医学
赫尔格
QT间期
复极
延长
心源性猝死
钾通道
药品
猝死
心脏病学
内科学
麻醉
药理学
电生理学
作者
Clifford TeBay,Jamie I. Vandenberg
出处
期刊:Heart Rhythm
[Elsevier]
日期:2024-03-01
卷期号:21 (3): 329-330
标识
DOI:10.1016/j.hrthm.2023.11.012
摘要
The increased risk of arrhythmias and sudden cardiac death (SCD) caused by drug-induced QT prolongation has been a prominent safety pharmacology concern for the last 30 years. Between 1994 and 2004, 9 drugs were either removed from the market or had their use restricted because of an unacceptably high risk of lethal ventricular arrhythmias,1 caused by inadvertent block of human ether-a-go-go-related gene (hERG) potassium channels, which encode the rapid delayed-rectifier potassium current, an important contributor to cardiac repolarization.
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