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Aspirin and Clopidogrel in Acute Coronary Syndromes
Author(s) -
Hani Jneid,
Deepak L. Bhatt,
Roberto Corti,
Juan J. Badimon,
Valentı́n Fuster,
Gary S. Francis
Publication year - 2003
Publication title -
archives of internal medicine
Language(s) - English
Resource type - Journals
eISSN - 1538-3679
pISSN - 0003-9926
DOI - 10.1001/archinte.163.10.1145
Subject(s) - clopidogrel , aspirin , medicine , cardiology , unstable angina , myocardial infarction , platelet , thromboxane a2 , acute coronary syndrome , coronary artery disease , coronary stent , thrombus , platelet activation , thienopyridine , stent , restenosis
Platelet adhesion, activation, and aggregation are central to thrombus formation, which follows atherosclerotic plaque disruption and causes acute coronary syndromes. Aspirin and clopidogrel exert their antiplatelet effects by inhibiting thromboxane A2 production and adenosine diphosphate-induced platelet aggregation pathways, respectively. Aspirin has proven benefits in primary and secondary prevention of coronary artery disease. Clopidogrel, an alternative antiplatelet agent used in patients with aspirin intolerance, is especially useful in combination with aspirin after coronary stent procedures. The CURE (Clopidogrel in Unstable Angina to Prevent Recurrent Events) study demonstrates for the first time the benefit of adding clopidogrel to aspirin rather than using aspirin alone in patients having acute coronary syndromes without ST-segment elevation myocardial infarction. Patients who are resistant to aspirin (up to 10%) have higher rates of cardiovascular events and may derive special benefit from the combination therapy. Aspirin resistance can be assessed through platelet aggregometry testing, measurement of urinary thromboxane metabolites, and, possibly, genomic testing in the future.

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