Suppr超能文献

普拉格雷:一种新型血小板 ADP P2Y 受体拮抗剂。

Prasugrel: a novel platelet ADP P2Y receptor antagonist.

作者信息

Wilson William, Gurvitch Ronen, Ajani Andrew E

机构信息

Department of Cardiology, Royal Melbourne Hospital, Melbourne, Victoria 3050, Australia.

出版信息

Cardiovasc Ther. 2009 Fall;27(3):194-8. doi: 10.1111/j.1755-5922.2009.00086.x.

Abstract

The antiplatelet drug prasugrel is one of the new generations of thienopyridines, drugs that inhibit the platelet P2Y(12) receptor. It is becoming clear that there is variability in individual responses to antiplatelet agents such as clopidogrel, which may limit their efficacy and widespread utility. A number of controversies remain, such as varied definitions of "nonresponders" to antiplatelet therapy, the optimal means of assessing platelet function, and the potential capacity of in vivo platelet function studies to predict future clinical events. Prasugrel provides more rapid and consistent platelet inhibition than does clopidogrel, yet its clinical utility is under scrutiny. We aim to review the available data evaluating the efficacy and safety of this novel antiplatelet agent.

摘要

抗血小板药物普拉格雷是新一代噻吩并吡啶类药物之一,这类药物可抑制血小板P2Y(12)受体。越来越明显的是,个体对氯吡格雷等抗血小板药物的反应存在差异,这可能会限制其疗效和广泛应用。仍存在一些争议,例如抗血小板治疗“无反应者”的不同定义、评估血小板功能的最佳方法以及体内血小板功能研究预测未来临床事件的潜在能力。普拉格雷比氯吡格雷能更快速、更持续地抑制血小板,但它的临床效用仍在接受审查。我们旨在综述评估这种新型抗血小板药物疗效和安全性的现有数据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验