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培哚普利降低稳定型冠状动脉疾病心脏事件的欧洲试验(EUROPA)。

The European trial on reduction of cardiac events with perindopril in stable coronary artery disease (EUROPA).

作者信息

Fox K M, Henderson J R, Bertrand M E, Ferrari R, Remme W J, Simoons M L

机构信息

The Royal Brompton and Harefield NHS Trust, London, UK.

出版信息

Eur Heart J. 1998 Sep;19 Suppl J:J52-5.

PMID:9796841
Abstract

BACKGROUND

Angiotensin-converting enzyme (ACE) inhibitors have an accepted place in the treatment of hypertension and heart failure. However, at present they have no specific role in the prevention or treatment of coronary artery disease: evidence from animal experiments and some of the large ACE inhibitor cardiac studies makes this effect well worth testing.

OBJECTIVE

The objective of EUROPA is to assess the effects of perindopril (an ACE inhibitor) on outcome in patients with stable coronary artery disease, but no clinical heart failure.

METHODS

This is a double-blind, placebo-controlled, multicentre study with a duration of 3.5 years. It is proposed to recruit 10500 patients from 24 countries in Europe. The primary end-point is a combined one: total mortality, non-fatal acute myocardial infarction, unstable angina pectoris and cardiac arrest with successful resuscitation are included; the outcome is studied in patients with proven coronary artery disease and no clinical heart failure. Secondary end-points consist of these events individually calculated. The first patient was recruited in October 1997, and it is planned to finish recruitment by the end of 1998.

摘要

背景

血管紧张素转换酶(ACE)抑制剂在高血压和心力衰竭的治疗中已得到认可。然而,目前它们在冠状动脉疾病的预防或治疗中没有特定作用:来自动物实验和一些大型ACE抑制剂心脏研究的证据表明这种作用很值得进行试验。

目的

EUROPA研究的目的是评估培哚普利(一种ACE抑制剂)对无临床心力衰竭的稳定型冠状动脉疾病患者预后的影响。

方法

这是一项为期3.5年的双盲、安慰剂对照、多中心研究。计划从欧洲24个国家招募10500名患者。主要终点是一个综合指标:包括总死亡率、非致命性急性心肌梗死、不稳定型心绞痛和复苏成功的心脏骤停;在已证实患有冠状动脉疾病且无临床心力衰竭的患者中研究该结果。次要终点由这些事件单独计算得出。第一名患者于1997年10月入组,计划于1998年底完成招募。

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