心脏移植后QT间期延长与心脏骤停：遗传性还是后天性？
Prolonged QT and cardiac arrest after heart transplantation: inherited or acquired?
作者信息
Liu Tong, Shehata Michael, Chang David, Patel Jignesh K, Kittleson Michelle M, Kobashigawa Jon A, Chugh Sumeet S, Wang Xunzhang
机构信息
The Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
出版信息
J Electrocardiol. 2011 May-Jun;44(3):350-2. doi: 10.1016/j.jelectrocard.2010.12.001. Epub 2011 Jan 26.
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.
长QT综合征是一种遗传性致心律失常疾病，其特征为QT间期延长、晕厥以及主要由尖端扭转型室性心动过速导致的心脏性猝死。我们报告一例原位心脏移植术后早期因尖端扭转型室性心动过速导致QT间期延长和心脏骤停的罕见病例。
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