Latent Causes of Sudden Cardiac Arrest

被引:9
|
作者
Krahn, Andrew D. [1 ,8 ]
Tfelt-Hansen, Jacob [2 ,3 ]
Tadros, Rafik [4 ]
Steinberg, Christian [5 ]
Semsarian, Christopher [6 ]
Han, Hui-Chen [1 ,7 ]
机构
[1] Univ British Columbia, Ctr Cardiovasc Innovat, Heart Rhythm Serv, Div Cardiol, Vancouver, BC, Canada
[2] Rigshosp, Copenhagen Univ Hosp, Heart Ctr, Dept Cardiol, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Med Sci, Dept Forens Med, Copenhagen, Denmark
[4] Univ Montreal, Montreal Heart Inst, Cardiovasc Genet Ctr, Dept Med, Montreal, PQ, Canada
[5] Laval Univ, Inst Univ Cardiol & Pneumol Quebec IUCPQ UL, Dept Cardiol & Cardiac Surg, Inherited Arrhythmia Serv, Quebec City, PQ, Canada
[6] Univ Sydney, Agnes Ginges Ctr Mol Cardiol Centenary Inst, Sydney, NSW, Australia
[7] Monash Univ, Victorian Heart Inst, Clayton, Vic, Australia
[8] Univ British Columbia, Ctr Cardiovasc Innovat, Heart Rhythm Serv, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
基金
英国医学研究理事会;
关键词
KEY WORDS inherited; sudden death; ventricular arrhythmia; POLYMORPHIC VENTRICULAR-TACHYCARDIA; SHORT QT SYNDROME; EARLY REPOLARIZATION PATTERN; SHORT-COUPLED VARIANT; RECEPTOR RYR2 GENE; ELECTROCARDIOGRAPHIC CHARACTERISTICS; BRUGADA SYNDROME; THERAPEUTIC STRATEGIES; EXPERIMENTAL-MODEL; ARRHYTHMIC EVENTS;
D O I
10.1016/j.jacep.2021.12.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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 suf-ficiently 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 repolari-zation 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. (J Am Coll Cardiol EP 2022;8:806-821) (c) 2022 by the American College of Cardiology Foundation.
引用
收藏
页码:806 / 821
页数:16
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