Key result
Review evaluates newer oral antiplatelets like prasugrel and ticagrelor for managing coronary disease.
This review summarizes recent literature and guidelines on oral antiplatelet agents, including newer P2Y12 inhibitors like prasugrel and ticagrelor, for managing coronary disease.
Informs antiplatelet choices amid high coronary disease burden; leaves open optimal prasugrel-ticagrelor selection in updated guidelines.
Ischemic heart disease is the major isolated cause of death worldwide, responsible for 7,249,000 deaths in 2008, 12.7% of deaths from any causes. The inhibition of platelet activation and aggregation is an important therapeutic target. Cyclooxygenase inhibitors and thienopyridines are currently the 2 most used pharmacological classes, but novel antiplatelet agents have currently an important role. The most recent thienopyridine, prasugrel, allows an irreversible inhibition of the P2Y12 platelet receptor associated to a faster and more consistent onset of action rather the previous antiplatelet agents of the same class. Cyclopentyl-triazolo-pyrimidines, a newer pharmacological class from which ticagrelor is an example, also act at the P2Y12 platelet receptor, and like prasugrel, ticagrelor inhibits platelet aggregation in a fast and consistent manner, however, in a reversible way. This article aims to conduct a review on the literature about the most recent information and guidelines on oral antiplatelet agents available for the management of coronary disease.
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Gonçalves et al. (2016) conducted a review in Coronary disease. Oral antiplatelet agents was evaluated. Oral antiplatelet agents, including newer drugs like prasugrel and ticagrelor, are reviewed for their role in managing coronary disease, which caused 7,249,000 deaths worldwide in 2008.
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