Outcomes of Percutaneous Endoscopic Gastrostomy in Children

You might also like

Download as pdf or txt
Download as pdf or txt
You are on page 1of 7

Curr Gastroenterol Rep (2011) 13:293–299

DOI 10.1007/s11894-011-0189-5

Outcomes of Percutaneous Endoscopic Gastrostomy


in Children
John E. Fortunato & Carmen Cuffari

Published online: 17 March 2011


# Springer Science+Business Media, LLC 2011

Abstract Percutaneous endoscopic gastrostomy (PEG) is a Introduction


relatively safe and minimally invasive surgical method for
providing enteral access in children. In pediatrics, the The enteral route remains the most practical means of
indications for PEG placement frequently include malnutri- providing nutrition in patients with a functional gastro-
tion or failure to thrive, as well as oropharyngeal dysphagia, intestinal tract but an inability to take food orally.
especially in children with neurological impairment (NI). The Although enteral nutrition can be accomplished simply
risk for postoperative complications is low. However, among by means of either a nasogastric or nasojejunal tube,
children with NI, gastroesophageal reflux disease (GERD) these conduits are fraught with an increased risk of
may necessitate fundoplication prior to gastrostomy tube aspiration, displacement, and mechanical failure [1]. In
placement. Preoperative pH probe testing has not been shown comparison, percutaneous endoscopic gastrostomy (PEG)
to be an effective screening tool prior to PEG placement provides enteral access that is much more conducive to
among patients with GERD. Laparoscopic gastrostomy tube long-term (>3 months) use. Although PEG requires
insertion was introduced in pediatric patients in an attempt to surgical placement, the procedure is often performed by
decrease complications associated with PEG. Although out- the pediatric gastroenterologist, and is considered less
comes were reported to be similar to or better than PEG invasive than traditional surgical gastrostomy. Further-
alone, future comparative studies are needed to better define more, the complication rate with PEG is lower (4–13.6%)
the optimal patient demographic for this technique. than with Stamm gastrostomy (24%) [2–5].
PEG was introduced in 1980, and has become an
Keywords Percutaneous endoscopic gastrostomy . effective method to establish gastrostomy tube feeds [6].
Children . Outcomes It is estimated that 11,000 PEGs are performed annually in
US children [7, 8•]. Historically, most of the early patients
C. Cuffari in whom PEG was performed were children with an
Department of Pediatrics, Division of Pediatric Gastroenterology inability to swallow. Over time, the indications have
and Nutrition, The Johns Hopkins University School of Medicine, broadened to include patients with oropharyngeal anatomic
Baltimore, MD, USA
abnormalities, as well as malnutrition and feeding problems
J. E. Fortunato related to conditions such as metabolic disorders, cystic
Department of Pediatrics, fibrosis, cardiac disease, malignancy, or neurological
Division of Pediatric Gastroenterology and Nutrition, impairment (NI) [8•]. The distribution of principal diagno-
The Wake Forest University School of Medicine,
Winston-Salem, NC, USA
ses and indications for PEG placement observed over
11 years at the Johns Hopkins Children’s Center are shown
J. E. Fortunato (*) in Table 1 [8•]. Although most studies have shown that
Department of Pediatrics, Division of Pediatric Gastroenterology PEG can be performed safely in the pediatric patient
and Nutrition, Wake Forest University School of Medicine,
Medical Center Boulevard,
population, the existence of concurrent pathological gastro-
Winston-Salem, NC 27157, USA esophageal reflux (GER), especially among children with
e-mail: jfortuna@wfubmc.edu NI, has warranted special consideration.
294 Curr Gastroenterol Rep (2011) 13:293–299

Table 1 Principal diagnoses for


pediatric patients undergoing Diagnosis No. of patients (% of all diagnoses)
percutaneous endoscopic gas-
trostomy at the Johns Hopkins Neurologic impairment 322 (35%)
Children’s Center from 1994 Diagnosis not defined 202 (22%)
to 2005 Chronic lung disease 152 (16%)
Metabolic/genetic syndrome 96 (10%)
Cardiac anomalies 61 (7%)
Cystic fibrosis 35 (4%)
Malignancy 30 (3%)
Oropharyngeal anatomic malformation 15 (2%)
Superior mesenteric artery syndrome 6 (<1%)
Chronic vomiting 4 (<1%)
(Adapted from Fortunato et al. Muscular dystrophy 3 (<1%)
[8].)

