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血管紧张素转换酶抑制剂在急性心肌梗死中的应用——综述

Angiotensine converting enzyme inhibitors In acute myocardial infarction--a review.

作者信息

Sawhney J P S

机构信息

Department of Cardiology, Sir Ganga Ram Hospital, Rajinder Nagar, New Delhi, India.

出版信息

Indian Heart J. 2011 Jan-Feb;63(1):71-8.

Abstract

Coronary artery diseases (CADs) are preventable and controllable disorders, but they continue to be a major cause of morbidity and premature mortality across globe. India is projected to have 62 million CAD patients by 2015, with nearly 1/3rd of this burden shared by patients younger than 40 years. The renin-angiotensin-aldosterone system (RAAS) plays a pivotal role in blood pressure (BP) regulation and fluid and electrolyte homoeostasis. Activation of RAAS has long been implicated in the pathogenesis of acute myocardial infarction (AMI) and benefits of inhibition of RAAS as an effective way to intervene in the pathogenesis of AMI is well documented. In the setting of AMI, angiotensin-II plays a significant detrimental role, contributing to cardiac remodeling, a process that predisposes to subsequent arrhythmia and cardiac failure. Angiotensin converting enzyme inhibitors (ACEls) play a key role in the clinical management of several cardiovascular disease (CVD)s such as AMI, by inhibiting the actions of angiotensin-II, ACEIs would be expected to modify unwanted post-AMI events. ACEIs trials have tested AMI patients with two different approaches: selective (those with left ventricular dysfunction (LVD) treated over a long-term) and relatively unselective (those treated early over the course and for a short-period, up to 6 weeks). In general, results are consistent and beneficial as regards to reduction in both short-term & long-term mortality and heart failure. There are evidences that suggest yielding of an extra protection (reduced mortality and occurrence of severe LVD) with early introduction of ACEIs in the course of AMI. Trials have also shown ACEIs effective and consistent protection against re-infarction and management of arrhythmias after AMI. Large clinical trials have proven ACEIs to be superior to ARB, in preventing CV deaths in high-risk AMI subjects. They have proven to be safe & effective in diabetic & older population. With wealth of evidence available supporting use of ACEIs in patients with MI, The use of ACEIs in AMI has moved form experimental to standard therapy.

摘要

冠状动脉疾病(CADs)是可预防和可控的疾病,但它们仍然是全球发病和过早死亡的主要原因。预计到2015年印度将有6200万CAD患者,其中近三分之一的负担由40岁以下的患者承担。肾素-血管紧张素-醛固酮系统(RAAS)在血压(BP)调节以及体液和电解质稳态中起关键作用。长期以来,RAAS的激活一直被认为与急性心肌梗死(AMI)的发病机制有关,并且抑制RAAS作为干预AMI发病机制的有效方法的益处已有充分记录。在AMI的情况下,血管紧张素-II起显著的有害作用,导致心脏重塑,这一过程易引发随后的心律失常和心力衰竭。血管紧张素转换酶抑制剂(ACEls)在几种心血管疾病(CVD)如AMI的临床管理中起关键作用,通过抑制血管紧张素-II的作用,预计ACEls会改变AMI后不良事件。ACEls试验采用两种不同方法对AMI患者进行了测试:选择性(对有左心室功能障碍(LVD)的患者进行长期治疗)和相对非选择性(在病程早期进行短期治疗,最长6周)。总体而言,在降低短期和长期死亡率以及心力衰竭方面,结果是一致且有益的。有证据表明,在AMI病程中早期引入ACEls可产生额外的保护作用(降低死亡率和严重LVD的发生率)。试验还表明ACEls对AMI后再梗死和心律失常的管理有效且具有持续保护作用。大型临床试验已证明,在预防高危AMI患者的心血管死亡方面,ACEls优于ARB。它们已被证明在糖尿病患者和老年人群中安全有效。有大量证据支持在心肌梗死患者中使用ACEls,ACEls在AMI中的使用已从实验性治疗转变为标准治疗。

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