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ttp://www.bsava.

com CAPSULE REVIEW

Intraperitoneal and incisional analgesia


in small animals: simple, cost-effective
techniques
P. V. M. Steagall 1,*, J. Benito*, B. Monteiro *, D. Lascelles†, P. W. Kronen‡, J. C. Murrell §
,
S. Robertson¶, B. Wright║ and K. Yamashita**
*
Department of Clinical Sciences, Université de Montréal, Montreal, Quebec J2S 2M2, Canada

Translational Research in Pain Program, Comparative Pain Research and Education Center, College of Veterinary Medicine,
North Carolina State University, Raleigh, North Carolina 27606, USA

Veterinary Anaesthesia Service – International, Winterthur 8400, Switzerland
§
Highcroft Veterinary Referrals, Whitchurch, Bristol BS14 9BE, UK

Lap of Love Veterinary Hospice, Lutz, Florida 33549, USA

Mistral Vet, Fort Collins, Colorado 80534, USA
**
Small Animal Clinical Sciences, Rakuno Gakuen University, Ebetsu, Hokkaido 069-8501, Japan
Corresponding author email: paulo.steagall@umontreal.ca

The World Small Animal Veterinary Association Global Pain Council (WSAVA-GPC) has recently pub-
lished its first “capsule review” by Monteiro et al. These are short articles that present a brief assess-
ment of the scientific evidence and practical recommendations on important, and sometimes
controversial, subjects in pain management. The capsules will be published regularly in the Journal of
Small Animal Practice, the official journal of the WSAVA. This second article discusses the use of
intraperitoneal and incisional analgesia in small animal practice, including their limitations and recom-
mendations by the authors.

Journal of Small Animal Practice (2019)


DOI: 10.1111/jsap.13084
Accepted: 30 September 2019

Local anaesthetics inhibit membrane depolarisation, nerve exci- CANINE STUDIES


tation and conduction primarily by blocking inward Na+ currents
through voltage-gated Na+ channels. These drugs are inexpen- The pharmacokinetics of lidocaine 2% after combined IP (8 mg/
sive, not scheduled, and are readily available world-wide. Intra- kg with epinephrine 1:400,000) and incisional (2  mg/kg with
peritoneal (IP) administration of local anaesthetics reduces early epinephrine 1:200,000) administration showed that plasma drug
postoperative analgesic requirements, time to first-intervention concentrations decreased rapidly after injection and did not reach
analgesia and pain scores after abdominal surgery in humans; it toxic concentrations (Wilson et al. 2004).
is currently recommended for laparoscopic surgery as an adju- In a randomised, clinical trial, dogs that received butorpha-
nol plus bupivacaine 0.75% IP (4.4 mg/kg) and at the incision
vant analgesic technique (Boddy et al. 2006, Kahokehr et al.
(splash of 2 mL over the incision site) required significantly less
2011, Hamill et al. 2017). Based on these results in the human
supplemental analgesia and had lower pain scores than control
literature, the WSAVA-GPC (Monteiro et al. 2019) guidelines
dogs (i.e. butorphanol only) (Carpenter et al. 2004). In this same
recommended IP and incisional analgesia for the management study, similar results were not observed after the administration
of pain, particularly as adjuvant techniques for pain relief in dogs of 8.8 mg/kg IP and incisional (2 mL total) lidocaine 2% with
and cats undergoing abdominal surgery (Mathews et al. 2014). epinephrine. However, at the 0.5-hour time point, the lidocaine
Both techniques are described and demonstrated in the following group was assessed to have a pain level intermediate between the
link (https://www.youtube.com/watch?v=76dwKuirqt0). Recent saline and bupivacaine groups. Based on the duration of action and
studies have corroborated these findings, which are summarised the results described above, longer-acting local anaesthetics such
in this capsule and in Tables 1 and 2. as bupivacaine or ropivacaine should be probably preferred for

Journal of Small Animal Practice • © 2019 British Small Animal Veterinary Association 1
P. V. M. Steagall et al.