The objective of this review is to examine the global comparing cost-effectiveness, indications for gastrostomy
experience in performing PEGs in the pediatric patient placement, or morbidity [16]. A preoperative diagnosis of
population. The difference in outcomes between surgical dysphagia may lengthen hospital stay in patients undergo-
gastrostomy and PEG also is discussed. This review ing PEG [8•].
addresses the influence of GERD, both preoperatively and About the same time PEG was first performed, another
postoperatively, on clinical outcome, and the need for method of placing a feeding gastrostomy, known as
preoperative diagnostic testing, especially among the percutaneous nonendoscopic or radiological gastrostomy,
neurologically impaired. Lastly, special consideration is was introduced [17]. Radiological gastrostomy has similar
given to the technical limitations associated with benefits to PEG, including ease of insertion and low major
performing PEGs in infants with significant prematurity complication rates, with the advantage of introducing an
[2–4, 9, 10]. uncontaminated catheter through the abdominal wall. In
contrast, radiologically placed tubes were observed to
exhibit higher clogging rates and overall inferior tube
Outcomes of Open Surgical, Percutaneous Radiologic, function rates after replacement [15]. In children, major
Laparoscopic, and PEG complications were uncommon in patients undergoing
either radiologic gastrostomy or PEG, but they were more
Until the early 1980s, surgically placed feeding tubes were frequent in the radiological group [18•]. Minor complica-
the only feasible means for feeding patients who could not tions were also significantly higher for radiologically
maintain adequate oral intake. Since that time, less invasive placed gastrostomies.
methods—including laparoscopically placed gastrostomy, The increasing use of laparoscopy to perform surgical
percutaneous radiologic gastrostomy, and PEG—have been techniques in a less invasive manner has introduced an
successfully introduced as alternatives. The best technique alternative for performing gastrostomy without the need for
in children remains uncertain. laparotomy. When conditions such as obstruction of the
Compared with PEG, surgical gastrostomy is generally upper gastrointestinal tract, prior abdominal surgery, or
associated with higher morbidity and mortality in most anatomic conditions (eg, hepatomegaly) exist, PEG may
adult series [11, 12]. However, some studies do not confirm not be a feasible option. Although most adult series agree
these results, demonstrating comparable complication rates that laparoscopic gastrostomy placement is a good choice
[13]. PEG is faster to perform in most cases, requiring for patients who are not candidates for PEG, PEG remains
fewer medical resources, decreased hospitalization time, the initial procedure of choice for placement of a gastro-
and less delay in starting feeds postoperatively [14]. When stomy [14, 19, 20]. For example, Bankhead et al. [14],
separated into minor versus major complications, open when comparing laparoscopic gastrostomy to PEG and
gastrostomy placement appears to be associated mainly open gastrostomy, showed that laparoscopic gastrostomy
with minor complications (eg, tube leaks and wound had the highest morbidity of the three techniques.
infections), which are less frequent with PEG (43–33%, In pediatric patients, the laparoscopic technique of
respectively), in one series [15]. Major complications were gastrostomy tube insertion was used in an attempt to
similar (14–17%, respectively) between open gastrostomy decrease complications associated with PEG. Laparoscopic
and PEG. In children, no significant difference was gastrostomy has the advantages of direct visualization of
observed between open gastrostomy and PEG when the tube’s placement into the stomach and of the stomach’s
Curr Gastroenterol Rep (2011) 13:293–299 295

