Brugada综合征
儿茶酚胺能多态性室性心动过速
心室颤动
医学
心源性猝死
长QT综合征
心脏病学
内科学
短QT综合征
心脏骤停
室性心动过速
病因学
心律失常
QT间期
心房颤动
兰尼碱受体2
兰尼定受体
钙
作者
Andrew D. Krahn,Jacob Tfelt‐Hansen,Rafik Tadros,Christian Steinberg,Christopher Semsarian,Hui‐Chen Han
标识
DOI:10.1016/j.jacep.2021.12.014
摘要
Inherited arrhythmia syndromes are a common cause of apparently unexplained cardiac arrest or sudden cardiac death. These include long QT syndrome and Brugada syndrome, with a well-recognized phenotype in most patients with sufficiently severe disease to lead to cardiac arrest. Less common and typically less apparent conditions that may not be readily evident include catecholaminergic polymorphic ventricular tachycardia, short QT syndrome and early repolarization syndrome. In cardiac arrest patients whose extensive testing does not reveal an underlying etiology, a diagnosis of idiopathic ventricular fibrillation or short-coupled ventricular fibrillation is assigned. This review summarizes our current understanding of the less common inherited arrhythmia syndromes and provides clinicians with a practical approach to diagnosis and management.
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