Key result
Aspirin resistance leaves up to 60% of long-term patients at high risk for thrombotic events.
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Review reveals varied benefits of aspirin in cardiovascular prevention, highlighting the trade-off between ischemic event reduction and bleeding risk.
Aspirin is well recognized as an effective antiplatelet drug for secondary prevention in subjects at high risk of cardiovascular events. However, most patients receiving long-term aspirin therapy still remain at substantial risk of thrombotic events due to insufficient inhibition of platelets, specifically via the thromboxane A2 pathway. Although the exact prevalence is unknown, estimates suggest that between 5.5% and 60% of patients using this drug may exhibit a degree of "aspirin resistance," depending upon the definition used and parameters measured. To date, only a limited number of clinical studies have convincingly investigated the importance of aspirin resistance. Of these, few are of a sufficient scale, well designed, and prospective, with aspirin used at standard doses. Also, most studies do not sufficiently address the issue of noncompliance to aspirin as a frequent, yet easily preventable cause of resistance to this antiplatelet drug. This review article provides a comprehensive overview of aspirin resistance, discussing its definition, prevalence, diagnosis, and therapeutic approaches. Moreover, the clinical implications of aspirin resistance are explored in various cardiovascular disease states, including diabetes mellitus, hypertension, heart failure, and other similar disorders where platelet reactivity is enhanced.
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Gasparyan et al. (2008) conducted a review in Cardiovascular disease and aspirin resistance. Aspirin was evaluated. Aspirin resistance is estimated to affect 5.5% to 60% of patients receiving long-term therapy, leaving them at substantial risk for thrombotic events despite treatment.
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