having been secured to the abdominal wall with sutures in their child’s health and quality of life after the tube was
the event of tube dislodgment [21]. Outcomes were placed [32]. However, a follow-up study the following year
reported to be similar to that of PEG insertion, with the examined the relatively low energy expenditure and high
exception of an increased rate of hollow organ injury in the body fat content of children with severe cerebral palsy,
PEG group in one study (3% vs 0%) [22]. In another report, highlighting the potential risk of overfeeding these children
PEG operative time was shorter than the laparoscopic [33]. This finding underscores the critical need for specific
approach, with similar intraoperative complication rates, dietary recommendations when considering gastrostomy in
but was associated with more serious postoperative com- NI patients, and the need for future studies to determine the
plications necessitating a higher rate of return to the most optimal preoperative and postoperative nutritional
operating room for complications (19.4% for PEG vs assessment.
8.7% for laparoscopic gastrostomy) [23•]. These complica-
tions included significant stomal problems, intraperitoneal
leak after tube exchange, early tube dislodgement, gastric Gastroesophageal Reflux Disease
separation, late gastrocolonic fistula, gastrocutaneous fistu-
la, colonic perforation, and pneumoperitoneum. The find- The risk of GERD after PEG has been the subject of many
ings in these retrospective studies underscore the need for trials and remains controversial. Although a study by
well-designed, randomized trials comparing PEG to lapa- Grunow et al. [34] suggested an increased incidence of
roscopic gastrostomy in pediatric patients matched not only GER after PEG in 6 of 10 patients, based on esophageal pH
for age and sex, but also for weight and underlying disease. monitoring before and after PEG, only one required
fundoplication. Subsequent larger trials have had different
conclusions. A prospective study in 68 patients showed that
Neurological Disorders pH monitoring after PEG did not differ significantly from
results before PEG, with the exception of PEG tubes placed
Neurological impairment is the most common indication for in the antrum [35]. The study further described poor
PEG in children and adults, because these patients are at correlation between clinical signs of GER and pH moni-
higher risk of becoming chronically malnourished [24, 25]. toring findings. These results are consistent with other
This situation is likely attributable to decreased oral intake, reports suggesting that PEG does not appear to precipitate
possibly from lack of oropharyngeal coordination or GERD [36, 37]. Interestingly, recent data have also raised a
dysphagia. PEG is a feasible option, particularly in the concern regarding the association between a preoperative
setting of a multidisciplinary clinic, and was shown to history of dysphagia or aspiration on modified barium
significantly reduce feeding time, choking events, and swallow study and GERD, with 10.6% and 11.2%,
incidence of pulmonary infections in these patients [26, respectively, of these patients requiring fundoplication after
27]. In several series, mortality and major complications, PEG [8•].
such as tract dehiscence, gastrocolonic fistula, volvulus, Patients with preexisting GERD or abnormal esophageal
peritonitis, or gastrointestinal bleeding, are rare after PEG pH study may require special attention, because these
in children with NI [8•, 9, 28, 29]. Most minor complica- patients may have a less favorable outcome from exacer-
tions are related to gastrostomy wound infections, granulo- bation of their symptoms after PEG [9, 38]. Sulaeman et al.
mas, or leakage from the tube [27]. Although major [9] showed that among 22 patients with normal preopera-
complications do not seem to differ between NI and non- tive 24-hour pH monitoring, only one later required Nissen
NI children, those with NI may have a higher incidence of fundoplication, compared to 7 of 24 with abnormal pH
long-term wound infections [8•]. In NI patients, PEG was before PEG. In contrast, in a series of 28 patients with an
also shown to have favorable outcomes in comparison to abnormal pregastrostomy pH study, the majority of subjects
Stamm gastrostomy, with decreased 30-day and 1-year with symptomatic GERD (19 of 25 patients) improved after
mortality, need for reoperation for bleeding, and incidence PEG alone, which raises questions about the need for
of fundoplication [30]. preoperative pH testing and the need for concomitant
Enteral feeding via PEG is an effective means of antireflux surgery [37].
improving growth and nutritional status of children with The patient with NI or cerebral palsy deserves special
severe neurological disabilities. Sullivan et al. [31], in a consideration because of the frequency of performing PEG
longitudinal, prospective, multicenter cohort study, demon- in these children. Increased GER is commonly seen in
strated significant increases in weight gain in children with patients with NI [39]. The evidence regarding an increase in
cerebral palsy, with median weight z-scores increasing from GER in children with NI after PEG is mixed: the clinical
−3 before PEG to −2.2 at 6 months and −1.6 at 12 months. severity of reflux was shown to increase in some studies,
Nearly all parents also reported a perceived improvement in but not in others [26, 37, 40, 41]. However, there seems to
296 Curr Gastroenterol Rep (2011) 13:293–299

