgery-related complications of ventral
hernia reported to the Finnish patient insurance centre. Scand J Surg. 2015;104:66–71.
80. Dietz UA, Winkler MS, Hartel RW, Fleischhacker A, Weigering A, Isbert C, et al. Importance
of recurrence rating, morphology, hernial gap size, and risk factors in ventral and incisional
hernia classification. Hernia. 2014;18:19–30.
81. Helgstrand F, Rosenberg J, Kehlet H, Jorgensen LN, Bisgaard T. Nationwide prospective study
of outcomes after elective incisional hernia repair. J Am Coll Surg. 2013;216:217–28.
82. Bellows CF, Alder A, Helton WS. Abdominal wall reconstruction using biological tissue
grafts: present status and future opportunities. Expert Rev Med Devices. 2006;3:657–75.
83. Ditzel M, Deerenberg EB, Grotenhuis N, Harlaar JJ, Monkhorst K, Bastiaansen-Jenniskens
YM, et al. Biologic meshes are not superior to synthetic meshes in ventral hernia repair: an
experimental study with long-term follow-up evaluation. Surg Endosc. 2013;27:3654–62.
84. Lowham AS, Filipi CJ, Fitzgibbons RJ Jr, Stoopa R, Wantz GE, et al. Mechanisms of her-
nia recurrence after preperitoneal mesh repair. Traditional and laparoscopic. Ann Surg.
1997;225:422.
85. Barzana D, Johnson K, Clancy TV, Hope WW. Hernia recurrence through a composite mesh
secondary to transfascial suture holes. Hernia. 2012;16:219–21.
86. Brahmbhatt R, Martindale R, Liang MK. Jumping the gun? Evaluating the evidence for syn-
thetic mesh in contaminated hernia repairs. J Am Coll Surg. 2014;218:498–9.
87. Cross W, Kumar A, ChandruKowdley G. Biological mesh in contaminated fields--overuse
without data: a systematic review of their use in abdominal wall reconstruction. Am Surg.
2014;80:3–8.
88. Mariette C, Briez N, Denies F, Guilbert M, Piessen G, Duhamel A, et al. Use of biological
mesh versus standard wound care in infected incisional ventral hernias, the SIMBIOSE study:
a study protocol for a randomized multicenter controlled trial. Trials. 2013;14:131.
89. Carbonell AM, Cobb WS. Safety of prosthetic mesh hernia repair in contaminated fields. Surg
Clin N Am. 2013;93:1227–39.
90. Carbonell AM, Criss CN, Cobb WS, Novitsky YW, Rosen MJ. Outcomes of synthetic mesh in
contaminated ventral hernia repairs. J Am Coll Surg. 2013;217:991–8.
Surgical Meshes Used in Laparoscopic Procedures 245
91. Deerenberg EB, Mulder IM, Grotenhuis N, Ditzel M, Jeekel J, Lange JF. Experimental study
on synthetic and biological mesh implantation in a contaminated environment. Br J Surg.
2012;99:1734–41.
92. Aube C, Caron C, Pessaux P, Tuech JJ, du Plesis R, Arnaud JP. Detection of peritoneal adhe-
sions using ultrasound examination for the evaluation of an innovative intraperitoneal mesh.
Surg Endosc. 2004;18:131–5.
93. Schreinemacher MH, van Barneveld KW, Dikmans RE, Gijbels MJ, Greve JW, Bouvy
ND. Coated meshes for hernia repair provide comparable intraperitoneal adhesion prevention.
Surg Endosc. 2013;27:4202–9.
94. Bringman S, Conze J, Cuccurullo D, Deprest J, Junge K, Klosterhalfen B, et al. Hernia repair:
the search for ideal meshes. Hernia. 2010;14:81–7.
95. Emans PJ, Schreinemacher MH, Gijbels MJ, Beets GL, Greve JW, Koole LH, et al.
Polypropylene meshes to prevent abdominal herniation. Can stable coatings prevent adhesions
in the long term? Ann Biomed Eng. 2009;37:410–8.
96. Koehler RH, Begos D, Berger D, Carey S, LeBlanc K, Ramshaw B, et al. Minimal adhesions
to ePTFE mesh after laparoscopic ventral incisional hernia repair: Reoperative findings in 65
cases. JSLS. 2003;7:335–40.
97. Schug-Pass C, Sommerer F, Tannapfel A, Lippert H, Kockerling F. Does the additional appli-
cation of a polylactide film (SurgiWrap) to a lightweight mesh (TiMesh) reduce adhesions
after laparoscopic intraperitoneal implantation procedures? Experimental results obtained
with the laparoscopic porcine model. Surg Endosc. 2008;22:2433–9.
98. Berger D. Diagnostics and therapy of chronic pain following hernia operation. Chirurg.
2014;85(2):117–20.
Staging Laparoscopy in Intra-Abdominal
Cancers
Sudhir Kumar Singh, Farhanul Huda,
Rajkumar Kottayasamy Seenivasagam,
and Somprakas Basu
Introduction
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 247
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_10
248 S. K. Singh et al.
probes and biopsy forceps (Fig. 1). Patients with previous abdominal surgeries may
require selective port placement to prevent intra-abdominal injuries.
After creating the pneumoperitoneum using carbon dioxide insufflation and
maintaining the intra-abdominal pressure at 10–12 mm of Hg, sufficient time should
be given for thorough inspection of the whole abdomen before any manipulation is
commenced. If ascites is present, the fluid must be collected for cytological exami-
nation (Fig. 2). Alternatively, in the absence of ascites, peritoneal lavage with
500 mL saline should routinely be performed to obtain fluid for cytological investi-
gation. To ensure that each site of the peritoneal cavity has been appropriately
cleaned, the operating table should be tilted to every side so that lavage fluid can
reach every part of the peritoneal cavity prior to reaspiration.
Abdominal exploration needs manipulation of the viscera and it should be started
from the left upper quadrant in reverse Trendelenburg position. Careful inspection
of the parietal and visceral peritoneum, the greater and lesser omentum, left lobe of
the liver, anterior wall of the stomach and spleen should be done. Inspection of
lesser omentum and cardia can be achieved by retraction of the left lobe of liver.
Sequential exploration of the right upper quadrant includes inspection of the perito-
neal surfaces, right lobe of the liver (especially inferior surface of the right liver),
the falciform ligament and the gallbladder. For lower abdominal exploration, the
patient is positioned in Trendelenburg position and rest of the abdominal and pelvic
viscera are examined subsequently.
Specific visceral exploration requires instrumentation and special manoeuvres.
To evaluate peritoneal metastasis in the lesser sac, it is preferably approached by
dividing the gastro colic ligament. Alternatively, it can be approached through divi-
sion of the gastro hepatic ligament. For detection of deep solid visceral lesions,
laparoscopic ultrasound is used with the help of a flexible ultrasound probe
(7.5 MHz) which is highly sensitive as compared to other radiological imaging
(Figs. 3 and 4). It is also helpful in evaluation of retroperitoneal lymph nodes and
tumour invasion or its proximity to the vessels.
Cancer of the Oesophagus
Even after R0 resection of oesophageal cancer, the 5-year survival is very low
(range: 10–20%) [6]. However, combined modality therapy may improve the out-
come of patients with operable disease [7, 8]. Accurate staging is also essential for
Staging Laparoscopy in Intra-Abdominal Cancers 251
inclusion of patients in clinical trials. Choice of therapy depends upon the tumour
stage e.g. T1/T2 tumour without lymphatic involvement can undergo upfront surgi-
cal resection while higher stages may require pre-operative chemo-radiotherapy fol-
lowed by surgery. Patients with metastatic disease require palliative treatment [6, 8].
Imaging techniques that are being used currently have a limitation in detection of
peritoneal carcinomatosis, small amount of malignant ascites and lesions smaller
than 1 cm in diameter [7]. Direct visualization by SL can bridge this diagnostic gap.
Thus staging laparoscopy can help detect disseminated disease and assess intra-
abdominal lymph nodes. Approximately in 20–30% of potentially resectable adeno-
carcinoma of distaloesophagus based on imaging, upfrontsurgery can be avoided by
laparoscopic staging with ultrasound as it leads to upstaging of the disease [9, 10].
SL, however, has no proven oncological benefit in squamous cell carcinoma of the
oesophagus as peritoneal carcinomatosis is rare [11].
After exploration of peritoneal, visceral surface metastasis and ascitic fluid sam-
pling, a 5 mm trocar is placed in the epigastric region for retraction of the left lobe
of liver which helps in further examination of the infra-hepatic space, esophago-
gastric junction and hepato-duodenal ligament. For lesser sac exploration, two addi-
tional ports are needed along the anterior axillary line in mid or upper abdomen.
After examination of the lower abdomen and pelvis, if there is no evidence of peri-
toneal spread, assessment of intra-parenchymal liver lesions and suspicious lymph
nodes in the hepatoduodenal ligament and para-aortic region is done by laparo-
scopic ultrasound. Biopsy is performed from the suspicious lesions. The lymph
nodal status in carcinoma oesophagus has a prognostic value on the outcome of the
disease, so laparoscopy and LUS should focus on the celiac axis lymph nodes which
is regional LN for the lower third of oesophagus while distant metastasis for upper
and mid oesophageal carcinomas. Assessment of para-aortic and hepatoduodenal
ligament lymph nodes must be done as their involvement is considered as distant
metastasis.
252 S. K. Singh et al.
Gastric Cancer
In most patients with gastric cancer, curative resection is not possible due to detec-
tion of the cancer in advanced stage. Resection with tumour free margin i.e. R0
resection in early stage is the most important prognostic factor in gastric cancer
[12]. Preoperative staging of gastric cancer consists of various modalities including
clinical examination, liver function tests, CECT abdomen and endoscopic ultra-
sound (EUS). For T and N staging, EUS is superior to CT scan [13]. Because of
limitation of imaging, the role of laparoscopy combined with LUS is of utmost
importance for its staging. The reason behind this is the biology of gastric cancer
which is prone to trans-peritoneal metastasis and palliative resection, leaving small
peritoneal/omental metastasis and/or liver metastasis, does not improve the overall
survival when compared to patients under observation alone [14] (Fig. 5).
Laparoscopy plays a major role in identifying and distinguishing the patients with
early disease, who can undergo upfront gastric resection and lymph node dissection
from patients with a locally advanced disease who may benefit from neo-adjuvant
chemotherapy or palliation.
During SL for gastric cancer, two 5 mm ports are placed in the left and right
upper quadrants for ascitic fluid aspiration and saline lavage from bilateral sub-
phrenic spaces and the pelvis. Peritoneal adhesions, if any, should be divided and
thorough examination of peritoneal cavity must be carried out including both the
anterior and inferior surfaces of bilateral lobes of liver, parietal peritoneum of
demonstration of gastric mobility with forceps, opening of lesser sac and elevation
of posterior gastric wall off the surface of the pancreas. Sometimes laparoscopic
staging may be compromised due to the presence of intra-abdominal adhesions and
difficult manoeuvring during the assessment of transverse mesocolon and lesser sac
(Fig. 8).
Pancreatic Cancer
clarified on LUS (Figs. 9, 10, and 11). Combined staging with LUS is more valuable
in patients with advanced cancer of the pancreatic head and body as compared to
patients with peri-ampullary cancers. Adenocarcinoma of pancreatic tail is notori-
ous for being metastatic and unresectable at presentation; thus, SL is beneficial
256 S. K. Singh et al.
Hepatobiliary Cancer
Gynaecologic Cancer
Most gynaecological cancers, except cervical and vaginal, are staged surgically. In
the past, staging was performed by laparotomy but with the advent of minimal inva-
sive surgery, laparoscopic staging of these cancers has gained popularity.
Carcinoma Cervix
Approximately 85% of cervical cancers occur in developing countries, where the
resources are limited. As a result, its staging is mainly dependent on clinical exami-
nation while expensive investigations like CT, MRI and PET-CT are not considered
mandatory. Even though lymph node metastasis is not included in the FIGO staging
of Carcinoma cervix, being an independent prognostic factor, lymphadenectomy
forms an integral part of the treatment of cervical cancer. The accuracy of CT, MRI
or PET-CT in detecting lymph node metastases is variable and the decision of
lymphadenectomy cannot be relied on these investigations. A systematic review
showed that 4%–35% of histologically proven para-aortic lymph node metastasis
was missed by CT, MRI or PET-CT. On the other hand, laparoscopic staging can
allow direct assessment of the lymph nodes in patients presenting with an early
disease. The mainstay of treatment in advanced cervical cancer is chemo-radiation.
Thus, by staging laparoscopy, the knowledge of the extent of lymph node involve-
ment can avoid unnecessary extended-field radiotherapy [21–23].
Carcinoma Endometrium
Laparoscopy in endometrial malignancies helps in collecting peritoneal washings
for cytology which has a prognostic significance in this malignancy along with
detection of lymph node involvement and need for lymphadenectomy. The need of
omentectomy can also be decided by laparoscopy [24, 25].
258 S. K. Singh et al.
Carcinoma Ovary
Laparoscopic staging in ovarian malignancy is important as 16–39.5% of appar-
ently early-stage ovarian cancers are upstaged after a staging procedure.
Laparoscopic scoring using parameters such as omental caking, peritoneal and dia-
phragmatic carcinomatosis, mesenteric retraction, bowel and stomach infiltration
and spleen and/or liver superficial metastasis has proved accurate in predicting
resectability in advanced ovarian cancers.
It could also avoid unnecessary up front laparotomies, which might otherwise
result in suboptimal debulking [26, 27] (Table 2).
Conclusion
Staging laparoscopy is a simple and safe diagnostic tool to exclude metastatic dis-
ease. With laparoscopic ultrasound, the clinical value of SL has further increased. It
increases the resectability rates, decreases non-therapeutic laparotomies and
Staging Laparoscopy in Intra-Abdominal Cancers 259
decreases the length of post-operative hospital stay in patients with advanced dis-
ease. Staging laparoscopy can help select those patients who would actually benefit
from neoadjuvant treatment, by upstaging the disease identified as early stage on
clinical and radiological staging. Another great advantage of SL is the palliative
laparoscopic procedures in patients with unresectable disease. Its disadvantages
include requirement of general anaesthesia and limited role in assessment of vascu-
lar invasion.
Editor’s Note1
References: Main chapter references are included after the “References Editor’s Note” section.
1
Staging Laparoscopy in Intra-Abdominal Cancers 261
Opposition: Detractors of the procedure have put forth that with the availability
of recent imaging techniques a high accuracy has been achieved in detection of
distant metastasis and additional staging laparoscopy may be of limited benefit [1].
Adjuncts: Different Adjunctive techniques have been used to detect peritoneal
hepatic and lymphnode metastasis as well as vascular invasion [2–6].
Adjuncts used in staging laparoscopy to increase yield
1. Laparoscopic USG
2. Lavage Cytology + RTPCR (e.g., for carcinoembryonic antigen)
3. Near Infra-red Fluorescence Laparoscopy/Indocyanine Green Fluorescence
4. Five aminolevulinic acid Fluorescence
5. Fluorescent antibody imaging
Table EN1 The results of trials evaluating staging laparoscopy in gastrointestinal and hepatobili-
ary and gynaecological malignancies [7–16]
Authors/year
Type of data Type of malignancy Outcome of SL
Convie L/2015 Esophagogastric cancer Macroscopic metastasis detected in esophageal
Prospective adenocarcinoma (11.8%)
collected data & gastric adenocarcinoma (22.6%). Positive
[7] peritoneal cytology is similar in both types of
malignancy
Ramos RF, Gastric cancer Sensitivity 84.6%, specificity 100% for detection
2016 of peritoneal metastasis
Meta-analysis
[8]
Hariharan D, Hepatobiliary Sensitivity in detection of metastasis in
2010 malignancy 1. Pancreatic cancer: Liver metastasis 88%,
Meta-analysis peritoneal metastasis 92%
[9] 2. Proximal biliary cancer: Liver metastasis 83%,
peritoneal metastasis 93%
Coelen R JS, Perihilar Diagnostic accuracy of staging laparoscopy with
2016 cholangiocarcinoma reference to sensitivity for detection of
Meta-analysis unresectable disease 52.2%
[10]
(continued)
262 S. K. Singh et al.
Table EN1 (continued)
Authors/year
Type of data Type of malignancy Outcome of SL
Tian Y, 2017 Gall bladder and hilar Detection of unresectable disease in:
Metaanalysis cholangiocarcinoma Gall bladder cancer: 27.6%, 0.642 (95% CI:
[11] 0.579–0.701)
Hilarcholangiocarcinoma: 32.4%, 0.556 (95% CI:
0.495–0.616)
Pooled specificity for the SL was 100% (95% CI:
0.993–1.000) for all studies
Ta R, 2019 Pancreatic cancer Of patients deemed resectable in imaging 20%
Metaanalysis (range:14%–38%) had unresectable disease.
[12] Among patients with locally advanced disease
in imaging 36% were detected to have
metastasis. Failure rate to detect non resectable
disease was 5%
Bastiaenen VP, Colonic cancer pT4 Peritoneal metastasis detected in second look:
2019 second look/third look 10% & third look: 10%
COLOPEC 2 laparoscopy
multicentre
randomized
trial [13]
Park HJ, 2013 Early-stage ovarian Reported lower blood loss, upstaging in 22.6%
Meta-analysis cancer and conversion in 3.7%
[14]
Lu Y, 2015 Comprehensive staging Less blood loss, shorter hospital stay, lower
Meta-analysis for early-stage ovarian recurrence in laparoscopic group. One study
[15] cancer showed lower incidence of tumor rupture in
laparoscopy group
Bogani G, 2017 Surgical staging in In laparoscopy a longer operative time (weighted
Meta-analysis early-stage ovarian mean difference [WMD] = 28.3 min; 95% [CI],
[16] cancer −2.59 to 59.2), a lower blood loss
(WMD = −156.5 mL; 95% CI, −216.4 to −96.5),
a shorter hospital stay (WMD = −3.7 days; 95%
CI, −5.2 to −2.1), and a lower postoperative
complication (odds ratio [OR] = 0.48; 95% CI,
0.29–0.81), shorter time to chemotherapy
(WMD = −5.16 days; 95% CI, −8.68 to −1.64)
than laparotomic procedures. Upstaging
(OR = 0.81; 95% CI, 0.55–1.20) and cyst rupture
(OR = 1.32; 95% CI, 0.52–3.38) were similar
Staging Laparoscopy in Intra-Abdominal Cancers 263
12. Ta R, O'Connor DB, Sulistijo A, Chung B, Conlon KC. The role of staging
laparoscopy in resectable and borderline resectable pancreatic cancer: a sys-
tematic review and meta-analysis. Dig Surg. 2019;36(3):251–60. https://doi.
org/10.1159/000488372.
13. Bastiaenen VP, Klaver CEL, Kok NFM, de Wilt JHW, de Hingh IHJT, Aalbers
AGJ, Boerma D, Bremers AJA, Burger JWA, van Duyn EB, Evers P, van
Grevenstein WMU, Hemmer PHJ, Madsen EVE, Snaebjornsson P, Tuynman
JB, Wiezer MJ, Dijkgraaf MGW, van der Bilt JDW, Tanis PJ. Second and third
look laparoscopy in pT4 colon cancer patients for early detection of peritoneal
metastases; the COLOPEC 2 randomized multicentre trial. BMC Cancer.
2019;19(1):254. https://doi.org/10.1186/s12885-019-5408-8.
14. Park HJ, Kim DW, Yim GW, Nam EJ, Kim S, Kim YT. Staging laparoscopy for
the management of early-stage ovarian cancer: a metaanalysis. Am J Obstet
Gynecol. 2013;209(1):58.e1–8. https://doi.org/10.1016/j.ajog.2013.04.013.
15. Lu Y, Yao DS, Xu JH. Systematic review of laparoscopic comprehensive stag-
ing surgery in early stage ovarian cancer: a meta-analysis. Taiwan J Obstet
Gynecol. 2015;54(1):29–38. https://doi.org/10.1016/j.tjog.2014.10.003.
16. Bogani G, Borghi C, Leone Roberti Maggiore U, Ditto A, Signorelli M,
Martinelli F, Chiappa V, Lopez C, Sabatucci I, Scaffa C, Indini A, Ferrero S,
Lorusso D, Raspagliesi F. Minimally invasive surgical staging in early-stage
ovarian carcinoma: a systematic review and meta-analysis. J Minim Invasive
Gynecol. 2017;24(4):552–62. https://doi.org/10.1016/j.jmig.2017.02.013.
Staging Laparoscopy in Intra-Abdominal Cancers 265
References
1. Metcalfe MS, Maddern GJ. Laparoscopic staging of upper gastrointestinal malignancy. ANZ J
Surg. 2003;73(10):782–3. https://doi.org/10.1046/j.1445-2197.2003.02788.x.
2. Zucker KA, Pitcher DE, Martin DT, Ford RS. Laparoscopic-assisted colon resection. Surg
Endosc. 1994;8(1):12–8. https://doi.org/10.1007/BF02909486.
3. Giger U, Schäfer M, Krähenbühl L. Technique and value of staging laparoscopy. Dig Surg.
2002;19(6):473–8. https://doi.org/10.1159/000067599.
4. Velanovich V. Staging laparoscopy in the management of intra-abdominal malignancies.
Surgery. 1998;124(4):773–81. https://doi.org/10.1067/msy.1998.91270.
5. Ramshaw BJ. Laparoscopic surgery for cancer patients. CA Cancer J Clin. 1997;47(6):327–50.
https://doi.org/10.3322/canjclin.47.6.327.
6. Zheng Z, Cai J, Yin J, Zhang J, Zhang ZT, Wang KL. Transthoracic versus abdominal-
transhiatal resection for treating Siewert type II/III adenocarcinoma of the esophagogastric
junction: a meta-analysis. Int J Clin Exp Med. 2015;8(10):17167–82.
7. Tirumani H, Rosenthal MH, Tirumani SH, Shinagare AB, Krajewski KM, Ramaiya
NH. Esophageal carcinoma: current concepts in the role of imaging in staging and manage-
ment. Can Assoc Radiol J. 2015;66(2):130–9. https://doi.org/10.1016/j.carj.2014.08.006.
8. Napier KJ, Scheerer M, Misra S. Esophageal cancer: a review of epidemiology, pathogen-
esis, staging workup and treatment modalities. World J Gastrointest Oncol. 2014;6(5):112–20.
https://doi.org/10.4251/wjgo.v6.i5.112.
9. Krasna MJ, Jiao X. Thoracoscopic and laparoscopic staging for esophageal cancer. Semin
Thorac Cardiovasc Surg. 2000;12(3):186–94. https://doi.org/10.1053/stcs.2000.9669.
10. de Graaf GW, Ayantunde AA, Parsons SL, Duffy JP, Welch NT. The role of staging laparoscopy
in oesophagogastric cancers. Eur J Surg Oncol. 2007;33(8):988–92. https://doi.org/10.1016/j.
ejso.2007.01.007.
11. Stein HJ, Kraemer SJ, Feussner H, Fink U, Siewert JR. Clinical value of diagnostic lapa-
roscopy with laparoscopic ultrasound in patients with cancer of the esophagus or cardia. J
Gastrointest Surg. 1997;1(2):167–73. https://doi.org/10.1016/s1091-255x(97)80105-9.
12. Villafranca E, Aristu J, Meiriño R, Dueñas MT, Marcos M. Prognostic factors of gastric car-
cinoma. Anales del Sistema Sanitario de Navarra. 2001;24:111–20. https://doi.org/10.23938/
ASSN.0438.
13.
Hallinan JT, Venkatesh SK. Gastric carcinoma: imaging diagnosis, staging and
assessment of treatment response. Cancer Imaging. 2013;13(2):212–27. https://doi.
org/10.1102/1470-7330.2013.0023.
14. Li Z, Ji J. Application of laparoscopy in the diagnosis and treatment of gastric cancer. Ann
Transl Med. 2015;3(9):126. https://doi.org/10.3978/j.issn.2305-5839.2015.03.29.
15.
Ryan DP, Hong TS, Bardeesy N. Pancreatic adenocarcinoma. N Engl J Med.
2014;371(11):1039–49. https://doi.org/10.1056/NEJMra1404198.
16. Sener SF, Fremgen A, Menck HR, Winchester DP. Pancreatic cancer: a report of treatment and
survival trends for 100,313 patients diagnosed from 1985-1995, using the National Cancer
Database. J Am Coll Surg. 1999;189(1):1–7. https://doi.org/10.1016/s1072-7515(99)00075-7.
17. John TG, Greig JD, Carter DC, Garden OJ. Carcinoma of the pancreatic head and periam-
pullary region. Tumor staging with laparoscopy and laparoscopic ultrasonography. Ann Surg.
1995;221(2):156–64. https://doi.org/10.1097/00000658-199502000-00005.
18. Furukawa H, Uesaka K, Boku N. Treatment decision making in pancreatic adenocarcinoma:
multidisciplinary team discussion with multidetector-row computed tomography. Arch Surg.
2008;143(3):275–81. https://doi.org/10.1001/archsurg.2007.78.
19. Callery MP, Strasberg SM, Doherty GM, Soper NJ, Norton JA. Staging laparoscopy with
laparoscopic ultrasonography: optimizing resectability in hepatobiliary and pancreatic malig-
nancy. J Am Coll Surg. 1997;185(1):33–9.
266 S. K. Singh et al.
Introduction
• Good signal to noise ratio (SNR) which provides high contrast such that only the
target area is visible not the background because of different wavelengths used
for illumination and recording.
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 267
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_11
268 D. Sharma et al.
All of the above features holds true for Indocyanine Green (ICG) with its well-
established clinical applications and is currently the most commonly used fluores-
cence agent. ICG was developed by the Kodak research laboratories in 1955 for
near infrared (NIR) photography and got US Food and Administration approval in
1959 for its clinical use [1].
ICG is sterile, non-toxic, anionic and water soluble. It is a hydrophobictricarbo-
cyanine compound with molecular weight of 751.4 Daltons, which is negatively
charged ion, belonging to large family of cyanine dyes [2]. Pharmaceutically avail-
able dry form is stable at room temperature [1].
As ICG is soluble in water (1 mg/mL) but not soluble in saline, it needs to be dis-
solved in water first and dilution with saline is done if it is required to make an iso-
tonic solution [1]. The solution can be administered intravenously or intra-arterially.
After intravascular administration, due to its high affinity towards plasma lipopro-
teins, it bind to them and confines itself to intravascular compartment with minimal
interstitial leakage. It is rapidly taken up selectively by hepatocytes and secreted in
bile after first pass metabolism for excretion within 3–5 min (half-life—t1/2) and
there is no absorption in intestinal mucous membrane, though this fluorophore has
tissue penetration of upto 5 mm. After a span of about 15 min a repeat dose can be
administered or until the ICG dye clears [3]. On extra vascular injection, it gets bind
to protein and reach the nearest draining lymph node within 15 min. After 1–2 h, it
binds to the regional lymph node and is also deposited into macrophages [4–7].
The toxicity of ICG is classified as low. However, in rare instances side effects
like sore throats, hot flushes, anaphylactic reaction (shock, tachycardia, dyspnoe
and utricaria) have been reported. Frequencies of mild, moderate and severe side-
effects are only 0.15%, 0.2% and 0.05% respectively; the mortality rate is 1:330000.
Its use should be avoided in patients allergic to iodine or iodinated contrast agents
(the agent contains 5% of sodium iodide) and in pregnant or lactating females [7].
The recommended dose of ICG for angiography to be injected peripherally is
0.1–0.5 mg/kg, with maximum dose not to increase 5 mg/kg body weight. The stan-
dard dose is injected into a peripheral vein as a bolus of 25 mg dissolved in 25 mL
of water. Within 1–2 s following injection, it binds to plasma lipoproteins and has a
half life of 3–5 min [1, 7].
The principle of ICG angiography in fluorescence imaging is simple that the tis-
sue of interest is illuminated at the excitation wavelength of about 750–800 nm
while observing it at longer emission wavelengths (over 800 nm). Both depend
largely on the solvent used and the concentration. Its maximum values are approx
810 nm in water and 830 nm in blood. ICG works in tissue optical window, that is,
the NIR light used both in excitation and fluorescence, penetrates tissue several mil-
limetres or even further [1].
Role of ICG Fluoroscence Imaging in Laparoscopic Bowel Anastomosis 269
The ICG device consists of a light source, and NIR sensitive sensor and filter
used to block the light at other wavelengths. This allows high resolution NIR images
without ambient and excitation light interference. Several intraoperative visualiza-
tion systems include: the AIM Platform, PINPOINT, the D-Light NIR/ICG,
IC-View, PDE-neo System, the SPY Elite Kit and the da Vinci Firefly robotic sys-
tem. These systems normally work in white light mode as a conventional laparo-
scope, and can be activated into NIR mode, in which ICG visualized as green on a
black background [8].
Colorectal Surgery
The overall anastomotic leak rate after colorectal anastomosis is 1–12% and about
10–14% after low or ultralow colorectal resections and anasotomosis [9–11]. Leaks
can lead to increase in length of hospital stay, rise in reoperation rates, and economi-
cal stress to patient and health-care system. Leaks after colorectal anastomo-
sis increase morbidity and mortality as well as predispose to local cancer recurrence
[12–18]. Revision surgical intervention is required in 10–35% of cases after leaks in
whom mortality rate ranges from 6 to 22% [19, 20].
Identified risk factors as the possible cause of anastomotic leak include: faulty
surgical techniques, patient risk factors, suture material or devices malfunction and
inadequate perfusion at the resection margins with subsequent ischemic changes
leading to leak [9, 20–22]. The mechanical causes can be checked intraoperatively
by doing air-water tightness with air or methylene blue, local site intraoperative
endoscopic visualization and assessment of anastomotic doughnut [16]. Inadequate
anastomotic site perfusion with local ischemic changes and poor oxygenation result
in failure of anastomotic healing and leakage which is difficult to be assessed on
table without perfusion studies, particularly in minimal access procedures [23].
During left sided colorectal cancer surgery after high ligation of inferior mesen-
teric artery, the blood supply to the bowel relies on patency of middle colic vessels
through the Marginal artery of Drummond and Arc of Riolan [24, 25]. Aberrant
anatomy such as absent middle colic artery or inadequate vascularization of the
splenic flexure is seen in upto 25% of cases and it becomes a major risk factor for
anastomotic leak [26–28].
Till now most widely used technique to assess adequate perfusion at resection
margin depends upon visual judgement based on clinical findings, such as tissue
color, temperature, marginal vessels pulsations, bleeding from resected margins and
peristalsis. The clinical assessment and surgeon’s subjective evaluation underesti-
mate the prediction of anastomotic leak [8].
The degree of tissue perfusion can be assessed by marginal vessel status [29].
(a) Brisk, bright red, ≥1 cm projectile bleeding or pulsatile bleeding denotes good
degree of perfusion
(b) Two colour bleeding with bright red arterial and the dark red venous blood, not
pulsatile represent moderate degree of perfusion
(c) Only dark red venous blood observed show poor perfusion
(d) No bleeding suggests no perfusion.
routine clinical practice and doesn’t have proven reliability hence are not widely
accepted [30–32].
Many a time even CT scan and water-soluble contrast enemas, could not identify
anastomotic leak early enough to allow timely intervention [16]. Proximal diverting
stoma doesn’t reduce the leak risk but do minimise the consequences after disinte-
gration of the anastomosis [33].
Indocyanine green angiography (ICG-A) has come into action and has been suc-
cessfully used for intraoperative real time assessment of tissue perfusion during
colorectal surgery. Fluorescence imaging has become especially important in era of
minimally invasive surgery, with little tactile feedback afforded during resection
[34]. This can lead to change in the site of resection and/or anastomosis, possibly
affecting anastomotic leak rate.
ICG in laparoscopic colorectal surgery can be used at three stages
C R
(3·1% vs 7·7%) and in those above 70 years (4·3% vs 11·9%) supporting the hypoth-
esis that indocyanine green fluorescence might substantially reduce the rate of
severe complications in colorectal surgery. The only problem with pre transaction
ICG injection is that, sometimes due to handling or stretching, the vascularity at the
transaction line of the same bowel gets changed after anastomosis. So the ICG test
should be ideally performed after the anastomosis to ensure vascularity (Fig. 5).
Some surgeons are exploring the idea to decide about creation of protective
ostomy based on ICG Fluorescence imaging. In future it might possible to avoid
ostomy after colorectal surgery based on ICG imaging, however as yet; it’s unan-
swered on evidence [8].
Major limitations of fluorescence imaging include:
The difference between maximum and baseline fluorescence is the most indica-
tive factor available to quantify anastomotic leak, with sensitivity and specificity of
100% and 92.5% respectively. However, there is no correlation between anasto-
motic leak and time of ICG injection to the first visible fluorescence signal [41].
274 D. Sharma et al.
Bariatric Surgery
Obesity can lead to numerous non communicable diseases like diabetes, hyperten-
sion, osteoarthritis, sleep apnoea etc. It can be the result of modern dietary habits,
sedentary lifestyle apart from endocrinal abnormalities. Bariatric surgery is the
most effective treatment for morbid obesity and helps to achieve or maintain signifi-
cant weight reduction, mitigating various morbid conditions associated with it.
Laparoscopic sleeve gastrectomy (LSG) is the most common bariatric procedure
performed. It is technically simpler and provides comparable weight loss and
improvement in co-morbidities with minimal metabolic complications as compared
to other procedures like Roux-en-Y gastric bypass [42].
Leakage from the staple line is one of the most dreaded complication that can
lead to reoperation, increased length of hospital stay, increased patient and financial
burden of health-care system and can even lead to mortality in up to 6–17% cases
[43–48]. Presentation of leak in these populations is often delayed due to muted
clinical presentation of the abdominal pathology. They often present with sepsis
multisystem organ failure [49]. After LSG, staple line leak rate ranges from 0–2%
and approximately 0.01–2.3% after Roux-en-Y gastric bypass from either gastroje-
junal anastomosis or directly from the gastric pouch [50–52].
Staple line leak after any bariatric procedure is divided according to the time of
its presentation as:
Early leaks are due to technical issue, such as staple misfire and tissue injury,
while intermediate and late leaks, are mainly a result of ischemia along the staple
line. Most common site for leak is the “Angle of His” due to combined factors of
mechanical stress and ischemic factors [52–55]. Advancement in surgical technique
and staple formation lead to decrease in leak rates, but still ischemic factors have not
been addressed formally.
