Power Rachel F, Hynes Brian G, Moran Darragh, Yagoub Hatim, Kiernan Gary, Ruggiero Nicholas J, Kiernan Thomas J
Department of Interventional Cardiology, Cork University Hospital, University College Cork School of Medicine, Cork, Ireland.
Expert Rev Cardiovasc Ther. 2012 Oct;10(10):1261-72. doi: 10.1586/erc.12.127.
Dual antiplatelet therapy is well recognized in the prevention of thrombotic complications of acute coronary syndrome and percutaneous coronary interventions. Despite clinical benefits of aspirin and clopidogrel therapy, a number of limitations curtail their efficacy: slow onset of action, variability in platelet inhibitory response and potential drug-drug interactions. Furthermore, the single platelet-activation pathway targeted by these agents allows continued platelet activation via other pathways, ensuring incomplete protection against ischemic events, thus, underscoring the need for alternate antiplatelet treatment strategies. A number of novel antiplatelet agents are currently in advance development and many have established superior effects on platelet inhibition, clinical outcomes and safety profile than clopidogrel in high-risk patients. The aim of this review is to provide an overview of the current status of P2Y12 receptor inhibition and PAR-1 antagonists in determining a future strategy for individualized antiplatelet therapy.
双联抗血小板治疗在预防急性冠状动脉综合征和经皮冠状动脉介入治疗的血栓形成并发症方面已得到广泛认可。尽管阿司匹林和氯吡格雷治疗具有临床益处,但一些局限性限制了它们的疗效:起效缓慢、血小板抑制反应存在变异性以及潜在的药物相互作用。此外,这些药物所靶向的单一血小板激活途径允许通过其他途径持续激活血小板,从而无法完全预防缺血事件,因此,凸显了需要替代抗血小板治疗策略。目前许多新型抗血小板药物正处于前期研发阶段,并且在高危患者中,许多药物已显示出比氯吡格雷在血小板抑制、临床结局和安全性方面具有更优的效果。本综述的目的是概述P2Y12受体抑制剂和PAR-1拮抗剂在确定未来个体化抗血小板治疗策略方面的现状。