Table 1. Summary of studies evaluating the effects after the administration of intraperitoneal and/or incisional
anaesthetics in dogs undergoing abdominal procedures
Technique Drug Dose Number Procedure Main findings References
of dogs
IP and IC Lidocaine 2% with IP: 8 mg/kg 6 OVH Plasma concentrations were Wilson et al. 2004
epinephrine IC: 2 mg/kg below toxic levels.
IP and IC Lidocaine 2% with Lido: 8.8 mg/kg 30 OVH Butorphanol with IP and Carpenter et al.
epinephrine or (IP) + 40 mg total (IC) IC anaesthesia using 2004
Bupivacaine 0.75% Bupi: 4.4 mg/kg bupivacaine resulted in
(IP) + 15 mg (IP) lower pain scores and less
need of rescue analgesia
than butorphanol only.
IP and IC Bupivacaine 0.5% IP: 4.4 mg/kg 16 Laparoscopic IP and IC anaesthesia Kim et al. 2012
IC: 5 mg total OVH resulted in lower pain
scores than IC anaesthesia
only.
IC Bupivacaine 0.25% IC: 2 mg/kg 60 Celiotomy Preoperative IC anaesthesia Savvas et al. 2008
resulted in lower pain
scores and less need
of rescue analgesia
than postoperative IC
anaesthesia.
Mesovarium Lidocaine 2% Mesovarium: 10 mg 20 OVH Methadone with local Bubalo et al. 2008
and IC total anaesthesia of the
IC: 2 mg/kg mesovarium and IC
anaesthesia did not reduce
autonomic responses to
surgery.
IC Bupivacaine (unknown IC: 2 mg/kg 92 OVH Morphine and carprofen Fitzpatrick et al.
concentration) with preoperative 2010
or postoperative IC
anaesthesia resulted in
similar pain scores than
morphine only.
IC Lidocaine with Lido: 4 mg/kg 59 OVH Morphine with or without IC McKune et al.
Bupivacaine Bupi: 1 mg/kg anaesthesia using lidocaine 2014
(unknown and bupivacaine resulted
concentrations) in similar pain scores to
controls (i.e. saline).
IP or IC Bupivacaine 0.5% with IP: 5 mg/kg 30 OVH Butorphanol with IP Campagnol et al.
epinephrine IC: 1 mg/kg anaesthesia resulted in 2012
lower pain scores than
controls (i.e. saline).
Butorphanol with IC
anaesthesia was not
different from controls.
IP alone or Bupivacaine 0.5% IP: 3 mg/kg 39 OVH Morphine and carprofen with Kalchofner
with IC IC: 1 mg/kg IP anaesthesia resulted Guerrero et al.
in similar pain scores to 2016
morphine and carprofen with
IP and IC anaesthesia.
IP Ropivacaine 0.75% or Ropi: 3 mg/kg 45 OVH Morphine and carprofen Lambertini et al.
Bupivacaine 0.5% Bupi: 3 mg/kg with IP anaesthesia using 2018
ropivacaine or bupivacaine
resulted in similar pain
scores and need of rescue
analgesia.
IP Intraperitoneal, IC Incisional, Lido Lidocaine, Bupi Bupivacaine, Ropi Ropivacaine, OVH Ovariohysterectomy

these techniques. In dogs undergoing laparoscopic ovariohyster- administration of incisional (i.e. subcutaneous and intramus-
ectomy, preoperative incisional (i.e. before the portal placement) cular infiltration) bupivacaine 0.25% (2 mg/kg) was associated
bupivacaine 0.5% (1 mL) and bupivacaine sprayed IP (4.4 mg/ with significantly lower pain scores and less need for postop-
kg; IP dose only) provided pain relief and prevented surgery- erative opioid administration when compared with postopera-
induced increases in cortisol concentration (Kim et al. 2012). It is tive administration of incisional bupivacaine or placebo in dogs
not known whether the postoperative analgesic effects observed in undergoing celiotomy (Savvas et al. 2008). This study demon-
these studies were due to the IP or incisional technique. strated the benefits of pre-emptive administration of incisional
The effects of incisional anaesthesia alone have been inves- anaesthesia. Conversely, incisional infiltration of the linea alba
tigated further and provide conflicting results. Preoperative with lidocaine 1% (2 mg/kg) and anaesthesia of the mesovarium