be agreement that concomitant antireflux surgery should series to date, consisting of 747 patients, immediate postop-
not automatically be performed in these patients, and that erative complications were observed in 4% of patients, and
routine investigation for GER in asymptomatic children included wound infection, pneumoperitoneum, skin necrosis,
should be avoided [41]. Further diagnostic assessment and inability to place PEG, and, most seriously, gastric separation
antireflux surgery should be considered if symptoms (Table 2) [8•]. Postoperative complications noted after
progress after PEG [42]. The discrepancies among studies hospital discharge occurred in 20% of patients and were
underscore the need for future studies to determine both the mostly minor, related to wound infection or granuloma
clinical relevance of pH monitoring before PEG as well as formation. Only one major complication, gastrocolonic
the need for antireflux surgery in both neurologically fistula, occurred [8•]. Other series have reported complica-
normal and NI patients. tions such as gastrocolonic fistula, pneumoperitoneum,
duodenal hematoma, necrotizing fasciitis, gastric perforation,
intestinal obstruction, and catheter migration [2, 3]. Only
PEG in Infants two deaths have been reported, both in patients with
advanced cardiac disease from one pediatric series [2].
Few studies have examined PEG placement in infants [43, These data compare favorably to adult series, in which
44]. Previous guidelines have considered the lower limit of complications were observed in 10% to 15% of patients after
body weight for PEG insertion to be about 10 kg [45]. PEG, with severe complications, often requiring surgical
However, infants weighing between 2.3 and 3.5 kg have intervention, occurring in 3.8% to 5.1% [5, 47, 48].
safely tolerated PEG insertion using the standard pull In the study by Fox et al. [3], acute cellulitis at the
technique [44]. With laparoscopic video-assisted technique gastrostomy site was the most frequent complication after
now well established in pediatric patients, some investi- PEG, occurring in 7.3% of patients (compared to a total
gators have suggested its use for gastrostomy tube complication rate of 12.4%). The use of prophylactic
placement in these small, medically complex infants. A antibiotics has been well described, most recently in a
recent series demonstrated that the procedure was well meta-analysis that included 10 randomized, controlled trials
tolerated in infants less than 1 year of age weighing as little with a pooled total of 1,059 patients [49]. The study
as 2.6 kg, with no reported complications [46]. demonstrated a relative risk reduction of 62% (95% CI: 48–
72%) and absolute risk reduction of 15% (95% CI: 10–
19%) with the use of prophylactic antibiotics. Patients who
Complications received penicillin-based prophylaxis had similar rates of
wound infections compared to those receiving
Although PEG tube insertion is generally a safe procedure, cephalosporin-based prophylaxis. In addition, administra-
major and minor complications have been reported, with a tion of three versus one antibiotic dose did not result in
variable incidence in published pediatric series. In the largest further reducing the risk of infection. Current guidelines for
Table 2 Complications ob-
served in the immediate postop- Immediate postoperative complications No. of complications in 747 patients
erative period after percutaneous Major
endoscopic gastrostomy and af- Gastric separation 1
ter discharge in pediatric
Minor
patients at the Johns Hopkins
Children’s Center from 1994 to Wound infection 19
2005 Pneumoperitoneum 4
Skin necrosis 2
Technical inability to place percutaneous endoscopic gastrostomy 2
Postoperative complications after hospital discharge No. of complications in 682 patients
Major
Gastrocolonic fistula 1
Minor
Granuloma 69
Wound infection 63
Pressure necrosis 9
Wound infection and granuloma 8
Wound infection and necrosis 1
(Adapted from Fortunato et al. Granuloma and necrosis 1
[8].)
Curr Gastroenterol Rep (2011) 13:293–299 297