Proximal gastric blood supply is unequivocally mainly derived from left gastric,
right gastric and inferior phrenic artery [56, 57]. Sometimes, accessory left gastric
arises from left hepatic artery and is present in gastrohepatic ligament supplying the
cardia and fundus of stomach. Injuries to any of these blood vessels can happen dur-
ing laparoscopic dissection.
During bariatric surgery if one or two branches of left gastric are severed, the
vascular submucosa plexus allows replacement of blood flow, but if three branches
are stapled, the blood supply gets compromised. Similarly branches of inferior
phrenic artery can be injured if associated hiatus hernia is repaired and accessory
gastric artery in gastro hepatic ligament may be inadvertently injured.
Over sewing the staple line, adding buttress material such as seam guard or
bovine pericardium and applying fibrin glue and other sealants are among the
Role of ICG Fluoroscence Imaging in Laparoscopic Bowel Anastomosis 275
techniques used to avoid complications, mainly bleeding. None have any significant
evidence in their efficacy in reducing leaks [50, 58–63].
Routine methods to detect staple line leak intraoperatively are [64]:
1. Methylene blue dye test: In this methylene blue at high pressure (to increase
sensitivity) is administered intraluminally via orogastric tubing near the staple
line and concurrently visualized by laparoscopic camera to detect extravasation
of blue dye. In addition a gauze pad can be placed adjacent to the staple line to
detect blue stain in case of any leak.
2. Gastroscopy with insufflation: The staple line is submerged in saline and gas-
troscopy is done. Air is insufflated into the remnant gastric lumen and presence
of air bubble if any visible by laparoscopic camera indicates a faulty staple line.
These tests may have an ill effect on the newly constructed anastomosis and
might induce the leak either due to the pressure of methylene blue instillation or
endoscope insertion and insufflation [55, 65]. Methylene blue leaves a permanent
stain and if it leaks, the operative field gets obscured, hence compromising safety of
subsequent leak repair. Gastroscopy with insufflation requires an experienced
endoscopist, an available endoscope in operation room, increase operative time
along with the cost of instruments and personnel involved.
These disadvantages can be simply avoided by instilling ICG via orogastric bou-
gie intraluminally to the remnant gastric lumen and checking the staple line.
Most importantly ICG is rendered invisible once the NIR spectrum light is dis-
engaged and does not interfere in further surgery.
Methods
coagulated along with the short gastric vessels using energy device. ICG, 1 mL
(1 mg/mL) is administered intravenously before sleeve creation to assess blood sup-
ply and its pattern. Placing 36-french lighted bougie in place the sleeve is created
with an attention to preserve the identified blood supply to the GE junction and
gastric tube. After the sleeve is created, 3 mL of ICG is injected to ensure preserva-
tion of pertinent blood vessels.
Intraluminal method: Laparoscopic bariatric procedure is performed in stan-
dard manner. ICG (2.5 mg) is mixed with water and then diluted in 100 mL of sterile
saline. After completion of procedure at the usual time of leak test (100 mL in LSG
and 60 mL in LRYGB laparoscopic Roux en Y gastric bypass) the ICG-saline dilu-
tion is instilled intraluminally by anaesthologist through orogastric bougie. Near
infrared laser of the camera is enabled and the passage of ICG observed and contin-
ued for approximately 30s afterwards. The staple line is highlighted with fluores-
cent green dye. If there is any leakage of fluorescence it denotes positive leak test
while absence of any leak depicts negative leak test. If positive, repair of the leak is
done in a standard fashion. Once the laser is disengaged the ICG is rendered invis-
ible and standard lighting is resumed facilitating leak repair unlike while using
methylene blue [65].
The intraluminal ICG method has sensitivity of 100% & specificity of 98.28% in
detecting clinically significant gastric staple line leakage, with negative predictive
value of 100% [65].
While we await randomised controlled trials to define the standards for use like dos-
age schedules and timings, fluorescence angiography continues to have a consider-
able clinical benefit in minimally invasive colorectal surgery and bariatric surgery.
Future studies will need to address the fluorophores used in fluorescence imaging.
At present, only two near-infrared fluorophores that support image-guided surgery
are available clinically: indocyanine green and methylene blue. However, neither
fluorophore provides optimum specificity and stability for targeted image guidance
[67]. Therefore, the development of near-infrared fluorophores to target this unmet
clinical need is of paramount importance. New fluorophores are being developed
that are water-soluble and biocompatible, with absorption and emission maxima
within the desired near-infrared spectra and have improved fluorescence perfor-
mance [68–70]. Novel fluorophores are being tested in animal models, and some are
being used as endoscopic molecular tools, providing an enhanced visual picture of
the mucosal and molecular targets [71, 72]. Fluorophores can also be used to label
antibodies and other biomarkers, converting a therapeutic tool into a diagnostic tool
[73–79]. Thus, development of fluorophores with the properties that are absent in
the dyes used at present might contribute towards the ongoing expansion of near-
infrared-fluorescence guidance in surgical practice. With this vast potential for
expanded use, studies will need to define the cost-effectiveness of fluorescence
imaging in laparoscopic surgery. The cost of the new technology can be prohibitive
for resource-limited health-care systems, restricting widespread application.
Role of ICG Fluoroscence Imaging in Laparoscopic Bowel Anastomosis 277
Conclusion
Initially developed for hepatic, cardiac, renal function evaluation and retinal artery
angiography, ICG fluorescence imaging has become a valuable tool and is now
widely used in laparoscopic gastrointestinal surgeries especially in colorectal and
bariatric procedures. As the location of these operative regions are difficult to
approach in case of a leak in post operative period and is associated with severe
morbidity and mortality, it is of paramount importance to identify such possi-
ble cases on table. The absence of tactile feedback sensation in laparoscopic era
makes the use of FI more important. The applications of fluorescence imaging using
ICG continue to evolve because of its safe, feasible and beneficial character.
Although fluorescence imaging seems to have a cost benefit in reducing compli-
cations and guiding appropriate resections, more studies on the true value of this
modality that consider outcomes, costs, and patient experience are warranted.
References
1. Alander JT, Kaartinen I, Laakso A, Pätilä T, Spillmann T, Tuchin VV, et al. A review of indo-
cyanine green fluorescent imaging in surgery. Int J Biomed Imaging. 2012;2012:1–26.
2. Mishra A, Behera RK, Behera PK, Mishra BK, Behera GB. Cyanines during the 1990s: a
review. Chem Rev. 2000;100(6):1973–2011.
278 D. Sharma et al.
3. Ris F, Hompes R, Cunningham C, Lindsey I, Guy R, Jones O, et al. Near-infrared (NIR) perfu-
sion angiography in minimally invasive colorectal surgery. Surg Endosc. 2014;28(7):2221–6.
4. Tajima Y, Murakami M, Yamazaki K, Masuda Y, Kato M, Sato A, Goto S, Otsuka K, Kato T,
Kusano M. Sentinel node mapping guided by indocyanine green fluorescence imaging during
laparoscopic surgery in gastric cancer. Ann Surg Oncol. 2010;17(7):1787–93.
5. Korn JM, Tellez-Diaz A, Bartz-Kurycki M, Gastman B. Indocyanine green SPY elite–assisted
sentinel lymph node biopsy in cutaneous melanoma. Plast Reconstr Surg. 2014;133(4):914–22.
6. Tanaka E, Choi HS, Fujii H, Bawendi MG, Frangioni JV. Image-guided oncologic surgery
using invisible light: completed pre-clinical development for sentinel lymph node mapping.
Ann Surg Oncol. 2006;13(12):1671–81.
7. Spota A, Al-Taher M, Felli E, et al. Fluorescence-based bowel anastomosis perfusion evalua-
tion: results from the IHU-IRCAD-EAES EURO-FIGS registry. Surg Endosc. 2021; https://
doi.org/10.1007/s00464-020-08234-8.
8. Keller DS, Ishizawa T, Cohen R, Chand M. Indocyanine green fluorescence imaging in
colorectal surgery: overview, applications, and future directions. Lancet Gastroenterol Hepatol.
2017;2(10):757–66.
9. Shogan BD, Carlisle EM, Alverdy JC, Umanskiy K. Do we really know why colorectal anas-
tomoses leak? J Gastrointest Surg. 2013;17(9):1698–707.
10. NasirKhan MU, Abir F, Longo W, Kozol R. Anastomotic disruption after large bowel resec-
tion. World J Gastroenterol: WJG. 2006;12(16):2497.
11. Trencheva K, Morrissey KP, Wells M, Mancuso CA, Lee SW, Sonoda T, Michelassi F, Charlson
ME, Milsom JW. Identifying important predictors for anastomotic leak after colon and rectal
resection: prospective study on 616 patients. Ann Surg. 2013;257(1):108–13.
12. Chadi SA, Fingerhut A, Berho M, DeMeester SR, Fleshman JW, Hyman NH, Margolin
DA, Martz JE, McLemore EC, Molena D, Newman MI. Emerging trends in the etiol-
ogy, prevention, and treatment of gastrointestinal anastomotic leakage. J Gastrointest Surg.
2016;20(12):2035–51.
13. Choi HK, Law WL, Ho JW. Leakage after resection and intraperitoneal anastomosis for
colorectal malignancy: analysis of risk factors. Dis Colon Rectum. 2006;49(11):1719–25.
14. Hyman NH, Osler T, Cataldo P, Burns EH, Shackford SR. Anastomotic leaks after bowel
resection: what does peer review teach us about the relationship to postoperative mortality? J
Am Coll Surg. 2009;208(1):48–52.
15. Alves A, Panis Y, Pocard M, Regimbeau JM, Valleur P. Management of anastomotic leakage
after nondiverted large bowel resection. J Am Coll Surg. 1999;189(6):554–9.
16. Hirst NA, Tiernan JP, Millner PA, Jayne DG. Systematic review of methods to predict and
detect anastomotic leakage in colorectal surgery. Color Dis. 2014;16(2):95–109.
17. Hammond J, Lim S, Wan Y, Gao X, Patkar A. The burden of gastrointestinal anastomotic leaks:
an evaluation of clinical and economic outcomes. J Gastrointest Surg. 2014;18:1176–85.
18. Goto S, Hasegawa S, Hida K, Uozumi R, Kanemitsu Y, Watanabe T, Sugihara K, Sakai
Y. Multicenter analysis of impact of anastomotic leakage on long-term oncologic outcomes
after curative resection of colon cancer. Surgery. 2017;162(2):317–24.
19. Buchs NC, Gervaz P, Secic M, Bucher P, Mugnier-Konrad B, Morel P. Incidence, conse-
quences, and risk factors for anastomotic dehiscence after colorectal surgery: a prospective
monocentric study. Int J Color Dis. 2008;23(3):265–70.
20. Asari SA, Cho MS, Kim NK. Safe anastomosis in laparoscopic and robotic low anterior resec-
tion for rectal cancer: a narrative review and outcomes study from an expert tertiary center. Eur
J Surg Oncol. 2015;41(2):175–85.
21. Frasson M, Flor-Lorente B, Rodríguez JL, Granero-Castro P, Hervás D, Alvarez Rico MA,
Brao MJ, Sánchez González JM, Garcia-Granero E, ANACO Study Group. Risk factors for
anastomotic leak after colon resection for cancer: multivariate analysis and nomogram from a
multicentric, prospective, national study with 3193 patients. Ann Surg. 2015;262(2):321–30.
22. Kingham TP, Pachter HL. Colonic anastomotic leak: risk factors, diagnosis, and treatment. J
Am Coll Surg. 2009;208(2):269–78.
Role of ICG Fluoroscence Imaging in Laparoscopic Bowel Anastomosis 279
23. Sheridan WG, Lowndes RH, Young HL. Tissue oxygen tension as a predictor of colonic anas-
tomotic healing. Dis Colon Rectum. 1987;30:867–71.
24. Al-Asari SF, Lim D, Min BS, Kim NK. The relation between inferior mesenteric vein ligation
and collateral vessels to splenic flexure: anatomical landmarks, technical precautions and clini-
cal significance. Yonsei Med J. 2013;54(6):1484.
25. Titu LV, Tweedle E, Rooney PS. High tie of the inferior mesenteric artery in curative surgery
for left colonic and rectal cancers: a systematic review. Dig Surg. 2008;25(2):148–57.
26. Goligher JC. The adequacy of the marginal blood-supply to the left colon after high ligation of
the inferior mesenteric artery during excision of the rectum. Br J Surg. 1954;41(168):351–3.
27. Griffiths J. Surgical anatomy of the blood supply of the distal colon: Arris and Gale Lecture
delivered at the Royal College of Surgeons of England on 27th March 1956. Ann R Coll Surg
Engl. 1956;19(4):241.
28. Sakorafas GH, Zouros E, Peros G. Applied vascular anatomy of the colon and rectum: clinical
implications for the surgical oncologist. Surg Oncol. 2006;15(4):243–55.
29. Ryu HS, Lim SB, Choi ET, Song I, Lee JL, Kim CW, Yoon YS, Park IJ, Yu CS, Kim
JC. Intraoperative perfusion assessment of the proximal colon by a visual grading sys-
tem for safe anastomosis after resection in left-sided colorectal cancer patients. Sci Rep.
2021;11(1):1–9.
30. Ambrosetti P, Robert J, Mathey P, Rohner A. Left-sided colon and colorectal anastomoses:
Doppler ultrasound as an aid to assess bowel vascularization. Int J Color Dis. 1994;9(4):211–4.
31. Seike K, Koda K, Saito N, Oda K, Kosugi C, Shimizu K, Miyazaki M. Laser Doppler assess-
ment of the influence of division at the root of the inferior mesenteric artery on anastomotic
blood flow in rectosigmoid cancer surgery. Int J Color Dis. 2007;22(6):689–97.
32. Hirano Y, Omura K, Tatsuzawa Y, Shimizu J, Kawaura Y, Watanabe G. Tissue oxygen satura-
tion during colorectal surgery measured by near-infrared spectroscopy: pilot study to predict
anastomotic complications. World J Surg. 2006;30(3):457–61.
33. Alberts JC, Parvaiz A, Moran BJ. Predicting risk and diminishing the consequences of anasto-
motic dehiscence following rectal resection. Color Dis. 2003;5:478–82.
34. Feingold DL, Addona T, Forde KA, Arnell TD, Carter JJ, Huang EH, Whelan RL. Safety and
reliability of tattooing colorectal neoplasms prior to laparoscopic resection. J Gastrointest
Surg. 2004;8(5):543–6.
35. Satoyoshi T, Okita K, Ishii M, et al. Timing of indocyanine green injection prior to lapa-
roscopic colorectal surgery for tumor localization: a prospective case series. Surg Endosc.
2021;35(2):763–9.
36. Jafari MD, Wexner SD, Martz JE, McLemore EC, Margolin DA, Sherwinter DA, Lee SW,
Senagore AJ, Phelan MJ, Stamos MJ. Perfusion assessment in laparoscopic left-sided/anterior
resection (PILLAR II): a multi-institutional study. J Am Coll Surg. 2015;220(1):82–92.
37. Cahill RA, Ris F, Mortensen NJ. Near-infrared laparoscopy for real-time intra-operative arte-
rial and lymphatic perfusion imaging. Color Dis. 2011;13:12–7.
38. Gröne J, Koch D, Kreis ME. Impact of intraoperative microperfusion assessment with Pinpoint
perfusion imaging on surgical management of laparoscopic low rectal and anorectal anastomo-
ses. Color Dis. 2015;17:22–8.
39. Hellan M, Spinoglio G, Pigazzi A, Lagares-Garcia JA. The influence of fluorescence imaging
on the location of bowel transection during robotic left-sided colorectal surgery. Surg Endosc.
2014;28(5):1695–702.
40. Kudszus S, Roesel C, Schachtrupp A, Höer JJ. Intraoperative laser fluorescence angiogra-
phy in colorectal surgery: a noninvasive analysis to reduce the rate of anastomotic leakage.
Langenbeck’s Arch Surg. 2010;395(8):1025–30.
41. Wada T, Kawada K, Takahashi R, Yoshitomi M, Hida K, Hasegawa S, Sakai Y. ICG fluo-
rescence imaging for quantitative evaluation of colonic perfusion in laparoscopic colorectal
surgery. Surg Endosc. 2017;31(10):4184–93.
42. Altieri MS, Yang J, Groves D, Obeid N, Park J, Talamini M, Pryor A. Sleeve gastrectomy: the
first 3 years: evaluation of emergency department visits, readmissions, and reoperations for
14,080 patients in New York state. Surg Endosc. 2018;32(3):1209–14.
280 D. Sharma et al.
43. Kirby GC, Macano CA, Nyasavajjala SM, Sahloul M, Nijjar R, Daskalakis M, Richardson
M, Singhal R. The Birmingham experience of high-pressure methylene blue dye test dur-
ing primary and revisional bariatric surgery: a retrospective cohort study. Ann Med Surg.
2017;23:32–4.
44. Bingham J, Kaufman J, Hata K, Dickerson J, Beekley A, Wisbach G, Swann J, Ahnfeldt E,
Hawkins D, Choi Y, Lim R. A multicenter study of routine versus selective intraoperative leak
testing for sleeve gastrectomy. Surg Obes Relat Dis. 2017;13(9):1469–75.
45. Špička P. Staple line leak with peritonitis after laparoscopic sleeve gastrectomy–a solution in
one to six steps. Videosurg Other Miniinvasive Tech. 2017;12(2):154.
46. Arndtz K, Steed H, Hodson J, Manjunath S. The hidden endoscopic burden of sleeve gastrec-
tomy and its comparison with Roux-en-Y gastric bypass. Ann Gastroenterol. 2016;29(1):44.
47. Puli SR, Spofford IS, Thompson CC. Use of self-expandable stents in the treatment of bariatric
surgery leaks: a systematic review and meta-analysis. Gastrointest Endosc. 2012;75(2):287–93.
48. Mohos E, Schmaldienst E, Richter D, Prager M. Examination of the efficacy and safety of
intraoperative gastroscopic testing of the gastrojejunal anastomosis in laparoscopic Roux Y
gastric bypass surgery. Obes Surg. 2011;21(10):1592–6.
49. Bingham J, Lallemand M, Barron M, Kuckelman J, Carter P, Blair K, Martin M. Routine
intraoperative leak testing for sleeve gastrectomy: is the leak test full of hot air? Am J Surg.
2016;211(5):943–7.
50. Kim J, Azagury D, Eisenberg D, DeMaria E, Campos GM. ASMBS position statement on
prevention, detection, and treatment of gastrointestinal leak after gastric bypass and sleeve
gastrectomy, including the roles of imaging, surgical exploration, and nonoperative manage-
ment. Surg Obes Relat Dis. 2015;11(4):739–48.
51. Aurora AR, Khaitan L, Saber AA. Sleeve gastrectomy and the risk of leak: a systematic analy-
sis of 4,888 patients. Surg Endosc. 2012;26(6):1509–15.
52. Ortega CB, Guerron AD, Portenier D. Endoscopic abscess septotomy: a less invasive
approach for the treatment of sleeve gastrectomy leaks. J Laparoendosc Adv Surg Tech.
2018;28(7):859–63.
53. Galloro G, Ruggiero S, Russo T, Telesca DA, Musella M, Milone M, Manta R. Staple-line leak
after sleve gastrectomy in obese patients: a hot topic in bariatric surgery. World J Gastrointest
Endosc. 2015;7(9):843.
54. AbouRached A, Basile M, El Masri H. Gastric leaks post sleeve gastrectomy: review of its
prevention and management. World J Gastroenterol: WJG. 2014;20(38):13904.
55. Sakran N, Goitein D, Raziel A, Keidar A, Beglaibter N, Grinbaum R, Matter I, Alfici R,
Mahajna A, Waksman I, Shimonov M. Gastric leaks after sleeve gastrectomy: a multicenter
experience with 2,834 patients. Surg Endosc. 2013;27(1):240–5.
56. Panagouli E, Venieratos D, Lolis E, Skandalakis P. Variations in the anatomy of the celiac
trunk: a systematic review and clinical implications. Ann Anat (Anatomischer Anzeiger).
2013;195(6):501–11.
57. Loukas M, Hullett J, Wagner T. Clinical anatomy of the inferior phrenic artery. Clin Anat.
2005;18(5):357–65.
58. Miller KA, Pump A. Use of bioabsorbable staple reinforcement material in gastric bypass: a
prospective randomized clinical trial. Surg Obes Relat Dis. 2007;3(4):417–21.
59. Shikora SA. The use of staple-line reinforcement during laparoscopic gastric bypass. Obes
Surg. 2004;14(10):1313–20.
60. Sapala JA, Wood MH, Schuhknecht MP. Anastomotic leak prophylaxis using a vapor-heated
fibrin sealant: report on 738 gastric bypass patients. Obes Surg. 2004;14(1):35–42.
61. Livingston EH, Liu CY, Glantz G, Li Z. Characteristics of bariatric surgery in an integrated VA
Health Care System: follow-up and outcomes. J Surg Res. 2003;109(2):138–43.
62. Silecchia G, Boru C, Pecchia A, Rizzello M, Casella G, Leonetti F, Basso N. Effectiveness of
laparoscopic sleeve gastrectomy (first stage of biliopancreatic diversion with duodenal switch)
on co-morbidities in super-obese high-risk patients. Obes Surg. 2006;16(9):1138–44.
63. Nandakumar G, Richards BG, Trencheva K, Dakin G. Surgical adhesive increases burst pres-
sure and seals leaks in stapled gastrojejunostomy. Surg Obes Relat Dis. 2010;6(5):498–501.
Role of ICG Fluoroscence Imaging in Laparoscopic Bowel Anastomosis 281
64. Kalmar CL, Reed CM, Peery CL, Salzberg AD. Intraluminal indocyanine green for intraopera-
tive staple line leak testing in bariatric surgery. Surg Endosc. 2020;34(9):4194–9.
65. Theodorou D, Doulami G, Larentzakis A, Almpanopoulos K, Stamou K, Zografos G,
Menenakos E. Bougie insertion: a common practice with underestimated dangers. Int J Surg
Case Rep. 2012;3(2):74–7.
66. Carrano FM, Di Lorenzo N. The use of indocyanine green in bariatric surgery: a systematic
review. J Gastric Surg. 2020;2(2):41–4.
67. Jo D, Hyun H. Structure-inherent targeting of near-infrared fluorophores for image-guided
surgery. Chonnam Med J. 2017;53(2):95.
68. Daly HC, Sampedro G, Bon C, Wu D, Ismail G, Cahill RA, O'Shea DF. BF2-azadipyrromethene
NIR-emissive fluorophores with research and clinical potential. Eur J Med Chem.
2017;135:392–400.
69. Sun Y, Ding M, Zeng X, Xiao Y, Wu H, Zhou H, Ding B, Qu C, Hou W, Er-Bu AG, Zhang
Y. Novel bright-emission small-molecule NIR-II fluorophores for in vivo tumor imaging and
image-guided surgery. Chem Sci. 2017;8(5):3489–93.
70. Hill TK, Kelkar SS, Wojtynek NE, Souchek JJ, Payne WM, Stumpf K, Marini FC, Mohs
AM. Near infrared fluorescent nanoparticles derived from hyaluronic acid improve tumor con-
trast for image-guided surgery. Theranostics. 2016;6(13):2314.
71. Burggraaf J, Kamerling IM, Gordon PB, Schrier L, De Kam ML, Kales AJ, Bendiksen R,
Indrevoll B, Bjerke RM, Moestue SA, Yazdanfar S. Detection of colorectal polyps in humans
using an intravenously administered fluorescent peptide targeted against c-Met. Nat Med.
2015;21(8):955–61.
72. Atreya R, Neumann H, Neufert C, Waldner MJ, Billmeier U, Zopf Y, Willma M, App C,
Münster T, Kessler H, Maas S. In vivo imaging using fluorescent antibodies to tumor necrosis
factor predicts therapeutic response in Crohn’s disease. Nat Med. 2014;20(3):313.
73. Lee JH, Wang TD. Molecular endoscopy for targeted imaging in the digestive tract. Lancet
Gastroenterol Hepatol. 2016;1:147–55.
74. Liu J, Zuo X, Li C, Yu T, Gu X, Zhou C, Li Z, Goetz M, Kiesslich R, Li Y. In vivo molecular
imaging of epidermal growth factor receptor in patients with colorectal neoplasia using confo-
cal laser endomicroscopy. Cancer Lett. 2013;330(2):200–7.
75. Mahmood U, Weissleder R. Near-infrared optical imaging of proteases in cancer. Mol Cancer
Ther. 2003;2(5):489–96.
76. Zhou J, Joshi BP, Duan X, Pant A, Qiu Z, Kuick R, Owens SR, Wang TD. EGFR overex-
pressed in colonic neoplasia can be detected on wide-field endoscopic imaging. Clin Transl
Gastroenterol. 2015;6(7):e101.
77. Joshi BP, Zhou J, Pant A, Duan X, Zhou Q, Kuick R, Owens SR, Appelman H, Wang
TD. Design and synthesis of near-infrared peptide for in vivo molecular imaging of HER2.
Bioconjug Chem. 2016;27(2):481–94.
78. Rabinsky EF, Joshi BP, Pant A, Zhou J, Duan X, Smith A, Kuick R, Fan S, Nusrat A, Owens
SR, Appelman HD. Overexpressed claudin-1 can be visualized endoscopically in colonic ade-
nomas in vivo. Cell Mol Gastroenterol Hepatol. 2016;2(2):222–37.
79. Foersch S, Kiesslich R, Waldner MJ, Delaney P, Galle PR, Neurath MF, Goetz M. Molecular
imaging of VEGF in gastrointestinal cancer in vivo using confocal laser endomicroscopy. Gut.
2010;59(8):1046–55.
Minimizing Pain in Laparoscopic Hernia
Surgery
Introduction
Hernia is one of the few conditions afflicting the human body which has only a
surgical cure. The most common type of hernia is the inguinal hernia and for ages,
recurrence was the bugbear of hernia repair and the huge number of types of hernia
repair only attested to the fact that most operations had less than optimal results.
This problem was mostly solved by the Lichtenstein tension free mesh repair which
many considered as gold standard as it consistently gave a low recurrence rate in the
hands of most surgeons. It also lent itself well to performance under local anes-
thetic. The Achilles’ heel of the Lichtenstein tension free mesh repair is the rela-
tively high frequency of chronic groin pain [1]. Over the years methods and
techniques with modifications have been suggested to overcome this chronic issue.
Most defined chronic pain as pain persisting beyond 3 months. However a range of
definitions is used ranging from 3–12 months. Pain in post operative period can be
due to neuropathic pain [Architectural damage of nerves] or Nociceptive pain
[Damage of tissue or organs leading to release of substance].
N. Sharma (*)
Department of Surgery, All India Institute of Medical Sciences, Jodhpur, India
D. Sharma · S. Meena
Department of Surgery, Lady Hardinge Medical College, New Delhi, India
Dr RML Hospital, New Delhi, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 283
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_12
284 N. Sharma et al.
Rives and Stoppa independently advocated the use of the preperitoneal space for
placement of a large mesh for management of groin hernia. This operation was
performed through a long lower midline incision. With laparoscopy coming of age
in the early 1990s, the same preperitoneal space was approached either extraperito-
neally during a totally extraperitoneal repair [TEP] or transabdominally while per-
forming a transabdominal preperitoneal repair [TAPP]. A large mesh of 15 × 10 cm
or larger could be deployed in the space after reducing the hernial sac using two
5 mm ports and one 10 mm port [Common technique].
Reducing the size of the large incision required for performing open inguinal
hernia to just 1 cm for laparoscopic surgery led to a remarkable decrease in early
postoperative pain and the large mesh kept the recurrence rates consistently low.
Research started shifting from recurrence as an endpoint to addressing endpoints
like acute postoperative pain and chronic groin pain [2].
Laparoscopic Repair
Laparoscopic [which would also include preperitoneal repairs for purpose of this
article] inguinal hernia repair [LIHR] is usually performed under general anesthe-
sia. While some papers have suggested that it is possible to perform LIHR under
spinal, epidural or even local anesthesia [3], very few surgeons perform LIHR under
these alternate anesthesia techniques; most repairs are performed under general
anesthesia. Some surgeons even advocate the use of a robot for minimal access
inguinal hernia repair but a large number of surgeons fail to appreciate the benefits
of using robot for inguinal hernia repair as compared to a LIHR [4].
Most LIHR surgery is performed using three ports, the commonest combination
being one 10 mm port and two 5 mm ports. Use of only two ports to accomplish
LIHR with and intent to further decrease pain and improve cosmesis is suggested,
but the technique never found its widespread use [5] (Table 1).
Table 1 Steps of surgery or modifications which can reduce acute postoperative pain
1. Preemptive analgesia
2. Choice of the type of ports used
3. Size of ports
4. Telescopic dissection vs balloon dissection
5. Completely reducing the indirect hernia sac vs proximal ligation and transection
6. Using a Transversus abdominis plane [TAP] block
7. Mesh material
8. Mesh size
9. Mesh fixation: Non fixation, Suture fixations, glue, absorbable tackers are modifications
over the conventional nonabsorbable titanium tack
10. Instillation of local anesthetic in dissected space
11. Closure of port sites and Skin closure
Minimizing Pain in Laparoscopic Hernia Surgery 285
Note: Most surgeons consider general anesthetic to be within the purview of the
anesthesiologist. This chapter will not address the nuances or difference in anesthe-
sia techniques used for laparoscopic inguinal hernia repair. There are mixed reports
regarding the role of Gabapentin or similar drugs administered preoperatively to
decrease the incidence of chronic postoperative inguinal pain.
Pre-emptive analgesia: It is the pre-incision port site infiltration with local anes-
thetic, so that the central pain circle is not created.
Pre-emptive analgesia using infiltration of port sites using lignocaine has proved
efficacious in laparoscopic cholecystectomy and decrease in postoperative pain has
also been demonstrated after infiltration of port sites during LIHR [6]. Infiltration
with local anesthetics can have benefits and specific effects have been seen in com-
parison to placebo. However no difference is seen in the long term to decrease
postoperative pain after infiltration of skin with local anesthetic either before mak-
ing the incision or before closure or at both times. In any case the risk of infection
and cost associated with this intervention is low and its routine use may be consid-
ered by the surgeon.
Radial dilating or cutting ports: A decrease in postoperative pain is seen after
using radially dilating trocars particularly in TAPP since these port sites do not
require suture closure [7, 8]. The trocars used during robotic surgery are also dilat-
ing trocars; therefore, the pain score after robotic surgery is reported to be the same
as after LIHR. However, a word of caution is sounded as port site hernias are gener-
ally reported after using 12 mm ports’ [9–14] incisional port site hernias have also
been reported through 8 mm robotic trocar port site [13, 14].
Size of ports: Reducing port size might help but it might not very significant.
Most surgeons perform LIHR using two 5 mm ports and one 10/12 mm port for the
telescope which is also used to insert the mesh. Some surgeons have attempted to
use 3 mm working ports instead of 5 mm working ports while using only a 5 mm
port as the optical port. They have reported that the pain is significantly less in the
early postoperative period with the use of smaller size ports [15–20]. However,
systematic review comparing single incision laparoscopic surgery versus multiple
incision laparoscopic surgery for inguinal hernia failed to reveal a statistically sig-
nificant difference in postoperative pain between the two groups [21].
Telescopic dissection vs balloon dissection: There are two commonly employed
techniques to create the initial space in totally extraperitoneal repair. The space is
either created using a forward viewing telescope or using either a commercial or
indigenous balloon made of glove fingers. Few RCTs comparing the two have
reported lower pain scores at 6 hrs in balloon dissection group compared to the
telescopic dissection [22] while similar trials have also given conflicting reports that
both techniques are similar in postoperative pain profile [23].
286 N. Sharma et al.
Concept of mapping the sites of pain (+, 0, −) have also been proposed. Images can
be preserved of the areas involved [abdomen, groin, thigh etc] and changes in site of
pain are compared with subsequent images to plan a management strategy [32].
These maps can provide broad ideas about the probable nerves involved [33] (Fig. 1,
Table 2).
Other recognized method of Quantitative sensory testing (QST) uses procedures
like pain on pin prick, pain on pressure, pain on contact with hot or cold. These are
regarded as a more conventional methods but is more time taking and difficult to
arrange in daily clinical scenario [34].
Incidence of chronic pain in hernia repair is less after laparoscopic surgery [28]. All
causes of chronic pain have their own special treatment hence knowing the probable
cause of pain is of paramount importance.
288 N. Sharma et al.
Hold back policy: Most pain after inguinal hernia repair tends to reduce with
time. So a complete explanation of the situation at times is helpful and active inter-
vention directed at pain can be hold back [35]. However few patients can get
depressed and start living an inactive life which should be particularly avoided [36].
Local anesthetic injection at site: These can cause temporary benefit depending
upon the half life of the drug used. However if these anaesthesia blocks are given
properly, they can definitely identify the nerve involved in the cause of pain [37].
Drug therapy: Advised medications vary from case to case. Mostly used are
NSAID, gabapentins, tricyclic antidepressants and selective serotonin/norepineph-
rine reuptake inhibitors with routine analgesics [38]. Lidocaine or diclofenac
patches have been used, but they generally don’t have any benefit [39].
Surgical management: Ranges from removal of the specific tack or removal of
the mesh to laparoscopic retroperitoneal neurectomy which should be done by
experts only. Patient need to understand that pain can be often due to damage of
nerves and removing the mesh might not alter the nerve injury and the patient can
still continue to perceive pain [31].
Minimizing Pain in Laparoscopic Hernia Surgery 289
Conclusion
Strategies for minimizing acute postoperative pain in LIHR which are likely to be
most useful are pre-emptive infiltration of port sites with local anesthetic, choosing
radially dilating ports [if costs are not a major concern], avoiding mesh fixation
whenever possible, using suture or glue when mesh fixation is deemed essential and
performing a TAP block [under laparoscopic vision]. The most important measure
for preventing chronic pain is to avoid any type of fixation below the iliopubic tract.
References
1. HerniaSurge Group. International guidelines for groin hernia management. Hernia.
2018;22(1):1–165.
2. Reinpold W. Risk factors of chronic pain after inguinal hernia repair: a systematic review.
Innov Surg Sci. 2017;2(2):61–8.
3. Baloyiannis I, Perivoliotis K, Sarakatsianou C, Tzovaras G. Laparoscopic total extraperitoneal
hernia repair under regional anesthesia: a systematic review of the literature. Surg Endosc.
