首页> 外文期刊>Cardiac electrophysiology clinics >Arrhythmias in Dilated Cardiomyopathy
【24h】

Arrhythmias in Dilated Cardiomyopathy

机译:扩张型心肌病的心律不齐

获取原文
获取原文并翻译 | 示例
           

摘要

Patients with dilated cardiomyopathies (DCM) face a significant burden of arrhythmias, including conduction defects such as atrioventricular block and interventricular delay in the form of left bundle branch block, resulting in altered electromechanical coupling that can exacerbate heart failure. Atrial fibrillation is common and carries an adverse prognosis. Ventricular arrhythmias and sudden cardiac death generally occur late in the disease course. Sustained monomorphic ventricular tachycardia accounts for most of the sustained ventricular arrhythmias in DCM. This article summarizes common forms of arrhythmias encountered in patients with DCM, and reviews the relevant electrophysiologic basis of these arrhythmias and their management.
机译:扩张型心肌病(DCM)患者面临严重的心律失常负担,包括传导缺陷,例如房室传导阻滞和左束支传导阻滞形式的心室延迟,导致机电耦合改变,从而加重心力衰竭。心房颤动很常见,预后不良。室性心律失常和心源性猝死通常发生在病程的后期。持续性单形性室性心动过速占DCM中持续性室性心律失常的大部分。本文总结了DCM患者常见的心律不齐形式,并回顾了这些心律不齐的相关电生理基础及其管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号