PEG insertion in children similarly recommend the use of trostomy tubes are very low when compared to PEG alone.
prophylactic antibiotics [50, 51]. The efficacy of single Future prospective studies are needed to better define the
dose versus multiple doses of antibiotics before PEG is not optimal patient demographic best suited for each technique.
clear. A recent prospective study using intravenous cef-
triaxone suggested that a single dose of antibiotic prophy-
laxis was just as effective as 48-hour prophylaxis using
Disclosure Conflicts of interest: J.E. Fortunato—none; C. Cuffari—
multiple doses [52]. none.
The influence of preoperative clinical factors on the risk
for complications after PEG is not entirely clear. This is
likely due in part to the heterogeneity of patient populations References
among medical centers performing PEG, as well as to the
number of cases and experience of the gastroenterologist. In Papers of particular interest, published recently, have been
children, preoperative conditions such as multisystem organ highlighted as:
failure, malignancy, NI, and AIDS have been shown to • Of importance
increase the risk for complications after PEG in some
reports, regardless of age, weight, or nutritional status [3, 1. Ciocon JO, Silverstone FA, Graver LM, Foley CJ. Tube feedings
53, 54]. In the larger series, preoperative diagnosis, in elderly patients. Indications, benefits, and complications. Arch
indication for PEG (including failure to thrive, dysphagia, Intern Med. 1988;148(2):429–33.
2. Gauderer MW. Percutaneous endoscopic gastrostomy: a 10-year
insufficient oral intake, and medication access), prematuri- experience with 220 children. J Pediatr Surg. 1991;26(3):288–92.
ty, or NI did not influence postoperative complications. discussion 292–284.
However, preoperative dysphagia and aspiration identified 3. Fox VL, Abel SD, Malas S, et al. Complications following
on modified barium swallow study and younger patient age percutaneous endoscopic gastrostomy and subsequent catheter
replacement in children and young adults. Gastrointest Endosc.
were associated with the need for PEG conversion to 1997;45(1):64–71.
fundoplication with gastrostomy [8•]. 4. Behrens R, Lang T, Muschweck H, et al. Percutaneous endoscopic
gastrostomy in children and adolescents. J Pediatr Gastroenterol
Nutr. 1997;25(5):487–91.
5. Amann W, Mischinger HJ, Berger A, et al. Percutaneous
Conclusions endoscopic gastrostomy (PEG). 8 years of clinical experience in
232 patients. Surg Endosc. 1997;11(7):741–4.
PEG is a relatively safe and minimally invasive method to 6. Gauderer MW, Ponsky JL, Izant Jr RJ. Gastrostomy without
provide enteral feeding access in most children, and is laparotomy: a percutaneous endoscopic technique. J Pediatr Surg.
1980;15(6):872–5.
associated with minimal complications in most patients. 7. Gauderer MW. Percutaneous endoscopic gastrostomy and the
The indications for PEG placement are broad, but frequent- evolution of contemporary long-term enteral access. Clin Nutr.
ly include malnutrition or failure to thrive, as well as 2002;21(2):103–10.
dysphagia. Little evidence exists to suggest that PEG 8. • Fortunato JE, Troy AL, Cuffari C, et al.: Outcome after
percutaneous endoscopic gastrostomy in children and young adults.
precipitates GERD, but its impact on preexisting reflux J Pediatr Gastroenterol Nutr. Apr 2010;50(4):390–393. This paper
symptoms remains unclear. Although esophageal pH examining the outcomes after PEG in children at the Johns
monitoring may better quantify the degree of reflux in Hopkins Children’s Center is the largest study to date, consisting
patients than reported GER symptoms, its preoperative role of 760 patients over an 11-year period. The report demonstrated
that preoperative diagnosis, indication, prematurity, and history of
before gastrostomy tube placement is not well defined. neurological impairment did not influence postoperative complica-
Because NI is the most common indication for PEG in tions. It did suggest that younger patients and those with a
children and adults, these patients require special attention preoperative history of dysphagia or aspiration on modified barium
before and after PEG placement. Although PEG is feasible swallow study had a higher incidence of subsequent fundoplication.
9. Sulaeman E, Udall Jr JN, Brown RF, et al. Gastroesophageal
in these patients, particularly after a multidisciplinary team reflux and Nissen fundoplication following percutaneous endo-
evaluation, these patients often have a high incidence of scopic gastrostomy in children. J Pediatr Gastroenterol Nutr.
GERD, which may not be detected preoperatively. Al- 1998;26(3):269–73.
though concomitant fundoplication and gastrostomy are 10. Avitsland TL, Kristensen C, Emblem R, et al. Percutaneous
endoscopic gastrostomy in children: a safe technique with major
generally not indicated initially in these patients, further symptom relief and high parental satisfaction. J Pediatr Gastro-
diagnostic assessment and antireflux surgery should be enterol Nutr. 2006;43(5):624–8.
considered if reflux symptoms progress after PEG. Finally, 11. Grant JP. Comparison of percutaneous endoscopic gastrostomy
the advent of minimally invasive laparoscopic surgery in with Stamm gastrostomy. Ann Surg. 1988;207(5):598–603.
12. Ljungdahl M, Sundbom M. Complication rate lower after
pediatric patients raises the question of what should be percutaneous endoscopic gastrostomy than after surgical gastro-
considered the ideal method for obtaining enteral access in stomy: a prospective, randomized trial. Surg Endosc. 2006;20
children. Complications from laparoscopically placed gas- (8):1248–51.
298 Curr Gastroenterol Rep (2011) 13:293–299

