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[先天性长QT综合征患者硫酸阿托品试验期间发生尖端扭转型室速]

[Torsade de pointes during an atropine sulfate test in a patient with congenital long QT syndrome].

作者信息

Beccaria E, Brun S, Gaita F, Giustetto C, Conti M

出版信息

Cardiologia. 1989 Dec;34(12):1039-43.

PMID:2634481
Abstract

After a brief revision about the long QT syndrome, we report the case of a 52 year old man admitted to hospital for a syncopal attack. His electrocardiogram was considered normal: sinus bradycardia and U waves were recorded. The echocardiogram revealed anterior mitral leaflet redundancy and possible tricuspid prolapse. During the atropine test, after a normal increment of sinus frequency, 2 runs of self-limited torsade de pointes appeared. The electrocardiogram showed lesion wave at first, and then prolonged QT. During the intracavitary study, premature ventricular stimulation caused torsade de pointes. After propranolol iv it was no more possible to induce major ventricular arrhythmias anymore. Coronarography was normal. Nadolol therapy was begun. On 6 months follow-up the patient is asymptomatic.

摘要

在对长QT综合征进行简要回顾后,我们报告一例52岁男性因晕厥发作入院的病例。他的心电图被认为正常:记录到窦性心动过缓和U波。超声心动图显示二尖瓣前叶冗长以及可能存在三尖瓣脱垂。在阿托品试验期间,窦性频率正常增加后,出现了2阵自限性尖端扭转型室速。心电图起初显示病变波,随后QT间期延长。在心腔内研究期间,室性早搏刺激诱发了尖端扭转型室速。静脉注射普萘洛尔后,不再能诱发严重室性心律失常。冠状动脉造影正常。开始使用纳多洛尔治疗。随访6个月时,患者无症状。

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