Analgesic effects of gabapentin and buprenorphine in cats undergoing ovariohysterectomy using two pain-scoring systems: a randomized clinical trial

Journal of Feline Medicine and Surgery - Tập 20 Số 8 - Trang 741-748 - 2018
Paulo V. Steagall1,2, Javier Benito2, Beatriz P. Monteiro1,3, Graeme M. Doodnaught1,2, Guy Beauchamp4, Marina C. Evangelista1,2
1Animal Pharmacology Research Group of Québec, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, Canada
2Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, Canada
3Department of Veterinary Biomedicine, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, Canada
4Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, Canada

Tóm tắt

Objectives

The aim of the study was to evaluate the analgesic efficacy of gabapentin–buprenorphine in comparison with meloxicam–buprenorphine or buprenorphine alone, and the correlation between two pain-scoring systems in cats.

Methods

Fifty-two adult cats were included in a randomized, controlled, blinded study. Anesthetic protocol included acepromazine–buprenorphine–propofol–isoflurane. The gabapentin–buprenorphine group (GBG, n = 19) received gabapentin capsules (50 mg PO) and buprenorphine (0.02 mg/kg IM). The meloxicam–buprenorphine group (MBG, n = 15) received meloxicam (0.2 mg/kg SC), buprenorphine and placebo capsules (PO). The buprenorphine group (BG, n = 18) received buprenorphine and placebo capsules (PO). Gabapentin (GBG) and placebo (MBG and BG) capsules were administered 12 h and 1 h before surgery. Postoperative pain was evaluated up to 8 h after ovariohysterectomy using a multidimensional composite pain scale (MCPS) and the Glasgow pain scale (rCMPS-F). A dynamic interactive visual analog scale (DIVAS) was used to evaluate sedation. Rescue analgesia included buprenorphine and/or meloxicam if the MCPS ⩾6. A repeated measures linear model was used for statistical analysis ( P <0.05). Spearman’s rank correlation between the MCPS and rCMPS-F was evaluated.

Results

The prevalence of rescue analgesia with a MCPS was not different ( P = 0.08; GBG, n = 5 [26%]; MBG, n = 2 [13%]; BG, n = 9 [50%]), but it would have been significantly higher in the BG (n = 14 [78%]) than GBG ( P = 0.003; n = 5 [26%]) and MBG ( P = 0.005; n = 4 [27%]) if intervention was based on the rCMPS-F. DIVAS and MCPS/rCMPS-F scores were not different among treatments. A strong correlation was observed between scoring systems ( P <0.0001).

Conclusions and relevance

Analgesia was not significantly different among treatments using an MCPS. Despite a strong correlation between scoring systems, GBG/MBG would have been superior to the BG with the rCMPS-F demonstrating a potential type II error with an MCPS due to small sample size.

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