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血小板功能和缺血性心脏病的抑制。

Platelet function and inhibition in ischemic heart disease.

机构信息

Department of Cardiovascular Sciences, Campus Bio-Medico University of Rome, Via Alvaro del Portillo 200, Rome, Italy.

出版信息

Curr Cardiol Rep. 2012 Aug;14(4):457-67. doi: 10.1007/s11886-012-0280-z.

Abstract

Platelets play an important role in the pathogenesis of thrombosis, the most common cause for the development of acute coronary syndromes such as complications occurring during percutaneous coronary intervention. Platelets act with a multiple step mechanism, in which different surface molecules are involved representing important therapeutic targets of antiplatelet agents. Despite clopidogrel efficacy which has been demonstrated in several studies, recurrent ischemic events remain considerably high in patients on treatment due to low clopidogrel responsiveness, a phenomenon influenced by environmental, clinical, and genetic factors. New P2Y12 blockers such as prasugrel and ticagrelor have been successfully introduced in clinical practice, whereas cangrelor, with a rapid offset and reversible platelet inhibition, may represent a useful bridging therapy in patients undergoing surgery. Moreover, the simultaneous inhibition of thrombin platelet aggregation by protease-activated receptor inhibitors may be an adjunctive approach in patients with coronary artery disease.

摘要

血小板在血栓形成的发病机制中起重要作用,血栓形成是经皮冠状动脉介入治疗等急性冠状动脉综合征并发症发生的最常见原因。血小板通过多步机制发挥作用,涉及不同的表面分子,这些分子是抗血小板药物的重要治疗靶点。尽管已有多项研究证实氯吡格雷的疗效,但由于氯吡格雷反应性低,接受治疗的患者仍存在相当高的复发性缺血事件,这种现象受环境、临床和遗传因素的影响。新型 P2Y12 抑制剂如普拉格雷和替格瑞洛已成功应用于临床实践,而具有快速消除和可逆性血小板抑制作用的坎格瑞洛可能是接受手术患者的有用桥接治疗方法。此外,蛋白酶激活受体抑制剂同时抑制凝血酶诱导的血小板聚集可能是冠心病患者的一种辅助治疗方法。

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