Abstract: Equine Gastric Ulcer Syndrome (EGUS) is common in horses, and nonsteroidal anti-inflammatory drugs (NSAIDs) are a known risk factor for gastrointestinal ulceration. Although COX-2 selective NSAIDs such as firocoxib theoretically offer a better safety profile, endoscopic evidence for their mucosal safety at high off-label doses is lacking. Objective: To compare the effects of label-dose flunixin meglumine and high-dose firocoxib on the gastric mucosa of a small selected group of horses using serial gastroscopy and histopathology in a descriptive pilot study. Methods: Twenty mixed-breed horses were allocated non-randomly to control (n = 10), flunixin meglumine (1.1 mg/kg IM, n = 5), or firocoxib (1.0 mg/kg PO, n = 5) groups, treated once daily for 5 days. Gastroscopic evaluation and histopathological analysis were performed before (Day 1) and after treatment (Day 6). Results: No glandular disease was observed. Low prevalence of pre-existing squamous lesions was found in all groups without progression after treatment. Histopathological scores revealed baseline incomparability, with marked cellular infiltrate present only in the flunixin group at Day 1 (60%). Within-group analyses showed no significant changes between time points (p > 0.05). The use of NSAIDs effectively resolved lameness. Conclusions: In this small descriptive pilot study, limited by non-randomised allocation and small sample size, the study found no detectable short-term gastric mucosal injury associated with high-dose firocoxib within the limits of this study. Due to the non-randomised design, no causal conclusions can be drawn. These hypothesis-generating findings require confirmation in adequately powered randomised trials.
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The research aimed to see if high-dose firocoxib, a COX-2 selective NSAID, caused less gastric damage compared to the commonly used flunixin meglumine.
NSAIDs, often used to reduce pain and inflammation, are known risk factors for causing ulcers and other gastrointestinal problems.
Traditional NSAIDs like flunixin meglumine inhibit both COX-1 and COX-2 enzymes, which can contribute to gastric damage.
COX-2 selective NSAIDs such as firocoxib ideally spare the COX-1 enzyme, potentially reducing gastrointestinal side effects.
Despite theoretical safety advantages, there is limited direct evidence from endoscopy about the effects of high doses of firocoxib on the horse’s gastric mucosa.
Study Objective
To compare the effects of label-dose flunixin meglumine and a high off-label dose of firocoxib on the gastric mucosa of horses.
Utilized serial gastroscopic examinations and histopathological tissue analyses to assess mucosal condition before and after treatment.
Methods
Twenty mixed-breed horses were assigned to three groups:
Control group: 10 horses receiving no NSAID treatment.
Flunixin meglumine group: 5 horses given 1.1 mg/kg intramuscularly once daily for 5 days.
Firocoxib group: 5 horses given 1.0 mg/kg orally once daily for 5 days (high-dose, off-label usage).
Gastroscopic evaluations (visual inspection using an endoscope) and histopathological (microscopic tissue) analyses were performed before (Day 1) and after treatment (Day 6).
Lameness was monitored to confirm NSAID effectiveness in pain relief.
Note the allocation was non-randomized, which is an important limitation affecting causal conclusions.
Low prevalence of pre-existing squamous (upper stomach lining) lesions was detected in all groups, but these lesions did not worsen following treatment.
Histopathological analysis showed differences at baseline:
The flunixin group showed a marked cellular infiltrate in 60% of horses at the start, indicating some pre-existing inflammation.
No significant changes in cellular infiltration or other markers were observed after treatment in any group, including the firocoxib group.
Within-group comparisons (before vs. after treatment) revealed no statistically significant changes in gastric mucosa condition (p > 0.05), suggesting no detectable short-term mucosal injury from either NSAID under the conditions tested.
Both NSAIDs effectively resolved lameness, confirming expected therapeutic effects.
Conclusions and Implications
The study found no evidence of acute gastric mucosal damage associated with high-dose firocoxib treatment over 5 days in this small group of horses.
Due to non-randomized allocation and the small sample size, these results are preliminary and cannot establish causality or generalize to broader populations.
The baseline differences, especially the pre-existing inflammation in the flunixin group, complicate direct comparisons between treatments.
These findings are important for generating hypotheses for future research but require confirmation with larger, randomized controlled trials for definitive safety assessments.
The study supports the potential mucosal safety of high-dose firocoxib but stresses caution in clinical use until further evidence is obtained.
Cite This Article
APA
de Oliveira RA, Correa ADS, Monteiro FDO, Teixeira PPM.
(2026).
Gastroscopic Evaluation of Gastric Mucosa in Horses Treated With Flunixin Meglumine or High-Dose Firocoxib: A Descriptive Pilot Study.
Vet Med Sci, 12(4), e71061.
https://doi.org/10.1002/vms3.71061
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