Key result
Short-term firocoxib or flunixin meglumine fails to clinically alter viscoelastic coagulation profiles in healthy horses.
Why the study?
To evaluate the effect of the cyclooxygenase-2-selective NSAID firocoxib compared to the nonselective NSAID flunixin meglumine on viscoelastic coagulation parameters in healthy horses.
Does firocoxib compared to flunixin meglumine alter viscoelastic coagulation profiles in healthy horses?
Does firocoxib compared to flunixin meglumine alter viscoelastic coagulation profiles in healthy horses?
p-value: p=0.02
Short-term administration of firocoxib or flunixin meglumine does not cause clinically significant alterations in viscoelastic coagulation profiles in healthy horses.
Short-term NSAID use shows no clinical coagulation effects in healthy horses; leaves open translation to diseased animals or practice.
OBJECTIVE: To evaluate the effect of the cyclooxygenase-2-selective NSAID firocoxib, compared to the nonselective NSAID flunixin meglumine on viscoelastic coagulation parameters in healthy horses. ANIMALS: 12 healthy adult mixed-breed horses. PROCEDURES: Following a crossover protocol, horses were administered flunixin meglumine (1.1 mg/kg, IV, q 12 h for 5 days), allowed a 6-month washout period, and then administered firocoxib (0.3 mg/kg, PO, once, then 0.1 mg/kg, PO, q 24 h for 4 days). Omeprazole (1 mg/kg, PO, q 24 h) was administered concurrently with each NSAID. Viscoelastic coagulation profiles and traditional coagulation parameters (prothrombin time, partial thromboplastin time, and fibrinogen) were measured before and after each treatment. RESULTS: Viscoelastic coagulation parameters were within reference intervals before and after both treatments. There was a statistically significant difference between treatments for amplitude at 10 minutes after clot time (P = .02) and maximum clot formation (P = .02); however, the magnitude of change was not clinically significant. CLINICAL RELEVANCE: Short-term administration of flunixin meglumine and firocoxib did not result in significant alteration of viscoelastic coagulation profiles in healthy horses. However, clinicians should be aware of possible coagulopathy secondary to NSAID administration with long-term use or critical illness, and further study is indicated.
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Bishop et al. (2022) studied Healthy horses (n=12). Firocoxib vs. Flunixin meglumine was evaluated on Viscoelastic coagulation parameters (p=0.02). Short-term administration of firocoxib or flunixin meglumine did not clinically alter viscoelastic coagulation profiles in healthy horses, despite differences in maximum clot formation (P=0.02).
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