Aspirin: Difference between revisions
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{{MedTemplate | {{MedTemplate | ||
| generic = Aspirin | | generic = Aspirin (acetylsalicylic acid; ASA) | ||
| brand | | brand = Bayer, Ecotrin, Bufferin, St. Joseph (low-dose 81 mg), Excedrin (with acetaminophen and caffeine) | ||
| classes = NSAID | | structure = | ||
| | | classes = [[:Category:NSAIDs|Non-steroidal anti-inflammatory (NSAID)]], [[:Category:Antiplatelets|Antiplatelet]], [[:Category:Analgesics|Analgesic]], [[:Category:Antipyretics|Antipyretic]] | ||
| uses = <vote slug="primary-cv-prevention-use">Primary cardiovascular prevention in selected patients (low-dose 81 mg, USPSTF guidance evolving)</vote>, <vote slug="secondary-cv-prevention-use">Secondary prevention of myocardial infarction and ischemic stroke (low-dose 81 mg daily, established benefit)</vote>, <vote slug="acute-mi-use">Acute myocardial infarction (162-325 mg chewed at first medical contact)</vote>, <vote slug="tia-acute-use">Transient ischemic attack / acute ischemic stroke management</vote>, <vote slug="preeclampsia-prophylaxis-use">Preeclampsia prophylaxis in pregnancy (81 mg after 12 weeks in high-risk patients, USPSTF)</vote>, <vote slug="mild-moderate-pain-use">Mild-to-moderate pain (FDA)</vote>, <vote slug="fever-use">Fever in adults (FDA; '''avoid in pediatric viral illness''')</vote>, <vote slug="kawasaki-disease-use">Kawasaki disease (FDA, pediatric)</vote> | |||
| starting_dose = Antiplatelet: 81 mg PO once daily. Acute MI/stroke: 162-325 mg chewed. Analgesic: 325-650 mg PO every 4-6 hours as needed | |||
| preparations = Tablets 81 (low-dose), 325, 500, 650 mg; chewable 81 mg; enteric-coated tablets; effervescent tablets; suppositories | |||
| fda_max = 4000 mg/day (analgesic) | |||
| pill_id = | |||
| routes = Oral, rectal | |||
| onset = Antiplatelet effect within 30-60 minutes; analgesic effect 30-60 minutes | |||
| duration = '''Antiplatelet effect lasts the platelet's lifetime (~7-10 days)''' due to irreversible COX-1 acetylation; analgesic 4-6 hours | |||
| halflife = Aspirin 15-30 minutes; salicylate metabolite 2-3 hours (concentration-dependent, saturable at high doses)<ref name="aspirin-label">FDA Prescribing Information, Bayer Aspirin (acetylsalicylic acid), Bayer HealthCare, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020589s015lbl.pdf</ref> | |||
| bioavailability = ~50% (oral; reduced by buffering and enteric coating but onset clinically similar)<ref name="aspirin-label" /> | |||
| pregnancy = Low-dose (81 mg) safe and indicated for preeclampsia prophylaxis after 12 weeks in high-risk patients per USPSTF; high-dose aspirin avoid third trimester due to premature ductus arteriosus closure and bleeding risk | |||
| legal = [[USLegal:Over-the-counter|OTC]] in US at all standard strengths | |||
| mechanism = <vote slug="aspirin-mech-claim">'''Irreversible''' covalent acetylation of cyclooxygenase enzymes (COX-1 and COX-2), distinguishing aspirin from all other NSAIDs, which inhibit reversibly. The platelet effect derives from COX-1 acetylation: platelets cannot synthesize new enzyme, so a single 81 mg daily dose abolishes thromboxane A2 production for the platelet's entire 7-10 day lifespan. Endothelial cells recover prostacyclin synthesis quickly because they have nuclei and can transcribe new COX. The analgesic, anti-inflammatory, and antipyretic effects come from the broader prostaglandin reduction.</vote> '''Reye syndrome''': rare hepatic encephalopathy in children given aspirin during viral illness, the basis of the firm pediatric viral-illness contraindication. Aspirin-exacerbated respiratory disease (Samter triad: asthma, nasal polyps, aspirin sensitivity) is a recognized cross-reactive hypersensitivity to all COX-1 inhibitors<ref name="aspirin-label" />. | |||
}} | }} | ||
== References == | |||
<references /> | |||
[[Category:NSAIDs]] | |||
[[Category:Antiplatelets]] | |||
[[Category:Analgesics]] | |||
[[Category:Antipyretics]] | |||