2018;32(5):2184–92. https://doi.org/10.1007/s00464-018-6083-6.
290 N. Sharma et al.
4. Bittner JG. Comment on robotic inguinal hernia repair: is technology taking over? Hernia.
2019;23(3):521–2. https://doi.org/10.1007/s10029-019-01984-y.
5. Iuamoto LR, Kato JM, Meyer A, Blanc P. Laparoscopic totally extraperitoneal [TEP] her-
nioplasty using two trocars: anatomical landmarks and surgical technique. Arq Bras Cir Dig.
2015;28(2):121–3. https://doi.org/10.1590/S0102-67202015000200009.
6. Pavlidis TE, Atmatzidis KS, Papaziogas BT, Makris JG, Lazaridis CN, Papaziogas TB. The
effect of preincisional periportal infiltration with ropivacaine in pain relief after laparoscopic
procedures: a prospective, randomized controlled trial. JSLS. 2003;7(4):305–10.
7. Mordecai SC, Warren OW, Warren SJ. Radially expanding laparoscopic trocar ports signifi-
cantly reduce postoperative pain in all age groups. Surg Endosc. 2012;26(3):843–6. https://doi.
org/10.1007/s00464-011-1963-z.
8. Lam TY, Lee SW, So HS, Kwok SP. Radially expanding trocar: a less painful alternative
for laparoscopic surgery. J Laparoendosc Adv Surg Tech A. 2000;10(5):269–73. https://doi.
org/10.1089/lap.2000.10.269.
9. Chiong E, Hegarty PK, Davis JW, Kamat AM, Pisters LL, Matin SF. Port-site hernias occur-
ring after the use of bladeless radially expanding trocars. Urology. 2010;75(3):574–80. https://
doi.org/10.1016/j.urology.2009.08.025.
10. Kocher NJ, Ilinsky D, Raman JD. Incarcerated right lateral trocar-site hernia as a rare compli-
cation of robot-assisted laparoscopic prostatectomy. J Endourol Case Rep. 2017;3(1):155–7.
https://doi.org/10.1089/cren.2017.0099.
11. Schmocker RK, Greenberg JA. An unusual trocar site hernia after prostatectomy. Case Rep
Surg. 2016;2016:3257824. https://doi.org/10.1155/2016/3257824.
12. Clark LH, Soliman PT, Odetto D, Munsell MF, Schmeler KM, Fleming N, Westin SN, Nick
AM, Ramirez PT. Incidence of trocar site herniation following robotic gynecologic surgery.
Gynecol Oncol. 2013;131(2):400–3. https://doi.org/10.1016/j.ygyno.2013.08.021.
13. Tsu JH, Ng AT, Wong JK, Wong EM, Ho KL, Yiu MK. Trocar-site hernia at the 8-mm robotic
port after robot-assisted laparoscopic prostatectomy: a case report and review of the literature.
J Robot Surg. 2014;8(1):89–91. https://doi.org/10.1007/s11701-013-0396-1.
14. Micelli E, Russo E, Mannella P, et al. Severe bowel incarceration in an eight-millimeter left-
lateral trocar site after robot-assisted laparoscopic colposacropexy: a case report. Case Rep
Women’s Health. 2019;24:e00151.
15. Malcher F, Cavazzola LT, Carvalho GL, Araujo GD, Silva JA, Rao P, Iglesias
AC. Minilaparoscopy for inguinal hernia repair. JSLS. 2016;20(4):e2016.00066. https://doi.
org/10.4293/JSLS.2016.00066.
16. Wada H, Kimura T, Kawabe A, Sato M, Miyaki Y, Tochikubo J, Inamori K, Shiiya
N. Laparoscopic transabdominal preperitoneal inguinal hernia repair using needlescopic instru-
ments: a 15-year, single-center experience in 317 patients. Surg Endosc. 2012;26(7):1898–902.
https://doi.org/10.1007/s00464-011-2122-2.
17. Chan YW, Hollinsky C. Needlescopic surgery versus single-port laparoscopy for inguinal her-
nia. JSLS. 2015;19(3):e2015.00056. https://doi.org/10.4293/JSLS.2015.00056.
18. Schmidt J. Minilaparoscopy With 5 Mm Optics and 3 Mm Trocars. Chirurg. 2017;88(8):647–55.
19. Gupta MK, Muley KK, Bethanbhatla MK, Nanavati JD, Manish K, Sarangi R. Mini totally
extra-peritoneal repair of inguinal hernia with all 5 mm ports: an innovative “555 technique”. J
Laparoendosc Adv Surg Tech A. 2017;27(3):295–301. https://doi.org/10.1089/lap.2016.0462.
20. Kamei A, Kanehira E, Nakagi M, Tanida T. Development of scar-less laparoscopic hernia
repair [TAPP-252] facilitated by new 2mm instruments. Minim Invasive Ther Allied Technol.
2016;25(6):314–8. https://doi.org/10.1080/13645706.2016.1193027.
21. Sajid MS, Khawaja AH, Sayegh M, Baig MK. A systematic review comparing single-incision
versus multi-incision laparoscopic surgery for inguinal hernia repair with mesh. Int J Surg.
2016;29:25–35. https://doi.org/10.1016/j.ijsu.2016.02.088.
22. Misra MC, Kumar S, Bansal VK. Total extraperitoneal [TEP] mesh repair of inguinal her-
nia in the developing world: comparison of low-cost indigenous balloon dissection ver-
sus direct telescopic dissection: a prospective randomized controlled study. Surg Endosc.
2008;22(9):1947–58. https://doi.org/10.1007/s00464-008-9897-9.
Minimizing Pain in Laparoscopic Hernia Surgery 291
Introduction
Inguinal hernia repair is one of the commonest surgeries performed worldwide [1].
New technology and advancement in technique which has improved the post opera-
tive quality of life has almost nullified the role of conservative treatment in hernia.
Recent universal acceptance of minimally invasive surgery in treatment of inguinal
hernia repair has led to its most significant metamorphosis [2]. Chronic groin pain
is almost negligible after laparoscopic repair and patients do return to normal activ-
ity and work earlier [3, 4]. Over the years of observation and familiarity, it has been
seen that laparoscopic procedures are absolutely safe in experienced hands.
Presently four laparoscopic techniques are commonly described in repairing an
inguinal hernia:
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 293
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_13
294 D. Sharma et al.
TEP all these years has shown a few drawbacks which surgeons all over face and
try to master with time. Among them confined space for dissection, difficulty in
mesh spreading due to inadequate space, cramped port placement and very impor-
tantly, a longer learning curve for young surgeons [1]. These limitations restrain its
use by the regular surgeon in spite of routine execution by laparoscopic experts
[9, 10].
Anatomically the inguinal extra peritoneal space can be reached from virtually
anywhere on the abdomen. The preperitoneal space in the lower abdomen is con-
tinuous with the retro rectus space beyond the arcuate line. Considering the above,
extended view totally extra peritoneal repair (eTEP) was designed [10, 11] and ini-
tially described by J Daes. “e” stands for extended view (Fig. 1).
Indications of eTEP
eTEP technique can be used to repair all cases of inguinal hernias; nonetheless, in
some specific scenarios eTEP is particularly helpful,
1. eTEP approach particularly is easier to grasp for the new surgeon. Concepts of
starting laparoscopic inguinal hernia surgery through TAPP and then moving to
TEP for trainees can be left aside, as eTEP technique can prime them early for
the extra-peritoneal approach.
2. Large abdomen or thick abdominal walls: Obesity is always a relative contrain-
dication for beginners because of the difficulty to negotiate the thick belly apron.
Further it is considered that the abdominal subcutaneous tissue is thinner in the
upper abdomen facilitating entry in eTEP.
3. In general the distance between umbilicus and pubic symphysis should be around
15–18 cm [13]. In patients in whom this length is lower it becomes very difficult
to accommodate the vertical three ports as it often leads to a chopstick effect of
the instruments during TEP.
4. TEP after pelvic surgery is difficult and is often avoided. However eTEP where
the dissection starts from far above the arcuate line creating space, previous pel-
vic surgeries don’t remain an absolute contraindication.
5. Difficult inguinal hernias in the form of large inguinoscrotal hernias occupying
most of groin space, and in patients with large irreducible hernias or large sliding
hernias, eTEP can be helpful as the ports are away from the area of dissection
and no cramping for space is felt.
Strong hernia repair mandates adequate dissection, proper mesh placement with
good overlap. eTEP technique can provide exactly the same without entering the
peritoneal cavity [14].
Instruments
Steps of Surgery
Patient is in a supine position with hands tucked at the side. Monitor is at the foot
end. Surgeons stand at the sides. Right handed surgeon generally prefer standing on
the left side of the patient while the camera holding assistant can be on the same side
or opposite side depending on the camera position. The operating table can be bro-
ken at the level of the costal margin which increases its distance to pubic symphysis
creating little more space to work with.
a b
Fig. 3 (a) Camera (C) and ports positions (P1 & P2) for Bilateral hernia (LH—Large Hernia &
SH—Small hernia). (b) Camera (C) and ports positions (P1 & P2) for Bilateral hernia (LH—Large
Hernia & SH—Small hernia)
298 D. Sharma et al.
In general during bilateral hernias, the camera is kept on the side of larger or
complicated hernia and working ports are off-axis on the opposite side (Fig. 3a, b).
While operating on unilateral uncomplicated hernia, the camera port can be on
the same side while maintaining triangulation of ports (Fig. 2). Right handed sur-
geons might at times find operating easy from the left side with the right hand work-
ing port to the right of the umbilicus. Port positioning overall is absolutely a surgeon
preference and can be acquired with practice.
Space Creation Through the 10–12 mm incision made at the decided site for cam-
era port, the anterior rectus fascia is exposed by sharp dissection and using the small
‘S’ retractor to retract the subcutaneous tissue and taking care not to create a subcu-
taneous tunnel. A no 11 size blade is used to incise the anterior rectus sheath in line
with the incision and both the lips of the cut rectus sheath are held with small Allis
clamps. Using a Kelly forceps the underlying rectus muscle is split in line of its
fibres and perpendicular to the sheath incision. Once that is done, the ‘S’ shaped
retractors are used to separate the fibres further. Then one can use a small peanut
swab (1 × 1 cm) mounted on the tip of a curved artery forceps or bluntly surgeon
can use his finger to create aspace between the muscle and the thick posterior sheath.
The dissecting finger or swab slides down into the retro rectus space and can be
swiped to right and left to create an initial space.
Once this space is created, hernia dissection can proceed further with either tele-
scopic dissection or working ports can be inserted to start dissecting. Every time
during dissection it should be checked that the inferior epigastric has not fallen
down and is always at the roof.
Working Ports Due to the large dissection, working port site can be flexible with
e-TEP. The initial entry port incision is placed in the upper quadrant on the same
side of the large hernia, usually 4 cm above and 4 cm lateral to the umbilicus. This
port might need to be higher in some cases particularly in very obese patients.
Subsequently 5 mm working port (Figs. 2 and 3 {P1}) is placed just below and lat-
eral (away from large hernia side) to the umbilicus and the next 5 mm port is placed
on the opposite lower inferior quadrant (Figs. 2 and 3 {P2}). An accessory 5-mm
port particularly in bilateral hernias is placed on the inferior quadrant opposite to PI/
P2 (Figs. 2 and 3 {A1}). Using this configuration hernias on both sides can be oper-
ated, however the surgeon some times needs to change sides and use ports P1 + P2
(Off-axis) or ports P1 + A1 (On-axis) for either hernia (Figs. 2 and 3). In Bilateral
hernias the working ports in general should be at a higher level to avoid interference.
Few authors advocate use of the flank opposite the hernia side about 3 cm above
and 5 cm lateral to the umbilicus for the first camera port. Following this one 5-mm
working port can be placed at or next to the umbilicus, and the other can be placed
inferior and lateral to the camera on the same inferior quadrant (Opposite to Hernia),
thus achieving perfect triangulation (Fig. 6).
Proponents advocating this approach mention about advantages of a large surgi-
cal field for large or complex hernias, less arcuate arch interference and achieving
visual triangulation for both sides.
Arcuate Arch Division If the visualization is not proper the arcuate arch which
extends midway between umbilicus and pubic tubercle might need division. This is
300 D. Sharma et al.
more frequent when the camera is used higher up in the abdomen. A small lateral
cut is usually good enough to improve vision. A midline cut on the arcuate line is
generally avoided as the posterior sheath and peritoneum are adherent in the midline
and it can create a rent leading to leakage of gas. (Fig. 7) Leakage of gas into peri-
toneal cavity is mostly not an issue in eTEP as the wide dissection helps to maintain
space inorder to perform surgery.
Extended-View Totally Extraperitoneal Approach (eTEP) for Inguinal Hernia Repair 301
Repair of Hernia Descriptive explanation is beyond this chapter but all principles
of laparoscopic inguinal hernia repair have to be followed which includes the con-
cept of critical view of Myopectineal orifice of Fruchaud(MPO) [15]. This is char-
acterized by proper exposure of the anatomy before placing a mesh.
Closure of Ports Preperitoneal space is then deflated under vision and fascial clo-
sure of all port sites above 10 mm are done using synthetic absorbable sutures.
Post-Operative Care Fluids are restricted orally for 4 hours after surgery and then
started on clear fluids and later soft diet on the same day evening or the morning
after. Patients are advised regarding early mobilization and are usually discharged
the next day of the procedure.
Conclusion
The concept of eTEP has recently revolutionized the approach for inguinal hernia
repair with young surgeons finding the learning curve less steep. It has been very
well documented that once the confluence of the arcuate line and semilunar line is
separated, it provides a limitless extraperitoneal space to work with. Regardless of
a difficult body habitus e-TEP provides a better anatomical and sound TEP repair,
compliant with the concepts of CV of the MPO, especially for residents / junior
faculty early in their experience.
References
1. Krishna A, Bansal VK, Misra MC, Prajapati O, Kumar S. Totally extraperitoneal repair in ingui-
nal hernia: more than a decade’s experience at a tertiary care hospital. Surg Laparosc Endosc
Percutan Technol. 2019 Aug;29(4):247–51. https://doi.org/10.1097/SLE.0000000000000682.
2. Daes J. Minimally invasive surgical techniques for inguinal hernia repair: the extended-view
totally extraperitoneal approach (eTEP). In: Davis Jr S, Dakin G, Bates A, editors. The SAGES
manual of hernia surgery, vol. 33. Springer; 2019. p. 449–60.
Extended-View Totally Extraperitoneal Approach (eTEP) for Inguinal Hernia Repair 303
Introduction
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 305
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_14
306 A. Poddar et al.
intolerable [2]. Here in the chapter we will try to focus on the correct technique in
creation of the gastric pouch, the Bilio-Pancreatic limb and end to side gastro-
jejunostomy during Mini Gastric Bypass.
Principles and Technique
Patient is placed in supine position and is under general anesthesia. Urethral cathe-
terization is done and dynamic limb compression device is applied. Patient is
strapped to the table and all pressure areas padded with soft cotton. The surgeon and
the camera surgeon are on the right side of the patient and assistant surgeon on the
left. The patient is placed in steep head rise and a tilt of 45° towards the right [4].
Antral Division
A 45-mm gold/green cartridge stapler is engaged across the antrum of the stomach
at right angles to its axis. More than 60% of the antral width should not be tran-
sected in the first firing. This takes care of the passage of the contents from the
bypassed remnant stomach. Twist should be avoided by grasping both the walls of
the stomach equally which will also help to avoid “bird beaking” of the edges
thereby avoiding trouble during gastro-jejunostomy as well in the next subsequent
firing [4].
The MGB pouch in contrast to RYGB pouch is different in the respect that it is
restrictive not obstructive. In contrast to RYGB, it also has a large pouch with a
wide GJ [2]. The MGB pouch is again different from the sleeve gastrectomy tube in
the respect that it’s a wide tube with no stress on OG junction dissection. The MGB
pouch is designed for relatively rapid non-obstructive transport of food from the
esophagus into small intestine which results in post gastrectomy syndrome. The
pouch length, GJ and loop Billroth II or GJ are designed to recapitulate the surgical
analogue of antrectomy and Billroth II reconstruction. The pouch should start just
distal to crow’s foot as this helps in prevention of Gastro-esophageal Reflux Disease
(GERD), pouch should lie as such that the medial aspect, formed by the mesentery
of the lesser curvature points directly to the 9 o’clock to the patient’s right and the
neo greater curvature points to the patient’s left at 3 o’clock with anterior and pos-
terior walls of the pouch being equal. Proper control of bleeding during pouch cre-
ation is a necessity; hence the prime maneuver is proper compression by the stapler
for around 30 seconds before firing. Rapid firings of stapler should be avoided as it
may lead to oozing and subsequent compromise of the staple line. After antral divi-
sion, gastric pouch creation is started by second firing, done from the right hypo-
chondrial port. The axis of division is kept perpendicular to the first firing (Antral
division) and parallel to lesser curvature [3] (Fig. 3).
Bougie of 36-Fr is then inserted and engaged until it reaches the tip of the pouch
Subsequent firings are done with the bougie as a guide. Care should be taken to cre-
ate a moderate-sized gastric pouch which is never too tight on the bougie (Fig. 4).
Dissection during MGB should be lateral to the left crus of the diaphragm and a
proper and safe dissection around the hiatus is mandatory to create an adequate
Fig. 5 Creation of
window near the angle of
his. MGB Pouch (P),
Remnant stomach®
space for stapler engagement. Care is taken to avoid inadvertent injury to short gas-
tric, inferior phrenic vessels and the spleen (Fig. 5). The final staple firing is to be
placed at least 2 cm lateral to the GE junction to avoid leaks near the junction in
spite of the fact that it is a low-pressure drainage system at the GJ (Fig. 6), so back
pressure at GE junction is minimum. During MGB it is even acceptable to leave a
small amount of fundus in exchange for leak prevention [5].
Bowel and stomach should be checked to avoid any kink or twist. One should
avoid a Bird’s beak deformity at the distal tip of gastric pouch and try to create a
310 A. Poddar et al.
wide cobra head effect of the distal tip to provide a wide perfusing field for the lat-
eral aspect of the distal gastric portion of the GJ [4] (Fig. 7).
BPL length of >200 cm should be reserved for revision cases. A longer bypass
results in more malnutrition without significant effect on co-morbidity resolu-
tion [6].
Creation of GJ is one of the most important steps in MGB. The goal is a wide open
and non-obstructive GJ that allows easy, rapid emptying of the gastric pouch which
is similar to the passage of food through esophagus. GJ thus created contributes to
the induction of post gastrectomy syndrome which ultimately modifies the type of
food intake, amount of foods along with timing of foods [2].
After identifying the site on jejunum for GJ, the small bowel loop is moved to the
left upper quadrant making sure not to twist the afferent and efferent limbs.
Anterior gastrostomy is made just above the gastric staple line midway between
the medial and lateral angle but the GJ anastomosis is always posterior. The size of
the gastrostomy should be equal to the diameter of the stapler anvil. The bougie can
be used to stabilize the pouch during gastrostomy and also act as a guide by stenting
the pouch (Fig. 8).
Since the gastrojejunostomy is posterior (i.e. made between the posterior wall of
stomach pouch and jejunum) the jejunostomy should be made 5 mm away from the
anti-mesenteric border of the jejunum towards the posterior wall to avoid twist. The
opening again should be made equal to the stapler cartridge [4] (Fig. 9).
Fig. 9 Creation of jejunotomy 5 mm posterior to anti mesenteric border (White arrow)
Fig. 10 Gastrojejunos-
tomy done to posterior
wall of gastric pouch.
Lateral stapler line of
gastric pouch (Green
Arrow) should be anterior
to the GJ (Blue arrow) as
shown in image (Image
Courtesy: Dr Deborshi
Sharma)
Mini Gastric Bypass 313
Fig. 12 Posterior
Gastrojejunostomy and the
gastric calibration tube
being pushed into jejunum
before closure (Green
Arrow) (Image Courtesy:
Dr Deborshi Sharma)
GJ Closure
Hemostasis
Leak Test
Leak test after MGB though not mandatory is done either by using intraluminal
75 mL diluted methylene blue or air leak test, after clamping both the efferent and
afferent loop. Recently Intraluminal ICG also has been used to check for any extrav-
asation. Recognizing leaks as early as possible is preferable and the mainstay for
any successful bariatric surgery, hence on table detection if any is the cornerstone of
management. A flat drain is placed between the gastric pouch and the bypassed
stomach [2, 4].
All the above advantages are the reasons why MGB is becoming one of the fast-
est acceptable metabolic procedures.
Mini Gastric Bypass 315
Complications
(a) Early complications—those occurring within the first 30 post operative days [8].
(b) Late complications—beyond 30 days to 10 years after surgery [9].
Early Complication
Late Complication
Late complications are seen in around 11% cases after primary surgery and 7% after
redosurgery.
T2DM is one of the most common non-communicable diseases and is the fourth
leading cause of death in first world countries. Now it is also reaching epidemic
propositions in developing countries [24]. The global prevalence of T2DM is on the
rise because of the increase in the factors which favors obesogenic environment,
like sedentary lifestyle and easier access to calorie dense foods [24].
Medications and lifestyle modifications require patient compliance but still con-
trol over T2DM remains elusive. Metabolic surgery is effective in the treatment and
prevention of T2DM, thereby reducing the mortality rate in the long term when
compared with medical treatment.
Metabolic surgery involves any intervention that alters the passage of food
through the GI tract resulting in improved control of T2DM. The control of T2DM
is not related to weight loss precluding a direct antidiabetic effect [25].
Various mechanisms have been put forward as the possible explanation for
improvement in T2DM after bariatric surgery. They are:
2. The ghrelin secretion from stomach also decreases which results in decreased
appetite and hence better T2DM control [28].
3. Foregut theory—There is an improvement or augmentation of the action of
Gastro Intestinal Peptide (GIP) from the foregut following metabolic surgery
which in turn helps to control the blood glucose level [28].
4. Hindgut theory—Post metabolic surgery there is an increase in secretion of
incretins such as Glucagon Like Peptide I (GLP-I) from the L-cells in the lower
ileum due to duodenal bypass, which results in early transit of nutrients to the
ileum and stimulation of β cells, which then results in good diabetic control
[29–31].
T2DM remission has been reported to be of varying degrees after all current
bariatric operations. However, after sleeve gastrectomy (leaks, weight regain,
GERD) and after RYGB (weight regain, malnutrition, internal hernias and others)
numerous complications can occur [21, 31]. MGB has been documented to be a
dependable bariatric procedure in large series. It has shown superiority in resolution
of comorbidities in comparative studies to RYGB and sleeve gastrectomy. MGB has
resulted in T2DM resolution in 85–95% of diabetic patients followed >5 years,
requiring no medication, which is superior to sleeve gastrectomy and RYGB
[32–36].
Following MGB with the rapid passage of food into the small bowel, rapid eleva-
tion of GLP-I levels have been found compared to other operations. MGB and
sleeve gastrectomy can rapidly augment the incretin effect which persists upto
5 years. However, the MGB has a better effect than sleeve gastrectomy at longer
follow-up due to the increase in serum GLP-I levels [31].
Future Perspective
Robotic surgery is one of the most rapidly developing and upcoming techniques in
the field of surgery. It offers 3D vision and gives the control of the camera to the
surgeon. Along with the degrees of freedom, the robotic arms provide a distinct
advantage while suturing in small confined spaces. Robotic MGB is possible with-
out hybrid or dual docking as all dissection and anastomosis is in the supracolic
compartment, hence MGB is suitable technically for robotic surgery [37].
Initial studies show no difference between robotic assisted and conventional
laparoscopic surgery with respect to surgical time, post operative hospital stay, com-
plications or rate of conversion to open surgery but the anastomosis leaks have been
shown to be significantly less after robotic surgeries. Use of the robot has reduced
the ergonomic challenges of bariatric surgery in comparison to conventional lapa-
roscopy. The robot controlled telescope, tissue manipulator with alignment, robotic
suturing etc are easier along with being more accurate. The time taken for the pro-
cedure in both the techniques is equivalent. The main disadvantage of robotic
Mini Gastric Bypass 319
Gastric banding was one of the most popular bariatric surgeries during 1990s and
early 2000s, because of its various complication like band slippage/erosion, inade-
quate weight loss to name a few, a large percentage of patients required a revision
surgery from LAGB. The various options for revision are LSG, LRYGB and
MGB. It has been seen that revision from an earlier restrictive procedure to a mal-
absorptive procedure leads to a more consistent and satisfactory weight loss. Hence
MGB is gaining consensus as a revisional surgery after LAGB.
The patient should learn dietary and behavioral changes atleast 3–6 months prior
to revision. A lack of willingness on the patient’s part for these changes should be
considered a contraindication for revision. The band has to be completely emptied
a few weeks before surgical procedure. Upper GI gastrograffin series, Upper GI
endoscopy and other routine necessary pre-operative bariatric investigations should
be done.
The surgeon may choose to go for a one stage or two stage surgery. The standard
technique for MGB is followed barring the following changes:
(a) Band is removed and the fibrous capsule is cut to prevent dysphagia in future.
(b) The vertical resection line while creating the gastric pouch is moved towards
the spleen to avoid the inflammatory tissue and band fibrous capsule in the last
stapler line. This helps to prevent complications in future and gives best results
post-operatively. Revision for LAGB to MGB can be a single and relatively safe
procedure which results in valid weight loss, rapid recovery with high level of
patient satisfaction [38].
Conversion from LSG to MGB is a safe, feasible and effective option and results in
significant weight loss. It is the operation of choice for morbidly obese patients who
are compliant in taking calcium and iron supplements. Patients having inadequate
weight loss following LSG due to non-anatomical causes are primary candidates for
conversion to MGB or RYGB, but the former is preferred because of its simple
technique, efficacy and reversibility [39].
320 A. Poddar et al.
Conclusion
Editor’s Note1
Late Complications
Gastro eosophageal reflux disease: Main concern over the years for MGB has been
the fear of increased GERD and is reported to vary from 0.5 to 4%. A shorter gastric
pouch of <9 cm and presence of preoperative GERD can be inciting factors while
de novo GERD after MGB is seen in 2% [1]. Rate of revision for GERD is very rare
(0–0.7%) due to intractable bile reflux, if standard operating protocol is followed
[2–4]. Intragastric pressure is significantly diminished after MGB hence GE reflux
is not increased. Endoscopy sometimes reveals bile in the stomach with mild to
moderate pouch gastritis, however evidence of any esophagitis on endoscopy after
MGB is rare [LC 3–5].
References: Main chapter references are included after the “References Editor’s Note” section.
1
322 A. Poddar et al.
Essentially, both MGB & OAGB is similar in theory, where main idea it is to avoid
two anastomosis and two limbs. Still MGB & OAGB differs in many aspects techni-
cally. In OAGB (Figure EN1) the following steps are stressed upon over MGB
Total small bowel measurement (TSB): Starting from DuodenoJejunal Junction
(DJ) downward to Ileocaecal junction (IC) total small bowel measurement is done
in OAGB [6]. This is done with the view point that differences will remain in the
metabolic setup of a younger vs older patient, obese vs super-obese, male with cen-
tral obesity vs female with gynecoid obesity and all these with a patient with severe
metabolic syndrome. After knowing the TSB, both BP limb and common channel
(CCh) can be tailored and a ratio of 0.37–0.44 (CCh/TSB) is regarded to give best
weight loss success rate and improve co-morbidities [7]. Length of CCh can be
maintained between 180 and 220 cm [8].
Bi-Valving the greater omentum: As more length of small bowel is bypassed in
OAGB compared to MGB, the greater omentum might exert more tension on anas-
tomosis. Omentum from its attachment on transverse colon upto the greater curve is
opened longitudinally to make it into two halves.
Complete dissection of “Angle of His”: Left side of Phreno-esophageal mem-
brane is dissected until the left crus of diaphragm, almost up to the posterior border
of spleen. Thick fat “Belsey’s fat” pad which surrounds the esophago-gastric junc-
tion (EGJ) is also dissected down. This manoeuvre allows creation of a wide aper-
ture of the retro-gastric window avoiding the short gastric vessels and any splenic
tissue injury. Ultimately endostapler is also optimally positioned at this demanding
position [6, 9].
Gastro-hepatic ligament dissection: Dissection starting at the Pars flaccid upto
right crus is done along with remains of right Phreno-esophageal membrane. This
release helps in lengthening of gastric pouch and decreasing anastomotic tension.
Any hiatal hernia if present is also selectively repaired [10].
Creation of long and narrow gastric pouch: In OAGB a long narrow pouch of
about 15–18 cm is made which usually lies over the gastric antrum of remnant stom-
ach with its tip at the level of the transverse colon [7].
Anti-reflux mechanism: Continous suturing for 8–10 cm using reabsorbable
material of anti-mesenteric border of small bowel to the vertical staple line of gas-
tric pouch is done. This continous suturing also is advantageous as it creates perma-
nent posterior fixation of small bowel and gastric pouch creating proper alignment
of two lumens, preventing twisting of pouch later on and ensures no gap between
them for any internal hernia [7].
GJ over anterior wall of pouch: The anterior wall of gastric pouch and small
bowel is anastomosed for 2.5 cm using linear endo stapler, anterior to the continous
anti reflux suture in a lateral-lateral fashion. The enterotomies are closed in standard
fashion.
This vertical 2.5 anastomosis makes the BP limb content to go down into afferent
limb (CCh channel) directly due to gravity preventing reflux or marginal ulcers [11].
Mini Gastric Bypass 323
RYGB is still considered by many to be the most effective and well balanced meta-
bolic/bariatric surgical technique [14]. RYGB is pulled down by some for its signifi-
cant unique complications such as internal hernias, marginal ulcers or
hyperinsulinemic hypoglycemias. Intermediate-term weight regain following
RYGB is also a concern [15, 16]. Weight regain or not maintaining 50% EWL on
follow up contributes to the overall failure rate [17]. dMGB proposes OAGB-MGB
procedure with a Roux-en-Y anastomosis added to the long narrow pouch.
After MGB-OAGB, a 100 cm into the efferent limb, from proximal to distal
beyond the gastro-jejunostomy a new side-to-side ileoileostomy or ileojejunostomy
is created between the afferent and efferent loop. The afferent is then disconnected
to the gastric pouch (Fig. EN2). The inter-mesenteric spaces hence created need
closure to prevent internal hernias. Initially this procedure was also called the Sleeve
gastric bypass. (Fig. EN3).
Fig. EN3 Schematic diagram of Sleeve Gastric bypass (Image Courtesy Dr. Gautam Anand)
Table EN1 Metaanalysis comparing various bariatric surgical procedures outcomes as: primary
procedure, for diabetes remission and as revisional procedure
Topic Study, author (first), year Result
Laparoscopic Comparison of safety and Advantages of MGBP over LSG
sleeve versus effectiveness between • Higher 1-year EWL% (excess weight
mini gastric laparoscopic mini-gastric loss),
bypass bypass and laparoscopic • Higher 5-year EWL%,
sleeve gastrectomy: A • Higher T2DM remission rate,
meta-analysis and • Higher hypertension remission rate,
systematic review. • Higher obstructive sleep apnea (OSA)
Wang F, 2017 [19] remission rate,
• Lower osteoarthritis remission rate,
• Lower leakage rate,
• Lower overall late complications rate,
• Higher ulcer rate,
• Lower gastroesophageal reflux disease
(GERD) rate,
• Shorter hospital stay and
• Lower revision rate.
Mini Gastric Bypass 325
Table EN1 (continued)
Topic Study, author (first), year Result
RYGB versus Outcomes of Mini vs Advantages MGBP over RYGBP
MGB Roux-en-Y gastric bypass: • A higher 1-year EWL% (P < 0.05),
A meta-analysis and • Higher 2-year EWL% (P < 0.05),
systematic review. • Higher type 2 diabetes mellitus remission
Wang FG, 2018 [20] rate,
• Shorter operation time (P < 0.05).
No significant statistical difference was
observed in hypertension remission rate,
mortality, leakage rate, GERD rate, or hospital
stay between mini gastric bypass and
Roux-en-Y gastric bypass.
Comparative Network meta-analysis of BPD and MGBP achieved higher diabetes
analysis MGB the relative efficacy of remission rates than the other procedures viz:
and other bariatric surgeries for LAGB, LSG, RYGBP, DJ Bypass, duodenal
bariatric diabetes remission. switch greater curvature plication.
surgeries in Kodama S, 2018 [21]
remission of Comparative effectiveness • MGBP has greatest probability of
type 2 DM of bariatric surgeries in achieving diabetes remission in adults
patients with obesity and with obesity and T2DM,
type 2 diabetes mellitus: A • BPD was the most effective in long-term
network meta-analysis of diabetes remission.
randomized controlled • RYGBP most favourable alternative
trials. treatment
Ding L, 2020 [22]
Efficacy of Laparoscopic MGBP compared with LAGB, LSG, and
Mini Gastric Bypass for RYGBP,
Obesity and Type 2 • MGBP showed significant weight loss
Diabetes Mellitus: A [WMD, −6.58 (95% CI, −9.37, −3.79),
Systematic Review and P < 0.01 and comparable/higher T2DM
Meta-Analysis. remission
Quan Y, 2015 [23] • MGBP also had shorter learning curve
and less operation time than RYGBP
[WMD, −35.2 (95% CI, −46.94,
−23.46)].
(continued)
326 A. Poddar et al.
Table EN1 (continued)
Topic Study, author (first), year Result
MGB as Roux-en-Y gastric bypass OAGBP/MGBP vs RYGBP
revisional versus one anastomosis- MGBP showed
surgery after mini gastric bypass as a • Lower rate of bleedings
restrictive rescue procedure following • Better weight loss (comparing pre vs post
bariatric failed restrictive bariatric revision BMI)
surgery surgery. A systematic • Shorter operative time
review of literature with • Similar rate of leaks
metanalysis.
Velotti N, 2021 [24]
One Anastomosis/ MGBP/OAGBP
Mini-Gastric Bypass • BMI/Weight loss mean initial BMI was
(OAGB/MGB) as 45.70 kg/m2, which decreased to 31.52,
Revisional Surgery 31.40, and 30.54 kg/m2 at 1, 3, and 5-year
Following Primary follow-ups, respectively.
Restrictive Bariatric • Remission of type-2 diabetes mellitus
Procedures: a Systematic (T2DM) following OAGB/MGB at 1-, 3-,
Review and and 5-year follow-up was 65.16 ± 24.43,
Meta-Analysis. 65.37 ± 36.07, and 78.10 ± 14.19%,
Kermansaravi M, 2021 respectively.
