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无症状性儿茶酚胺能性多形性室性心动过速的治疗

Treatment of asymptomatic catecholaminergic polymorphic ventricular tachycardia.

作者信息

Obeyesekere Manoj N, Sy Raymond W, Leong-Sit Peter, Gula Lorne J, Yee Raymond, Skanes Allan C, Klein George J, Krahn Andrew D

机构信息

The University of Western Ontario, Division of Cardiology, London, Ontario, Canada.

出版信息

Future Cardiol. 2012 May;8(3):439-50. doi: 10.2217/fca.12.12.

Abstract

Catecholaminergic polymorphic ventricular tachycardia is a rare genetic disorder caused by mutations in genes involved in the intracellular calcium homeostasis of cardiac cells. Affected patients typically present with life-threatening ventricular arrhythmias precipitated by emotional/physical stress. The diagnosis is based on the demonstration of polymorphic or bidirectional ventricular tachycardia associated with adrenergic stress. Genetic testing can be confirmatory in some patients. Treatment for catecholaminergic polymorphic ventricular tachycardia includes medical and surgical efforts to suppress the effects of epinephrine at the myocardial level and/or modulation of calcium homeostasis. Mortality is high when untreated and sudden cardiac death may be the first manifestation of the disease. First-degree relatives of a proband should be offered genetic testing if the causal mutation is known. If the family mutation is not known, relatives should be clinically evaluated with provocative testing. In the absence of rigorous trials, prophylactic treatment of the asymptomatic catecholaminergic polymorphic ventricular tachycardia patient appears to reduce morbidity and mortality.

摘要

儿茶酚胺能性多形性室性心动过速是一种罕见的遗传性疾病,由参与心脏细胞内钙稳态的基因突变引起。受影响的患者通常会出现由情绪/身体应激诱发的危及生命的室性心律失常。诊断基于与肾上腺素能应激相关的多形性或双向性室性心动过速的证实。基因检测在某些患者中可作为确诊依据。儿茶酚胺能性多形性室性心动过速的治疗包括在心肌水平抑制肾上腺素作用和/或调节钙稳态的药物及手术措施。未经治疗时死亡率很高,心脏性猝死可能是该疾病的首发表现。如果已知致病突变,先证者的一级亲属应接受基因检测。如果家族突变未知,亲属应通过激发试验进行临床评估。在缺乏严格试验的情况下,对无症状的儿茶酚胺能性多形性室性心动过速患者进行预防性治疗似乎可降低发病率和死亡率。

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