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[索他洛尔致一名15个月大婴儿尖端扭转型室性心动过速]

[Sotalol-induced torsade de pointes tachycardia in a 15-month-old infant].

作者信息

Sasse M, Paul T, Bergmann P, Kallfelz H C

机构信息

Abteilung Kinderheilkunde III und Pädiatrische Kardiologie Kinderklinik Medizinische Hochschule Hannover.

出版信息

Z Kardiol. 1995 Oct;84(10):863-6.

PMID:7502575
Abstract

Torsade de pointes (tdp) is a form of ventricular tachycardia whose occurrence in childhood is very rare. In adults treated with sotalol (Sotalex), tdp has been reported to have an incidence of 2-4%. There have been no reports of its occurrence in children treated with sotalol. We report about a 15-month-old girl with Wolff-Parkinson-White syndrome who developed recurrent syncopal attacks. She had been treated with sotalol at 1.5 mg/kg daily since being a newborn because of recurrent episodes of paroxysmal supraventricular tachycardia. Electrocardiogram exhibited frequent tdp tachycardia. Serum electrolyte levels were normal. Echocardiography excluded a structural heart defect and showed no signs of myocardial infection. After sotalol was ceased, infusion with lidocain was started. Despite this therapy the tdp continued. Magnesium aspartate (Magnesiocard) was then administered, and this finally stopped the tdp. As no other cause was evident, tdp in this child must be judged as a proarrhythmia related to sotalol therapy.

摘要

尖端扭转型室性心动过速(TdP)是室性心动过速的一种形式,在儿童中极为罕见。在使用索他洛尔(施太可)治疗的成人中,据报道TdP的发生率为2%至4%。尚无关于使用索他洛尔治疗的儿童发生TdP的报道。我们报告了一名15个月大患有预激综合征的女孩,她反复出现晕厥发作。自出生以来,由于阵发性室上性心动过速反复发作,她每天接受1.5毫克/千克的索他洛尔治疗。心电图显示频繁的TdP心动过速。血清电解质水平正常。超声心动图排除了结构性心脏缺陷,未显示心肌感染迹象。停用索他洛尔后,开始输注利多卡因。尽管进行了这种治疗,TdP仍持续。随后给予门冬氨酸镁(心镁),最终终止了TdP。由于没有其他明显原因,该患儿的TdP必须被判定为与索他洛尔治疗相关的致心律失常作用。

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