[25] • Remission/improvement rate from
gastroesophageal reflux disease (GERD).
• 7.4% of the patients developed de novo
GERD following OAGB/MGB.
• Leakage was the most common major
complication. OAGB/MGB
MGBP minigastric bypass, LSG laparoscopic sleeve gastrectomy, RYGBP Roux en Y gastric
bypass, LAGB laparoscopic adjustable gastric banding, BPD biliopancreatic diversion, OAGBP
one anastomosis gastric bypass, EWL excess weight loss, T2DM type 2 diabetes mellitus, GERD
gastroesophageal reflux disease, BMI body mass index
Mini Gastric Bypass 327
References
1. Cowan GS Jr, Smalley MD, Defibaugh N, et al. Obesity stereotypes among physi-
cians, medical and college students, bariatric surgery patients and families. Obes Surg.
1991;1:171–6.
2. Rutledge R, Kular KS, Chiappetta S, Manchanda N. Understanding the technique of MGB:
clearing the confusion. In: Essentials of mini–one anastomosis gastric bypass. Cham: Springer;
2018. p. 17–30.
3. Rutledge R. The mini-gastric bypass: experience with the first 1,274 cases. Obes Surg.
2001;11:276–80.
4. Shivakumar S, Tantia O, Chaudhuri T, Khanna S, Ahuja A, Goyal G. Ten crucial steps for
the MGB operation. In: Essentials of mini-one anastomosis gastric bypass. Cham: Springer;
2018. p. 39–49.
5. Iossa A, Abdelgawad M, Watkins BM, Silecchia G. Leaks after laparoscopic sleeve
gastrectomy: overview of pathogenesis and risk factors. Langenbeck’s Arch Surg.
2016;401:757–66.
6. Ahuja A, Tantia O, Goyal G, Chaudhuri T, Khanna S, Poddar A, Gupta S, Majumdar
K. MGB-OAGB: effect of biliopancreatic limb length on nutritional deficiency, weight loss,
and comorbidity resolution. Obes Surg. 2018 Nov;28(11):3439–45. https://doi.org/10.1007/
s11695-018-3405-7.
7. Rancaño RS, Pernaute AS, Garcia AJ. Single anastomosis malabsorptive procedures. In:
Prevention and management of complications in bariatric surgery. Oxford University Press;
2018. p. 361–80.
8. Musella M, Velotti N. Early complications of the MGB: prevention and treatment. In:
Essentials of mini-one anastomosis gastric bypass. Cham: Springer; 2018. p. 75–80.
9. Musella M, Bocchetti A. Late complications of the MGB: prevention and treatment. In:
Essentials of mini-one anastomosis gastric bypass. Cham: Springer; 2018. p. 81–6.
10. Musella M, Susa A, Manno E, et al. Complications following the mini/one anastomosis gastric
bypass (MGB/OAGB): a multi-institutional survey on 2678 patients with a mid-term (5 years)
follow-up. Obes Surg. 2017;27:2956–67.
11. Lee WJ, Yu PJ, Wang W, et al. Laparoscopic Roux-en-Y versus mini-gastric bypass for the
treatment of morbid obesity: a prospective randomized controlled clinical trial. Ann Surg.
2005;242:20–8.
12. Woodward GA, Morton JM. Stomal stenosis after gastric bypass. In: Deitel M, Gagner M,
Dixon JB, Himpens J, editors. Handbook of obesity surgery. Toronto: FD-Communications;
2010. p. 102–7.
13. Sifrim D. Management of bile reflux. Gastroenterol Hepatol (NY). 2013;9:179–80.
14. Vaezi MF, Richter JE. Duodenogastroesophageal reflux and methods to monitor nonacidic
reflux. Am J Med. 2001;111(Suppl 8A):160S–8S.
15. Carbajo MA, Luque-de-León E, et al. Laparoscopic one-anastomosis gastric bypass: tech-
nique, results, and long-term follow-up in 1200 patients. Obes Surg. 2017;27:1153–67.
16. Georgiadou D, Sergentanis TN, Nixon A, et al. Efficacy and safety of laparoscopic mini-
gastric bypass. A systematic review. Surg Obes Relat Dis. 2014;10:984–91.
17. Kular KS, Manchanda N, Rutledge R. A 6-year experience with 1,054 mini-gastric bypasses:
first study from Indian subcontinent. Obes Surg. 2014;24:1430–5.
18. Chen MC, Lee YC, Lee W-J, Liu HL, Ser KH. Diet behavior and low hemoglobin level after
laparoscopic mini-gastric bypass surgery. Hepato-Gastroenterology. 2012;59:2530–2.
330 A. Poddar et al.
19. Musella N, Sousa A, Greco F, De Luca FM, Manno E, Di Stefano C, Milone M, et al. The
laparoscopic mini-gastric bypass: the Italian experience: outcomes from 974 consecutive cases
in a multicenter review. Surg Endosc. 2014;28:156–63.
20. Wang W, Wei PL, Lee YC, Huang MT, Chiu CC, Lee WJ. Short-term results of laparoscopic
mini-gastric bypass. Obes Surg. 2005;15:648–54.
21. Rutledge R, Walsh TR. Continued excellent results with the mini-gastric bypass: six-year
study in 2,410 patients. Obes Surg. 2005;15:1304–8.
22. Jammu GS, Sharma R. A 7-year clinical audit of 1107 Cases comparing sleeve gastrectomy,
Roux-en-Y gastric bypass, and mini-gastric bypass, to determine an effective and safe bariatric
and metabolic procedure. Obes Surg. 2016;26:926–32.
23. Luger M, Kruschitz R, Langer F, Prager G, Walker M, Marculescu R, et al. Effects of omega-
loopgastric bypass on vitamin D and bone metabolism in morbidly obese bariatric patients.
Obes Surg. 2015;25:1056–62.
24. International Diabetes Federation. IDF diabetes atlas. 6th ed. IDF; 2013. https://w.idf.org/sites/
default/files/EN_6E_Atlas_Full_0.pdf
25. Forieg AM. Effects of MGB on type 2 diabetesin morbid obesity, and comparison with other
operations. In: Essentials of mini-one anastomosis gastric bypass. Cham: Springer; 2018.
p. 119–30.
26. Herbst CA, Hughes TA, Gwynne JT, et al. Gastric bariatric operation in insulin-treated adults.
Surgery. 1984;95:209–13.
27. Kelley DE, Wing R, Buonocore C, et al. Relative effects of caloric restriction and weight loss
in noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab. 1993;77:1287–93.
28. Mahdy T, Gado W. Effects of MGB on type 2 diabetesin lower BMI patients. In: Essentials of
mini-one anastomosis gastric bypass. Cham: Springer; 2018. p. 131–8.
29. Fetner R, McGinty J, Russell C, et al. Incretins, diabetes, and bariatric surgery: a review. Surg
Obes Relat Dis. 2005;1:589–98.
30. Laferrere B, McGinty J, Heshka S, et al. Incretin levels and effect are markedly enhanced 1
month after Roux-en-Y gastric bypass surgery in obese patients with type 2 diabetes. Diabetes
Care. 2007;30:1709–16.
31. Lee WJ, Chong K, Lin YH, Wei JH, Chen SC. Laparoscopic sleeve gastrectomy versus single
anastomosis (mini-) gastric bypass for the treatment of type 2 diabetes mellitus: 5-year results
of a randomized trial and study of incretin effect. Obes Surg. 2014;24:1552–62.
32. Carbajo MA, Jimenez JM, Castro MJ, et al. Outcomes and weight loss, fasting blood glu-
cose and glycosylated hemoglobin in a sample of 415 obese patients, included in the data-
base of the European Accreditation Council for Excellence Centers for Bariatric Surgery with
Laparoscopic One Anastomosis Gastric Bypass. Nutr Hosp. 2014;30:1032–8.
33. Kim Z, Hur K. Laparoscopic mini-gastric bypass for type 2 diabetes: the preliminary report.
World J Surg. 2011;35:631–6.
34. Kular KS, Manchanda N, Cheema GK. Seven years of mini-gastric bypass in type II diabe-
tespatients with a body mass index <35 kg/m2. Obes Surg. 2016;26:1457–62.
35. Guenzi M, Arman G, Rau C, Cordun C, Moszkowicz D, Voron T, et al. Remission of type
2diabetes after omega loop gastric bypass for morbid obesity. Surg Endosc. 2015;29:2669–74.
36. Habashi AB, Sakr M, Hamaza Y, Sweidan A, Tacchino R, Frieg A. The role of mini-
gastricbypass in the control of type 2 diabetes mellitus. Biolife. 2016;4:255–60.
37. Prasad A. Robotic mini-gastric bypass. In: Essentials of mini-one anastomosis gastric bypass.
Cham: Springer; 2018. p. 171–9.
38. Soprani A, Carandina S, et al. Revision of lap-band to MGB. In: Essentials of mini-one anas-
tomosis gastric bypass. Cham: Springer; 2018. p. 185–99.
39. Jammu GS. Comparison of results of mini-gastric bypass to sleeve gastrectomy and Roux-en-Y
gastric bypass. Technique of conversion of failed sleeve gastrectomy to MGB. In: Essentials
of mini-one anastomosis gastric bypass. Cham: Springer; 2018. p. 201–13.
Robotic Roux-en-Y Gastric Bypass
Vivek Bindal
Introduction
In the last decade, bariatric surgery has witnessed an ever-increasing demand with
rise in the prevalence of obesity. Laparoscopic Roux-en-y gastric bypass (LRYGB)
was described in 1990s [1] and currently more than 100,000 procedures are esti-
mated to be performed annually alone in United States [2]. According to American
Society for Metabolic & Bariatric Surgery (ASMBS) estimate published in July
2015, RYGB constitutes 26.8% of total bariatric surgery volume.
Bariatric surgery is a technically demanding surgery particularly in situations with
huge patients with large livers, thick abdominal walls and substantial visceral fat making
exposure, dissection and reconstruction difficult [3]. The super obese patients (SO) with
a body mass index (BMI) greater than or equal to 50 kg/m2 is a difficult to manage popu-
lation because of limited working space, excessive torque, on instruments due to thick
abdominal wall, co-morbidities and high-risk anesthesia [4]. The maneuvering of instru-
ments while performing LRYGB often becomes difficult, particularly while doing intra-
corporeal suturing. All these lead to a longer learning curve for LRYGB, which has been
estimated to be around 75–100 cases [5, 6]. Along with the difficulty, the surgeons
encounter very difficult ergonomic positions during LRYGB which can potentially be
career shortening, and whereas on one hand methods to improve the patient outcomes,
surgical technique and decrease complications are being targetted, on the other hand
concomitant reduction of the learning curve is being aimed.
Use of robotics in bariatric surgery has been evolving since Cadiere GB et al.
reported the first such case in 1999 [7]. Robotic surgery has provided the surgeons
with the advantage of three-dimensional vision, increased dexterity and precision
by downscaling surgeon’s movements enabling a fine tissue dissection and filtering
V. Bindal (*)
Institute of Minimal Access, Bariatric and Robotic Surgery, Max Super Speciality Hospitals,
Noida & Mohali, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 331
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_15
332 V. Bindal
out physiological tremor [8, 9]. In morbidly obese it overcomes the restraint of
torque on ports from thick abdominal wall and minimizes port site trauma by remote
centre technology [10]. Consensus document on robotic surgery prepared by the
SAGES-MIRA Robotic Surgery Consensus Group, claims robotic surgery to hold
particular value for gastric bypass amongst general surgical procedures.
The main limitation of robotic surgery is its higher cost and robot setting up time
compared to laparoscopy, but with increased experience, it is seen that setup times
reduce and costs may also come down as material prices reduces [11].
RYGB is often considered as the gold standard surgical procedure for morbid obe-
sity [12, 13]. Overall results are good in terms of both weight loss and comorbidity
resolution [14]. RYGB leads to an excess weight loss to the tune of 65.7%, while
remission rates of type 2 DM being 66.7% and for dyslipidemia being 60.4% [15].
RYGB is done by creating two gastrointestinal anastomoses namely gastrojejunos-
tomy and jejunojejunostomy. Robotic surgery is currently considered as a valuable
technology that could help perform RYGB, given its well described benefits [16].
Robotic RYGB (R-RYGB) is today the most studied robotic bariatric procedure
[17, 18].
Surgical Technique
There are many ways by which R-RYGB can be performed. The major variations in
technique are listed below:
Instrumentation (Fig. 1)
All three arms of the robotic system are used with third arm coming from the left
side of the patient (explained in docking).
The patient is positioned in supine position with 15–200 reverse trendelenberg tilt
under general anesthesia. This position helps to complete the procedure in a single
docking, as both infracolic and supracolic portions of the procedure can be done
without changing the position. The abdomen is cleaned and draped and orogastric
tube/urinary catheter (optional) are placed. Assistant surgeon stands by the side of
the patient along with the scrub nurse. The master console should be placed in such
a way that the surgeon is able to freely visualize the operative field while sitting on
the console. It is important that two video monitors are placed on both sides of the
patient to enable the assistants to easily watch the monitor and if required to help at
every step of procedure, with ergonomic comfort. The anesthesia machine is also
kept on one side of the head end as patient cart comes in from the head end.
334 V. Bindal
Fig. 2 Operating room setup and patient cart positioning for robot assisted RYGB
a b
Liver
Retractor
2 3
Camera 1
Assistant
Fig. 3 (a) Schematic diagram of port positions for Robot assisted RYGB; (b) Port position for
Robot assisted RYGB
• R1: (8 mm da vinci® cannula) is placed in left mid clavicular line approx. 20 cm
from xiphisternum
• R2 (8 mm da vinci® cannula) is placed in right hypochondrium in mid clavicular
line taking care that the entry of port is below the margin of liver.
• R3 (8 mm da vinci® cannula) is placed in left flank at the level of camera port.
• Assistant port (12 mm diameter) is placed in between camera port and R2 with a
distance of at least 10 cm from both of them.
336 V. Bindal
• A 5 mm epigastric port is made and used for placing Nathanson liver retractor for
retracting left lobe of liver.
The da Vinci® patient cart is brought from head end of the patient, and the arms
are docked to the ports placed. The third arm of the robot comes from left side of the
patient. To start the procedure, a permanent cautery hook is taken in R1, fenestrated
bipolar forceps in R2 and a Cadiere forceps in R3. The assistant surgeon stands by
the side for complementary maneuvers (i.e., suction, stapling, retraction etc.). A
sample OR setup for RRYGB is depicted in Fig. 2. Diagnostic laparoscopy is done
to look for any adhesions/hernias/inadvertent injury during abdominal wall access.
Dissection should be started from the left crus by bringing the phrenoesophageal
membrane down using the hook after caudally retracting the fundus of stomach
(Fig. 5). Gastric pouch is created using perigastric dissection starting at the second
vessel from gastroesophageal junction. Third arm is used to retract stomach later-
ally while harmonic scalpel opens the gastro-hepatic ligament. Perigastric dissec-
tion is done using hook avoiding injury to vagus nerve and lesser sac is entered.
Stapler is fired horizontally which is done by the assistant using a 60 mm blue
The camera now needs to focus towards the infracolic part. The transverse colon is
lifted up and ligament of trietz is identified. Jejunum is measured from ligament of
treitz for 60 cm and divided using stapler. Biliopancreatic limb is held static by the
third arm while 120 cm of roux limb is measured and the site for jejuno-jejunostomy
identified. Then the bowel loops are held together while enterotomy is created using
cautery hook (Fig. 6). Using the third arm to hold limbs together, time for a stay
suture is saved and the operation runs more efficiently.
A jejuno-jejunostomy is created using a 60 mm stapler (Fig. 7). The enterotomy
is closed using PDS 3-0 running suture with large needle driver. Omentum is divided
using harmonic scalpel and roux limb is taken up to gastric pouch for gastro-
jejunostomy (GJ). Polypropylene suture is used to close the mesentric defect after
GJ creation to avoid tension on the mesentery while roux limb is taken up to the
gastric pouch.
Fig. 7 Creation of
stappled jejunojenostomy
corner of anastomosis. Similar full thickness anterior layer of GJ is also done from
left to right with the ends of sutures knotted securely at the right side. Finally, the
anterior sero-serosal layer is completed from left to right side. Ambidexterity is the
basis of a robotic platform which allows the needle holder to be driven effectively
in all directions during creation of GJ. Often four pieces of 6 inches PDS 3-0 is
required to complete the 4 layered GJ (Fig. 10).
340 V. Bindal
Peterson defect is closed starting from the base of the ‘V’ type opening basically
by lifting up the transverse mesocolon and working towards the top. This is also
done using polypropylene suture, taking care that no mesentric vessel is injured in
this maneuvre. An intraoperative check esophago-gastroscopy is done with air leak
test in all the cases at end of the procedure.
Perioperative Care
Outcomes and Results
Robotic surgery is a team effort, and more so in bariatric surgery, where the role of
an experienced OT table side surgeon cannot be understated, as he is also respon-
sible for stapling (if robotic staplers are used). Main surgeon in the console is always
slightly away from the patient while performing robotic surgery, hence the assistant
surgeon also has to be trained to perform difficult tasks and also to take care of any
emergency situation arising during the procedure. The entire team has to learn with
the surgeon and develop knowledge about patient safety, operating room setup,
types of instruments used or needed, thus leading to better OR times and better
patient outcomes. The role of a trained scrub nurse and operating room technician
is also very important in streamlining the conduct of the procedure and prevent any
wastage of time and resources.
Lesser operator fatigue and improved ergonomics are the main advantages of a
robotic platform. Ergonomics in laparoscopic surgery can be very challenging par-
ticularly with big patients and uncomfortable postures, which leads to fatigue and
work-related musculoskeletal problems [19]. Robotics provides the advantage of
more degrees of freedom, which is advantageous in performing difficult dissection
and sutured anastomosis. Many significant published series compare outcomes of
R-RYGB vs L-RYGB [20–29] where they primarily compare intra-operative and
post operative outcomes.
Duration of Surgery: Initially time taken for totally R-RYGB or Hybrid
R-RYGB is more compared to L-RYGB, as additional time is taken in docking and
undocking which is compounded by the fact that mostly a sutured anastomosis is
done in the robotic surgery while a stapled anastomosis is done in laparoscopic arm.
Robotic Roux-en-Y Gastric Bypass 341
Conclusion
Big question to be answered is whether the use of robotics is going to stay or will it
perish with time like many fancy technologies. Looking at the basic concept of
computer assisted navigational surgery, robotics provide an enabling platform in
between surgeon and the patient. It provides augmented and higher quality inputs
from the patient to the surgeon and his output is refined to a superior quality before
reaching back to the target. All this should not be analyzed in terms of features of
the present machine that is available for use, but in terms of the potential in the
concept of using a digital interface to interact with patients and enhance the perfor-
mance of the surgeon. With the advent of newer technologies in robotics like fluo-
rescence, integration of images, virtual and augmented reality, telesurgery, single
site platforms, natural orifice surgery and haptic feedback, it is believed that digital
platforms will provide an empowering tool to the surgeons which can potentially
change the way surgery is practised today.
Editor’s Note1
RYGB can be done as a primary procedure in (1) super obese (2) obese patients with
comorbidity (3) revisional procedure after failed restrictive surgery. Long term
nutritional deficiency remains an important concern with the procedure. The other
complications related to the anastomosis are bleeding from staple line, anastomotic
leak, gastro jejunal stomal stricture, marginal ulcers, bowel obstruction and forma-
tion of internal hernia. A higher incidence of biliary disease has also been reported
in patients undergoing RYGB [1].
Minimally invasive techniques viz. laparoscopic and robotic RYGB have definite
distinctive advantages over open surgery. In a systematic review and Bayesian net-
work meta-analysis comparing open, laparoscopic, and robotic approach the laparo-
scopic and robotic approaches had better outcome as compared to open related to
complication, surgical site infection, pulmonary infection and anastomotic leak
rates [2].
References: Main chapter references are included after the “References Editor’s Note” section.
1
Robotic Roux-en-Y Gastric Bypass 345
Table EN1 Meta-analysis on outcome of robotic RYGB compared with laparoscopic and open
procedures
Study title, first author, year of
publication Result/conclusion
Roux-en-Y gastric bypass: Laparoscopic RYGB(L-RYGB) & Robotic RYGB
Systematic review and Bayesian (R-RYGB) vs Open RYGB (O-RYGB)
network meta-analysis comparing • 30-day mortality was significantly lower LapRYGB and
open, laparoscopic, and robotic RoRYGB versus OpenRYGB(risk ratio RR = 0.64, 95%
approach. Aiolfi A, 2019 [2] Crl 0.46–0.97, and RR = 0.49, 95% Crl 0.24–0.99,
respectively).
• Complication rate was significantly lower L-RYGB and
R-RYGB versus O-RYGB (RR = 0.63, 95% CrI
0.42–0.91, and RR = 0.60, 95% CrI 0.33–0.95,
respectively).
• Surgical site infection lower for LapRYGB and
RoRYGB versus OpenRYGB
(RR = 0.42, 95% CI 0.30–0.75, and RR = 0.24; 95% CI
0.13–0.58, respectively)
• Pulmonary complications lower for L-RYGB &
R-RYGB versus O-RYGB (RR = 0.57, 95% CrI
0.45–0.77, and RR = 0.42; 95% CrI 0.25–0.76,
respectively.
• Anastomotic leak rate was similar for L-RYGB and
R-RYGB versus O-RYGB(RR = 1.10, 95% CrI
0.67–1.81, and RR = 0.95, 95% CrI 0.45–2.12,
respectively).
No differences were found in:
• Postoperative bleeding,
• Thromboembolic complication,
• 30-day reoperation,
• 30-day hospital readmission rates.
Robotic Versus Laparoscopic Robotic RYGB (R-RYGB) versus laparoscopic RYGB
Roux-en-Y Gastric Bypass for (L-RYGB)
Morbid Obesity: a Systematic R-RYGB was associated with a longer mean operative
Review and Meta-Analysis. Wang time.
L 2018 [3] R-RYGB was not found to be superior to LRYGB.
Robotic vs. Laparoscopic Robotic-assisted RYGB vs laparoscopic RYGB
Roux-En-Y Gastric Bypass: a Robotic procedure had significantly less:
Systematic Review and • Anastomotic stricture,
Meta-Analysis. • Reoperations,
Economopoulos KP, 2015 [4] • Length of hospital stay
Robotic versus laparoscopic Robotic RYGB versus laparoscopic RYGB
Roux-en-Y gastric bypass (RYGB) No difference in:
in obese adults ages 18 to • Overall major or minor complications
65 years: a systematic review and • Anastomotic leak,
economic analysis. • Bleeding,
Bailey JG, 2014 [5] • Stricture,
• Reoperation
As expected costs for robotic RYGB ($15,447) were
higher than for laparoscopic RYGB ($11,956).
RYGB Roux-en-Y gastric bypass, R-RYGB Robotic RYGB, L-RYGB laparoscopic RYGB, O-RYGB
Open RYGB, RR risk ratio, CrI Credible interval
346 V. Bindal
bowel obstruction and internal hernias were reported in the retro colic/retro gastric
group (bowel obstruction in 1.4% patients in the AC/AG group and 5.2% patients in
the RC/RG group, P < 0.001). Internal hernias were reported 1.3%patients in the
AC/AG group and 2.3% patients in the RC/RG group (P < 0.001) [8].
Revisional RYGB
1. Cunningham RM, Jones KT, Kuhn JE, Dove JT, Horsley RD, Daouadi M,
Gabrielsen JD, Petrick AT, Parker DM. Asymptomatic Cholelithiasis and
Bariatric Surgery: a Comprehensive Long-Term Analysis of the Risks of Biliary
Disease in Patients Undergoing Primary Roux-en-Y Gastric Bypass. Obes Surg.
2021 Mar;31(3):1249–55. https://doi.org/10.1007/s11695-020-05125-8. Epub
2020 Nov 23. PMID: 33230759.
2. Aiolfi A, Tornese S, Bonitta G, Rausa E, Micheletto G, Bona D. Roux-en-Y gas-
tric bypass: systematic review and Bayesian network meta-analysis comparing
open, laparoscopic, and robotic approach. SurgObesRelat Dis. 2019
Jun;15(6):985–94. https://doi.org/10.1016/j.soard.2019.03.006. Epub 2019 Mar
20. PMID: 31104958.
3. Wang L, Yao L, Yan P, Xie D, Han C, Liu R, Yang K, Guo T, Tian L. Robotic
Versus Laparoscopic Roux-en-Y Gastric Bypass for Morbid Obesity: a
Systematic Review and Meta-Analysis. Obes Surg. 2018 Nov;28(11):3691–700.
https://doi.org/10.1007/s11695-018-3458-7. PMID: 30178157.
4. Economopoulos KP, Theocharidis V, McKenzie TJ, Sergentanis TN, Psaltopoulou
T. Robotic vs. Laparoscopic Roux-En-Y Gastric Bypass: a Systematic Review
and Meta-Analysis. Obes Surg. 2015 Nov;25(11):2180–9. https://doi.
org/10.1007/s11695-015-1870-9. PMID: 26344797.
5. Bailey JG, Hayden JA, Davis PJ, Liu RY, Haardt D, Ellsmere J. Robotic versus
laparoscopic Roux-en-Y gastric bypass (RYGB) in obese adults ages 18 to
65 years: a systematic review and economic analysis. SurgEndosc. 2014
Feb;28(2):414–26. https://doi.org/10.1007/s00464-013-3217-8. Epub 2013 Oct
3. PMID: 24196545.
6. Hagen ME, Jung MK, Fakhro J, Buchs NC, Buehler L, Mendoza JM, Morel
P. Robotic versus laparoscopic stapling during robotic Roux-en-Y gastric bypass
surgery: a case-matched analysis of costs and clinical outcomes. SurgEndosc.
2018 Jan;32(1):472–7. https://doi.org/10.1007/s00464-017-5707-6. Epub 2017
Jul 19. PMID: 28726136.
7. Beckmann JH, Kersebaum JN, von Schönfels W, Becker T, Schafmayer C,
Egberts JH. Use of barbed sutures in robotic bariatric bypass surgery: a single-
center case series. BMC Surg. 2019 Jul 23;19(1):97. https://doi.org/10.1186/
s12893-019-0563-z. PMID: 31337375; PMCID: PMC6651907.
8. Al Harakeh AB, Kallies KJ, Borgert AJ, Kothari SN. Bowel obstruction rates in
antecolic/antegastric versus retrocolic/retrogastric Roux limb gastric bypass: a
meta-analysis. Surg ObesRelat Dis. 2016 Jan;12(1):194–8. https://doi.
org/10.1016/j.soard.2015.02.004. Epub 2015 Feb 11. PMID: 26003892.
348 V. Bindal
References
1. Wittgrove AC, Clark GW, Tremblay LJ. Laparoscopic gastric bypass, Roux-en-Y: preliminary
report of five cases. Obes Surg. 1994 Nov;4(4):353–7.
2. Nguyen NT, Masoomi H, Magno CP, Nguyen XM, Laugenour K, Lane J. Trends in use of
bariatric surgery, 2003–2008. J Am Coll Surg. 2011 Aug;213(2):261–6.
3. Wilson EB, Sudan R. The evolution of robotic bariatric surgery. World J Surg. 2013;37:2756–60.
4. Parikh MS, Shen R, Weiner M, Siegel N, Ren CJ. Laparoscopic bariatric surgery in
super-obese patients (BMI>50) is safe and effective: a review of 332 patients. Obes Surg.
2005;15(6):858–63.
5. Schauer P, Ikramuddin S, Hamad G, Gourash W. The learning curve for laparoscopic Roux-
en-Y gastric bypass is 100 cases. Surg Endosc. 2003 Feb;17(2):212–5.
6. Shikora SA, Kim JJ, Tarnoff ME, Raskin E, Shore R. Laparoscopic Roux-en-Y gastric
bypass: results and learning curve of a high-volume academic program. Arch Surg. 2005
Apr;140(4):362–7.
7. Cadiere GB, Himpens J, Vertruyen M, Favretti F. The world’s first obesity surgery performed
by a surgeon at a distance. Obes Surg. 1999;9:206–9.
8. Talamini MA, Chapman S, Horgan S, Melvin WS. The academic robotic group. A prospective
analysis of 211 robotic-assisted procedures. Surg Endosc. 2003;17:1521–4.
9. Bindal V, Bhatia P, Kalhan S, Khetan M, John S, Ali A, et al. Robot-assisted excision of a large
retroperitoneal schwannoma. JSLS. 2014;18(1):150–4.
10. Cadiere GB, Himpens J, Vertruyen M, Bruyns J, Germay O, Leman G, et al. Evaluation of
telesurgical (robotic) Nissen fundoplication. Surg Endosc. 2001 Sep;15(9):918–23.
11. Nakadi IE, Melot C, Closset J, DeMoor V, Betroune K, Feron P, et al. Evaluation of da Vinci
Nissen fundoplication clinical results and cost minimization. World J Surg. 2006;30(6):1050–4.
12. Schauer PR, Ikramuddin S. Laparoscopic surgery for morbid obesity. Surg Clin North Am.
2001;81(5):1145–79.
13. Buchwald H, Williams SE. Bariatric surgery worldwide 2003. Obes Surg. 2004;14(9):1157–64.
14. Sjostrom L, Lindroos AK, Peltonen M, Torgerson J, Bouchard C, Carlsson B, et al. Lifestyle,
diabetes, and cardiovascular risk factors 10 years after bariatric surgery. N Engl J Med.
2004;351(26):2683–93.
15. Puzziferri N, Roshek TB, Mayo HG, Gallagher R, Belle SH, Livingston EH. Long-term fol-
low-up after bariatric surgery: a systematic review. JAMA. 2014 Sep 3;312(9):934–42.
16. Buchs NC, Pugin F, Bucher P, Hagen ME, Chassot G, Koutny-Fong P, et al. Learning curve for
robot-assisted Roux-en-Y gastric bypass. Surg Endosc. 2012;26:1116–21.
17. Bindal V, Gonzalez-Heredia R, Masrur M, Elli EF. Technique evolution, learning curve, and
outcomes of 200 robot-assisted gastric bypass procedures: a 5-year experience. Obes Surg.
2015 Jun;25(6):997–1002.
18. Bindal V, Gonzalez-Heredia R, Elli EF. Outcomes of robot-assisted roux-en-Y gastric bypass
as a reoperative bariatric procedure. Obes Surg. 2015 Oct;25(10):1810–5.
19. Esposito C, El Ghoneimi A, Yamataka A, Rothenberg S, Bailez M, Ferro M, et al. Work-related
upper limb musculoskeletal disorders in paediatric laparoscopic surgery. A multicenter survey.
J Pediatr Surg. 2013;48(8):1750–6.
20. Sanchez BR, Mohr CJ, Morton JM, Safadi BY, Alami RS, Curet MJ. Comparison of totally
robotic laparoscopic Roux-en-Y gastric bypass and traditional laparoscopic Roux-en-Y gastric
bypass. Surg Obes Relat Dis. 2005;1:549–54.
21. Snyder BE, Wilson T, Leong BY, Klein C, Wilson EB. Robotic-assisted Roux-en-Y gastric
bypass: minimizing morbidity and mortality. Obes Surg. 2010;20(3):265–70.
22. Ayloo SM, Addeo P, Buchs NC, Shah G, Giulianotti PC. Robot-assisted versus laparoscopic
Roux-en-Y gastric bypass: is there a difference in outcomes? World J Surg. 2011;35(3):637–42.
23. Park CW, Lam ECF, Walsh TM, Karimoto M, Ma AT, Koo M, et al. Robotic-assisted Roux-
en-Y gastric bypass performed in a community hospital setting: the future of bariatric surgery?
Surg Endosc. 2011;25:3312–21.
350 V. Bindal
Introduction
Scar less surgery has always fascinated the surgeons and patients alike. As the tech-
nology has improved in vision and optics, laparoscopic surgery has become the
mainstream. Still the incision less surgery eludes the medical field.
As the surgical field was developing, parallel development in the flexible endo-
scopes was going on during the period. Flexible endoscopes allowed us to go deep
into the stomach and intestine to visualize the lumen. Intraluminal procedures like
polypectomies and stricture dilatation are performed relatively with ease now a days
with these endoscopes.
In between, there were thoughts of moving into the peritoneum from the lumen,
through its wall and performing few surgical procedures [1], which was known as
Natural orifice transluminal endoscopic surgery (NOTES). “NOTES” was univer-
sally handicapped by the poor closing techniques of the lumen after the procedure.
Much new advancements were practised to perfect the lumen closure technique.
A mucosal flap technique was discovered where a potential space was created
between muscularis mucosae and muscularis propria by injecting a fluid and
expanding the space, thus allowing dissection within the space. This technique
allowed the closure of the mucosal side relatively well. Soon other applications of
this technique were discovered and the era of third space endoscopy started.
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 351
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_16
352 A. Dalal et al.
First space refers to the lumen; Second space is outside lumen, usually peritoneal cav-
ity. Third space refers to the potential space between muscularis mucosa and muscula-
ris propria. Initially multiple experiments were done on animal models and the
accessories and instruments were invented to perfect this technique. First POEM (Per
oral endoscopic myotomy) in a human subject was first performed in 2008 [2]. Since
then, POEM has become the most commonly performed third space surgery worldwide.
Many other new applications of the third space have been invented since then.
These are enumerated as below:
POEM is usually done for the treatment of achalasia cardia. It can be performed as
the initial procedure and also for the recurrent cases, both post endoscopic as well
as post surgical achalasia management.
The indications to do POEM are [3]:
1. Achalasia (Types 1, 2 and 3)
2. Previous failed Heller’s myotomy
3. Previous failed pneumatic dilatation
4. Previous failed botulism toxin injection
5. Diffuse esophageal spasm
6. Jackhammer esophagus
The contraindications to do POEMS are [3]:
1. History of radiation therapy to esophagus
2. Previous ablation/resection of esophageal mucosa
3. Cirrhosis with portal hypertension
4. Any other comorbid condition of a patient making him/her unfit for surgery.
Patient has to be nil per mouth for 12 h before the procedure and it is not a bad
idea to place a nasoesophageal tube for lavage and suction of the residual food in the
dilated oesophagus just before the procedure. Preoperative antibiotics should be
started 12 h before the procedure.