13. Stiegmann GV, Goff JS, Silas D, et al. Endoscopic versus 32. Sullivan PB, Juszczak E, Bachlet AM, et al. Impact of
operative gastrostomy: final results of a prospective randomized gastrostomy tube feeding on the quality of life of carers of
trial. Gastrointest Endosc. 1990;36(1):1–5. children with cerebral palsy. Dev Med Child Neurol. 2004;46
14. Bankhead RR, Fisher CA, Rolandelli RH. Gastrostomy tube (12):796–800.
placement outcomes: comparison of surgical, endoscopic, and 33. Sullivan PB, Alder N, Bachlet AM, et al. Gastrostomy feeding in
laparoscopic methods. Nutr Clin Pract. 2005;20(6):607–12. cerebral palsy: too much of a good thing? Dev Med Child Neurol.
15. Cosentini EP, Sautner T, Gnant M, et al. Outcomes of surgical, 2006;48(11):877–82.
percutaneous endoscopic, and percutaneous radiologic gastro- 34. Grunow JE, al-Hafidh A, Tunell WP. Gastroesophageal reflux
stomies. Arch Surg. 1998;133(10):1076–83. following percutaneous endoscopic gastrostomy in children. J
16. Goretsky MF, Johnson N, Farrell M, Ziegler MM. Alternative Pediatr Surg. 1989;24(1):42–4. Discussion 44–45.
techniques of feeding gastrostomy in children: a critical analysis. J 35. Razeghi S, Lang T, Behrens R. Influence of percutaneous
Am Coll Surg. 1996;182(3):233–40. endoscopic gastrostomy on gastroesophageal reflux: a pro-
17. Preshaw RM. A percutaneous method for inserting a feeding spective study in 68 children. J Pediatr Gastroenterol Nutr.
gastrostomy tube. Surg Gynecol Obstet. 1981;152(5):658–60. 2002;35(1):27–30.
18. • Nah SA, Narayanaswamy B, Eaton S, et al.: Gastrostomy 36. Launay V, Gottrand F, Turck D, et al. Percutaneous endoscopic
insertion in children: percutaneous endoscopic or percutaneous gastrostomy in children: influence on gastroesophageal reflux.
image-guided? J Pediatr Surg. Jun 2010;45(6):1153–1158. This Pediatrics. 1996;97(5):726–8.
paper compared gastrostomy insertion via PEG placed by 37. Wilson GJ, van der Zee DC, Bax NM. Endoscopic gastrostomy
surgeons versus interventional radiologists. The authors demon- placement in the child with gastroesophageal reflux: is concom-
strated that although major complications were rare, they were itant antireflux surgery indicated? J Pediatr Surg. 2006;41
more frequent in those tubes placed by radiologists. (8):1441–5.
19. Nagle AP, Murayama KM. Laparoscopic gastrostomy and 38. Samuel M, Holmes K. Quantitative and qualitative analysis of
jejunostomy. J Long Term Eff Med Implants. 2004;14(1):1–11. gastroesophageal reflux after percutaneous endoscopic gastro-
20. Ho HS, Ngo H. Gastrostomy for enteral access. A comparison stomy. J Pediatr Surg. 2002;37(2):256–61.