2 Journal of Small Animal Practice • © 2019 British Small Animal Veterinary Association
WSAVA global pain council capsules

Table 2. Summary of studies evaluating the effects after the administration of intraperitoneal and/or incisional
anaesthetics in cats undergoing abdominal procedures
Technique Drug Dose Number of cats Procedure Main findings References
IP Bupivacaine 0.25% Bupi: 2 mg/kg 8 OVH Plasma concentrations were below Benito et al. 2016a
toxic levels.
IP Bupivacaine 0.25% Bupi: 2 mg/kg 45 OVH Buprenorphine administered in Benito et al. 2016b
combination with IP anaesthesia
resulted in similar pain scores and
need for rescue analgesia when
compared with buprenorphine and
meloxicam, and in lower pain scores
than buprenorphine alone.
IP Bupivacaine 0.25% Bupi: 2 mg/kg 16 OVH Plasma concentrations of IP Benito et al. 2018
with epinephrine or anaesthesia using bupivacaine with
dexmedetomidine epinephrine or dexmedetomidine
were below toxic levels.
Buprenorphine and meloxicam
with IP anaesthesia using
bupivacaine with epinephrine or
dexmedetomidine provided similar
analgesia.
IP Bupivacaine 0.25% Bupi: 2 mg/kg 60 OVH In terms of prevalence of rescue Benito et al. 2019
alone or with analgesia, but not duration of
dexmedetomidine action, the analgesic efficacy of
bupivacaine-dexmedetomidine was
similar to bupivacaine alone.
IP Intraperitoneal, IC Incisional, Bupi Bupivacaine, Epi Epinephrine, Dex Dexmedetomidine, OVH Ovariohysterectomy

(0.5  mL of lidocaine 2%) did not blunt autonomic responses analgesia when administered in combination with morphine and
to surgery (Bubalo et al. 2008). Furthermore, two other stud- carprofen (Lambertini et al. 2018) but 15 out 44 dogs required
ies did not show any benefits of incisional anaesthesia in dogs the administration of rescue analgesia.
undergoing ovariohysterectomy either because the technique So-called incisional “splash block” techniques have, as
was administered as part of multimodal analgesia (Epstein et al. described above, been incorporated into several studies. How-
2010, Fitzpatrick et al. 2010) or because of the challenges of rec- ever, thus far, no studies have evaluated the efficacy of an inci-
ognising pain in the clinical setting (McKune et al. 2014). sional “splash” block, and indeed, it is unclear what is meant
IP and incisional techniques were compared in a prospective, by a splash block. For example, the IP technique has been also
randomised, placebo-controlled, clinical study. IP (5 mg/kg) or referred as a “splash block”. Carpenter et al. 2004 placed local
incisional (i.e. subcutaneous infiltration of linea alba at 1 mg/kg) anaesthetic on the wound and “no attempt was made to prevent
bupivacaine 0.5% with epinephrine was evaluated in dogs under- it from running off during closure”. Conversely, a “splash block”
going ovariohysterectomy and receiving butorphanol. Pain scores was described where sutures were used to elevate wound edges to
based on a visual analog scale were significantly lower after IP keep the local anaesthetic in contact with the wound tissues for
bupivacaine than in controls (i.e. butorphanol only). Although 20 minutes in dogs undergoing ear canal ablation (Buback et al.
there was a trend for a decreased need for rescue analgesia in the 1996). The WSAVA-GPC cautions against relying on splashing
IP bupivacaine group, this was not significantly different between local anaesthetic onto a wound since there is usually not enough
saline and bupivacaine treatments, most likely due to small sam- time for drug absorption. Of note is that this early description in
ple size and scoring systems used for acute pain assessment (Cam- human paediatrics described the technique as “installation”, not
pagnol et al. 2012). Based on these findings, the WSAVA-GPC “splash” – the term splash was used later.
suggests that the IP route of administration should be given prior-
ity over the incisional technique when maximum recommended
doses and volumes of local anaesthetics are used, to avoid toxic- FELINE STUDIES
ity. Finally, a recent study did not show any benefits of using IP
(3 mg/kg) and incisional (i.e. subcutaneous “splash” of 1 mg/kg) The pharmacokinetics, safety and efficacy of IP bupivacaine
bupivacaine over the IP technique alone before complete closure have recently been published in cats (Benito et al. 2016a,
of the linea alba after ovariohysterectomy in dogs. However, as 2016b, 2018). The IP technique was always performed imme-
previously observed with incisional anaesthesia (Fitzpatrick et al. diately before ovariohysterectomy by the same experienced
2010), the results were likely confounded by the concurrent use surgeon. A pharmacokinetic study revealed that plasma con-
of other analgesics such as morphine and carprofen (Kalchofner centrations of IP bupivacaine 0.25% (2 mg/kg) were detectable,
Guerrero et al. 2016). In a follow-up study, the IP administration but at much lower concentrations than those associated with
of ropivacaine 0.75% (3 mg/kg) or bupivacaine 0.5% (3 mg/kg) toxic effects (Benito et al. 2016a); outwardly detectable adverse
without incisional anaesthesia provided similar postoperative effects were not observed in these cats. In a randomised, pro-

