Prasugrel provides a more rapid and potent antiplatelet effect with less interindividual variability compared to clopidogrel, but is associated with an increased risk of bleeding.
Prasugrel offers a more potent and consistent antiplatelet effect than clopidogrel for ACS patients undergoing PCI, though its use requires careful consideration of the increased bleeding risk.
INTRODUCTION: Prasugrel (CS-747, LY640315) is a third-generation thienopyridine, which gained approval by the FDA in 2009 for its use in patients with acute coronary syndrome undergoing percutaneous coronary intervention. AREAS COVERED: This article focuses on the preclinical profile of prasugrel. Using published preclinical and clinical studies, the authors summarize the pharmacokinetics, pharmacodynamics, and pharmacogenomics of prasugrel and their distinguishing features in efficacy and safety. EXPERT OPINION: Prasugrel has a more rapid, more potent antiplatelet effect with less interindividual response variability when compared to clopidogrel. Those therapeutic advantages are attributed to features of its chemical structure that favor the metabolic conversion of prasugrel to its active metabolite. However, the increased risk of bleeding has been associated with a greater antiplatelet effect and dosing profile; this is especially the case in those patients who are at a higher risk of bleeding complications. It is therefore important for an optimal dosing strategy of prasugrel to be identified to provide a formulation that has the best balance for efficacy and safety.
Shan et al. (Wed,) conducted a review in Acute coronary syndrome undergoing percutaneous coronary intervention. Prasugrel vs. Clopidogrel was evaluated. Prasugrel provides a more rapid and potent antiplatelet effect with less interindividual variability compared to clopidogrel, but is associated with an increased risk of bleeding.
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