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What is the risk of intensifying platelet inhibition beyond clopidogrel? A systematic review and a critical appraisal of then role of prasugrel

机译:除氯吡格雷外,增强血小板抑制作用的风险是什么?普拉格雷的作用的系统评价和关键评价

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摘要

Thienopyridines are a class of drug targeting the platelet adenosine diphosphate 2 receptor. They have been shown to significantly reduce platelet activity exerting an important role in those clinical settings in which such an effect is beneficial. Ticlopidine was first to be introduced several years ago but it was quickly replaced by clopidogrel as it had a better risk/benefit profile. Recently, prasugrel has been developed and tested in several ex vivo studies and clinical trials showing able to provide a more powerful antiplatelet effect at the expense of a higher risk of bleeding complications. Great debate rose around its recent approval in the US as well as in Europe. This review aims at exploring the development and available clinical data of this third-generation thienopyridine while discussing its practical implementation in routine practice.
机译:噻吩并吡啶类是针对血小板二磷酸腺苷2受体的药物。已显示它们显着降低血小板活性,在有益于此类效果的那些临床环境中发挥重要作用。噻氯匹定是几年前首次引入的,但由于它具有更好的风险/获益特征,因此被氯吡格雷迅速取代。最近,普拉格雷已在多项体外研究和临床试验中得到开发和测试,显示能够以更高的出血并发症风险为代价提供更强大的抗血小板作用。关于其最近在美国和欧洲的批准,引起了广泛的争论。这篇综述旨在探讨这种第三代噻吩并吡啶的开发和临床数据,同时讨论其在常规实践中的实际应用。

著录项

  • 来源
    《QJM》 |2010年第6期|p.367-377|共11页
  • 作者

    F. Bedogni;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 01:07:08

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