Key result
Oral antiplatelet agents, including newer options like prasugrel and ticagrelor, are reviewed for their pharmacology, safety, and efficacy in preventing complications in ischemic heart disease.
This review summarizes the pharmacology, safety, and efficacy of newer oral antiplatelet agents like prasugrel and ticagrelor compared to clopidogrel in the management of ischemic heart disease.
Consolidates evidence on prasugrel and ticagrelor versus clopidogrel in IHD; leaves open optimal use in evolving real-world populations.
Platelet activation and aggregation play a central role in the pathophysiology of thrombogenesis in ischemic heart disease. Dual antiplatelet therapy with aspirin and clopidogrel is currently the golden standard in the prevention of cardiovascular complications after percutaneous coronary intervention. Newer antiplatelet drugs are continuously marketed to respond to the limitations of clopidogrel, namely a delayed onset of action, an irreversible inhibition of platelet aggregation as well as a substantial variability in antiplatelet effect, in part due to genetic polymorphism. The second-generation thienopyridine prasugrel is more potent than clopidogrel, but also manifests a greater bleeding risk. Ticagrelor, a third-generation thienopyridine, seems to have a better safety profile and has recently been approved as a first-choice antiplatelet treatment in acute coronary syndrome in Europe. This article will review the different oral antiplatelet drugs currently available, compare pharmacology and safety/e...
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Dridi et al. (2011) conducted a review in Ischemic heart disease. Oral antiplatelet agents (e.g., aspirin, clopidogrel, prasugrel, ticagrelor) was evaluated. Oral antiplatelet agents, including newer options like prasugrel and ticagrelor, are reviewed for their pharmacology, safety, and efficacy in preventing complications in ischemic heart disease.
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