Journal of Small Animal Practice • © 2019 British Small Animal Veterinary Association 3
P. V. M. Steagall et al.

spective, controlled clinical trial, IP bupivacaine 0.25% (2 mg/ • IP and incisional analgesia should be used as part of a mul-
kg) in cats premedicated with buprenorphine showed similar timodal analgesic plan (Benito et al. 2018). For example, the
postoperative pain scores and prevalence of rescue analgesia combination of an opioid, NSAID and IP and incisional
when compared with cats receiving meloxicam and buprenor- anaesthesia provides adequate postoperative analgesia in cats
phine, and superior analgesia than buprenorphine alone. Anal- undergoing ovariohysterectomy (Benito et al. 2018).
gesic effects were observed for up to 8  hours postoperatively • Total doses of bupivacaine 0.5% should not exceed 4 mg/kg in
(Benito et al. 2016b). The efficacy and pharmacokinetics of IP dogs and 2 mg/kg in cats (Benito et al. 2016a, 2016b, 2018).
bupivacaine 0.25% in combination with epinephrine (2  μg/ Based on the experience of the authors, if both techniques are
kg) or dexmedetomidine (1 μg/kg) in cats undergoing ovario- used, one-fourth of the total dose is administered for inci-
hysterectomy have also been investigated (Benito et al. 2018). sional anaesthesia whereas the remaining volume is used for
These adjuvant drugs can produce local vasoconstriction which IP analgesia.
delays systemic absorption and improves the safety and efficacy • In cats, bupivacaine 0.5% can be diluted in equal parts with
of IP anaesthesia. Both treatments produced plasma concen- saline to increase the volume of IP injection. The final concen-
trations below toxic levels and similar analgesic effects when tration before drug administration is then 0.25% (Benito et al.
administered with buprenorphine and meloxicam. These adju- 2016a, 2016b, 2018).
vant drugs produced delayed absorption and a longer terminal • Based on the concept of pre-emptive analgesia and the study by
half-life when compared with bupivacaine alone (Benito et al. Savvas et al. (2008), preoperative administration of incisional
2018). However, the prevalence of rescue analgesia was not sig- anaesthesia is preferred over postoperative use.
nificantly different between IP bupivacaine alone and bupiva-
caine in combination with dexmedetomidine in a clinical trial
involving 60 cats undergoing ovariohysterectomy (Benito et al. LIMITATIONS
2019). It appears that the use of such vasoactive drugs for IP
analgesia is not supported by strong evidence at this time. The The current literature on IP and incisional analgesia has several
intraoperative effects of incisional anaesthesia on physiologic limitations. Published studies used different surgeons and anaes-
parameters have been reported in cats anaesthetised with ket- thetists with different clinical experience (including veterinary
amine-medetomidine-buprenorphine for ovariohysterectomy. students and other individuals under training), and with differ-
The technique partially blunted sympathetic responses to sur- ent doses, drugs and volumes of local anaesthetics (Tables 1 and
gery when using preoperative incisional lidocaine 1% (1.5 mg/ 2). The definition of incisional anaesthesia, timing of incisional
kg) or the combination of lidocaine 1% and bupivacaine injection (pre- versus post-operative) and location of IP adminis-
