实用心电学杂志2016，Vol.25Issue(5)：313-316,4.DOI:10.13308/j.issn.2095-9354.2016.05.003
继发性长 QT 综合征与尖端扭转型室性心动过速
Acquired long-QT syndrome and torsade de pointes
刘志红 1王晓燕 1张云哲 1智亚欣1
作者信息
- 1. 050011 河北 石家庄，石家庄市第三医院心内科
- 折叠
摘要
Abstract
Long-QT syndrome(LQTS)is characterized by prolongation of ventricular repolar-ization time,and increase of inhomogeneity and dispersion.LQTS is dangerous because it may lead to torsade de pointes(TdP)and ventricular fibrillation.The clinical manifestations include syncope,tetany or sudden death.LQTS includes congenital long-QT syndrome(cLQTS)and ac-quired long-QT syndrome(aLQTS).The latter is more frequently seen in clinical practice than the former,and is potentially lethal,which makes it one of the most important reasons for sudden car-diac death in hospital.In the calculation of QT/QTc intervals,to evaluate ventricular repolariza-tion as accurately as possible in different methods within the recommended range of critical value of QT/QTc interval prolongation time can predict the occurrence of TdP and further reduce the rate of sudden death.关键词
继发性长QT综合征/尖端扭转型室性心动过速/QT/QTc间期Key words
acquired long-QT syndrome/torsade de pointes/QT/QTc interval分类
医药卫生引用本文复制引用
刘志红,王晓燕,张云哲,智亚欣..继发性长 QT 综合征与尖端扭转型室性心动过速[J].实用心电学杂志,2016,25(5):313-316,4.
