Evaluation of the analgesic effects of phenylbutazone administered at a high or low dosage in horses with chronic lameness.
Abstract: To compare analgesic effects of phenylbutazone administered at a dosage of 4.4 mg/kg/d (2 mg/lb/d) or 8.8 mg/kg/d (4 mg/lb/d) in horses with chronic lameness. Methods: Controlled crossover study. Animals-9 horses with chronic forelimb lameness. Methods: Horses were treated i.v. with phenylbutazone (4.4 mg/kg/d or 8.8 mg/kg/d) or saline (0.9% NaCl) solution once daily for 4 days. All horses received all 3 treatments with a minimum of 14 days between treatments. Mean peak vertical force (mPVF) was measured and clinical lameness scores were assigned before initiation of each treatment and 6, 12, and 24 hours after the final dose for each treatment. Results: Compared with values obtained after administration of saline solution, mPVF was significantly increased at all posttreatment evaluation times when phenylbutazone was administered. Clinical lameness scores were significantly decreased 6 and 12 hours after administration of the final dose when phenylbutazone was administered at the low or high dosage but were significantly decreased 24 hours after treatment only when phenylbutazone was administered at the high dosage. No significant differences in mPVF and clinical lameness scores were found at any time when phenylbutazone was administered at the low versus high dosage. Conclusions: Results suggest that the high dosage of phenylbutazone was not associated with greater analgesic effects, in terms of mPVF or lameness score, than was the low dosage. Considering that toxicity of phenylbutazone is related to dosage, the higher dosage may not be beneficial in chronically lame horses.
Publication Date: 2005-02-11 PubMed ID: 15702692DOI: 10.2460/javma.2005.226.414Google Scholar: Lookup
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- Clinical Trial
- Journal Article
- Randomized Controlled Trial
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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This study evaluates the pain-relieving effects of two different doses of the drug phenylbutazone on horses with chronic lameness. The researchers found that a higher dose does not yield superior pain-relief compared to a lower dose, suggesting that the higher dose may not be needed and could potentially avoid unnecessary side effects.
Research Methodology
- The researchers conducted a controlled crossover study using nine horses which were all suffering from chronic forelimb lameness.
- The treatment administered to these horses included either a low dose of phenylbutazone (4.4 mg/kg/d), a high dose of phenylbutazone (8.8 mg/kg/d), or a saline solution (as a control group).
- All horses received each of the three treatments, with a minimum of a 14-day interval between each treatment cycle to prevent overlap or interference from one treatment to the next.
- Before each treatment cycle began, and at 6, 12, and 24-hour intervals after the final dose, the researchers measured each horse’s mean peak vertical force (mPVF) – a measure of the horse’s weight-bearing ability – and assigned a clinical lameness score to assess the severity of the horse’s lameness.
Results
- Compared to the saline solution treatment, both doses of phenylbutazone resulted in a significant increase in the mPVF and a significant decrease in lameness scores at all times of post-treatment evaluation.
- While both the high and low doses of phenylbutazone significantly reduced clinical lameness scores 6 and 12 hours after administration, reduction of lameness at 24 hours was only significantly observed when the high dose was used.
- However, there were no substantial differences between the low and high doses on both mPVF and clinical lameness scores at any of the assessment times.
Conclusions
- The researchers concluded that there was no significant difference in the pain-relief effect between the lower and higher dose of phenylbutazone.
- The study therefore suggests that the use of a higher dose of the drug may not offer additional benefits for chronically lame horses. This is particularly important because the toxicity of phenylbutazone is dependent on the dose – therefore, using a lower dose could possibly minimize side effects without compromising the analgesic effect.
Cite This Article
APA
Hu HH, MacAllister CG, Payton ME, Erkert RS.
(2005).
Evaluation of the analgesic effects of phenylbutazone administered at a high or low dosage in horses with chronic lameness.
J Am Vet Med Assoc, 226(3), 414-417.
https://doi.org/10.2460/javma.2005.226.414 Publication
Researcher Affiliations
- Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Oklahoma State University, Stillwater, OK 74078, USA.
MeSH Terms
- Animals
- Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
- Cross-Over Studies
- Dose-Response Relationship, Drug
- Female
- Horse Diseases / drug therapy
- Horses
- Lameness, Animal / drug therapy
- Male
- Phenylbutazone / therapeutic use
- Treatment Outcome
Citations
This article has been cited 4 times.- Jacobs CC, Schnabel LV, McIlwraith CW, Blikslager AT. Non-steroidal anti-inflammatory drugs in equine orthopaedics.. Equine Vet J 2022 Jan 25;54(4):636-48.
- Whitfield-Cargile CM, Coleman MC, Cohen ND, Chamoun-Emanuelli AM, DeSolis CN, Tetrault T, Sowinski R, Bradbery A, Much M. Effects of phenylbutazone alone or in combination with a nutritional therapeutic on gastric ulcers, intestinal permeability, and fecal microbiota in horses.. J Vet Intern Med 2021 Mar;35(2):1121-1130.
- Martin LM, Johnson PJ, Amorim JR, DeClue AE. Effects of Orally Administered Resveratrol on TNF, IL-1β, Leukocyte Phagocytic Activity and Oxidative Burst Function in Horses: A Prospective, Randomized, Double-Blinded, Placebo-Controlled Study.. Int J Mol Sci 2020 Feb 20;21(4).
- Whitfield-Cargile CM, Chamoun-Emanuelli AM, Cohen ND, Richardson LM, Ajami NJ, Dockery HJ. Differential effects of selective and non-selective cyclooxygenase inhibitors on fecal microbiota in adult horses.. PLoS One 2018;13(8):e0202527.
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