Using room air for doing POEM procedures may lead to more incidences of
pneumomediastinum, gas embolism and cardiac arrest. Thus POEM is typically
performed using the carbon dioxide gas. General anaesthesia and endotracheal intu-
bation is advocated to minimize any risk of aspiration.
Instruments Required:
Steps of POEM
Mucosal Incision: A high definition scope with an attached distal cap is inserted
into the esophagus. The first step is to identify the site of mucosal incision.
Two types of approaches are described (Anterior & Posterior). Posterior approach
is usually done at a 5 o’clock position just adjacent to the spine impression around
8–10 cm proximal to GEJ junction. In the anterior approach, mucosal incision is
made at 2 o’ clock position approximately 8–10 cm proximal to GEJ junction. Both
the approaches are similar in most aspects and considered equally effective for the
treatment of achalasia [4]. However in a patient of previously failed surgical Heller’s
myotomy, a posterior approach is favoured. In spasmodic disorders of oesophagus
a more proximal site is chosen as the myotomy in these cases can be quite long.
At the pre-decided site of mucosal incision, mucosal injection of saline mixed
with methylene blue or indigo carmine is done to create a submucosal bleb (Fig. 2).
This step raises the mucosa over the muscularis propria. It thus provides a space to
make an incision limited to mucosa and submucosa but not reaching up to the mus-
cularis propria as it provides a cushion effect. After raising this submucosal bleb a
linear incision is made using the knife and electrosurgical cautery (Fig. 3). Careful
dissection of the surrounding submucosal tissue is done to facilitate the entry of
scope into the submucosal area. The edges of the mucosal incision site may be
trimmed with electrosurgical cautery to prevent bleeding and later facilitating easy
mucosal closure.
Creation of submucosal tunnel: A submucosal tunnel is then created with the
dissection of submucosal tissue (Fig. 4). The submucosal tissue is also injected with
saline mixed with methylene blue to facilitate dissection. Dissection is done with a
knife using an electrosurgical unit. Maintaining orientation is of utmost importance
during this step. Utmost care should be taken to preserve the mucosal integrity. Any
large vessel seen is coagulated by soft coagulation grasper. The submucosal tunnel
is extended till 3–5 cm from the gastroesophageal junction (GEJ). The GEJ is
identified by appearance of small blood vessels, longitudinal muscle fibres and nar-
rowing of the submucosal space. This can be confirmed during endoscopy by the
blanching of mucosa just below cardia. If the endoscopist doesn't want to remove
his scope from the tunnel then another ultrathin scope can be passed by the side and
blanching below cardia can be noted to see the adequacy of submucosal tun-
nel length.
Myotomy: After creating this submucosal tunnel, Myotomy is performed
(Fig. 5). The circular muscle fibres are cut starting 3–4 cm above GEJ and till 2 cm
below GEJ. Ideally selective circular fibre myotomy is performed but it becomes
really difficult to distinguish between circular and longitudinal fibres. Endoscopist
many times perform a full thickness myotomy as no difference is seen between
partial thickness and full thickness myotomy [5]. It is more important to maintain
mucosal integrity rather than worrying about the myotomy thickness. Adequate
myotomy can be assessed by the ease of passing scope across the GE junction.
356 A. Dalal et al.
Fig. 5 Creation of
myotomy (Image
Courtesy: Dr Pravin
Suryavanshi)
• Clips
• Endoscopic suturing
• OTSC (Over the scope clip)
Usually, hemoclips are most commonly used given that they are cheaper, easily
applicable and removable. Endoscopic suturing is relatively new technique, yet to
be easily available commercially. Over the scope clip is a recent addition in clips
Third Space Endoscopy 357
which has to be loaded on scope, their cost and difficulty in removing if misfired has
limited their use.
The patient can be kept nil by mouth for next 12 h. A gastrografin swallow is
done to rule out any leak. Patients can be started orally on a soft diet after 48 h. Oral
antibiotics should be prescribed for the next 7 days and Proton Pump inhibitors
should be advised for the next 2 weeks. Figure 7 is a schematic diagram of the space
of dissection in POEM (Fig. 7).
Outcomes of Poem
POEM has now established itself as a safe and reliable surgery for achalasia cardia.
Multiple meta-analyses of various studies have been done now. Clinical success
reported is around 98% in one year follow up [6]. In the long-term results have
shown a sustained clinical efficacy of 83–95% [7, 8].
POEM is very safe procedures as the incidence of serious adverse effects are very
low [6]. The adverse effects may be due to:-
Z-POEM is used for the treatment of Zenker’s diverticulum [13]. Zenker’s diver-
ticulum is a pulsion diverticulum at the upper end of the esophagus. It can lead to
dysphagia and can also lead to aspiration. The usual treatment of Zenker’s diverticu-
lum has been by open surgery and septostomy using either endoscopy or flexible
endoscopy. Third space endoscopy technique is now being also used in management
of Zenker’s diverticulum. In this technique, a submucosal tunnel is created on the
septum and the muscular septum is cut beneath the mucosa. The advantage of
Z-POEM over the endoscopic septostomy is that the muscular septum can be cut for
a longer length and thus chances of recurrence are lesser as compared to the septos-
tomy (Fig. 10). However, the success rate of endoscopic septostomy is 91% which
is similar to that of Z-POEM which is around 92% [13]. Recurrences can be suc-
cessfully managed by a repeat septostomy.
D-POEM is used for management of esophageal diverticula other than the Zenker’s
diverticulum. It is simple, safe and effective to relieve symptoms such as dysphagia,
reflux and chest pain caused by esophageal diverticulum, while avoiding invasive
surgery. The technique is similar to Z-POEM. Here after creating the submucosal
tunnel, the muscular septum is divided and then the mucosal incision site is closed.
Fig. 10 Schematic
diagram showing site of
myotomy in Zenker’s
Diverticulum
Third Space Endoscopy 361
Fig. 11 Schematic
diagram showing G-POEM
being done
After the success of POEM in achalasia, a similar procedure was developed for the
management of gastroparesis in the stomach, where a submucosal tunnel is created
from 7 to 8 cm proximal to pylorus and pyloromyotomy is done (Fig. 11) [14]. The
results are so far good in gastroparesis but not for diabetic patients. So a careful
evaluation and selection of patients is mandatory before doing this procedure. As in
POEM where GERD is a major symptom post procedure, bile reflux is a common
sequel after G-POEM.
Subepithelial tumours in GI tract are traditionally removed when the size is more
than 3 cm. With the advent of third space endoscopy technique a submucosal tunnel
is created 4–5 cm proximal to the lesion and the lesion is dissected from the sur-
rounding tissue using electrosurgical knives. The tumour is then removed through
the mucosal opening site. This technique can be challenging if the tumour is located
in fundus or lesser curvature of the stomach, tumour is larger >4.5 cm in size,
tumour is multilobulated or adherent to the deep structures.
Conclusion
Third space endoscopy has evolved over the last decade after the introduction of the
first case of POEM in 2008. It is now the method of choice for the type 3 achalasia
and other esophageal spasmodic disorders. For the management of type 1 and type
2 achalasia also it compares equally with LHM. Third space endoscopy is evolving
in the management of oesophageal diverticula and gastroparesis. STER is now
being routinely performed for excision of subepithelial tumours.
362 A. Dalal et al.
Editor’s Note1
The prominent application currently has been in the treatment of achalasia cardia.
Table EN1 enlists various published meta-analyses comparing outcome of laparo-
scopic Hellers myotomy (LHM) and Peroral endoscopic myotomy [4–13]. Most
studies report better dysphagia control with POEM than LHM [4–7, 9, 11, 12].
The quoted advantages of POEM are that it is a scarless surgery and has a relatively
shorter operative time and hospital stay [6–8]. Complications and serious adverse
events have been comparable between POEM and LHM across studies [6–13]. One of
the noted disadvantages of POEM in treatment of achalasia is the higher incidence of
GERD (gastroesophageal reflux disease) as compared to Laparoscopic Hellers myot-
omy in both subjective and objective assessments as evidenced by higher GERD
symptoms, abnormal pH studies and erosive esophagitis [4, 8, 9, 14].
POEM has been observed to have better dysphagia relief than PD (pneumatic
dilatation) with comparable adverse events [9–11]. As most Hellers myotomy is
coupled with a fundoplication, addition of an trans oral endoscopic treatment of
GERD to POEM viz: transoral incisionless fundoplication or electrical stimulators
might be able to decrease the incidence of GERD and thus emerge as a potential
topic of research in the near future. POEM can also be considered as a safe alterna-
tive in failed Hellers myotomy [15].
References: Main chapter references are included after the “References Editor’s Note” section.
1
364 A. Dalal et al.
Third space endoscopy essentially uses the SEMF (submucosal endoscopy with
mucosal flap technique) [16]. Technical issues like ensuring a good vision and hae-
mostasis in POEM are paramount. Use of a lighted LED probe to help improve
visibility in submucosal tunnel creation as also for assessing completeness of myot-
omy has been proposed to be beneficial in this regard [17]. Use of saline jet or water
pump assisted dissection, balloon dilators and various knives are being evaluated.
Table EN1 Meta-analyses comparing POEM (Per oral endoscopic myotomy) with LHM (Laparoscopic Hellers myotomy)
Postoperative GERD gastroesophageal Other outcome parameters POEM
Study, Author (first), Year Dysphagia Relief POEM vs LHM reflux disease POEM vs LHM vs LHM
Laparoscopic Heller Myotomy Improvement in dysphagia at 12 Patients undergoing POEM were more Length of hospital stay was 1.03
Versus Peroral Endoscopic months were 93.5% for POEM and likely to develop following days longer after POEM (P = 0.04).
Myotomy (POEM) for Achalasia: 91.0% for LHM (P = 0.01) 1. GERD symptoms
A Systematic Review and (OR 1.69, 95% CI 1.33–2.14,
Third Space Endoscopy
Meta-analysis P < 0.0001),
Schlottmann F, 2018 [4] 2. Erosive esophagitis
(OR 9.31, 95% CI 4.71–18.85,
P < 0.0001),
3. GERD evidenced by pH monitoring
(OR 4.30, 95% CI 2.96–6.27,
P < 0.0001).
Meta-analysis of clinical outcome POEM more successful than LHM
after treatment for achalasia based for both type I and type III
on manometric subtypes. achalasia (odds ratio (OR) 2·97,
Andolfi C, 2019 [5] 95% CI 1·09 to 8·03; P = 0.032) &
(OR 3·50, 1·39 to 8·77; P = 0.007)
The likelihood of success of POEM
and LHM for type II achalasia was
similar.
Peroral (poem) or surgical Greater mean reduction in Eckardt Post-Operative Gastroesophageal Reflux • No difference in operative time
myotomy for the treatment of score in POEM patients no significant difference (MD = −10,26, 95% CI (−5,6 to
achalasia: a systematic review and (MD = −0.257, 95% CI: (−0.512 to (RD: −0.00, 95%CI: (−0.09, 0.09), I2: 8,2), P < 0.001
meta-analysis. −0.002), P = 0.048) 0%) • Decreased length of hospital stay
Martins RK 2020 [6] for POEM (MD: −0.6, 95% CI
(−1.11, −0.09), P = 0.02),
• Similar rates of adverse events.
(continued)
365
Table EN1 (continued)
366
a systematic review and network 0·15–0·71; P-score 0·89), then LHM 2. Need for re-intervention or
meta-analysis. (RR 0·45, 0·26–0·78, P-score 0·61). surgery
Mundre P 2021 [11] 3. Serious adverse events
Per-Oral Endoscopic Myotomy POEM group had a lower Eckardt No differences between the POEM
Versus Laparoscopic Heller score after surgery compared with and LHM groups in:
Myotomy for Achalasia: A those in the LHM group 1. Length of myotomy,
Meta-Analysis of Nonrandomized (MD = −0.30, 95% CI −0.42 to 2. Operation time,
Comparative Studies. −0.18; P < 0.001 3. length of hospital stay,
Zhang Y 2016 [12] 4. Complications
Peroral esophageal myotomy Symptomatic recurrence by Eckardt Gastroesophageal reflux not significant No significant difference between
versus laparoscopic Heller’s score not significant (OR = 1.00, 95% CI 0.38–2.61, POEM and LHM in:
myotomy for achalasia: a (OR = 0.24, 95% CI 0.04–1.55, P = 1.00). 1. Complications
meta-analysis. P = 0.13). 2. Pain score,
Wei M, 2015 [13] 3. Operating time,
4. Hospital stay
OR odds ratio, MD mean difference, WMD weighted mean difference, RD risk difference, CI confidence interval, RR relative risk
367
368 A. Dalal et al.
References
1. Kalloo AN, et al. Flexible transgastricperitoneoscopy: a novel approach to diagnostic and
therapeutic interventions in the peritoneal cavity. Gastrointest. Endosc. 2004;60:114–7.
2. Inoue H, et al. Peroral endoscopic myotomy (POEM) for esophageal achalasia. Endoscopy.
2010;42:265–71.
3. Jawaid S, Draganov PV, Yang D. Esophageal POEM: the new standard of care. Transl.
Gastroenterol. Hepatol. 2020;5:47.
4. Rodríguez de Santiago E, et al. Anterior versus posterior myotomy during poem for the
treatment of achalasia: systematic review and meta-analysis of randomized clinical trials. J
Gastrointest Liver Dis. 2019;28:107–15.
5. Li C, et al. Clinical outcomes and safety of partial full-thickness myotomy versus circular
muscle myotomy in peroral endoscopic myotomy for achalasia patients. Gastroenterol. Res.
Pract. 2017;2017:1–7.
6. Akintoye E, Kumar N, Obaitan I, Alayo QA, Thompson CC. Peroral endoscopic myotomy: a
meta-analysis. Endoscopy. 2016;48:1059–68.
7. Zhang X, et al. Per-oral endoscopic myotomy in patients with or without prior Heller’s
myotomy: comparing long-term outcomes in a large U.S. single-center cohort (with videos).
Gastrointest. Endosc. 2018;87:972–85.
8. Teitelbaum EN, et al. Peroral esophageal myotomy (POEM) and laparoscopic Heller myotomy
produce a similar short-term anatomic and functional effect. Surgery. 2013;154:885–91; dis-
cussion 891–92.
9. Nabi Z, Reddy DN, Ramchandani M. Adverse events during and after per-oral endoscopic
myotomy: prevention, diagnosis, and management. Gastrointest. Endosc. 2018;87:4–17.
10. Schlottmann F, Luckett DJ, Fine J, Shaheen NJ, Patti MG. Laparoscopic heller myotomy
versus peroral endoscopic myotomy (POEM) for achalasia: a systematic review and meta-
analysis. Ann. Surg. 2018;267:451–60.
11. Ponds FA, et al. Effect of peroral endoscopic myotomy vs pneumatic dilation on symptom
severity and treatment outcomes among treatment-naive patients with achalasia: a randomized
clinical trial. JAMA. 2019;322:134.
12. Park CH, et al. Comparative efficacy of per-oral endoscopic myotomy and Heller myotomy in
patients with achalasia: a meta-analysis. Gastrointest. Endosc. 2019;90:546–58.e3.
13. Yang J, et al. An international study on the use of peroral endoscopic myotomy in the manage-
ment of Zenker’s diverticulum. Gastrointest Endosc. 2020;91:163–8.
14. Xu J, et al. Gastric peroral endoscopic myotomy (G-POEM) as a treatment for refractory gas-
troparesis: long-term outcomes. Can. J. Gastroenterol. Hepatol. 2018;2018:6409698.
Endoscopic Management of Pancreatic
Fluid Collection
Vaishali Bhardwaj and Vikram Bhatia
Introduction
V. Bhardwaj (*)
Department of Gastroenterology, ABVIMS & Dr RML Hospital, New Delhi, India
V. Bhatia
Department of Hepatology, ILBS, New Delhi, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 371
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_17
372 V. Bhardwaj and V. Bhatia
APFC normally develops after an episode of IEP and progresses to PPC if not
resolved in 4 weeks whereas, ANC develops after acute necrotizing pancreatitis and
if unresolved develops into WON. CECT further helps to classify the various pan-
creatic fluid collection. Pseudocysts have clear contents and a defined wall whereas
WON have walled off variable amount of solid necrotic debris. Cross-sectional
imaging after the first week can differentiate ANC and acute PFC. PFC have clear
contents whereas ANC appears loculated with variable amount of debris within the
fluid [2].
Acute collections (APFC or ANC) usually do not require any intervention as they
improve with conservative management [3]. However, a proportion of symptomatic
WON and pseudocysts require intervention. The various drainage options of PFCs
are: (1) percutaneous drainage (2) endoscopic drainage/stenting (3) surgical drain-
age, which may be open or by minimally invasive approaches. With advent of tech-
nical innovations in interventional endoscopy, invasive surgical procedures can be
avoided in majority of PFC patients.
Certain newer insights have come to picture, namely
(a) Outcome of a drainage procedure is better if performed once the collection gets
walled off or encapsulated (>4 week).
(b) Minimally invasive approach to the management of PFCs is better than the
conventional open surgical methods
(c) The outcome of endoscopic drainage depends on the nature of PFC i.e. pseudo-
cyst or WON [4–7].
Specific Technology
It is prudent to rule out other causes of pancreatic cysts such as cystic neoplasm,
duplication cyst, as also complications like presence of pseudoaneurysm before
intervention. Evaluation of pancreatic duct integrity is also helpful to rule out DPDS
(disconnected pancreatic duct syndrome), which is associated with WON and com-
munication of pseudocyst with the duct. The following investigations can aid in
assessment:
• occlusion of catheter,
• peri catheter cellulitis,
• sepsis and prolonged pancreatic fistula in presence of cysto-ductal
communication.
1. Anatomic proximity of the PFC to the stomach and duodenum. This is an impor-
tant factor which helps in decision making regarding the choice of lumen for
drainage. If the collection is near the stomach and is producing a visible intramu-
ral bulge on the gastric wall (Fig. 1), it is amenable to drainage via EGD alone
method described in details later in this chapter. EUS is recommended if the PFC
is not bulging (Fig. 2) or is slightly away from the lumen wall.
2. Anatomy of the pancreatic duct with cystoductal communication (CDC) is
another factor. If the collection is communicating with main pancreatic duct
trans-papillary drainage is possible via ERCP.
3. Size of the collection with presence of necrosis in the cyst, helps in decision
making as collection with large necrotic content compared to fluid component
are not amenable to simple drainage procedures. Presence of necrosis might
require multiple attempts for total clearance.
4. Number of cysts and internal communication between them is an important fac-
tor while making decisions as communicating cysts are better amenable to endo-
scopic procedures compared to non-communicating ones.
5. Thickness of cysts wall: Cyst wall must be mature before attempting any kind of
drainage procedure so pre procedure radiological evaluation is mandatory prior
to venturing into any kind of drainage procedure.
Preprocedure Preparation
• identification of the ideal puncture site under endoscopic guidance over the bulge,
• needle puncture at the site and through the PPC wall into the cyst and diagnostic
aspiration to look for haemorrhage or infection. The aspirated fluid should be
sent for microbiological analysis.
• insertion of guide wire through the needle
• coiling of guidewire inside the cyst cavity (can be confirmed with fluoroscopy)
• removal of needle
• dilatation of cystogastric tract using cystotome and balloon over guide wire
causes cyst fluid to gush into the stomach
• placement of stents (commonly double pigtail stents) communicating the cyst to
the stomach cavity (Figs. 3 and 4).
a b
c d
Fig. 3 (a) Needle knife papillotome making incision at the bulging site, (b) Balloon dilatation of
the tract, (c) Fluoroscopy picture of guide wire in situ, (d) Double pigtail stent draining from the
cyst into stomach
378 V. Bhardwaj and V. Bhatia
Spleen
Stents in
Cystogastrostomy
Pseudocyst
Pancreas
Transverse Colon
Benefits: The EUS guided transmural PFC drainage technique is similar to only
EGD guided technique with added perceived benefits as follows:
a b
c d
Fig. 5 EUS aided transmural drainage of PFC. (a) EUS image of pancreatic fluid collection, (b)
EUS guided dilatation of tract (Green arrow), (c) Placement of Lumen apposing metal stent
(LAMS), (d) LAMS in position draining fluid (Guide wire is also seen)
for necrosectomy in some cases. Necrotic debris in the cyst cavity can be flushed
with normal saline solution (100 mL every 4 h until the aspirate is clear) [9].
Techniques have evolved for insertion of multiple catheters using a single puncture
more commonly known as “one step double wire technique” [15, 16].
Pre procedure ERCP: Preprocedure ERCP has been used by some authors to
delineate ductal disruptions and perform a sphincterotomy or stenting before drain-
age (as discussed below).
• Identification of optimal site by EUS (site of PFC <1 cm from posterior gastric/
medial duodenal wall with no interceding vascular abnormalities or viscera).
Rarely distal esophagus has been described as portal of drainage.
• Puncture of PFC and diagnostic aspiration of fluid content is performed with a
19-gauge needle under real time EUS guidance (to exclude any misdiagnosis and
to look for infection and hemorrhage within the cyst).
• Under simultaneous EUS and fluoroscopic guidance a guidewire (0.035-
inch × 440 cm) is inserted through the needle into PFC cavity with sufficient
length for looping it in the cavity. More than one guidewire may be placed if
multiple stents are to be used.
• Needle is removed after placement of guidewires
• Enlargement of the tract by sequential dilatation of the tract done with 6–10 mm
hydrostatic balloon dilator and/or cystotome to facilitate insertion of multiple
plastic stent (gush of cyst fluid occurs into the stomach following dilatation)
• Insertion of double-pigtail plastic stents (sizes between 7 and 10 Fr) under EUS
and fluoroscopic guidance. The double pigtail is designed to make it self-
retaining and prevention of migration into the cyst or bowel lumen.
• Most frequently two plastic double-pigtailed biliary stents are placed. Multiple
stents or a nasocystic catheter is deployed if indicated.
• In uncomplicated cases, number and size of plastic stent used or number of inter-
ventions done, does not affect outcome
• To evaluate response to intervention a repeat CT scan is done after 4–6 weeks [9].
Complications and Outcome
• bleeding
• perforation of viscera
• pneumoperitoneum
• fistula formation
• stent related problems (migration/occlusion) [17, 18].
Endoscopic Management of Pancreatic Fluid Collection 381
Use of electrocautery along with knife cystotome has been tried to reduce bleed-
ing complications [18]. In a prospective randomized trial comparing only EGD
based (Blind Technique) and EUS-based approach in cysts >4 cm size, equivalent
results were noted [17]. It needs to be emphasized that whereas bulging PFCs are
drained with EGD only non-bulging PFCs are drained with combined EGD and
EUS technique which can confound comparisons [18]. Another prospective ran-
domized trial noted a higher technical success rate and lower complications with
EUS guided EGD when compared to EGD alone technique [19]. EUS should be
preferred as a first-line of treatment in all, particularly in nonbulging cysts [17–19].
Before the advent of advanced imaging systems for the pancreatic duct like MRCP,
an ERCP-based algorithm was advocated to guide treatment of PFCs based on pan-
creatic duct morphology viz. ductal disruption, strictures, complete cutoff of the
duct and cystoductal communication (CDC) necessitating the need for pre proce-
dure ERCP [20, 21]. However, due to availability of noninvasive imaging like
MRCP, pre drainage ERCP pancreatogram is now not regularly used to guide the
drainage approach.
PFCs communicating with the main pancreatic duct can be managed with transpap-
illary stenting of the main pancreatic duct through the main or minor papilla which
may be accompanied with a sphincterotomy. Alternatively, drainage of the PFCs
through the transpapillary stent (cystopancreatic stents) has been advocated. Thus,
the stent may be placed into the collection or positioned close to the collection in a
Fig. 6 Schematic
illustration of
transpapillary stenting
Pseudocyst
Endoscope
Pancreas Disruption in
main pancreatic duct
Transpapillary Duodenum
Stent
382 V. Bhardwaj and V. Bhatia
manner to bridge the duct disruption/stricture, by coursing into the pancreatic tail
[22–24]. Insertion of a transpapillary nasocystic catheter can be used for irrigation
of the cyst cavity [22]. Even a simple stenting can improve flow dynamics of the
pancreatic duct by promoting flow of pancreatic secretions through the papilla (a
low resistance tract) rather than into the PFCs (a relatively high resistance tract).
Complete bridging of the disruption is preferable particularly in pancreatic body
and tail disruptions [25].
• completely intact PD
• completely disrupted/disconnected pancreatic duct syndrome with no communi-
cation between the downstream PD and PPC [9].
• Stent migration
• Plastic stents have narrow lumen necessitating placement of multiple stents
which is labor intensive and time consuming
• Due to their small luminal diameter, they are prone to occlusion
• Larger plastic stents are difficult to deploy through small calibre channels of the
endoscope [27].
• Stent end abutting against luminal wall can lead to incomplete drainage.
• If apposition of cyst wall and GI lumen walls is lacking plastic stents can cause
fluid leakage in the intervening space.
SEMS: Fully covered SEMS which are commonly used to stent gastrointestinal
strictures were initially tested in drainage of PFCs to overcome the shortcomings of
DPS [27]. The main advantage of fully covered SEMS is having a larger diameter
384 V. Bhardwaj and V. Bhatia
than DPS and only a single stent is needed instead of multiple stents. However fully
covered SEMS still has potential risk of migration and modification with fins or
placement of DPS across the fully covered SEMS has been suggested to prevent
overt migration [28]. SEMS has not been beneficial over DPS for PPC but may be
more useful in WON [28].
LAMS: LAMS (AXIOS; Xlumena Mountain View CA, approved in USA &
NAGI; approved in Europe) are saddle-shaped, nitinol, braided, flexible stents fully
covered with a silicon membrane designed to overcome the drawbacks of DPS and
SEMS. The stent has bilateral double-walled anchoring barbell flanges designed to
hold the stomach or duodenal wall in direct opposition to the PFC wall, reducing the
risk of migration. This stent is available in 10 and 15 mm size diameters and mea-
sures 10 mm in length. A 15-mm diameter allows for the passage of conventional
upper GI endoscope for reinterventions such as repeated debridement, irrigation or
necrosectomy [9].
Management of WON differs from PPC as the former requires debridement, often
multiple interventions, which may be:
Open necrosectomy for pancreatic necrosis is reported to have very high morbid-
ity (34%–95%), and mortality ranging from 6% to 25% [30]. It also causes long-
term complications like pancreatic exocrine insufficiency. Novel endoscopic
approaches have revolutionized the treatment of infected pancreatic necrosis
386 V. Bhardwaj and V. Bhatia
• Sterile acute pancreatic necrosis does not require intervention neither early nor
delayed unless symptomatic
• Infected early pancreatic necrosis seldom require early intervention and it is pru-
dent to delay interventions by 4–6 weeks.
• If it is necessary to intervene in early pancreatic necrosis because of clinical
deterioration with signs of sepsis, radiological or endoscopic approach should be
preferred over surgery
• Only symptomatic WON with discrete encapsulation should undergo interven-
tion after 4–6 weeks
• Asymptomatic WON irrespective of size and duration does not require interven-
tion [30].
The procedure is performed under general anaesthesia with C02 insufflation. The
initial steps of Direct Endoscopic Necrosectomy (DEN) is similar to EUS guided
endoscopic transmural drainage but involves dilatation of the cysto-gastric tract
with a balloon of larger size upto 20 mm and placement of LAMS which can allow
subsequent multiple sessions of DEN without need for repeated dilatation. After the
initial establishment of cystogastric tract, the echoendoscope is replaced with a
larger single channel or double channel endoscope which is advanced into the cavity
of WON for direct necrosectomy. The cavity is lavaged with normal saline and
necrotic debris is removed under direct vision using forceps, snares or baskets
(Fig. 9) [33]. Diluted Hydrogen peroxide irrigation can also be used to help in loos-
ening up of necrotic tissue. Newer stents have wider lumen which allow multiple
sessions of DEN without need for repeated dilatations. Multiple sessions may be
required for completing the procedure which is regarded as a distinct disadvantage
of the DEN procedure.
Waterjet necrosectomy device (WAND): Previously there was no device
designed exactly for endoscopic necrosectomy and retrieval of necrotic material
was done with all available snares, forceps or baskets which appeared to be subop-
timal. Bulky or adherent necrotic slough may pose difficulty during removal A
recent innovation is the waterjet necrosectomy device (WAND) which has been
tested in preclinical series (Fig. 10). It can be introduced through a 2.8-mm working
channel of a standard adult upper GI endoscope. (Fig. 11) The principle of WAND
Endoscopic Management of Pancreatic Fluid Collection 387
Fig. 10 Waterjet
necrosectomy device
(WAND) (Image courtesy
Dr. Patrick Stephen
Yachimski, Nashville, TN,
USA. Published with his
permission)
b
388 V. Bhardwaj and V. Bhatia
Complications
Conclusion
The management of PFCs has evolved from primarily open surgical drainage to
endoscopic/radiological based minimally invasive approach. Only symptomatic
PFCs need intervention preferably after 4 weeks. Endoscopic procedures with
endoprosthesis insertion can manage most PFCs that require intervention. EUS
guidance whenever available should be used with endoscopic procedures to decrease
complications. Whereas PPC often resolve with drainage procedures like endo-
scopic transmural drainage or endoscopic transpapillary drainage, necrosectomy
may be necessary in addition to drainage in WON a complication of necrotizing
pancreatitis. Lately patients with WON have safely undergone endoscopic necro-
sectomy, obviating the need for surgical exploration. If PD disruption is suspected,
ERCP with PD stenting should be done to prevent recurrence of PFCs after drain-
age. An individualized patient centric team approach comprising of gastroenterolo-
gist, endoscopists, interventional radiologists, intensivists and the surgeon is
desirable.
1. PFCs are classified based on duration and type of collection i.e. necrotic versus
clear into APFC, ANC, PPC and WON.
Endoscopic Management of Pancreatic Fluid Collection 389
2. Intervention for drainage is usually not required in APFC and ANC as they
often improve with conservative management.
3. Only a proportion of symptomatic Walled of Necrosis (WON) and Pseudocysts
(PPC) require intervention.
4. Asymptomatic PFCs do not require interventions irrespective of size and
duration
5. Interventions in symptomatic PFCs are best delayed until after 4 weeks unless
there are compelling evidence for early intervention like sepsis
6. PFCs can be drained surgically, percutaneously under radiologic guidance or
endoscopically
7. Minimally invasive approaches have less morbidity than open surgical proce-
dures for drainage of PFCs
8. Pre procedure radiological investigations, CT scan, MRI, MRCP can provide
information regarding the maturity of cyst wall, necrosis, location i.e. proximity
to bowel, complications like pseudoaneurysm and status of the pancreatic duct
which are important determinants of the route and mode of intervention
9. Anatomic relationship of the PFC to the stomach and duodenum (distance from
gastric or duodenal wall) helps in decision making regarding the choice of
lumen for drainage
10. Endoscopic drainage of PFCs can be done either transmurally or through trans-
papillary route with or without EUS
11. Only EGD based transmural approach requires presence of a luminal compres-
sion visible as endoluminal bulge of the cyst during endoscopy
12. In non-bulging PFCs EUS along with EGD is required for transmural drainage
13. Transpapillary approach has decreased risk of bleeding or perforation com-
pared to transmural drainage.
14. Added advantage of transpapillary approach is that concomitant ductal pathol-
ogy can be addressed viz. intraductal pancreatic stones and pancreatic duct
strictures, ductal disruptions, thus promoting early cyst resolution and decreas-
ing recurrence
15. Endoscopic drainage of the cyst can be achieved with plastic DPS or metallic
fully covered SEMS/ LAMS.
16. WON may require necrosectomy along with drainage
17. Necrosectomy can be performed as a step up procedure with repeated irrigation
and drainage or direct endoscopic necrosectomy
18. Direct Endoscopic Necrosectomy (DEN) involves advancement of the endo-
scope into the cavity of WON through the tract and removal of necrotic material
through, snares, baskets and forceps
19. A large, 15 mm, LAMS can facilitate passage of conventional upper GI endo-
scope into the cyst to enable necrosectomy
20. DEN has significant complications therefore it should not be performed unless
indicated and should be done by experts
21. Waterjet necrosectomy device (WAND) is a recent innovative aid devised for
necrosectomy which has been evaluated in preclinical studies and may prove
promising in future.
390 V. Bhardwaj and V. Bhatia
Editor’s Note1
1. Percutaneous drainage
2. Endoscopic drainage
3. Surgical drainage (laparoscopic/open).
References: Main chapter references are included after the “References Editor’s Note” section.
1
Endoscopic Management of Pancreatic Fluid Collection 391
Table EN1 (continued)
Study author (first), year Result
Endoscopic versus percutaneous management Endoscopic versus percutaneous drainage:
for symptomatic pancreatic fluid collections: Results in favor of endoscopy for:
a systematic review and meta-analysis. • Clinical success
Khan MA, 2018 [3] RR 0.40 (0.26, 0.61), i2 = 42%.
• Technical success: Pooled RR 1.50
(0.52, 4.37).
• Adverse event: Pooled RR 0.77 (0.46,
1.28)
• Rate of recurrence Pooled RR 0.60
(0.29, 1.24)
• Hospital stay Pooled MD − 8.97
(−12.88, −5.07)
• Rate of re-intervention Pooled md
−0.66 (−0.93, −0.38)
PD percutaneous drainage, RR risk ratio, MD mean difference, WMD weighted mean difference,
OR odds ratio, LOH length of hospital stay
Table EN2 (continued)
Study author (first), year Result
Time for a changing of guard: From minimally Endoscopic drainage (ED) versus
invasive surgery to endoscopic drainage for minimally invasive surgical
management of pancreatic walled-off necrosis. necrosectomy (MISN)
Khan MA, 2019 [7] Significantly lower in ED group:
• Mortality
(8.5% and 14.2%, for ED and
MISN POR 0.59; 0.35–0.98),
• New onset MOF
12% and 54% for ED and MISN,
POR 0.12 (0.06–0.31),
• Adverse events: Pooled or was
0.25 (0.10–0.67),
• Pancreatic fistula rate
[OR, 0.20 (0.11–0.37)],
• Length of stay
MD −21.07 (−36.97 to −5.18) days
No difference in:
• Risk of bleeding
Interventions for necrotising pancreatitis. MISN vs ED:
Gurusamy KS, 2016 [8] • Higher adverse events in MISN
(rate ratio 11.70, 95% CI 1.52 to
89.87; 22 participants; 1 study),
• Lower number of interventions per
patient with MIS
Inconsistent results on
• Number of serious adverse events,
• Organ failure rate,
• Hospital stay,
• Intensive therapy unit stay
ED endoscopic drainage, MISN minimally invasive surgical necrosectomy, RR risk ratio, MD mean
difference, WMD weighted mean difference, OR odds ratio, POR Pooled odds ratio, LOH length
of hospital stay, MOF multiorgan failure
Table EN3 Meta-analyses on use of metallic versus plastic stent for drainage of pancreatic fluid
collection
Study author (first), year Result
Metal versus plastic stents for drainage of pancreatic Higher clinical success rate with
fluid collection: A meta-analysis. Yoon SB, 2018 [10] metallic stent and lower adverse
event
Metal stents vs plastic stent:
• Clinical success rate
(OR) 3.39, (95% ci) 2.05–5.60)
• Adverse event rate
(OR 0.37, 95% ci 0.21–0.66)
The results were seen in subgroup
analysis both for pseudocyst and
walled-off necrosis.