among placement by laparotomy, laparoscopy, and endoscopy. 39. Sondheimer JM, Morris BA. Gastroesophageal reflux among
Surg Endosc. 1999;13(10):991–4. severely retarded children. J Pediatr. 1979;94(5):710–4.
21. Rothenberg SS, Bealer JF, Chang JH. Primary laparoscopic 40. Novotny NM, Jester AL, Ladd AP. Preoperative prediction of
placement of gastrostomy buttons for feeding tubes. A safer and need for fundoplication before gastrostomy tube placement in
simpler technique Surg Endosc. 1999;13(10):995–7. children. J Pediatr Surg. 2009;44(1):173–6. discussion 176–
22. Zamakhshary M, Jamal M, Blair GK, et al. Laparoscopic vs 177.
percutaneous endoscopic gastrostomy tube insertion: a new 41. Puntis JW, Thwaites R, Abel G, Stringer MD. Children with
pediatric gold standard? J Pediatr Surg. 2005;40(5):859–62. neurological disorders do not always need fundoplication con-
23. • Akay B, Capizzani TR, Lee AM, et al.: Gastrostomy tube comitant with percutaneous endoscopic gastrostomy. Dev Med
placement in infants and children: is there a preferred technique? J Child Neurol. 2000;42(2):97–9.
Pediatr Surg. Jun 2010;45(6):1147–1152. This report compares 42. Hament JM, Bax NM, van der Zee DC, et al. Complications of
placement of gastrostomy tubes in infants and children using PEG percutaneous endoscopic gastrostomy with or without concomi-
alone and laparoscopic-assisted PEG. Although operative time tant antireflux surgery in 96 children. J Pediatr Surg. 2001;36
for PEG alone was shorter than laparoscopically assisted (9):1412–5.
gastrostomy placement, there were more complications requiring 43. Ni YH, Chang MH, Hsu HY, et al. Percutaneous endoscopic
a second operation in the PEG-alone group. gastrostomy in infants. J Formos Med Assoc. 1995;94(10):635–7.
24. Nicholson FB, Korman MG, Richardson MA. Percutaneous 44. Wilson L, Oliva-Hemker M. Percutaneous endoscopic gastro-
endoscopic gastrostomy: a review of indications, complications stomy in small medically complex infants. Endoscopy. 2001;33
and outcome. J Gastroenterol Hepatol. 2000;15(1):21–5. (5):433–6.
25. Miller RE, Castlemain B, Lacqua FJ, Kotler DP. Percutaneous 45. Loser C, Aschl G, Hebuterne X, et al. ESPEN guidelines on
endoscopic gastrostomy. Results in 316 patients and review of artificial enteral nutrition–percutaneous endoscopic gastrostomy
literature. Surg Endosc. 1989;3(4):186–90. (PEG). Clin Nutr. 2005;24(5):848–61.
26. Heine RG, Reddihough DS, Catto-Smith AG. Gastro-oesophageal 46. Backman T, Arnbjornsson E, Berglund Y, Larsson LT. Video-
reflux and feeding problems after gastrostomy in children with assisted gastrostomy in infants less than 1 year. Pediatr Surg Int.
