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Mavacoxib and meloxicam for canine osteoarthritis: a randomised clinical comparator trial
M B Walton1, E C Cowderoy1, B Wustefeld-Janssens1
1Musculoskeletal Biology and Small Animal Teaching Hospital, University of Liverpool, Neston, Cheshire, UK.
Abstract:
NSAIDs are the cornerstone of medical management of canine osteoarthritis (OA). Meloxicam is a daily-administered NSAID widely available in a liquid formulation and manufacturer's summary of product characteristics (SPC) advise that it is given at the lowest effective dose. Mavacoxib is a long-acting NSAID given as a monthly tablet. This study compares these drugs in the management of canine OA. In all, 111 dogs with OA of the elbow, hip or stifle were randomly assigned to receive one of these NSAIDs for a 12-week period, and to administer them as per the manufacturer's SPC. Outcomes, including ground reaction forces and three validated clinical metrology instruments, were measured at baseline, 6 and 12 weeks. Improvements were seen in all outcome measures for both groups to a similar degree, and adverse events occurred at a similar rate. There were significant improvements in outcome measures from week 6 to week 12, as well as from baseline. Long-term meloxicam dose was more important than recent dose. Clinical efficacy and adverse event rates are similar for meloxicam and mavacoxib when administered as per their UK SPC. This is relevant information for veterinary surgeons when prescribing NSAID treatment for canine OA.
Insights
For canine osteoarthritis (OA), daily meloxicam and monthly mavacoxib showed similar clinical efficacy and adverse event rates. Long-term meloxicam dosage proved more critical than recent dosage for managing OA in dogs.
Area of Science:
- Veterinary Medicine
- Pharmacology
- Canine Health
Background:
- Nonsteroidal anti-inflammatory drugs (NSAIDs) are essential for managing canine osteoarthritis (OA).
- Meloxicam is a daily NSAID, while mavacoxib is a long-acting monthly NSAID.
- Manufacturer's guidelines recommend using the lowest effective NSAID dose.
Purpose of the Study:
- To compare the clinical efficacy and safety of meloxicam and mavacoxib in managing canine OA.
- To evaluate outcomes using ground reaction forces and validated clinical metrology instruments.
- To assess the impact of NSAID administration timing and dosage on OA management.
Main Methods:
- 111 dogs with elbow, hip, or stifle OA were randomly assigned to receive either meloxicam or mavacoxib for 12 weeks.
- Drugs were administered according to manufacturer's Summary of Product Characteristics (SPC).
- Outcome measures, including ground reaction forces and clinical metrology instruments, were assessed at baseline, 6 weeks, and 12 weeks.
Main Results:
- Both meloxicam and mavacoxib groups showed similar improvements in all measured outcome parameters.
- Adverse event rates were comparable between the two NSAID groups.
- Significant improvements in outcome measures were observed from baseline to 12 weeks, and specifically from week 6 to week 12.
Conclusions:
- Meloxicam and mavacoxib demonstrate similar clinical efficacy and safety profiles for canine OA when used per UK SPC guidelines.
- Long-term meloxicam dosage is a more significant factor than recent dosage in managing canine OA.
- This comparative data is valuable for veterinary surgeons prescribing NSAIDs for canine OA.
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