Aspirin, or acetylsalicylic acid, is a salicylate NSAID with analgesic, anti-inflammatory and antipyretic actions. At lower exposure it is also used to inhibit platelet function. Veterinary use has declined for many painful conditions because other agents offer more suitable species-specific evidence or tolerability.
Analgesic and antiplatelet uses involve different therapeutic objectives and exposure requirements. Platelet response is variable in animals, and species differences in salicylate elimination substantially affect persistence and accumulation.
Aspirin irreversibly acetylates cyclooxygenase enzymes, reducing formation of prostaglandins from arachidonic acid. Lower prostaglandin production reduces inflammatory sensitization of pain pathways and contributes to analgesia, anti-inflammatory activity and antipyresis. Reduced protective prostaglandins also explain important gastrointestinal and renal effects.
In platelets, inhibition of COX-1 reduces thromboxane A2 formation and thereby limits platelet activation and aggregation. Because platelets cannot readily replace the acetylated enzyme, inhibition can persist beyond the presence of aspirin in plasma. The degree of suppression is nevertheless inconsistent among veterinary patients.
After absorption aspirin is hydrolyzed to salicylate, which contributes additional pharmacologic effects and is eliminated at markedly different rates between species. Aspirin’s platelet action is therefore distinct from simply selecting any NSAID, and an analgesic dose is not automatically an appropriate antithrombotic regimen.
Salicylate poisoning can cause vomiting, hyperthermia, hyperventilation, acid–base disturbances, weakness, seizures and coma. Monitor blood gases, electrolytes, hydration and renal function. Decontamination, gastrointestinal protection and carefully monitored urinary alkalinization may be indicated; dialysis may be considered for severe poisoning.
Monitor gastrointestinal signs and bleeding. Enteric-coated absorption in dogs can be erratic and incomplete; buffering does not prevent serious ulceration or perforation.
Aspirin can suppress measured thyroid hormone values after 2–4 weeks; values returned to baseline about 14 days after stopping in the described observation.
Keep tightly sealed and dry at room temperature; moisture causes hydrolysis. Extended-release Durlaza capsules must not be opened or broken.
For an avian drinking-water preparation, 5 g in 250 mL as the sole water source is described; exposure depends on intake. Because of hydrolysis, prepare fresh every 12 hours at room temperature or every 4 days refrigerated at 5°C. Monitor PCV and fecal blood when indicated; stop before planned surgery when clinically appropriate, with 1 week described for platelet recovery.
Routine aspirin after heartworm adulticide treatment lacks convincing clinical benefit and can be inappropriate; it is not a preferred prophylactic protocol. Use the metric strength of the exact bolus rather than an assumed grain conversion.