Effect of meloxicam or robenacoxib administration timing on renal function and postoperative analgesia in cats undergoing ovariohysterectomy: A randomized, blinded, controlled clinical trial

Author:

Krekis Alex1ORCID,King Jonathan N.2,D'Arcy‐Howard Duncan3,Stapleton Nadene3,Elliott Jonathan4ORCID,Pelligand Ludovic45ORCID

Affiliation:

1. Davies Veterinary Specialists Hitchin UK

2. J.N.King Consulting Bennwil Switzerland

3. Department of Clinical Science and Services, Beaumont Sainsbury Animal Hospital, Royal Veterinary College University of London London UK

4. Department of Comparative Biomedical Sciences, Royal Veterinary College University of London London UK

5. Department of Clinical Science and Services, Queen Mother Hospital for Animals, Royal Veterinary College University of London London UK

Abstract

AbstractWe evaluated the effect of administration timing of meloxicam and robenacoxib on renal function, platelet cyclo‐oxygenase and perioperative analgesia in 60 cats undergoing ovariohysterectomy, in a prospective randomized blinded controlled study. Twelve cats were randomly allocated to one subcutaneous treatment group: meloxicam (0.2 mg/kg) or robenacoxib (2 mg/kg) at admission (MA, RA), at induction (MI, RI) and robenacoxib at the end of surgery (RE). All cats received the same anaesthesia protocol. Plasma renin activity (PRA), plasma creatinine, drug concentrations and serum thromboxane (TxB2) were measured sequentially. Anaesthesia significantly increased PRA, as activity at end of the surgery was higher than 2 h later (mean ± SD: 26.6 ± 2.8 versus 10.0 ± 3.9 ng/mL/h). PRA remained higher at 2 h post‐surgery in admission groups compared to induction groups (p = .01). Serum TxB2 was lower with meloxicam than robenacoxib (p = .001), and was lower in the MA than each robenacoxib group at catheter placement. Admission groups (16/24 from RA and MA groups) received earlier rescue analgesia than other groups (p = .033). In conclusion, the renin‐angiotensin system was activated during anaesthesia despite cyclo‐oxygenase inhibition, possibly due to hypotension or surgical stimulation. There was no effect of drug or timing on the markers of renal function.

Funder

Novartis Animal Health

Publisher

Wiley

Subject

General Veterinary,Pharmacology

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