Clinical features of Brugada syndrome

被引：5
作者：
Shimizu, Wataru [1 ,2 ]
机构：
[1] Natl Cerebral & Cardiovasc Ctr, Dept Cardiovasc Med, 5-7-1 Fujishiro Dai, Suita, Osaka, Japan
[2] Nippon Med Sch, Dept Internal Med, Div Cardiol, Bunkyo Ku, Tokyo 1138603, Japan
来源：
JOURNAL OF ARRHYTHMIA | 2013年 / 29卷 / 02期
关键词：
Brugada syndrome; ST segment; Ventricular fibrillation; Diagnosis Risk stratification;
D O I：
10.1016/j.joa.2013.01.009
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Brugada syndrome is a clinical entity characterized by type -1 (coved) ST-segment elevation in the right precordial electrocardiographic leads (V1-V3) and an aborted sudden cardiac death due to ventricular fibrillation (VF) in the absence of structural heart disease. Since 1992, when Brugada and Brugada reported the first case, numerous studies across the world have characterized the clinical, electrocardiographic, electrophysiologic, and prognostic features of Brugada syndrome. Several multicenter studies also suggested the natural history and proposed the risk stratification for subsequent cardiac events. In this review article, the clinical features of Brugada syndrome will be updated. (C) 2013 Japanese Heart Rhythm Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码：65 / 70
页数：6
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