(continued)
394 V. Bhardwaj and V. Bhatia
Table EN3 (continued)
Study author (first), year Result
Lumen apposing metal stents in drainage of Higher clinical success rate with
pancreatic walled-off necrosis, are they any better metallic stent and lower adverse
than plastic stents? A systematic review and event
meta-analysis of studies published since the revised Metal vs plastic stent:
Atlanta classification of pancreatic fluid collections. • Clinical-success rate
Mohan BP, 2019 [11] 88.5% (95% CI 82.5–92.6,
I2 = 71.7) and 88.1% (95% CI
80.5–93.0, I2 = 78.1) P = 0.93.
• Adverse-event
11.2% vs 15.9% P = 0.38.
Efficacy and safety of lumen-apposing metal stents Higher clinical success rate with
in management of pancreatic fluid collections: Are metallic stent and lower adverse
they better than plastic stents? A systematic review event
and meta-analysis. Metal versus plastic stent
Hammad T, 2018 [12] • Clinical success rate
0.37 (0.20, 0.67)
• Adverse events rate
0.39 (0.18, 0.84)
A systematic review and meta-analysis of metal Higher clinical success rate, lower
versus plastic stents for drainage of pancreatic fluid adverse event, lower additional
collections: Metal stents are advantageous. intervention with metallic stent
Saunders R, 2018 [13] Metal versus plastic stent
• Clinical success
93.8% versus 86.2% RR 1.08
[95% CI 1.02–1.14]; p = 0.009.
• Adverse events
(10.2% vs. 25.0%), RR 0.42 [95%
CI 0.22–0.81]; p = 0.010.
Metal stent usage
• Reduced bleeding
(2.8% vs. 7.9%), RR 0.37; [95%
CI 0.18–0.75]; p = 0.006.
• Lower number of intervention
12.4% versus 26.7%, RR 0.54;
[95% CI 0.22–1.29]; p = 0.165.
Efficacy and safety of metallic stents in comparison Higher clinical success rate, lower
to plastic stents for endoscopic drainage of adverse event and lesser need for
peripancreatic fluid collections: a meta-analysis and additional intervention with metallic
trial sequential analysis. stent
Panwar R, 2017 [14] Metal versus plastic stent
• Clinical success rate
OR 3.22; 95% CI 1.87–5.54;
P < 0.001.
• Adverse events
OR 0.40; 95% CI 0.24–0.65;
P < 0.001
• Need for additional salvage
procedures lower with metallic
stents.
OR 0.31; 95% CI 0.13–0.70;
P = 0.01
Endoscopic Management of Pancreatic Fluid Collection 395
Table EN3 (continued)
Study author (first), year Result
Metal versus plastic stents for pancreatic fluid Higher clinical success rate, lower
collection drainage: A systematic review and adverse event and lower recurrence
meta-analysis. with metallic stent
Zhou X, 2021 [15] Metal versus plastic stent
• Clinical success rate
92% versus 82% (P < 0.01)
• Adverse event rate
20% versus 31% (P < 0.01)
• Recurrence rate
3% versus 10% (P < 0.01)
Comparison between lumen-apposing metal stents Higher clinical success rate, lower
and plastic stents in endoscopic ultrasound-guided recurrence and fewer additional
drainage of pancreatic fluid collection: A meta- intervention with metallic stent
analysis and systematic review. Metal versus plastic stent
Lyu Y, 2021 [16] • Clinical success
(90.01% vs 82.56%) (odds ratio
[OR], 2.44; [CI], 1.79–3.33;
P < 0.00001),
• Less recurrence
(OR, 0.44; 95% CI, 0.29–0.68;
P = 0.0002), and
• Fewer additional interventions
(OR, 0.34; 95% CI, 0.211–0.55;
P < 0.001).
Adverse event: Lumen-apposing metal
stents have slightly more perforations
(OR, 7.10; 95% CI, 1.22–41.30;
P = 0.03) in studies of walled-off
necrosis.
RR risk ratio, MD mean difference, OR Odds Ratio, CI Confidence interval
396 V. Bhardwaj and V. Bhatia
atic walled-off necrosis, are they any better than plastic stents? A systematic
review and meta-analysis of studies published since the revised Atlanta classi-
fication of pancreatic fluid collections. Endosc Ultrasound. 2019;8(2):82–90.
https://doi.org/10.4103/eus.eus_7_19.
12. Hammad T, Khan MA, Alastal Y, Lee W, Nawras A, Ismail MK, Kahaleh
M. Efficacy and safety of lumen-apposing metal stents in management of pan-
creatic fluid collections: are they better than plastic stents? A systematic review
and meta-analysis. Dig Dis Sci. 2018;63(2):289–301. https://doi.org/10.1007/
s10620-017-4851-0.
13. Saunders R, Ramesh J, Cicconi S, Evans J, Yip VS, Raraty M, Ghaneh P, Sutton
R, Neoptolemos JP, Halloran C. A systematic review and meta-analysis of
metal versus plastic stents for drainage of pancreatic fluid collections: metal
stents are advantageous. Surg Endosc. 2019;33(5):1412–25. https://doi.
org/10.1007/s00464-018-6416-5.
14. Panwar R, Singh PM. Efficacy and safety of metallic stents in comparison to
plastic stents for endoscopic drainage of peripancreatic fluid collections: a
meta-analysis and trial sequential analysis. Clin J Gastroenterol.
2017;10(5):403–14. https://doi.org/10.1007/s12328-017-0763-y.
15. Zhou X, Lin H, Su X, Zhang P, Fu C, Kong X, Jin Z, Li Z, Du Y, Zhu H. Metal
versus plastic stents for pancreatic fluid collection drainage: a systematic review
and meta-analysis. J Clin Gastroenterol. 2021; https://doi.org/10.1097/
MCG.0000000000001539.
16. Lyu Y, Li T, Wang B, Cheng Y, Chen L, Zhao S. Comparison between lumen-
apposing metal stents and plastic stents in endoscopic ultrasound-guided drain-
age of pancreatic fluid collection: a meta-analysis and systematic review.
Pancreas. 2021;50(4):571–8. https://doi.org/10.1097/MPA.0000000000001798.
398 V. Bhardwaj and V. Bhatia
References
1. Rogers BH, Cicurel NJ, Seed RW. Transgastric needle aspiration of pancreatic pseudocyst
through an endoscope. Gastrointest Endosc. 1975;21:133–4.
2. Banks PA, Bollen TL, Dervenis C, Gooszen HG, Johnson CD, Sarr MG, Tsiotos GG, Vege
SS, Acute Pancreatitis Classification Working Group. Classification of acute pancreati-
tis--2012: revision of the Atlanta classification and definitions by international consensus. Gut.
2013;62(1):102–11. https://doi.org/10.1136/gutjnl-2012-302779.
3. van Santvoort HC, Bakker OJ, Bollen TL, Besselink MG, Ahmed Ali U, Schrijver AM,
Boermeester MA, van Goor H, Dejong CH, van Eijck CH, van Ramshorst B, Schaapherder
AF, van der Harst E, Hofker S, Nieuwenhuijs VB, Brink MA, Kruyt PM, Manusama ER, van
der Schelling GP, Karsten T, Hesselink EJ, van Laarhoven CJ, Rosman C, Bosscha K, de Wit
RJ, Houdijk AP, Cuesta MA, Wahab PJ, Gooszen HG, Dutch Pancreatitis Study Group. A
conservative and minimally invasive approach to necrotizing pancreatitis improves outcome.
Gastroenterology. 2011;141(4):1254–63. https://doi.org/10.1053/j.gastro.2011.06.073.
4. Bakker OJ, van Santvoort HC, van Brunschot S, Geskus RB, Besselink MG, Bollen TL, van
Eijck CH, Fockens P, Hazebroek EJ, Nijmeijer RM, Poley JW, van Ramshorst B, Vleggaar
FP, Boermeester MA, Gooszen HG, Weusten BL, Timmer R, Dutch Pancreatitis Study Group.
Endoscopic transgastric vs surgical necrosectomy for infected necrotizing pancreatitis: a ran-
domized trial. JAMA. 2012;307(10):1053–61. https://doi.org/10.1001/jama.2012.276.
5. van Santvoort HC, Besselink MG, Bakker OJ, Hofker HS, Boermeester MA, Dejong CH, van
Goor H, Schaapherder AF, van Eijck CH, Bollen TL, van Ramshorst B, Nieuwenhuijs VB,
Timmer R, Laméris JS, Kruyt PM, Manusama ER, van der Harst E, van der Schelling GP,
Karsten T, Hesselink EJ, van Laarhoven CJ, Rosman C, Bosscha K, de Wit RJ, Houdijk AP, van
Leeuwen MS, Buskens E, Gooszen HG, Dutch Pancreatitis Study Group. A step-up approach
or open necrosectomy for necrotizing pancreatitis. N Engl J Med. 2010;362(16):1491–502.
https://doi.org/10.1056/NEJMoa0908821.
6. Guenther L, Hardt PD, Collet P. Review of current therapy of pancreatic pseudocysts. Z
Gastroenterol. 2015;53(2):125–35. https://doi.org/10.1055/s-0034-1385713.
7. Varadarajulu S, Bang JY, Sutton BS, Trevino JM, Christein JD, Wilcox CM. Equal efficacy of
endoscopic and surgical cystogastrostomy for pancreatic pseudocyst drainage in a randomized
trial. Gastroenterology. 2013;145(3):583–90.e1. https://doi.org/10.1053/j.gastro.2013.05.046.
8. Parks RW, Tzovaras G, Diamond T, Rowlands BJ. Management of pancreatic pseudocysts.
Ann R Coll Surg Engl. 2000;82(6):383–7.
9. Muniraj T, Jamidar PA, Nealon WH, Aslanian HR. Endoscopic management of pancre-
atic fluid collections. J Clin Gastroenterol. 2017;51(1):19–33. https://doi.org/10.1097/
MCG.0000000000000644.
10. Vitale GC, Lawhon JC, Larson GM, Harrell DJ, Reed DN Jr, MacLeod S. Endoscopic drainage
of the pancreatic pseudocyst. Surgery. 1999;126(4):616–21; discussion 621–3.
11. Voermans RP, Eisendrath P, Bruno MJ, Le Moine O, Devière J, Fockens P, ARCADE Group.
Initial evaluation of a novel prototype forward-viewing US endoscope in transmural drainage
of pancreatic pseudocysts (with videos). Gastrointest Endosc. 2007;66(5):1013–7. https://doi.
org/10.1016/j.gie.2007.02.057.
12. Fusaroli P, Ceroni L, Caletti G. Forward-view endoscopic ultrasound: a systematic review
of diagnostic and therapeutic applications. Endosc Ultrasound. 2013;2(2):64–70. https://doi.
org/10.4103/2303-9027.117689.
13. Fusaroli P, Cortecchia S, Caletti G. EUS-FNA using a forward-view echoendoscope in difficult
cases. J Gastrointestin Liver Dis. 2011;20(2):216–7.
14. Iwashita T, Nakai Y, Lee JG, Park DH, Muthusamy VR, Chang KJ. Newly-developed, forward-
viewing echoendoscope: a comparative pilot study to the standard echoendoscope in the imag-
ing of abdominal organs and feasibility of endoscopic ultrasound-guided interventions. J
Gastroenterol Hepatol. 2012;27(2):362–7. https://doi.org/10.1111/j.1440-1746.2011.06923.x.
Endoscopic Management of Pancreatic Fluid Collection 399
15. Seewald S, Thonke F, Ang TL, Omar S, Seitz U, Groth S, Zhong Y, Yekebas E, Izbicki J,
Soehendra N. One-step, simultaneous double-wire technique facilitates pancreatic pseudo-
cyst and abscess drainage (with videos). Gastrointest Endosc. 2006;64(5):805–8. https://doi.
org/10.1016/j.gie.2006.07.049.
16. Khashab MA, Lennon AM, Singh VK, Kalloo AN, Giday SA. Endoscopic ultrasound (EUS)-
guided pseudocyst drainage as a one-step procedure using a novel multiple-wire inser-
tion technique (with video). Surg Endosc. 2012;26(11):3320–3. https://doi.org/10.1007/
s00464-012-2297-1.
17. Varadarajulu S, Christein JD, Tamhane A, Drelichman ER, Wilcox CM. Prospective random-
ized trial comparing EUS and EGD for transmural drainage of pancreatic pseudocysts (with
videos). Gastrointest Endosc. 2008;68(6):1102–11. https://doi.org/10.1016/j.gie.2008.04.028.
18. Kahaleh M, Shami VM, Conaway MR, Tokar J, Rockoff T, De La Rue SA, de Lange E,
Bassignani M, Gay S, Adams RB, Yeaton P. Endoscopic ultrasound drainage of pancreatic
pseudocyst: a prospective comparison with conventional endoscopic drainage. Endoscopy.
2006;38(4):355–9. https://doi.org/10.1055/s-2006-925249.
19. Park DH, Lee SS, Moon SH, Choi SY, Jung SW, Seo DW, Lee SK, Kim MH. Endoscopic ultra-
sound-guided versus conventional transmural drainage for pancreatic pseudocysts: a prospective
randomized trial. Endoscopy. 2009;41(10):842–8. https://doi.org/10.1055/s-0029-1215133.
20. Nealon WH, Walser E. Main pancreatic ductal anatomy can direct choice of modal-
ity for treating pancreatic pseudocysts (surgery versus percutaneous drainage). Ann Surg.
2002;235(6):751–8. https://doi.org/10.1097/00000658-200206000-00001.
21. Ahearne PM, Baillie JM, Cotton PB, Baker ME, Meyers WC, Pappas TN. An endoscopic
retrograde cholangiopancreatography (ERCP)-based algorithm for the management of
pancreatic pseudocysts. Am J Surg. 1992;163(1):111–5; discussion 115–6. https://doi.
org/10.1016/0002-9610(92)90262-p.
22. Barthet M, Sahel J, Bodiou-Bertei C, Bernard JP. Endoscopic transpapillary drainage of
pancreatic pseudocysts. Gastrointest Endosc. 1995;42(3):208–13. https://doi.org/10.1016/
s0016-5107(95)70093-5.
23. Catalano MF, Geenen JE, Schmalz MJ, Johnson GK, Dean RS, Hogan WJ. Treatment of pan-
creatic pseudocysts with ductal communication by transpapillary pancreatic duct endoprosthe-
sis. Gastrointest Endosc. 1995;42(3):214–8. https://doi.org/10.1016/s0016-5107(95)70094-3.
24. Kraft M, Simon P, Nitsche C, Runge S, Hahn N, Puls R, Lerch MM. Successful drain-
age of recurrent pancreatic pseudocyst via a transpapillary and transpancreatic approach,
using a conventional cystotome. Endoscopy. 2012;44 Suppl 2 UCTN:E186–7. https://doi.
org/10.1055/s-0032-1306793.
25. ASGE Standards of Practice Committee, Muthusamy VR, Chandrasekhara V, Acosta RD,
Bruining DH, Chathadi KV, Eloubeidi MA, Faulx AL, Fonkalsrud L, Gurudu SR, Khashab
MA, Kothari S, Lightdale JR, Pasha SF, Saltzman JR, Shaukat A, Wang A, Yang J, Cash BD,
DeWitt JM. The role of endoscopy in the diagnosis and treatment of inflammatory pancre-
atic fluid collections. Gastrointest Endosc. 2016;83(3):481–8. https://doi.org/10.1016/j.
gie.2015.11.027.
26. Trevino JM, Tamhane A, Varadarajulu S. Successful stenting in ductal disruption favor-
ably impacts treatment outcomes in patients undergoing transmural drainage of peri-
pancreatic fluid collections. J Gastroenterol Hepatol. 2010;25(3):526–31. https://doi.
org/10.1111/j.1440-1746.2009.06109.x. Erratum in: J Gastroenterol Hepatol. 2010
Mar;25(3):526. Tevino, Jessica M [corrected to Trevino, Jessica M]
27. Penn DE, Draganov PV, Wagh MS, Forsmark CE, Gupte AR, Chauhan SS. Prospective
evaluation of the use of fully covered self-expanding metal stents for EUS-guided transmu-
ral drainage of pancreatic pseudocysts. Gastrointest Endosc. 2012;76(3):679–84. https://doi.
org/10.1016/j.gie.2012.04.457.
28. Shamah S, Okolo PI 3rd. Systematic review of endoscopic cyst gastrostomy. Gastrointest
Endosc Clin N Am. 2018;28(4):477–92. https://doi.org/10.1016/j.giec.2018.06.002.
400 V. Bhardwaj and V. Bhatia
29. Baron TH, Kozarek RA. Endotherapy for organized pancreatic necrosis: perspectives after
20 years. Clin Gastroenterol Hepatol. 2012;10(11):1202–7. https://doi.org/10.1016/j.
cgh.2012.07.009.
30. Freeman ML, Werner J, van Santvoort HC, Baron TH, Besselink MG, Windsor JA, Horvath
KD, van Sonnenberg E, Bollen TL, Vege SS, International Multidisciplinary Panel of
Speakers and Moderators. Interventions for necrotizing pancreatitis: summary of a multi-
disciplinary consensus conference. Pancreas. 2012;41(8):1176–94. https://doi.org/10.1097/
MPA.0b013e318269c660.
31. Mathew A, Biswas A, Meitz KP. Endoscopic necrosectomy as primary treatment for infected
peripancreatic fluid collections (with video). Gastrointest Endosc. 2008;68(4):776–82. https://
doi.org/10.1016/j.gie.2008.05.010.
32. Seewald S, Ang TL, Richter H, Teng KY, Zhong Y, Groth S, Omar S, Soehendra N. Long-term
results after endoscopic drainage and necrosectomy of symptomatic pancreatic fluid collec-
tions. Dig Endosc. 2012;24(1):36–41. https://doi.org/10.1111/j.1443-1661.2011.01162.x.
33. Kumar N, Conwell DL, Thompson CC. Direct endoscopic necrosectomy versus step-up
approach for walled-off pancreatic necrosis: comparison of clinical outcome and health care
utilization. Pancreas. 2014;43(8):1334–9. https://doi.org/10.1097/MPA.0000000000000213.
34. Yachimski P, Landewee CA, Campisano F, Valdastri P, Obstein KL. The waterjet necrosectomy
device for endoscopic management of pancreatic necrosis: design, development, and preclini-
cal testing (with videos). Gastrointest Endosc. 2020;92(3):770–5. https://doi.org/10.1016/j.
gie.2020.04.024.
35. Seifert H, Biermer M, Schmitt W, Jürgensen C, Will U, Gerlach R, Kreitmair C, Meining
A, Wehrmann T, Rösch T. Transluminal endoscopic necrosectomy after acute pancreatitis: a
multicentre study with long-term follow-up (the GEPARD Study). Gut. 2009;58(9):1260–6.
https://doi.org/10.1136/gut.2008.163733.
36. Yasuda I, Nakashima M, Iwai T, Isayama H, Itoi T, Hisai H, Inoue H, Kato H, Kanno A,
Kubota K, Irisawa A, Igarashi H, Okabe Y, Kitano M, Kawakami H, Hayashi T, Mukai T, Sata
N, Kida M, Shimosegawa T. Japanese multicenter experience of endoscopic necrosectomy for
infected walled-off pancreatic necrosis: the JENIPaN study. Endoscopy. 2013;45(8):627–34.
https://doi.org/10.1055/s-0033-1344027.
37. van Brunschot S, Fockens P, Bakker OJ, Besselink MG, Voermans RP, Poley JW, Gooszen
HG, Bruno M, van Santvoort HC. Endoscopic transluminal necrosectomy in necrotising pan-
creatitis: a systematic review. Surg Endosc. 2014;28(5):1425–38. https://doi.org/10.1007/
s00464-013-3382-9.
38. Lakhtakia S, Basha J, Talukdar R, Gupta R, Nabi Z, Ramchandani M, Kumar BVN, Pal
P, Kalpala R, Reddy PM, Pradeep R, Singh JR, Rao GV, Reddy DN. Endoscopic “step-up
approach” using a dedicated biflanged metal stent reduces the need for direct necrosectomy
in walled-off necrosis (with videos). Gastrointest Endosc. 2017;85(6):1243–52. https://doi.
org/10.1016/j.gie.2016.10.037.
39. Azeem N, Baron TH, Topazian MD, Zhong N, Fleming CJ, Kendrick ML. Outcomes of
endoscopic and percutaneous drainage of pancreatic fluid collections arising after pan-
creatic tail resection. J Am Coll Surg. 2012;215(2):177–85. https://doi.org/10.1016/j.
jamcollsurg.2012.03.015.
Management of Solitary Pulmonary
Nodule
Kamran Ali and Sabyasachi Bal
Introduction
Apart from knowing what a SPN is, it is also important to understand the concept of
Solid and Subsolid nodules (SSN).
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 401
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_18
402 K. Ali and S. Bal
• Part-solid nodule (PSN): has both solid and ground glass component ≤3 cm in
diameter.
• Pure ground-glass nodule (PGGN): ground glass opacity ≤3 cm in diameter.
Solid component: the term is used to describe part of a nodule that obscures the
underlying broncho-vascular structure.
Ground-glass component: it refers to opacification, which is more than the
background, but visibility of underlying vascular structure is not hampered [1].
Approach to a SPN
Despite minor discrepancies, all proposed approaches take into consideration the
following factors:
No
Yes Assess risk of lung cancer according
Previous imaging?
to survillance algorithm 2
No
Yes
Nodule <8mm diameter or <300mm3 volume?
No
Fig. 2 BTS algorithm for solid nodules on CT scan [1] (published with permission from British
Thoracic Society)
The BTS guidelines recommend the use of two risk prediction models (Brock
University model and Herder model) for nodules >300 mm3 volume or >8 mm
diameter [1]. These models are readily available for anyone to use in the form of a
calculator-app on all smartphones (“BTS Pulmonary Nodule Risk Calculator” on
App Store or Google Play Store). The examples of malignancy risk prediction by
Brock model and Herder model can be seen in Fig. 3 and Fig. 4 respectively.
Whereas the Brock model is primarily based on clinical parameters supple-
mented with CT findings, PET CT is an additional modality of assessment in the
Herder model. CT surveillance is recommended for patients with nodules that have
<10% risk of malignancy as assessed by the Brock University model, whereas PET
CT is advisable for patients with higher risk who are further re-evaluated with the
Herder model [6]. The Herder model further classifies FDG (fluorodeoxyglucose)
uptake in PET as absent, faint, moderate or intense [7].
Brock Calculator
26 65
1 Male Female
Emphysema
Solid
Yes No
Nodule in Upper Lobe
Brock Model Probability
Yes No
67.7%
Spiculation
Yes No Calculate
Fig. 3 Example of Brock University Model in a 65-year Male with a 26 mm solid nodule
406 K. Ali and S. Bal
Herder Calculator
Spiculation
Never Smoked
Yes No
Previous History of Extra-Thoracic Ca
PET-CT Avidity Findings i
Yes No
NO FDG Faint FDG
10.4%
Calculate
Fig. 4 Example of Herder Model in a 65 year with a non FDG avid 26 mm nodule
and the time interval between the two scans [8–10]. Using automated volumetry,
growth of nodule, defined as increase in volume >25%, can be reliably predicted at
a 3 month interval CT. Another advantage of a 3-month CT is that most nodules
which resolve do so in 3 months interval. On the other hand, for small nodules,
5–6 mm size, the CT surveillance interval may be extended to 12 months to detect
appreciable growth. Stable disease at 1 year is indicative of benign aetiology [8].
SSNs are often benign, preinvasive or early invasive malignant lesions with an indo-
lent disease which carry a better prognosis and calls for a different management
strategy than solid nodules (Fig. 5). The pathological correlates [11–13] of a SSN
are tabulated in Table 3:
Thus, SSNs may represent both preinvasive and invasive lesions. Clinical and
morphological variables that are more likely to be associated with malignancy in
SSNs are:
• advanced age,
• prior history of lung cancer,
• size,
• part-solid nature (independent predictor of malignancy)
• pleural retraction
• indentation
• bubble-like appearance in a pGGN
Sub-solid nodule(s) on CT
Yes
Nodule <5mm, patient unfit for any treatment or stable over 4 years?
No
Yes Assess interval change, If stable over less than
Previous imaging?
4 years, assess risk of malignancy as below.
No
Fig. 5 The BTS algorithm for sub solid nodules on CT scan (reproduced with permission from
British Thoracic Society)
Biopsy Techniques
• Nonsurgical
• Surgical
• fluoroscopy
• EBUS, radial endobronchial ultrasound
• ENB, electromagnetic navigation bronchoscopy.
A 65%–84% yield with ENB and 46%–77% with radial EBUS has been
reported [18].
The relative draw backs of bronchoscopic guided technique are:
• access limitations of small lesions <2 cm located in peripheral third of the lung
• time consuming
• lack of wide availability (particularly EBUS AND ENB)
Surgical biopsy: Excision biopsy for SPN may be performed in the following
situations:
Thoracoscopic wedge resection remains the gold standard for surgical lung
biopsy (Figs. 6 and 7). The morbidity and mortality of the surgical procedure should
be weighed in contrast to the possibility of progression during radiological surveil-
lance when considering surgical resection as an option. A 0.4% mortality for wedge
resection/ segmentectomy has been reported by the UK and Ireland Society of
Cardio-Thoracic Surgeons. A 30-day mortality of 2.1% and a 90-day mortality of
4.2% has been reported in patients undergoing wedge resection or segmentectomy
(The English National Lung Cancer Audit) [19].
Fig. 6 Intraoperative
picture of a thoracoscopic
wedge resection using an
endostapler
Once a decision to resect a SPN has been taken, few issues regarding the optimal
surgical treatment need to be addressed. The two major considerations are the
approach and the extent of resection.
1. VATS rather than an open surgery should be the preferred surgical approach in SPN
2. In the context of a pulmonary nodule biopsy confirmed as lung cancer preopera-
tively or following a wedge resection with intraoperative frozen section analysis,
lobectomy should be offered as definitive management which may be attempted
at the same anaesthetic setting.
412 K. Ali and S. Bal
Bi-digital palpation in thoracotomy makes it easy to localize and resect even deep-
seated small lesions, if a limited resection is planned. Certain characteristics of the
nodules make it difficult to locate in thoracoscopy viz.: small size, located deep to
the visceral pleura and nodules exhibiting a ground-glass morphology.
Several preoperative marking techniques have been developed to facilitate local-
ization of these nodules, their use is subject to availability of the facility and exper-
tise (Table 4) [24–29].
Yes No
Fit for surgery?
Fig. 8 The BTS protocol for excision of a SPN (reproduced with permission from British Thoracic
Society) (RFA radiofrequency ablation, SABR stereotactic ablative body radiotherapy)
Patients with SPN who are deemed unfit for surgical treatment and patients who
choose to opt out of surgical treatment can be offered non-surgical treatment options.
An attempt should be made to obtain a histological confirmation, however if such is
not possible, treatment may proceed without biopsy, provided the risk of malig-
nancy is higher than 70%. The main alternatives to surgery are:
Editor’s Note1
References: Main chapter references are included after the “References Editor’s Note” section.
1
Management of Solitary Pulmonary Nodule 415
localization techniques enlisted are: (1) tumor to visceral pleura distance >4 cm
results in increased complications (2) location of tumor close to heart/ great vessel
(3) accessibility of localization hampered by scapula or ribs. There are less chances
of complications like pneumothorax and bleeding in bronchoscopic localization
however the procedure is complex and has higher costs as well as limited accuracy.
References
1. Callister ME, Baldwin DR, Akram AR, Barnard S, Cane P, Draffan J, Franks K, Gleeson F,
Graham R, Malhotra P, Prokop M, Rodger K, Subesinghe M, Waller D, Woolhouse I, British
Thoracic Society Pulmonary Nodule Guideline Development Group, British Thoracic Society
Standards of Care Committee. British Thoracic Society guidelines for the investigation and
management of pulmonary nodules. Thorax. 2015;70 Suppl 2:ii1–54. Erratum in: Thorax.
2015 Dec;70(12):1188. https://doi.org/10.1136/thoraxjnl-2015-207168.
2. MacMahon H, Naidich DP, Goo JM, Lee KS, Leung ANC, Mayo JR, Mehta AC, Ohno Y,
Powell CA, Prokop M, Rubin GD, Schaefer-Prokop CM, Travis WD, Van Schil PE, Bankier
AA. Guidelines for management of incidental pulmonary nodules detected on CT images:
from the Fleischner Society 2017. Radiology. 2017;284(1):228–43. https://doi.org/10.1148/
radiol.2017161659.
3. Gould MK, Donington J, Lynch WR, Mazzone PJ, Midthun DE, Naidich DP, Wiener
RS. Evaluation of individuals with pulmonary nodules: when is it lung cancer? Diagnosis and
management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based
clinical practice guidelines. Chest. 2013;143(5 Suppl):e93S–e120S. https://doi.org/10.1378/
chest.12-2351.
4. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Non-small cell lung
cancer version 2.2019; 21 November, 2018.
5. Horeweg N, van Rosmalen J, Heuvelmans MA, van der Aalst CM, Vliegenthart R, Scholten
ET, ten Haaf K, Nackaerts K, Lammers JW, Weenink C, Groen HJ, van Ooijen P, de Jong
PA, de Bock GH, Mali W, de Koning HJ, Oudkerk M. Lung cancer probability in patients
with CT-detected pulmonary nodules: a prespecified analysis of data from the NELSON trial
of low-dose CT screening. Lancet Oncol. 2014;15(12):1332–41. https://doi.org/10.1016/
S1470-2045(14)70389-4.
6. McWilliams A, Tammemagi MC, Mayo JR, Roberts H, Liu G, Soghrati K, Yasufuku K, Martel
S, Laberge F, Gingras M, Atkar-Khattra S, Berg CD, Evans K, Finley R, Yee J, English J,
Nasute P, Goffin J, Puksa S, Stewart L, Tsai S, Johnston MR, Manos D, Nicholas G, Goss
GD, Seely JM, Amjadi K, Tremblay A, Burrowes P, MacEachern P, Bhatia R, Tsao MS, Lam
S. Probability of cancer in pulmonary nodules detected on first screening CT. N Engl J Med.
2013;369(10):910–9. https://doi.org/10.1056/NEJMoa1214726.
7. Herder GJ, van Tinteren H, Golding RP, Kostense PJ, Comans EF, Smit EF, Hoekstra
OS. Clinical prediction model to characterize pulmonary nodules: validation and added value
of 18F-fluorodeoxyglucose positron emission tomography. Chest. 2005;128(4):2490–6.
https://doi.org/10.1378/chest.128.4.2490.
8. Baldwin DR. Management of pulmonary nodules according to the 2015 British Thoracic Society
guidelines. Key messages for clinical practice. Pol Arch Med Wewn. 2016;126(4):262–74.
https://doi.org/10.20452/pamw.3379.
9. Korst RJ, Lee BE, Krinsky GA, Rutledge JR. The utility of automated volumetric growth anal-
ysis in a dedicated pulmonary nodule clinic. J Thorac Cardiovasc Surg. 2011;142(2):372–7.
https://doi.org/10.1016/j.jtcvs.2011.04.015.
10. Ko JP, Berman EJ, Kaur M, Babb JS, Bomsztyk E, Greenberg AK, Naidich DP, Rusinek
H. Pulmonary Nodules: growth rate assessment in patients by using serial CT and
three-
dimensional volumetry. Radiology. 2012;262(2):662–71. https://doi.org/10.1148/
radiol.11100878.
11. Travis WD, Brambilla E, Noguchi M, Nicholson AG, Geisinger KR, Yatabe Y, Beer DG, Powell
CA, Riely GJ, Van Schil PE, Garg K, Austin JH, Asamura H, Rusch VW, Hirsch FR, Scagliotti
G, Mitsudomi T, Huber RM, Ishikawa Y, Jett J, Sanchez-Cespedes M, Sculier JP, Takahashi T,
Tsuboi M, Vansteenkiste J, Wistuba I, Yang PC, Aberle D, Brambilla C, Flieder D, Franklin W,
Gazdar A, Gould M, Hasleton P, Henderson D, Johnson B, Johnson D, Kerr K, Kuriyama K,
Lee JS, Miller VA, Petersen I, Roggli V, Rosell R, Saijo N, Thunnissen E, Tsao M, Yankelewitz
D. International association for the study of lung cancer/american thoracic society/european
Management of Solitary Pulmonary Nodule 417
racoscopic resection of small pulmonary nodules: experience with 174 nodules. J Thorac
Cardiovasc Surg. 2006;132(2):320–4. https://doi.org/10.1016/j.jtcvs.2006.04.012.
28. Vandoni RE, Cuttat JF, Wicky S, Suter M. CT-guided methylene-blue labelling before thoraco-
scopic resection of pulmonary nodules. Eur J Cardiothorac Surg. 1998;14(3):265–70. https://
doi.org/10.1016/s1010-7940(98)00160-2.
29. Ambrogi MC, Melfi F, Zirafa C, Lucchi M, De Liperi A, Mariani G, Fanucchi O, Mussi
A. Radio-guided thoracoscopic surgery (RGTS) of small pulmonary nodules. Surg Endosc.
2012;26(4):914–9. https://doi.org/10.1007/s00464-011-1967-8.
