Role of implantable cardioverter defibrillator therapy in patients with long OT syndrome

被引：26

作者：

Daubert, James P. ^{[1
]}

Zareba, Wojciech ^{[1
]}

Rosero, Spencer Z. ^{[1
]}

Budzikowski, Adam ^{[1
]}

Robinson, Jennifer L. ^{[1
]}

Moss, Arthur J. ^{[1
]}

机构：

[1] Univ Rochester, Med Ctr, Dept Med, Div Cardiol, Rochester, NY 14642 USA

来源：

AMERICAN HEART JOURNAL | 2007年 / 153卷 / 04期

关键词：

D O I：

10.1016/j.ahj.2007.01.025

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Long QT syndrome (LQTS) is one of several primary electrical disorders or hereditary arrhythmia syndromes along with the short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. Since its initial recognition in 1957 by Jervell and Lange-Nielsen (Am Heart J. 1957;54:59-68), LQTS has been intimately associated with risk for sudden cardiac death. The implantable defibrillator was developed by Morowski et al (N Engl J Med. 1980;303:322-4) as a treatment to prevent sudden cardiac death. Consequently, implanted cardioverter-defibrillator therapy deserves serious consideration as an important therapy for LQTS.

引用

页码：53 / 58

页数：6

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