ASPIRIN
Aspirin’s long use and
availability without prescription diminishes its glamour compared with that of
the newer NSAIDs. Aspirin is now rarely used as an anti-inflammatory medication
and will be reviewed only in terms of its anti-platelet effects (ie, doses of
81–325 mg once daily).
Salicylic acid is a
simple organic acid with a pKa of 3.0. Aspirin (acetylsalicylic acid; ASA) has a pKa of 3.5 (see Table
1–3). The salicylates are rapidly absorbed from the stomach and upper small
intestine yielding a peak plasma salicylate level within 1–2 hours. Aspirin is
absorbed as such and is rapidly hydrolyzed (serum half-life 15 minutes) to
acetic acid and salicylate by esterases in tissue and blood (Figure 36–3).
Salicylate is nonlinearly bound to albu-min. Alkalinization of the urine
increases the rate of excretion of free salicylate and its water-soluble
conjugates.
Aspirin
irreversibly inhibits platelet COX so that aspirin’s anti-platelet effect lasts
8–10 days (the life of the platelet). In other tissues, synthesis of new COX
replaces the inactivated enzyme so that ordinary doses have a duration of
action of 6–12 hours.
Aspirin decreases the
incidence of transient ischemic attacks, unstable angina, coronary artery
thrombosis with myocardial infarction, and thrombosis after coronary artery
bypass grafting .Epidemiologic studies suggest that long-term use of aspirin at
low dosage is associated with a lower incidence of colon cancer, possibly
related to its COX-inhibiting effects
In addition to the
common side effects listed above, aspirin’s main adverse effects at
antithrombotic doses are gastric upset (intolerance) and gastric and duodenal
ulcers. Hepatotoxicity, asthma, rashes, GI bleeding, and renal toxicity rarely
if ever occur at antithrombotic doses.
The antiplatelet
action of aspirin contraindicates its use by patients with hemophilia. Although
previously not recommended during pregnancy, aspirin may be valuable in treating
preeclampsia-eclampsia.
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