severe neurological impairment. Dev Med Child Neurol. 1995;37 2006;22(3):243–6.
(4):320–9. 47. Erdil A, Saka M, Ates Y, et al. Enteral nutrition via
27. Mathus-Vliegen EM, Koning H, Taminiau JA, Moorman- percutaneous endoscopic gastrostomy and nutritional status
Voestermans CG. Percutaneous endoscopic gastrostomy and gastro- of patients: five-year prospective study. J Gastroenterol
jejunostomy in psychomotor retarded subjects: a follow-up covering Hepatol. 2005;20(7):1002–7.
106 patient years. J Pediatr Gastroenterol Nutr. 2001;33(4):488–94. 48. Loser C, Wolters S, Folsch UR. Enteral long-term nutrition
28. Brant CQ, Stanich P, Ferrari Jr AP. Improvement of children’s via percutaneous endoscopic gastrostomy (PEG) in 210
nutritional status after enteral feeding by PEG: an interim report. patients: a four-year prospective study. Dig Dis Sci. 1998;43
Gastrointest Endosc. 1999;50(2):183–8. (11):2549–57.
29. Borowitz SM, Sutphen JL, Hutcheson RL. Percutaneous endo- 49. Jafri NS, Mahid SS, Minor KS, et al. Meta-analysis: antibiotic
scopic gastrostomy without an antireflux procedure in neurolog- prophylaxis to prevent peristomal infection following percutane-
ically disabled children. Clin Pediatr (Phila). 1997;36(1):25–9. ous endoscopic gastrostomy. Aliment Pharmacol Ther. 2007;25
30. Cameron BH, Blair GK, Murphy 3rd JJ. Fraser GC: Morbidity in (6):647–56.
neurologically impaired children after percutaneous endoscopic 50. Rey JR, Axon A, Budzynska A, et al. Guidelines of the
versus Stamm gastrostomy. Gastrointest Endosc. 1995;42(1):41–4. European Society of Gastrointestinal Endoscopy (E.S.G.E.)
31. Sullivan PB, Juszczak E, Bachlet AM, et al. Gastrostomy tube antibiotic prophylaxis for gastrointestinal endoscopy. European
feeding in children with cerebral palsy: a prospective, longitudinal Society of Gastrointestinal Endoscopy. Endoscopy. 1998;30
study. Dev Med Child Neurol. 2005;47(2):77–85. (3):318–24.
Curr Gastroenterol Rep (2011) 13:293–299 299

51. Snyder J, Bratton B. Antimicrobial prophylaxis for gastrointestinal 53. Marin OE, Glassman MS, Schoen BT, Caplan DB. Safety and
procedures: current practices in North American academic pediatric efficacy of percutaneous endoscopic gastrostomy in children. Am
programs. J Pediatr Gastroenterol Nutr. 2002;35(4):564–9. J Gastroenterol. 1994;89(3):357–61.
52. Rawat D, Srivistava A, Thomson M. Antibody prophylaxis for 54. Khattak IU, Kimber C, Kiely EM, Spitz L. Percutaneous
children undergoing percutaneous endoscopic gastrostomy. J endoscopic gastrostomy in paediatric practice: complications and
Pediatr Gastroenterol Nutr. 2005;40(2):234–5. outcome. J Pediatr Surg. 1998;33(1):67–72.

You might also like