Minimally Invasive Thymectomy
Introduction
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 419
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_19
420 A. J. Mukherjee et al.
Indications
Indications of Thymectomy
1. Thymoma
(a) Small (<2 cm) intra thymic thymoma
(b) Large well encapsulated thymoma (preferably <5 cm)
(c) Minimally invasive thymoma
2. Generalized MG unresponsive to medical treatment
3. MG with ocular disease refractory to treatment
Classification of Thymectomy
1. T1 Transcervical thymectomy
(a) Basic
(b) Extended
2. T2 Videoscopic thymectomy
(a) Classic VATS
Minimally Invasive Thymectomy 421
(i) unilateral
(ii) bilateral
(iii) subxiphoid
(b) VATET
(i) Extended-bilateral thoracoscopy + open cervical exploration
3. T3 Transsternal thymectomy
(a) Standard
(b) Extended
4. T4 Transcervical and transsternal thymectomy
Preoperative Evaluation
Preoperative Preparation
Operative Technique
Patient and Port Position: The patient is placed in a 30-degree semi recumbent
supine position, with ipsilateral arm abducted and a bag placed under the shoulder.
Right-side approach is more commonly preferred for non thymomatous myasthenia
gravis, as it provides greater manipulation workspace with the heart out of the way
(Fig. 1). A left sided approach is usually reserved for a left sided thymoma.
Pneumothorax is created by inserting 10 mm trocar by open technique into the
thoracic cavity at fourth/fifth ICS in mid-axillary line (Fig. 1) similar way like inser-
tion of chest drainage tube and connecting it to gas insufflation setting pressures to
6–8 mmHg. This results in compression of lung thus providing space for surgical
manoeuvrings. Lung exclusion can also be done with a double lumen endotracheal
tube supplemented with insufflation of carbon dioxide (5–8 mmHg pressure at 4 L/
min flow rate). Once the lung is adequately deflated the carbon dioxide insufflation
is discontinued. Carbon dioxide insufflation alone can be used for lung collapse
keeping the pressures to 6–8 mmHg throughout the surgery which alleviates the
need of a double lumen tube. A 5 mm 30-degree camera makes it easy to change
camera position among all the ports. The surgeon and camera man stand on the
same side while the scrub nurse and second assistant positioned on the contalateral
side (Fig. 2).
The 3-port technique is commonly used. The initial 10 mm port incision should
always be directed in front of the tip of the scapula along the mid/posterior axillary
line. The second and third 5-mm instrument ports should be inserted guided under
direct thoracoscopic vision at the 2nd/3rd intercostal space and sixth/seventh inter-
costal space respectively in midaxillary line/anterior axillary line (Fig. 1). A sub
mammary fold approach for port placement can be adopted in females for cosmetic
reasons. The initial/first 10 mm port is used for specimen removal and after the end
of procedure a chest drain with water seal is placed through it.
Dissection of the gland: Dissection begins just anterior to the phrenic nerve, by
incising the mediastinal pleura with hook electrocautery/ultrasonic shears. The thy-
mus and pericardial fat are carefully mobilized from the right phrenic nerve. Care
should be exercised to prevent thermal or stretch injury to the nerve (Figs. 3 and 4).
monitor
assisting
doctor
scrub
nurse
surgeon
424 A. J. Mukherjee et al.
The pleural incision is extended along the length of the nerve toward the dia-
phragm, and all thymic tissue and pericardial fat are swept from the pericardium,
starting near the diaphragm (Fig. 5). Dissection is achieved via combination of blunt
and sharp dissection. Additionally, the thymus is mobilized superiorly by incising
the mediastinal pleura along the medial border of the internal mammary vessels.
This dissection is carried superiorly, freeing all soft tissue from the retro sternum
and eventually the thymus from the innominate vein. Gentle traction of the thymus
is initiated, which facilitates the identification of all vein branches draining into the
innominate vein. All thymic veins and attachments are controlled with endoclips
along the innominate vein (Figs. 6 and 7).
Complete gland removal: Once all thymic veins and attachments are dissected,
the superior poles can be identified with gentle downward traction of the gland.
Care should be taken as number and position of thymic veins are not definite and at
times may be incongruous. Using careful countertraction, the cephalad attachments
of the superior poles can be freed under direct visualization. All arterial connections
with the internal mammary arteries in this region are clipped and ligated. Also, care
is to be taken to identify the inferior thyroid vein while dissecting the superior horns
of the thymus in the thyro-thymic tract as it can be a source of torrential bleed.
Following mobilization of the superior poles, medial dissection can continue toward
the left chest, taking all thymic tissue and fat from the pericardium (Fig. 8).
Minimally Invasive Thymectomy 425
Dissection from left side: Left side can be part of thoracoscopic unilateral or in
general thoracoscopic bilateral approach. A 5-mm port is inserted into the left chest
for dissection of left thymus. Before this, right lung ventilation is started again and
maintained till the end of surgery. A 30-degree thoracoscope is inserted into the left
chest and is controlled by the surgical assistant. Output from this scope is displayed
separate from the primary surgeon’s scope/monitor, allowing simultaneous bilateral
mediastinal visualization. For more dissection from left side two additional ports
can be inserted under direct visualisation on the left side as done in right sided
approach.
426 A. J. Mukherjee et al.
a b
Fig. 9 (a) Bare area after complete en bloc dissection, phrenic-to-phrenic resection of all thymic
tissue and anterior mediastinal fat. (b) Final view from the right side in c/o bilateral approach
Chest drainage: If only right sided approach was adopted a single chest
drain suffices. However, in cases where the left pleura is also opened or when
left thoracoscopic dissection is added (Bilateral VATS), a chest drain can be
passed trans-mediastinal under direct visualization as it is a single cavity.
Adequate lung expansion is directly visualized before closing all port sites
sequentially in layers with absorbable sutures and skin with glue/sutures
(Fig. 13).
428 A. J. Mukherjee et al.
Operative Setup
The patient is placed in supine position and induced under general anaesthesia
with a dual lumen endotracheal tube. In most thymic lesions a semi right lateral
decubitus position is helpful particularly for non-thymomatous myasthenia
Minimally Invasive Thymectomy 429
Anesthesiologist 30° up or
a b
new port placement
Robot
Monitor
Scrub
nurse
Monitor
Instrument
Robotic
table
console
Fig. 14 The robotic platform can be docked from either side of the patient depending on surgical
approach and/or operating room layout
gravis, however one may choose a right/left sided approach depending on location
of the disease. The patient’s chest and hip are elevated, and the position is secured
with a de-sufflated bean bag with proper padding of pressure points. The upper
arm (side of approach) is outstretched, and the lower arm is secured at the patient’s
side. The robotic platform can be docked from either side of the patient depending
on surgical approach and/or operating room layout (Fig. 14). It is regarded that the
left sided approach is possible easily with robotic surgery in spite of less space,
leads to more complete removal of all thymic tissue thus preventing myasthenia
gravis from developing post-operatively even in patients only presenting with
thymoma.
Once the patient has been positioned, prepped, and draped, the left lung is collapsed
and single right lung ventilation is initiated. A Veress needle is inserted into the
chest and intrathoracic placement is confirmed with a saline column drop test. The
left chest is then insufflated with CO2 to expedite and augment lung collapse and
depression of the diaphragm and ventricle from the chest wall and sternum. This is
typically well tolerated at a pressure of 8 mmHg on high flow. Alternately 8 mm
port can be introduced into thoracic cavity under direct vision by open technique
when patient is on single lumen tube and gas insufflation at 8 mmHg works very
well in collapsing the lung.
430 A. J. Mukherjee et al.
Port position: An 8-mm camera port is inserted into the fifth intercostal space
within the inframammary fold at the anterior to mid-axillary line. Rest three trocars
are placed under direct vision.
An 8-mm port is placed in the third intercostal space on the anterior axillary line.
The next 8-mm port is placed in the fifth intercostal space, just lateral to the sternum
(left robotic working arm). Lastly, a 12-mm assistant port is placed caudally in the
midaxillary line, typically in the seventh intercostal space for suctioning.
The robotic console is then brought in proximity to the bedside with the central
column positioned over the patient’s contralateral shoulder. Appropriate instrumen-
tation is then inserted though the trocars under direct visualization and docked to the
robot; In general, an ultrasonic shears is preferred energy source in the right work-
ing robotic arm port and a bipolar grasper in the left robotic arm port.
Dissection of the gland: Once all instrumentation is docked to the robotic con-
sole, direct visualization of the left phrenic nerve is achieved. En bloc resection is
initiated through incision of the mediastinal pleura, just medial to the left
phrenic nerve.
Careful mobilization of the phrenic nerve is performed, preserving the nerve if
adequate oncologic margins are feasible. Pleural incision is carried along the length
of the nerve, taking care to prevent stretch injury to the nerve or damage to the adja-
cent perineural vessels. Dissection is continued medially, using a combination of
sharp and blunt dissection. All thymic tissue and pericardial fat are taken off from
the pericardium in all directions medially, caudally and cephalad towards the
innominate vein.
Upwards, the pleural incision goes anteriorly adjacent to the internal mammary
artery and phrenic nerve junction. This dissection is extended downwards to the
diaphragm, running medial to the internal mammary vessels. All tissue is then
excised from the retro sternum with blunt and sharp dissection to the level of the
innominate vein superiorly, and medial to the contralateral internal mammary ves-
sels (better visualized after contralateral pleural incision). The left and right thymic
horns are identified at the top which are fully mobilized, and resected en bloc with
the specimen.
Following division of the thymic horns, dissection is carried toward the right
pleura. At this point in the operation, risk of injury to the contralateral phrenic
nerves and/or mammary vessels can be high if adequate visualization is not obtained.
It is found that identification of the contralateral nerve and/or internal mammary
vessels can be difficult in certain cases and therefore two strategies have been iden-
tified to facilitate this. One method is through utilization of simultaneous bilateral
visualization of the mediastinum. In this method, we insert a 5-mm thoracoscopic
port into the contralateral chest at the level of the infra mammary crease.
Thoracoscopic video output from this port, is controlled by the bed side assistant
surgeon, can be directly linked to existing robotic platforms, allowing bilateral and
simultaneous mediastinal visualization while sitting at the robotic console. The bed-
side assistant maintains visualization of vital contralateral structures as the primary
surgeon operates from the left side.
Minimally Invasive Thymectomy 431
Post-Operative Care
With advent of modern anaestheisa and minimally invasive surgeries early extu-
bation add further to the advocated better outcomes of minimally invasive thy-
mectomy. Normal diet is given, unless there is bulbar weakness due to MG. Chest
physiotherapy as well as incentive spirometry is mandated for speedy recovery
along with chest x-ray monitoring. It is imperative to monitor Spo2 and bedside
spirometry serves well in the early postoperative period to detect early respira-
tory muscle weakness. A volume of <15 mL/kg, or continuous fall in forced vital
capacity should raise an alarm towards respiratory failure. Preoperative medica-
tions should be resumed in early postop for the control of MG In the absence of
air leak or bleeding intercostal chest drainage tube can be removed after postop-
erative day 1. Steroids and immune suppressants should also be resumed after
surgery and should be gradually tapered over several months. In non-thymoma-
tous MG, there is improvement in 85% of patients of whom 35% of achieve drug-
free remission [20]. However, the effect of thymectomy may be observed only
after 1–2 years. Remission rate increases with time and reaches 40–60% after
7–10 years.
Advantages of VATS
1. The VATS and Robotics approaches minimize chest wall trauma which results in
lower morbidity, enabling early discharges, and improved patient acceptability
for surgery.
2. Conversion from VATS to sternotomy is low ranging from 2.6 to 5.5% [21].
3. The VATS approach is preferred for many reasons.
(a) Excellent vision: A panoramic vision of thorax and wide angle manipulation
is major advantage of VATS
(b) Handling bleeding: As the thymus, is more an anterior mediastinal structure,
chest offers direct approach than the neck and it is easy to handle any
bleeding.
(c) Completion thymectomy: Residual thymic tissue can be taken with ease, in
cases where transcervical approach had failed.
Minimally Invasive Thymectomy 433
(d) Cosmesis: VATS offers better cosmesis which although not arguable to jus-
tify a particular approach yet serves better to larger young female population
with the disease.
(e) Pulmonary function: A randomized prospective study has clearly attributed
an advantage of VATS over open approach in terms of better pulmonary
function and a faster recovery for MG [22]. This adds to earlier extubation
and thus significant reduction in postoperative pulmonary infections.
1. Severe coagulopathy
2. Pleural symphysis.
3. Patients with poor lung function, COPD, ILD or other severe underlying lung
disease in whom single lung ventilation may be difficult to manage.
4. Young children may not be suitable candidates due to smaller airways which are
not amenable to the smallest double-lumen tube andone-lung ventilation with
other methods can be more hazardous.
5. Previous surgery in the ipsilateral chest is a relative contraindication
Future
The uniportal technique could be described as a way of performing surgery with the
least number of devices possible, reducing this way a possible compression over the
intercostal space when multiple instruments are introduced through a single inci-
sion. The use of two specific instruments: a long curved stainless-steel Dennis suc-
tion device on the left hand and an energy device on the right hand is the key. The
434 A. J. Mukherjee et al.
coordination enables a fast and effective dissection and coagulation and exposure in
addition, the use of an external articulated camera support allows for a firm and
stable handling without an assistant. Future experience gained with the uniportal
approach will favour this type of surgery, therefore enabling the optimization of
hospital resources [23].
Non-intubated thoracic surgery (NITS) has been the hot topic in past decade. It
offers potential advantages over general anaesthesia of avoiding side effects of
endotracheal intubation, mechanical ventilation, and general anaesthetic drugs.
Thoracic centres are enthusiastic about NITS, although the criteria for patient selec-
tion and the standard anaesthetic care for NITS are yet to be established.
The rationale here is to avoid muscle relaxants, which would lower the risk of
postoperative muscle weakness and respiratory insufficiency, thus improving patient
recovery. Awake endoscopic thymectomy has been reported which allows the
patient to eat, drink, and walk in immediate postoperative period. With iatrogenic
opening of the pleurae, continuous suction through a nasogastric tube to the pleural
hole would help to expand the lung passively [24].
A systematic review of the literature was done comparing open to minimally inva-
sive thymectomy, both nonrobotic and robotic VATS included a total of 20 compara-
tive studies encompassing 2068 patients receiving either open [1230 (59.5%)] or
minimally invasive [838 (40.5%)] thymectomy [25]. There was considerable varia-
tion regarding patient age, sex, and indication for thymectomy across studies, but all
studies were individually well matched between comparison groups. Across stud-
ies, there was a consistent trend of significantly lower mean blood loss (VATS:
20–200 mL; Open 86–466 mL), pleural drainage duration (VATS: 1.3–4.1 days;
open 2.4–5.3 days), and hospital length of stay (VATS: 1.0–10.6 days; Open
4.0–14.6 days) in patients treated with minimally invasive thymectomy. No consis-
tent differences could be found in terms of operative time, rate of R0 resection of
malignancy, or perioperative complications. Long-term outcomes such as remission
of myasthenia gravis and thymoma recurrence were similar in open and minimally
invasive groups, although follow-up time was limited across studies. Friedant et al.
performed a systematic review and meta-analysis of minimally invasive versus open
thymectomy for malignancy [26]. They too reported a lower estimated blood loss
during minimally invasive thymectomy with a standardized mean difference of
−0.78 (95% CI: −1.05, −0.51). Length of hospital stay was also shorter for mini-
mally invasive groups (standardized mean difference −0.88; 95% CI: −1.52, −0.24).
There were no significant differences in operative time, rates of R0 resection, com-
plications, or locoregional cancer recurrence.
Minimally Invasive Thymectomy 435
Few studies have directly compared outcomes for robotic and nonrobotic VATS
thymectomy. Ye et al. reported a series of 25 unilateral VATS procedures compared
to 21 unilateral robotic VATS procedures for Masaoka stage I thymoma. No signifi-
cant differences was noted in operating time or estimated blood loss, but a shorter
pleural drainage time (1.1 days vs. 3.6 days; P < 0.01) and length of hospital stay
(3.7 vs. 6.7; P < 0.01) was seen in the robotic VATS group. There were similar con-
versions to open surgery (VATS-1; robotic VATS-0) and incidence of postoperative
complications (VATS-1; robotic VATS-1). Robotic VATS as anticipated incurred a
significantly higher mean hospitalization cost ($8662 vs. $6097; P < 0.01) [27].
Ruckert et al. conducted a cohort study of 79 VATS versus 74 robotic VATS thymec-
tomies for myasthenia gravis. Both groups were well matched with respect to age,
sex, and disease severity, and there were similar operating times (198 ± 48 vs.
187 ± 48 min), rates of open conversion [1(1.3%) vs. 1(1.4%)], and postoperative
morbidity [2(2.5%) vs. 2(2.7%)] in the VATS and robotic VATS groups, respec-
tively [28].
Marulli and colleagues reported a series of 100 patients undergoing robotic thy-
mectomy for myasthenia gravis. Postoperative complications occurred in 6 (6%) of
patients, and median hospital stay was 3 days (range 2 to 14 days) [29]. Ruckert
et al. reported a series of 106 consecutive robotic thymectomies for myasthenia
gravis, with a 1% rate of open conversion and 2% rate of postoperative morbid-
ity [30].
The purported benefits of a robotic approach are related to its narrow nature and
the rigid chest wall. With the use of CO2 this space is widened, resulting in improved
visualization and operability. In comparison to VATS, the complications are similar.
With regard to clinical outcomes, there appears to be no significant difference,
although some suggest that there is a quicker improvement in quality of life and
shorter hospital stay.
Conclusion
Editor’s Note1
References: Main chapter references are included after the “References Editor’s Note” section.
1
Table EN1 Comparison of various approaches for VATS thymectomy - advantages and disadvantages [31]
438
Vessel Nerves
Intrathoracic Thymic Recurrent
Working Brachiocephalic vein and vein and Phrenic nerve Anatomical
Approach space vein artery artery nerve (left) Lung Pericardium Tumor resection problem
Trans- Limited Possible Possible Possible Difficult Good Impossible Difficult Limited to Impossible to
cervical and small tumor resect large
partially tumor;
difficult Impossible to
approach lower
portion of
thymus
One-sided Limited Possible and Same side: Possible Same Impossible Good Good Needed Impossible to
Trans- but partially Good and side: intercostal resect cervical
intrathoracic same difficult Other side: partially Good thoracotomy; portion;
side: Difficult difficult Other postoperative difficult to
Good side: pain approach
Other Difficult another part of
side: thymus
Limited
Bilateral Good Possible Good Good Good Impossible Good Good Needed Difficult to
trans- intercostal resect cervical
intrathoracic thoracotomy; portion
postoperative
pain
(continued)
A. J. Mukherjee et al.
Table 1 (continued)
Vessel Nerves
Intrathoracic Thymic Recurrent
Working Brachiocephalic vein and vein and Phrenic nerve Anatomical
Approach space vein artery artery nerve (left) Lung Pericardium Tumor resection problem
Trans- Limited Possible and Possible Possible Possible Impossible Possible Possible No need for Difficult to
subxiphoid partially and and and thoracotomy resect cervical
difficult partially partially partially fat portion
difficult difficult difficult completely;
difficult to
Minimally Invasive Thymectomy
approach the
upper portion
of left
innominate
vein
439
440 A. J. Mukherjee et al.
References
1. Jaretzki A, Steinglass KM, Sonett JR. Thymectomy in the management of myasthenia gravis.
Semin Neurol. 2004;24(1):49–62.
2. Mack MJ. Video-assisted thoracic surgery. In: Kaiser LR, Kron IL, Spray TL, editors. Mastery
of cardiothoracic surgery. Philadelphia: Lippincott-Raven; 1998. p. 92–104.
3. Rückert JC, Walter M, Müller JM. Pulmonary function after thoracoscopic thymectomy versus
median sternotomy for myasthenia gravis. Ann Thorac Surg. 2000;70:1656–61.
4. Meyer DM, Herbert MA, Sobhani NC, et al. Comparative clinical outcomes of thymectomy
for myasthenia gravis performed by extended transsternal and minimal invasive approaches.
Ann Thorac Surg. 2009;87:385–91.
5. Sauerbruch F. Thymektomie bei einem Fall von Morbus Basedowimit Myasthenia. Mitt
Grenzgeb Med Chir. 1913;25:746.
6. Blalock A, Mason MF, Morgan HG, et al. Myasthenia gravis and tumors of the thymic region.
Ann Surg. 1939;110:544–61.
7. Blalock A, Harvey A, Ford F, Lilienthal J Jr. The treatment of myasthenia gravis by removal of
the thymus gland. JAMA. 1941;117:1529–31.
8. Blalock A. Thymectomy in the treatment of myasthenia gravis. J Thorac Surg. 1944;13:316.
9. Sugarbaker DJ. Thoracoscopy in the management of anterior mediastinal masses. Ann Thorac
Surg. 1993;56:653–6.
10. Coosemans W, Lerut TE, Van Raemdonck DE. Thoracoscopic surgery: the Belgian experi-
ence. Ann Thorac Surg. 1993;56:721–30.
11. Yim AP. Paradigm shift in surgical approaches to thymectomy. ANZ J Surg. 2002;72:40–5.
12. Yim AP, Low JM, Ng SK, Ho JK, Liu KK. Video-assisted thoracoscopic surgery in the paedi-
atric population. J Paediatr Child Health. 1995;31:192–6.
13. Novellino L, Longoni M, Spinelli L, et al. “Extended” thymectomy without sternotomy, per-
formed by cervicotomy and thoracoscopic techniques in the treatment of myasthenia gravis.
Int Surg. 1994;79:378–81.
14. Gronseth GS, Barohn RJ. Practice parameter: thymectomy for autoimmune myasthenia gravis
(an evidence-base review): report of the Quality Standards Subcommittee of the American
Academy of Neurology. Neurology. 2000;55:7–15.
15. Papatestas AE, Genkins G, Kornfeld P, et al. Effects of thymectomy in myasthenia gravis. Ann
Surg. 1987;206:79–88.
16. Seggia JC, Abreu P, Takatani M. Plasmapheresis a preparatory method for thymectomy in
myasthenia gravis. Arq Neuropsiquiatr. 1995;53:411–5.
17. Wagner OJ, Louie BE, Vallieres E, et al. Near-infrared fluorescence imaging can help
identify the contralateral phrenic nerve during robotic thymectomy. Ann Thorac Surg.
2012;94(2):622–5.
18. Soon JL, Agasthian T. Harmonic scalpel in video-assisted thoracoscopic thymic resections.
Asian Cardiovasc Thorac Ann. 2008;16(5):366–9.
19. Agasthian T. Beyond the limits, extreme minimally invasive surgery in invasive thymic
tumours. J Vis Surg. 2017;3:58.
20. Nieto IP, Robledo JP, Pajuelo MC, et al. Prognostic factors for myasthenia gravis treated by
thymectomy: review of 61 cases. Ann Thorac Surg. 1999;67(6):1568–71.
21. Ng CSH, Wan IYP, Yim APC. Video-assisted thoracic surgery thymectomy: the better
approach. Ann Thorac Surg. 2010;89(6):S2135–41.
22. Rückert JC, Walter M, Müller JM. Pulmonary function after thoracoscopic thymectomy versus
median sternotomy for myasthenia gravis. Ann Thorac Surg. 2000;70:1656–61.
23. Gonzalez-Rivas D, Sihoe ADL. Important technical details during uniportal video-assisted
thoracoscopic major resections. Thorac Surg Clin. 2017 Nov;27(4):357–72. https://doi.
org/10.1016/j.thorsurg.2017.06.004.
24. Zhao ZR, Lau RWH, Ng CSH. Anaesthesiology for uniportal VATS: double lumen, single
lumen and tubeless. J Vis Surg. 2017;3:108. https://doi.org/10.21037/jovs.2017.07.05.
442 A. J. Mukherjee et al.
25. Hess NR, Sarkaria IS, Pennathur A, et al. Minimally invasive versus open thymectomy: a sys-
tematic review of surgical techniques, patient demographics, and perioperative outcomes. Ann
Cardiothorac Surg. 2016;5(1):1–9.
26. Friedant AJ, Handorf EA, Su S, et al. Minimally invasive versus open thymectomy for thymic
malignancies: systematic review and meta-analysis. J Thorac Oncol. 2016;11(1):30–8.
27. Ye B, Tantai JC, Li W, et al. Video-assisted thoracoscopic surgery versus robotic-assisted tho-
racoscopic surgery in the surgical treatment of Masaoka stage I thymoma. World J Surg Oncol.
2013;11:157.
28. Ruckert JC, Swierzy M, Ismail M. Comparison of robotic and nonrobotic thoracoscopic thy-
mectomy: a cohort study. J Thorac Cardiovasc Surg. 2011;141(3):673–7.
29. Marulli G, Schiavon M, Perissinotto E, et al. Surgical and neurologic outcomes after robotic
thymectomy in 100 consecutive patients with myasthenia gravis. J Thorac Cardiovasc Surg.
2013;145(3):730–735; discussion 735–6.
30. Ruckert JC, Ismail M, Swierzy M, et al. Thoracoscopic thymectomy with the da Vinci robotic
system for myasthenia gravis. Ann N Y Acad Sci. 2008;1132:329–35.
31. Takeo S, Shoji F, Toyokawa G, Kozuma Y, Yamazaki K. Video-assisted thoracoscopic thymec-
tomy for early-stage thymoma: A review, Open access text, keynote lecture at the 68th Annual
Scientific Meeting of the Japanese Association for Thoracic Surgery. https://doi.org/10.15761/
GOS.1000208.
Retroperitoneoscopic Minimally
Invasive Adrenalectomy
Sameer Rege
Introduction
Surgical excision for adrenal pathologies was conventionally done with open
method and required large abdominal incisions to reach these small glands. The
vasculature being small and lean in these glands, there was a propensity for easy
damage to these structures during open surgery with resultant bleeding and added
morbidity for the patient. Further the deep position of these small friable glands
makes access in open surgery difficult, often requiring large incisions to retrieve the
small gland. Minimal access surgery with magnification and pinpoint precision
have not only made adrenal surgery more meticulous, but long reach of laparo-
scopic instruments through small ports also have reduced the morbidity of abdomi-
nal incision leading to less hospital stay, postoperative pain and additionally offers
better cosmesis.
Adrenalectomies with minimal access techniques have been described with
transperitoneal and retroperitoneal approaches which can be via posterior or lateral
approach. We in this chapter describe the retroperitoneal (RP) technique of minimal
access surgery for removing a diseased adrenal.
Anatomy and Physiology
Adrenal or suprarenal glands are situated in deep retroperitoneum just at the upper
pole of the kidneys. These are in close proximity to inferior vena cava, liver and the
kidney on right side while aorta, tail of the pancreas, spleen, duodenojejunal flexure
and hilum of the kidney on left side.
S. Rege (*)
Seth GS Medical College and KEM Hospital, Mumbai, India
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 443
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_20
444 S. Rege
These endocrine glands are responsible for secretion of various hormones which
regulate the blood pressure, electrolytes and hormones for stress response.
Anatomically, adrenal gland has a peripheral cortex and central medulla and disor-
ders vary with pathological affection of these areas.
History
Higashihara from Japan and Gagner from Canada are credited with first laparo-
scopic adrenalectomy in 1992 [1]. Gaur et al from India in 1992, initiated work in
retroperitoneum for renal procedures such as laparoscopic ureterolithotomy and
paraaortic lymph node biopsies [2] and in1993, endoscopic model for retroperito-
neal adrenalectomy was demonstrated by Brunt et al. [3] with CO2 insufflation and
retroperitoneoscopy, which laid the foundation for retroperitoneal surgeries. Mercan
et al. [4] are credited for posterior retroperitoneal approach described in 1995 for 11
cases which was modified and popularized by Walz et al. [5].
Adrenalectomies with minimal access techniques have been described with trans-
peritoneal and retroperitoneal approaches which can be via posterior or lateral
approach.
There are advantages and disadvantages of either approach. Transperitoneal
approach offers better visibility and working space. The surgeons are usually famil-
iar with landmark and structures however one has to mobilize few organs and struc-
tures to reach the adrenal and hence they are liable for damage. Tumors more than
5 cms were better amenable with transperitoneal approach but recently retroperito-
neal approach has also proved to be safe for them. Previous abdominal surgery may
pose a difficulty in reaching adrenal gland via transperitoneal approach due to adhe-
sions. In obese patients with friable hepatomegaly one may have difficulty in access-
ing the right adrenal vein. Bilateral lesions would entail change of positions and
hence longer operative times in the transperitoneal approach.
Retroperitoneal approach is direct and does not interfere with the intraabdominal
organs, hence damage to them is rare. It may also be a preferred approach with a
scarred abdomen with prior history of abdominal surgery. The incisions are on the
back leading to less postoperative pain so that the patients can be mobilized early
requiring shorter hospital stay. However, the smaller space in the retroperitoneum,
crowding of instruments and unfamiliar anatomy with unclear landmarks at the
beginning of procedure requires specialized training at high volume centers and still
has a long learning curve [1].
Lateral retroperitoneal approach familiarized by Zhang et al has been shown to
be effective in the management of larger tumors (more than 5 cms) and has impro-
vised dissection so as to shorten the intra operative time as compared to transperito-
neal approach. However bilateral lesions require change of position and hence a
longer operative time [6–8].
Retroperitoneoscopic Minimally Invasive Adrenalectomy 445
Posterior approach developed and popularized by Walz et al could deal with
bilateral lesion in same prone position of the patient or even simultaneous surgery
with two specialized teams decreasing the operative time [5]. The standardized
operative steps allow management of large adrenal lesion with minimized blood
loss and pain. Training is a must to work in the small retroperitoneal space with
decreased freedom of movement of instruments below the ribs. The principle of the
retroperitoneal surgery is based on adrenal being enclosed in loose Gerota’s fascia
and can directly be accessed from posterior aspect after opening the deep thoraco-
lumbar fascia, the same approach being followed in conventional lumbotomy
approach for renal surgeries.
All patients need an extensive workup with hormonal assay, computerized
tomography with special cuts at the level above kidney to delineate the vascular
supply, drainage and relations with adjoining structures. Endocrinology and cardiac
opinions are usually sought for. It is imperative that the surgical team should be well
versed with the radiology of the patient to plan the surgery. Sestambi and MIBG
scan should be done if indicated. Tables 1 and 2 enumerates the various common
approaches adopted and indications for minimally invasive adrenalectomy.
Monitor
Laparoscopic
Cart
accommodated in between (Fig. 1). This special pillow placed also suspends the
upper torso allowing about 90 degrees flexion of the hips which ensures the flatness
of the spine opening up the retroperitoneal space between diaphragm and the
pelvis [5].
The knees can be flexed at right angle and are supported with adequate padding.
The legs are separated providing space for the assistant. The operating surgeon usu-
ally stands on the side to be operated (patient being prone it’s the opposite side of
the table) with the camera monitor on the opposite head end side and another moni-
tor for assistant on the operating surgeon’s side. For unilateral lesions, the lateral
edge of the patient coincides with the lateral edge of the table allowing a better
mobility of instruments, however for bilateral lesions; the patient is placed in the
centre of the table. The scrub assistant stands on the opposite side of the lesion.
Instruments: A 10 mm 30-degree telescope is preferred; however, a 5 mm tele-
scope may be helpful for retrieving the specimen and also if single port surgery is
being planned with posterior approach. The carbon dioxide insufflators should be
able to maintain pressure of minimum of 20 mmHg and higher. Special energy
device such as bipolar or ultrasonic scissors are preferable as adrenal veins can be
sealed and tackled with them, however hemoclips and harmonic scalpel can also be
used. Disposable blunt trocar with inflatable balloon and adjustable sleeve is prefer-
able as the first port. Conventional laparoscopic instruments can be used; however,
a clamp which can hold a peanut of gauze piece may be useful for blunt dissection.
The entire back is scrubbed and draped to keep the lumbar area open with lateral
drapes placed below the anterior axillary line. First landmark to identify is the tip of
the 12th rib on the side and transverse 1.5 cm incision is taken just below the tip. A
straight scissors is pushed vertically inside to pierce the thoracolumbar fascia
Retroperitoneoscopic Minimally Invasive Adrenalectomy 447
Fig. 2 Intra-operative
image of straight scissor
being used to create the
first port
noticed with a sudden give-way feel and the tract is adequately dilated to allow the
surgeons finger to go in (Fig. 2).
Index finger of left hand is inserted for right adrenalectomy and vice versa. This
dissection is done laterally closer to the abdominal wall to dissect the Gerota’s down
from the abdominal wall. First working port, a 5 mm port (preferably spiral/ ringed)
is introduced laterally in the space created by the tip of index finger through the
midaxillary line pointing towards the spine which should ideally be more than
10–12 cm lateral from the first trocar. A 10 mm blunt trocar with inflatable balloon
with adjustable sleeve is introduced through the first incision. This optical port is
self- retaining and being transparent allows vision through port at the near site also.
The space in insufflated with carbon dioxide and a pressure of 20 mmHg is kept
which allows to open up spaces between the abdominal wall and the areolar tissue.
A 30- degree telescope is introduced with vision facing the spine. Blunt dissection
is done to take all areolar tissue down from the abdominal wall so that the kidney
falls down. Third 10 mm port is introduced in oblique direction towards the apex of
the space from the midpoint of the first port and the spine at the same level to avoid
torque at the abdominal wall. This port is also used for the optics to provide a sec-
toral vision, when the first two ports are used as working ports (Fig. 3).
On either side, the initial aim is to dissect all retroperitoneal loose areolar tissue
from the posterior abdominal wall so that the working space is developed (Fig. 4).
The dissection is deemed complete when the inferior vena cava is seen bare till apex
on the right side and the entire apex is seen on either side (Figs. 5 and 6).
On right side, the upper pole of the kidney is cleared from inferior vena cava
medially to lateral abdominal wall (9 to 3 ‘0’clock) to identify the peritoneum seen
as a shiny glistening layer and the bare area of the liver. Accidental fenestration of
the peritoneum and Toldt’s membrane should be prevented, however the pneumo-
peritoneum always does not interfere with retroperitoneal dissection. The adrenal
gland with the loose areolar tissue is never grasped but only retracted with the pea-
nut grasper or blunt grasper, which prevents fragmentation of the gland irrespective
of the pathology.
The retrocaval arteries traverse medially and are coagulated during dissection to
lift the adrenal from the lateral border of the inferior vena cava. The dissection
gradually moves cranially to identify the adrenal vein, which is coagulated and
448 S. Rege
transected with an energy device or clipped and cut (Figs. 7, 8 and 9). In general,
ultrasonic shears are used and after identifying the adrenal vein is clipped. One has
to be very sure to clip the specimen side of the vein first and also ensure complete
clipping.
