儿茶酚胺能多态性室性心动过速
医学
Brugada综合征
心源性猝死
短QT综合征
心室颤动
室性心动过速
长QT综合征
内科学
心脏病学
病因学
重症监护医学
QT间期
兰尼碱受体2
钙
兰尼定受体
作者
Claire Kirkby,Catherine Renwick,Joanne Hargrave,Liam Tobin,Katie Frampton,Elizabeth Wilson,Soraya Nuthoo,Teofila Bueser
标识
DOI:10.12968/bjca.2022.0127
摘要
This article is the third instalment of the British Journal of Cardiac Nursing’s series on cardiac genetic concepts. Inherited arrhythmias are a group of conditions that affect the cardiac electrical system, typically resulting from changes in the way sodium, potassium or calcium ions are handled in the cell. Inherited arrhythmias can cause sudden cardiac death, especially in people who are undiagnosed and untreated. Most inherited arrhythmias are inherited in an autosomal dominant pattern. This article provides an overview of the aetiology, diagnosis, risk-management and treatment of patients with inherited arrhythmias at different ages and stages of life. The focus will be on inherited arrhythmias, specifically long QT, Brugada and catecholaminergic polymorphic ventricular tachycardia. There will be a brief mention of idiopathic ventricular fibrillation and sudden arrhythmic death syndrome.
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