Prolonged QT and cardiac arrest after heart transplantation: inherited or acquired?

被引：4
|
作者：
Liu, Tong [1 ]
Shehata, Michael [1 ]
Chang, David [1 ]
Patel, Jignesh K. [1 ]
Kittleson, Michelle M. [1 ]
Kobashigawa, Jon A. [1 ]
Chugh, Sumeet S. [1 ]
Wang, Xunzhang [1 ]
机构：
[1] Cedars Sinai Med Ctr, Inst Heart, Los Angeles, CA 90048 USA
来源：
JOURNAL OF ELECTROCARDIOLOGY | 2011年 / 44卷 / 03期
关键词：
Long QT syndrome; Torsades de Pointes; Sudden cardiac death; Heart transplantation; LONG;
D O I：
10.1016/j.jelectrocard.2010.12.001
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The long QT syndrome is an inherited arrhythmogenic disease characterized by prolongation of QT interval, syncope, and sudden cardiac death because of ventricular tachycardia, mainly in the form of Torsades de Pointes. We present an unusual case of prolonged QT interval and cardiac arrest caused by Torsades de Pointes in the early phase after orthotopic heart transplant. (c) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码：350 / 352
页数：3
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