On the left side the adrenal lies at an upper level than right side and also
extends more medially and till the hilum of left kidney. Hence the left kidney is
additionally dissected on posterior aspect till the hilum and bared medially and
the left kidney is lowered so as have access to the left adrenal vein which joins
Fig. 6 Schematic diagram showing venous drainage of both adrenals as viewed from the posterior
approach
the renal vein (Fig. 10). Attempts are made to preserve the inferior phrenic vein
which travels on posterior abdominal wall lateral to aorta and joins the adrenal
vein to drain into the left renal vein (Fig. 11). The adrenal vein is secured and
then the adrenal gland is than dissected from caudal to cranial along with the
areolar tissue.
The resected gland is placed in endobag (Fig. 12) and retrieved. Occasional sur-
geon has mentioned morcellating the specimen in the endobag prior to removal [5].
The fascia and the ports are sutured and drains are seldom required.
Retroperitoneoscopic Minimally Invasive Adrenalectomy 451
In the lateral approach, the dissection is again in a smaller space like the posterior
retroperitoneoscopic approach and is more difficult in males as compared to females
because of more muscle mass.
The patient is operated in total lateral decubitus position with elevation of the
kidney/lumbar bridge of the table and straightening the ipsilateral lower limb to
maximize the distance between iliac crest and the 12th rib. All pressure points over
the hips, legs, and bony prominences are well padded and care should be taken not
to over extend the axilla to prevent brachial plexus injuries. The operating surgeon
stands on the contralateral side of the patient (the right-side adrenal operated from
left side of the table meaning facing the abdomen of the patient) along with the
camera assistant. The second assistant stands towards the back of the patient. The
position is similar to that for lateral transperitoneal laparoscopic adrenalectomy and
nephrectomy.
Retroperitoneoscopic Minimally Invasive Adrenalectomy 453
Scrubbing is done from nipple to knee in anterior and lateral aspect and posteri-
orly entire back on the operating side till below the iliac crest. The first incision is a
longitudinal 2 cm incision taken below the tip of 12th rib in posterior axillary line.
A straight scissors as described earlier is inserted through the thoracolumbar fascia
and the muscles are separated by blunt dissection. Retroperitoneal space is identi-
fied by a sudden give way and the once the space is confirmed, finger dissection to
push the Gerota’s fascia upwards and the peritoneum downwards is done blindly
with the index finger. A 10 mm balloon trocar with adjustable sleeve is then inserted
in this space and inflated and the space is created with about 600–800 mL balloon
distension. Then a 10 mm optical trocar is inserted about 2 fingerbreadths above the
iliac crest in the mid-axillary line and used as the camera port. Second trocar of
5 mm as a working port is inserted under vision below the costal margin in the ante-
rior axillary line. The site of balloon trocar insertion is used as the third port or as
the second working port in the posterior axillary line. Digitally controlled place-
ment of trocars is essential to avoid inadvertent injury to the peritoneum and the
Gerota’s fascia. CO2 insufflation pressure is maintained above 20 mmHg. Some
surgeons prefer a 12 mm working trocar instead 10 mm for using endo-GI sealing
devices usually on the dominant hand side [6–8].
Mobilization of retroperitoneal adipose tissue from Gerota’s fascia is done.
Gerota’s fascia is incised longitudinally just posterior to the peritoneal reflection;
superiorly from the indentation that is the meeting point of peritoneal reflection and
psoas muscle to the iliac fossa inferiorly. Dissection is carried out in the avascular
plane between perirenal fat capsule and anterior layer of prerenal fascia. The dissec-
tion is then done medially to reach the anterior surface of adrenal gland and identi-
fication of the vascular structures.
In creating the retroperitoneal space, the important aspect is orientation of the
vascular structures—IVC on the right side and the renal vein on the left. For the
right side the adrenal vein is usually located postero-laterally to the vena-cava and
for the left side, the left adrenal vein is usually located on the upper surface of the
renal vein. If the surgery is being done for pheochromocytoma, it is essential that
the adrenal gland is retracted with blunt instruments and not grasped to prevent
inadvertent tumor rupture [6, 7]. Also, it is necessary to identify the adrenal vein
first to secure and clip the vein. On the right side the adrenal vein drains into the
IVC, so identification of vena cava is essential whereas on the left dissection of
renal hilum is to be done first as left adrenal vein drains into the left renal vein. One
needs to be cautious about the variant anatomy of right adrenal vein.
In this approach it is better to use blunt dissectors because of proximity of vascu-
lar structures especially on the right because troublesome bleeding will make the
surgery difficult and may need conversion to open. Care should be taken to avoid
inadvertently touching the IVC with heated vessel sealing devices. Another risk on
the left side is the close proximity of tail of pancreas on the ventral aspect and care-
ful blunt dissection should be done to avoid injury. The lateral approach is better in
the way that no position change will be required if need for open conversion arises.
The inferior and medial aspects of the gland are then dissected and the adrenal
arteries are identified and clipped. Use of hemoclips is preferred for adrenal artery
454 S. Rege
and vein. On the left side the branches of phrenic vein need to be tackled and
clipped. The superior aspect of the gland is dissected followed by lateral aspects
which is poorly vascularised. The specimen is retrieved through the camera port in
an endobag. The fascia of the ports greater than 10 mm are closed followed by skin
closure. Drains are usually not required.
The posterior approach seems to have greater incidence of intraoperative risks than
those with a lateral approach owing to following reasons
I. A particular drawback seen in the lateral approach is that bilateral tumours are
difficult to operate owing to position change requirement for each side.
II. The inferior vena cava on the right side and the aorta on the left side lie deeper
to the adrenal and the kidney, hence very careful dissection has to be done in the
lateral approach as the weight of the tumor presses on to space between these
vital structures, with minimal space left for retraction and managing the
vasculature.
III. Higher learning curve compared to the posterior approach.
Size of the tumour was initially a limiting factor for the lateral approach. But
with improvement of laparoscopic instruments and better understanding of anat-
omy, size is no longer a limiting factor of lateral retroperitoneal approach versus
transperitoneal approach [7]. Tables 3 and 4 summarizes the quoted advantages and
disadvantages of minimally invasive retroperitoneal approaches for adrenalectomy.
Reasons for Conversion
The relative reasons for conversion quoted in literature are surgeons’ inexperience,
bleeding, failure to progress, failure to maintain a working space due to
pneumoperitoneum.
Minor complication rates vary from 0 to 15% for unilateral while increase to 23%
for bilateral surgeries and no significant difference is observed in laparoscopic intra-
peritoneal and retroperitoneal approaches [11]. Splenic, liver and peritoneal injuries
have been documented along with relaxation of abdominal wall especially for pos-
terior approach. Injury to subcostal nerve leading to pain has also been documented
with posterior approach [12] (Table 5).
increased operative time in the lateral approach [14]. They mentioned the lateral
approach to have all the other advantages of the posterior approach, over transperi-
toneal approach [4].
The retroperitoneal procedures have a steep learning curve, require a thorough
knowledge of retroperitoneal anatomy and should be initially attempted for tumours
less than 6 cm and non-functional or benign cases in patients with normal BMI [10,
15, 16].
Recently there have been studies on the use of ICG (Indocyanine Green) dye for
delineating the vascular anatomy in laparoscopic transperitoneal and retroperitoneal
adrenal surgeries. ICG is a nontoxic dye that can aid in the identification of vascular
structures and parenchymal tissue planes in real time. It requires a special camera
and monitor system compatible with the fluorescence imaging. The green intraop-
erative fluorescence helps to delineate the margins of resection and guide towards a
more precise operation. The role of ICG is especially important in lateral approach
owing to close proximity of vascular structures at the start of the dissection. ICG
should be given IV (intravenous) after a test dose just after the insertion of ports.
Conclusion
Minimal access surgery for adrenal has many benefits and the posterior retro-
peritoneal approach among them though initially technical difficult can be used
simultaneous for bilateral cases. Retroperitoneal space is small hence needs immac-
ulate dissection of tissue but it hardly causes systemic problem.
Retroperitoneoscopic Minimally Invasive Adrenalectomy 457
Editor’s Note1
Adrenalectomy
Approach
Adrenalectomy may be performed by minimally invasive or open approach. Both
open and minimally invasive surgery can be performed by transperitoneal or retro-
peritoneal approach. Minimally invasive approach maybe: laparoscopic transab-
dominal, laparoscopic retroperitoneal or laparoscopic robot assisted. Further they
may be multiport or uniport technique. Retroperitoneal approaches can be lateral or
posterior whereas the transabdominal approach is usually a lateral approach with
rare reports of an anterior transmesocolic transabdominal approach.
References: Main chapter references are included after the “References Editor’s Note” section.
1
Retroperitoneoscopic Minimally Invasive Adrenalectomy 459
MI and Retroperitoneal Adrenalectomy
B
BMI and increased retroperitoneal fat mass has been shown to be associated with
adverse outcomes related to operative time and complications in retroperitoneal
adrenalectomy [15,16]. Periadrenal fat volume rather than BMI is associated with
460 S. Rege
of the perirenal fat and third plane on the parenchymal surface of the upper renal
pole. In the single plane adrenalectomy the authors approach the anterior aspect of
the adrenal first and dissect between the upper pole of the kidney and capsule of
adrenal gland [31].
References
1. Alesina PF. Retroperitoneal adrenalectomy- learning curve, practical tips and tricks, what lim-
its its wider uptake. Gland Surgery. 2019;8:36–40.
2. Gaur DD. Laparoscopic operative retroperitoneoscopy: use of a new device. J Urol.
1992;148:1137–9.
3. Brunt LM, Molmenti EP, Kerbl K, et al. Retroperitoneal endoscopic adrenalectomy: an experi-
mental study. Surg Laparosc Endosc. 1993;3:300–6.
4. Mercan S, Seven R, Ozarmagan S. Endoscopic retroperitoneal adrenalectomy. Surgery.
1995;118(6):1071–5.
5. Walz MK, Peitgen K, Walz MV, et al. Posterior retroperitoneoscopic adrenalectomy: lessons
learned within five years. World J Surg. 2001;25:728–34.
6. Zhang X, Fu B, Lang B, Zhang J, Xu K, Li HZ, Ma X, Zheng T. Technique of anatomical
retroperitoneoscopic adrenalectomy with report of 800 cases. J Urol. 2007;177(4):1254–7.
7. Zhang X, Fu B, Lang B, et al. Technique of anatomical retroperitoneoscopic adrenalectomy.
Chin J Urol. 2007;28(3):5–8.
8. Chen W, Lin W, Han D-J, Liang Y. Lateral retroperitoneoscopic adrenalectomy for compli-
cated adrenal tumour larger than 5 centimeters. Afri Health Sci. 2017;17(1):293–300.
9. Walz MK, Peitgen K, Hoermann R, et al. Posterior retroperitoneoscopy as a new minimally
invasive approach for adrenalectomy: results of 30 adrenalectomies in 27 patients. World J
Surg. 1996;20:769–74.
10. Vrielink OM, Engelsman AF, Hemmer PHJ, et al. Multicentre study evaluating the surgical
learning curve for posterior retroperitoneoscopic adrenalectomy. Br J Surg. 2018;105:544–51.
11. Alesina PF. Complications of minimally invasive adrenalectomy. Chirurg. 2015;86:29–32.
12. Walz MK, Alesina PF, Wenger FA, Deligiannis A, Szuczik E, Petersenn S, Ommer A, Groeben
H, Peitgen K, Janssen OE, Philipp T, Neumann HPH, Schmid KW, Mann K. Posterior ret-
roperitoneoscopic adrenalectomy—results of 560 procedures in 520 patients. Surgery.
2006;140(6):943–50.
13. Lang B, Fu B, Ouyang JZ, Wang BJ, Zhang GX, Xu K, Zhang J, Wang C, Shi TP, Zhou HX,
Ma X. Zhang X; Retrospective comparison of retroperitoneoscopic versus open adrenalectomy
for pheochromocytoma. J Urol. 2008;179(1):57–60. discussion 60
14. Ju Yong O, Chung HS, Yu SH, et al. Comparison of surgical outcomes between lateral and
posterior approaches for retroperitoneal laparoscopic adrenalectomy: a single surgeon’s expe-
rience. Investig Clin Urol. 2020;61(2):180–7.
15. Zhang X, Lang B, Ouyang JZ, et al. Retroperitoneal adrenalectomy without previous control
of adrenal vein is feasible and safe for pheochromocytoma. Urology. 2007;69:849–53.
16. Zhang X. Anatomical retroperitoneoscopic adrenalectomy: operative technique and our expe-
rience. J Clin Urol. 2007;22(8):561–4.
17. Moore EC, Berber E. Fluoroscence techniques in adrenal surgery. Gland Surg. 2019 Jul;8(Suppl
1):S22–7.
Laparoscopic Donor Nephrectomy
Umesh Sharma and Hemant Goel
Introduction
Annually 735,000 deaths are attributed to chronic kidney disease globally and an
equivalent number is also observed in India [1, 2]. End stage renal disease (ESRD)
is best treated with renal transplantation. According to United Network for Organ
Sharing registry data there are many benefits of living donor renal transplantation
such as (1) shorter waiting period (2) better graft (3) improved patient survival (4)
optimization of medical health of the recipient and (5) an overall reduced cost when
compared long term with cadaveric transplantation [3]. However, organ shortage is
a key limiting factor that mars the success of kidney transplantation.
The first laparoscopic nephrectomy was reported by Clayman et al. [4] in 1990.
Following the demonstration of the feasibility of “Laparoscopic donor nephrec-
tomy” (LDN) in the animal models by Gill and colleagues, Ratner et al. [5] per-
formed the first laparoscopic live donor nephrectomy in 1995. Today most centres
performing “Open donor nephrectomy” (ODN) are slowly adopting minimal access
donor nephrectomy like LDN & “Robotic Assisted Donor Nephrectomy” (RADN).
LDN, overcomes some of the inherent disincentives of open organ donation by
making donor nephrectomy less painful, shortening the convalescence period, and
improving the cosmetic outcome thereby exhibiting the potential to increase the
number of living kidney donations. In this chapter we describe different surgical
techniques related to LDN (Table 1).
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 469
D. Sharma, P. Hazrah (eds.), Recent Concepts in Minimal Access Surgery,
https://doi.org/10.1007/978-981-16-5473-2_21
470 U. Sharma and H. Goel
Various strategies have been adopted to increase the number of living donors and
organ donation:
Surgical Techniques
Position & Port site The operation is commenced with the donor positioned in a
left lateral decubitus position and the operation table flexed (Fig. 1). A 12 mm cam-
era trocar, is inserted two fingerbreadths above and lateral to umbilicus and if the
donor is obese then it can be placed even more laterally at lateral border of rectus.
Pneumoperitoneum is created to maintain an intraabdominal pressure of 12 mmHg
Laparoscopic Donor Nephrectomy 471
so as not to compromise renal perfusion. Additional ports of 12 mm and 5 mm are
inserted under vision at midway between spino-umbilical line and in left subcostal
region in the mid clavicular line. Another 5mm port is inserted in left anterior axil-
lary line for retraction (Fig. 1).
Peri-Renal and Hilar Dissection Lumbar veins, sometimes multiple, are seen
inferior and posterior to renal vein. The adrenal vein is found medially and superior
to renal vein. The adrenal and lumbar veins are clipped and divided (Fig. 3). The
gonadal vein is left attached to renal vein for vascular reconstruction if required
later; additionally, it is hypothesized to help in preserving vascularity to upper ureter
though the issue is controversial as orchialgia is a perceived complication of the
manoeuvre. Thereafter the renal vein is identified, dissected, and hooked to expose
the renal artery which is traced till its origin (Fig. 4). After dividing the adrenal vein,
an upper window is created between the adrenal gland and the kidney. The ureter is
dissected down to the point of its crossing of iliac vessels, wherein it is clipped and
divided, one should be careful not to damage the nerves running on the psoas mus-
cle particularly the genitofemoral nerve in the process.
a b
Fig. 5 (a) Clipping of left renal artery; (b) Clipping of left renal vein
Extraction of the Kidney The kidney can be removed with an Endo-Catch bag or
manually, either through a 5-cm periumbilical incision, or alternatively through a
Pfannenstiel incision or muscle-splitting Gibson incision which is prepared in
advance before the division of renal hilum (Fig. 6). In the manual extraction tech-
nique, the perirenal fat lateral to the kidney is held with two fingers inserted into the
abdominal cavity through the small incision, and the graft gently extracted. The
retrieved kidney is immediately flushed with preservation fluid and stored on ice.
The main advantage of the manual extraction technique as compared with
laparoscopic bag technique is that it exhibits a shorter warm ischemia time, without
any significant increase in donor morbidity, also the additional costs of the endobag
is mitigated.
Drawbacks of LDN
The most important drawback of LDN is that it exhibits a steep learning curve. The
transperitoneal approach makes it vulnerable to the associated complications of
bowel injury from trocar insertion or instrumentation and intestinal adhesions.
Shorter operative time, warm ischaemia time and greater vessel lengths are the rela-
tive advantages of open procedure [6]. Other complications reported in laparoscopic
474 U. Sharma and H. Goel
LDN vs ODN
Hand-Assisted LDN
trial of laparoscopic donor nephrectomy with and without hand assistance observed
similar outcome, complications and quality of life in both the groups [16].
The right renal vein being shorter and the constraints of space due to the liver over-
lying the right kidney, it is always a technical challenge to laparoscopically harvest
the right kidney for transplant. After transplant, as the right renal artery is long, it
can get kinked while the right vein which is short (particularly in laparoscopic
approach where an additional 1 cm length of the vessel is lost due to stapling),
makes it more prone to compression by the kidney leading to higher incidence of
venous thrombosis in in right kidney grafts making surgeons prefer the left for
LDN. However, the important principle of leaving the better kidney with the donor
needs to be adhered to and experts working particularly in high volume institutions,
take up RLDN in spite of the difficulties [17]. Contrarily it has been reported that
the right kidney is easy to extract and decreases risk of splenic injury [13].
Due to the inherent anatomical challenges discussed earlier, the right kidney is used
only in approximately 20% cases. To circumvent the drawbacks various modifica-
tions advocated in transperitoneal approach of laparoscopic right donor nephrec-
tomy include 1) dissection of the inter aortocaval space to allow division of the renal
artery at its origin from the aorta, 2). Control of renal vein at its junction with the
vena cava to ensure a maximal possible length 3) inclusion of a cuff of vena cava,
using a laparoscopic vascular clamp which is thereafter repaired by intracorporeal
suturing 4) use of recipient saphenous vein graft supplement to reconstruct the renal
vein in case harvested renal vein is very short. On the right side there is no need to
control the lumbar, gonadal and adrenal vein as they do not drain into the renal vein.
The advantage of ERDN is that the peritoneal cavity is not breached. ERDN can be
performed with and without hand assistance. The procedure is performed with the
donor in full lateral position. Initially a retroperitoneal workspace is created by
blunt dissection using a balloon or the operator’s hand which is further maintained
at a pressure of 12mm by insufflation of carbon dioxide (CO2). Further dissection
and mobilization of the kidney, ureter and vascular pedicles are performed on prin-
ciples as described for LDN. In limited studies it has been observed that hand
assisted retroperitoneoscopic nephrectomy yields similar intraoperative and postop-
erative outcome both for donors and recipients as compared to laparoscopic
approach [18–20].
port is necessary for liver retraction. The operative steps mirror the laparoscopic
approach described earlier. Though robotic donor nephrectomy is feasible, it does
not appear to have overt advantages over other minimally invasive techniques and
has added costs [24, 25]. There are anecdotal reports of robotic donor nephrectomy
being performed through trans vaginal route (hybrid NOTES) [26].
Complications
Conclusion
A variety of techniques both open and laparoscopic have been described for living
donor nephrectomy. Minimally invasive techniques due to its association with
decreased morbidity and improved recovery time should be viewed as the preferred
approach for majority of these patients. The key principle of donor safety is para-
mount in making final decisions regarding donation techniques. Also different cen-
tres and surgeons may have varied approaches that result in good and safe outcomes.
Thus, the experience of the surgeon in a particular approach becomes an important
consideration in determining the best approach for each patient.
Editor’s Note1
Live donor nephrectomy has evolved with time from conventional open approaches
to the newer minimally invasive techniques. The initial scepticism of laparoscopic
donor nephrectomy has waned with emerging studies which vouched for its safety
and efficacy as equivalent to open donor nephrectomy. In a recently published meta-
analysis on longterm outcome of laparoscopic versus open donor nephrectomy, the
authors observed, similar 1-year outcomes as compared with open technique with
respect to serum creatinine levels, proteinuria, donation attitude, donor health-
related quality of life and recipient graft survival between the groups [1]. Since
laparoscopic procedures have longer operative times as compared to conventional
open procedures a longer ischaemia time has been noted in laparoscopic donor
nephrectomy which however does not translate into a worse outcome and given the
attractive attributes of less pain shorter hospital stay and better cosmesis it has
gained an overall modest acceptability [2]. Many variations in technique have been
investigated such as use of retroperitoneal versus transperitoneal approach, use of
hand assisted versus total laparoscopic approach, laparoscopic single site technique
as compared to multiport laparoscopic approach, right versus left laparoscopic
donor nephrectomy and recently robotic versus laparoscopic approach. Most stud-
ies show some differences in the short-term end points viz: warm ischaemia time,
operative time blood loss, conversion, postoperative pain/ analgesic requirement
complication and hospital stay in published systematic reviews/metanalysis. Overall
the retroperitoneal approach appeared to have lesser complications than transperito-
neal laparoscopic approach and warm ischaemia time as well as mean operative
time was observed to be less in hand assisted technique as compared to total laparo-
scopic approach. The laparoscopic single site donor nephrectomy appears to be
technically more challenging as evidenced by higher conversion rates and operative
time. Pertinent long term outcome like graft survival and function appears to be
largely independent of these technical modifications (Table EN1) [3–12].
Recently an attempt has been made to classify difficulty of laparoscopic donor
nephrectomy and the following variables were noted to significantly influence dif-
ficulty: gender, BMI, technique (hand assisted versus pure), presence of multiple
renal arteries and veins. Interestingly age and side of operation (left versus right)
was not found to be significant [13].
Other variations reported in literature are in modes of pedicle ligature viz the
vessel sealing devices for renal pedicle for example use of clips versus staplers for
vascular control [12], single stapler technique for pedicle control [14] and routes of
extraction of specimen through extended port site compared to delivering through
Pfannensteilor periumbilical incision (Table EN1) [11].
References: Main chapter references are included after the “References Editor’s Note” section.
1
480 U. Sharma and H. Goel
Table EN1 (continued)
Study, first author name, year Results
Determining the Superior Technique for Retro-peritoneoscopic approach had the
Living-donor Nephrectomy: the Laparoscopic following advantages as compared to
Intraperitoneal Versus the Retroperitoneoscopic laparoscopic transperitoneal group:
Approach.He B, 2016 [7] • lower blood transfusion
• less delayed graft functions
• less vessel injuries
• less conversion to open surgical
procedure
A comparison of technique modifications in • Retroperitoneoscopic group had less
laparoscopic donor nephrectomy: a systematic complications
review and meta-analysis. • Hand-assisted techniques had shorter
Özdemir-van Brunschot DM, 2015 [8] first warm ischemia and operation times
Laparoendoscopic single-site (LESS) vs Laparoscopic live donor nephrectomy had
laparoscopic living-donor nephrectomy: a the following benefits over LESS LDN:
systematic review and meta-analysis.Autorino R, • shorter operative time P = 0.003
2015 [9] • less likelihood for conversion
No significant difference was observed in:
• warm ischaemia time
• estimated blood loss
• hospital stay
• visual analogue pain score at discharge
• postoperative complication
• postoperative renal function of recepient
analgesic requirement was lower for LESS
LDN (P = 0.04)
Should hand-assisted retroperitoneoscopic Hand assisted retroperitoneoscopic
nephrectomy replace the standard laparoscopic nephrectomy HARP was superior to Total
technique for living donor nephrectomy? A Laparoscopic Nephrectomy with respect to:
meta-analysis. • shorter operative duration
Elmaraezy A, 2017 [10] • shorter warm ischemia time
No significant difference with respect to:
• blood loss
• hospital stay
• graft survival
• intraoperative complications
Laparoscopic nephrectomy - Pfannenstiel or Pfannensteil extraction site had benefits
expanded port site specimen extraction: a of:
systematic review and meta-analysis. • Less in patient stay (p = 0.03)
Amer T, 2015 [11] • Lower blood loss (p = 0.03)
Staplers or clips? A systematic review and Hem-o-Lok clips versus staplers
meta-analysis of vessel controlling devices Disadvantages of Hem-o-Lok clips:
for renal pedicle ligation in laparoscopic live • greater blood loss
donor nephrectomy.Liu Y, 2018 [12] • longer warm ischemia time (WIT)
Advantages of Hem-o-Lok clips:
Longer vascular graft length in clip group
longer as compared to stapler group.
Lower Cost
No difference in outcome as regards:
• device failure rate
• death rate
• severe hemorrhage rate.
482 U. Sharma and H. Goel
References
1. Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. Global and regional
mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analy-
sis for the Global Burden of Disease Study 2010. Lancet 2012 Dec 15;380(9859):2095–128.
https://doi.org/10.1016/S0140-6736(12)61728-0.
2. Modi G, Jha V. Incidence of ESRD in India. Kidney Int. 2011 Mar;79(5):573. https://doi.
org/10.1038/ki.2010.477. PMID: 21321559.
3. US Renal Data System (USRDS): 1994 Annual Data Report. The National Institute of Health,
National Institute of Diabetes and Diabetes and Kidney Disease, Betheseda, MD. June 1994.
4. Clayman RV, Kavoussi LR, Soper NJ, Dierks SM, Merety KS, Darcy MD, Long SR, Roemer
FD, Pingleton ED, Thomson PG. Laparoscopic nephrectomy. N Engl J Med. 1991 May
9;324(19):1370–1. https://doi.org/10.1056/NEJM199105093241917. PMID: 1826761
5. Ratner LE, Ciseck LJ, Moore RG, Cigarroa FG, Kaufman HS, Kavoussi LR. Laparoscopic live
donor nephrectomy. Transplantation. 1995 Nov 15;60(9):1047–9. PMID: 7491680.
6. Øyen O, Andersen M, Mathisen L, Kvarstein G, Edwin B, Line PD, Scholz T, Pfeffer
PF. Laparoscopic versus open living-donor nephrectomy: experiences from a prospec-
tive, randomized, single-center study focusing on donor safety. Transplantation. 2005 May
15;79(9):1236–40. https://doi.org/10.1097/01.tp.0000161669.49416.ba. PMID: 15880077.
7. Leventhal JR, Kocak B, Salvalaggio PR, Koffron AJ, Baker TB, Kaufman DB, Fryer JP,
Abecassis MM, Stuart FP. Laparoscopic donor nephrectomy 1997 to 2003: lessons learned with
500 cases at a single institution. Surgery. 2004 Oct;136(4):881–90. https://doi.org/10.1016/j.
surg.2004.06.025. PMID: 15467675.
8. Nanidis TG, Antcliffe D, Kokkinos C, Borysiewicz CA, Darzi AW, Tekkis PP, Papalois
VE. Laparoscopic versus open live donor nephrectomy in renal transplantation: a meta-
analysis. Ann Surg. 2008 Jan;247(1):58–70. https://doi.org/10.1097/SLA.0b013e318153fd13.
9. Antcliffe D, Nanidis TG, Darzi AW, Tekkis PP, Papalois VE. A meta-analysis of mini-
open versus standard open and laparoscopic living donor nephrectomy. Transpl Int. 2009
Apr;22(4):463–74. https://doi.org/10.1111/j.1432-2277.2008.00828.x. Epub 2009 Jan 20.
PMID: 19175543.
10. Lewis GR, Brook NR, Waller JR, Bains JC, Veitch PS, Nicholson ML. A comparison of tra-
ditional open, minimal-incision donor nephrectomy and laparoscopic donor nephrectomy.
Transpl Int. 2004 Nov;17(10):589–95. https://doi.org/10.1007/s00147-004-0770-z. Epub 2004
Oct 29. PMID: 15517169.
11. Maartense S, Idu M, Bemelman FJ, Balm R, Surachno S, Bemelman WA. Hand-assisted lapa-
roscopic live donor nephrectomy. Br J Surg. 2004 Mar;91(3):344–8. https://doi.org/10.1002/
bjs.4432. PMID: 14991637.
12. Minnee RC, Idu MM. Laparoscopic donor nephrectomy. Neth J Med. 2010 May;68(5):199–206.
PMID: 20508268.
13. Hoda MR, Greco F, Reichelt O, Heynemann H, Fornara P. Right-sided transperitoneal hand-
assisted laparoscopic donor nephrectomy: is there an issue with the renal vessels? J Endourol.
2010 Dec;24(12):1947–52. https://doi.org/10.1089/end.2010.0116. Epub 2010 Oct 7. PMID:
20929411.
14. El-Galley R, Hood N, Young CJ, Deierhoi M, Urban DA. Donor nephrectomy: A compari-
son of techniques and results of open, hand assisted and full laparoscopic nephrectomy. J
Urol. 2004 Jan;171(1):40–3. https://doi.org/10.1097/01.ju.0000100149.76079.89. PMID:
14665839.
15. Wolf JS Jr, Merion RM, Leichtman AB, Campbell DA Jr, Magee JC, Punch JD, Turcotte
JG, Konnak JW. Randomized controlled trial of hand-assisted laparoscopic versus open
surgical live donor nephrectomy. Transplantation. 2001 Jul 27;72(2):284–90. https://doi.
org/10.1097/00007890-200107270-00021. PMID: 11477354.
16. Bargman V, Sundaram CP, Bernie J, Goggins W. Randomized trial of laparoscopic donor
nephrectomy with and without hand assistance. J Endourol. 2006 Oct;20(10):717–22. https://
doi.org/10.1089/end.2006.20.717. PMID: 17094745.
Laparoscopic Donor Nephrectomy 485
17. Tsoulfas G, Agorastou P, Ko D, Hertl M, Elias N, Cosimi AB, Kawai T. Laparoscopic living
donor nephrectomy: is there a difference between using a left or a right kidney? Transplant
Proc. 2012 Nov;44(9):2706–8. https://doi.org/10.1016/j.transproceed.2012.09.019. PMID:
23146499.
18. Gjertsen H, Sandberg AK, Wadström J, Tydén G, Ericzon BG. Introduction of hand-assisted
retroperitoneoscopic living donor nephrectomy at Karolinska University Hospital Huddinge.
Transplant Proc. 2006 Oct;38(8):2644–5. https://doi.org/10.1016/j.transproceed.2006.07.042.
PMID: 17098026.
19. Sundqvist P, Feuk U, Häggman M, Persson AE, Stridsberg M, Wadström J. Hand-assisted
retroperitoneoscopic live donor nephrectomy in comparison to open and laparoscopic proce-
dures: a prospective study on donor morbidity and kidney function. Transplantation. 2004 Jul
15;78(1):147–53. https://doi.org/10.1097/01.tp.0000133280.74695.34. PMID: 15257054.
20. Wadström J, Lindström P, Engström BM. Hand-assisted retroperitoneoscopic living donor
nephrectomy superior to laparoscopic nephrectomy. Transplant Proc. 2003 Mar;35(2):782–3.
https://doi.org/10.1016/s0041-1345(03)00041-1. PMID: 12644134.
21. Lewandowski PM, Leslie S, Gill I, Desai MM. Laparo-endoscopic single-site donor nephrec-
tomy: techniques and outcomes. Arch Esp Urol. 2012 Apr;65(3):318–28. PMID: 22495272.
22. Kim JM, Jeong WJ, Choi BJ, Yuk SM, Hwang JK, Lee SC. Transumbilical pure single-port
laparoscopic donor nephrectomy. Ann Surg Treat Res. 2015 Nov;89(5):278–83. https://doi.
org/10.4174/astr.2015.89.5.278. Epub 2015 Oct 28. PMID: 26576409; PMCID: PMC4644910.
23. Gill IS, Canes D, Aron M, Haber GP, Goldfarb DA, Flechner S, Desai MR, Kaouk JH,
Desai MM. Single port transumbilical (E-NOTES) donor nephrectomy. J Urol. 2008
Aug;180(2):637–41; discussion 641. https://doi.org/10.1016/j.juro.2008.04.028. Epub 2008
Jun 12. PMID: 18554653.
24. Shin TY, Lee YS. Robot-assisted laparoscopic donor nephrectomy: surgical feasibility and
technique. Heliyon. 2019 Aug 5;5(8):e02204. https://doi.org/10.1016/j.heliyon.2019.e02204.
PMID: 31428713; PMCID: PMC6695282.
25. Serni S, Pecoraro A, Sessa F, Gemma L, Greco I, Barzaghi P, Grosso AA, Corti F, Mormile N,
Spatafora P, Caroassai S, Berni A, Gacci M, Giancane S, Tuccio A, Sebastianelli A, Li Marzi
V, Vignolini G, Campi R. Robot-Assisted Laparoscopic Living Donor Nephrectomy: The
University of Florence Technique. Front Surg. 2021 Jan 15;7:588215. https://doi.org/10.3389/
fsurg.2020.588215. PMID: 33521044; PMCID: PMC7844329
26. Kaouk JH, Khalifeh A, Laydner H, Autorino R, Hillyer SP, Panumatrassamee K, Modlin C,
Goldman HB. Transvaginal hybrid natural orifice transluminal surgery robotic donor nephrec-
tomy: first clinical application. Urology. 2012 Dec;80(6):1171–5. https://doi.org/10.1016/j.
urology.2012.08.061. PMID: 23206759.
27. Breda A, Veale J, Liao J, Schulam PG. Complications of laparoscopic living donor nephrec-
tomy and their management: the UCLA experience. Urology. 2007 Jan;69(1):49–52. https://
doi.org/10.1016/j.urology.2006.09.030. PMID: 17270612.
28. Ramdhani K, Malessy MJA, Simon MJG, Huurman VAL. Nerve Surgery to Treat Intractable
Genitofemoral Neuropathic Pain following Laparoscopic Live Kidney Donation. Case
Rep Transplant. 2018 Jun 6;2018:9326975. https://doi.org/10.1155/2018/9326975. PMID:
29977640; PMCID: PMC6011110.