0.25% (1  mg/kg for each drug), but not saline (0.3 mL/kg) tration varied which renders results difficult to interpret. Acute
(Vicente & Bergstrom 2018). pain assessment was performed using different pain scoring sys-
tems that have variable validity. The amount of observer training
in pain assessment is not often described and may be a significant
INDICATIONS FOR IP AND INCISIONAL source of bias in the interpretation of these results.
ANAESTHESIA In conclusion, based on current evidence, the WSAVA-GPC
supports both techniques for the treatment of perioperative pain
Based on the aforementioned study findings and a consensus of as part of a multimodal analgesia regimen. IP and incisional anaes-
the WSAVA GPC members, some recommendations are pre- thesia are simple, safe and cost-effective adjunct methods to reduce
sented below: pain after abdominal surgery in companion animals and are not
limited by geographical drug availability. However, readers should
• It is our consensus that these techniques should be used be aware that some of our recommendations were based on a con-
for any type of abdominal surgery such as intestinal for- sensus and low-level of evidence provided by the current litera-
eign body removal, enterotomy, splenectomy, etc. Further ture. Future studies should continue to investigate the efficacy and
research should investigate and provide evidence on the ben- safety of both techniques in a large number of clinical patients.
efits of incisional and IP techniques for these procedures.
• Based on the safety and efficacy of IP analgesia with bupiva-
Conflict of interest
caine as part of multimodal analgesia in dogs and cats (Car-
penter et al. 2004, Campagnol et al. 2012, Benito et al. 2016a,
2016b, 2018), this technique should be readily applied in ster- No conflict of interest has been declared.
ilisation programs, especially in countries with limited drug
availability. References
Benito, J., Monteiro, B. P., Beaudry, F., et al. (2016a) Pharmacokinetics of bupi-
• They should always be performed under strict aseptic condi- vacaine after intraperitoneal administration to cats undergoing ovariohysterec-
tomy. American Journal of Veterinary Research 77, 641-645
tions and general anaesthesia. There is no evidence that these Benito, J., Monteiro, B., Lavoie, A. M., et al. (2016b) Analgesic efficacy of intra-
techniques should replace other analgesics such as nonsteroidal peritoneal administration of bupivacaine in cats. Journal of Feline Medicine and
Surgery 18, 906-912
anti-inflammatory drugs (NSAIDs) but, rather, should be used Benito, J., Monteiro, B., Beaudry, F., et al. (2018) Efficacy and pharmacokinetics of
in addition. bupivacaine with epinephrine or dexmedetomidine after intraperitoneal admin-

4 Journal of Small Animal Practice • © 2019 British Small Animal Veterinary Association
WSAVA global pain council capsules

istration in cats undergoing ovariohysterectomy. Canadian Journal of Veterinary Kahokehr, A., Sammour, T., Srinivasa, S., et al. (2011) Systematic review and
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of bupivacaine or bupivacaine-dexmedetomidine after intraperitoneal adminis- Kalchofner Guerrero, K. S., Campagna, I., Bruhl-Day, R., et al. (2016) Intraperi-
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Journal of Small Animal Practice • © 2019 British Small Animal Veterinary Association 5

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