In cats after ovariohysterectomy, does gabapentin vs placebo reduce postoperative pain scores and rescue opioid need?
Shelf #745 · gate-verified and displayed under the developer's blinded-trial rule
POSSIBLE (the treatment made no difference): In the one randomised, masked, placebo-controlled trial of exactly this question, a single preoperative gabapentin dose did not reduce postoperative pain or rescue need after ovariohysterectomy. In Harris 2026 (34 healthy female shelter cats randomized to liquid gabapentin 20 mg/kg or placebo orally, 2 to 4 hours before anaesthesia and surgery, with all scoring by 2 masked individuals), there was no evidence of a difference between treatment groups, or of a treatment-by-time interaction, for any outcome measure: Feline Grimace Scale pain scores rose after recovery in both groups (gabapentin at 30 to 90 minutes; placebo at 30 and 60 minutes), and no cat in either group required rescue analgesia at any time point. Design class (a): randomisation and blinding are established by the pivotal record's own wording — cats were 'randomized' and scored by 'masked' assessors — and the trial answers this shelf's own comparison (gabapentin versus placebo) in this shelf's own population (cats undergoing ovariohysterectomy). The cross-pointed second trial points the same way on its primary scale: in Steagall 2018 (52 cats, all receiving buprenorphine; gabapentin 50 mg capsules at 12 hours and 1 hour before surgery versus placebo capsules), pain and sedation scores were not different among treatments and rescue prevalence on the primary multidimensional composite pain scale was not significantly different (gabapentin-buprenorphine 5 of 19 [26%] versus buprenorphine with placebo capsules 9 of 18 [50%], overall P = 0.08) — that record is already carded as a claim-carrier in Shelf #197 and is cross-pointed here, not re-carded. Limits stated plainly: the pivotal trial is small (34 cats), follows pain only to 180 minutes after recovery, uses one single 20 mg/kg liquid dose, and its zero rescue need in both groups means the trial cannot show an opioid-sparing effect even in principle — there was no rescue use to spare; whether repeated or higher dosing, or gabapentin added to an opioid, changes later pain is a different question (Steagall's second scoring system, the revised Glasgow scale, would have separated the groups, which is why this stamp is POSSIBLE, not a stronger null). Drafted Nov 10, 2026 (VetMed build, topic #745); all figures from the abstract fetched and verified at drafting.
Randomized, placebo-controlled trial with masked outcome scoring (record's own wording: cats 'were randomized', scored by '2 masked individuals'; publication type: Journal Article)
Who: Cats: 34 healthy female shelter cats undergoing ovariohysterectomy. Randomized, placebo-controlled trial with masked scoring: cats were randomized to receive liquid gabapentin 20 mg/kg or a placebo orally, 2 to 4 hours prior to anaesthesia and surgery. Cats were scored by 2 masked individuals for stress, sedation, tolerance to handling and pain using the cat stress score, the feline multiparametric sedation score, a previously published handling score and the Feline Grimace Scale (FGS). Scores were assigned prior to the first dose of medication, at anaesthetic induction, and at 30, 60, 90, 120 and 180 minutes after recovery. Data were analysed with a linear mixed model evaluating treatment, time, and treatment-by-time interaction. Per-arm group sizes are not stated in the abstract.
Result: There was no evidence of a difference between treatment groups or treatment-by-time interaction for any outcome measure. Cat stress score decreased and tractability score increased at 30 minutes after recovery in both treatments. Sedation score was higher than baseline at 30 to 90 minutes after recovery in both treatments. Cats treated with gabapentin had an increased FGS score at 30 to 90 minutes, and those that received placebo had an increased FGS score at 30 and 60 minutes. No cat required rescue analgesia at any time point. The authors conclude that gabapentin use in shelter cats presenting for ovariohysterectomy did not significantly decrease stress or pain or increase ease of handling perioperatively, and that the results suggest a lack of evidence for gabapentin decreasing stress or providing perioperative analgesia when administered prior to anaesthesia and surgery for ovariohysterectomy in shelter cats.
Watch out: A null result with a floor problem for the rescue outcome: no cat in either group needed rescue analgesia, so the trial shows no detectable pain-score benefit but cannot estimate an opioid-sparing effect. Pain was followed only to 180 minutes after recovery and on a single scale (Feline Grimace Scale); the abstract reports directions of change without FGS values, and does not detail the background anaesthetic or analgesic protocol, so how much other analgesia the cats received cannot be verified from the record. One single 20 mg/kg oral liquid dose in healthy shelter cats — the null does not extend to repeated dosing, higher doses, client-owned cats, or more painful surgery.
Harris T, Reger E, Kleine S, DeBolt R, Cannon S, Weisent J, Seabolt M, Reed R. Evaluation of the effects of gabapentin on stress and pain in shelter cats undergoing ovariohysterectomy. J Am Vet Med Assoc. 2026;264(6):724-729. PMID: 41534210. Registry ID: none in the record. MeSH: Animals · Gabapentin*/therapeutic use, administration & dosage · Cats/surgery · Hysterectomy*/veterinary, adverse effects · Ovariectomy*/veterinary, adverse effects · Female · Analgesics*/therapeutic use, administration & dosage · Postoperative Pain*/veterinary, prevention & control · Stress, Physiological*/drug effects
Synthesis
Who: Synthesis of the card above (Harris 2026, 34 shelter cats, single-dose gabapentin 20 mg/kg versus placebo, Feline Grimace Scale to 180 minutes), with Steagall 2018 (52 cats, gabapentin capsules on a buprenorphine background versus placebo capsules) cross-pointed from Shelf #197, not re-carded.
Result: (1) Pain scores: no difference between gabapentin and placebo on any outcome at any time point (Harris). (2) Rescue analgesia: 0 cats in either group required rescue (Harris); on Steagall's primary multidimensional scale, rescue prevalence was not significantly different between gabapentin-buprenorphine (26%) and buprenorphine plus placebo capsules (50%), P = 0.08 overall. (3) The discordant note: on Steagall's second scale (revised Glasgow), rescue would have been significantly higher without gabapentin (78% versus 26%, P = 0.003) — the two validated scales disagree, so a small benefit of gabapentin added to buprenorphine cannot be excluded, but no trial shows one on its primary pain measure.
Watch out: One-home collisions handled by cross-pointing, not re-carding: Steagall 2018 (PMID: 28920534) is a claim-carrier in Shelf #197 (buprenorphine-based versus NSAID-based analgesia in cats), where its gabapentin arm serves that shelf's comparison; gabapentin for pre-visit stress in cats homes in Shelf #304 (PMIDs: 29099247, 35481442) and gabapentin for feline osteoarthritis in Shelf #742 (PMID: 30110208) — none of those records is re-carded here, and none answers this shelf's postoperative question. A postoperative-hospitalization study of gabapentin or alprazolam in cats (PMID: 38997952) measured hospitalisation stress/sedation outcomes, not post-ovariohysterectomy pain against placebo, and was not carded. This pack covers a single preoperative dose for ovariohysterectomy only — not gabapentin as part of a multimodal protocol over several days, and not other operations.
Synthesis of Harris T et al. PMID: 41534210. Cross-pointed, not carded: Steagall PV et al. PMID: 28920534 (Shelf #197). Registry IDs as on the individual cards.
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