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Ventricular tachycardia and exercise related syncope in children with structurally normal hearts: emphasis on repolarisation abnormality.

机译:心脏结构正常的儿童的室性心动过速和运动相关性晕厥:强调复极异常。

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摘要

OBJECTIVE--To emphasize the importance of ventricular tachycardia associated with repolarisation abnormality in syncope associated with exercise. DESIGN--Retrospective analysis of data on children presenting with syncope between 1985 and 1993. PATIENTS--5 apparently normal children with recurrent exercise related syncope associated with electrocardiographically abnormal TU complexes. RESULTS--3 children were diagnosed as having an intermediate form of the long QT syndrome and catecholamine sensitive ventricular tachycardia because the abnormal TU complexes were associated with polymorphic ventricular tachycardia that was not typical of torsades de pointes. Tachycardia was induced by exercise in all patients and by isoprenaline in the one patient who was tested. One patient also had sinus node dysfunction. One child had incessant salvos of polymorphic ventricular arrhythmias and intermittent abnormal TU complexes suggestive of repolarisation abnormalities. The other had typical congenital long QT syndrome. Treatment was effective in three patients; two patients took a beta blocker alone and one took a beta blocker and low doses of amiodarone. One patient died suddenly, death being associated with sinus node dysfunction. In one patient with incessant ventricular arrhythmias treatment with a beta blocker, amiodarone, or Ic drugs was ineffective and always associated with proarrhythmia or syncope. He was not given further treatment and was asymptomatic despite having mild cardiomegaly. CONCLUSIONS--Ventricular tachycardia associated with repolarisation abnormality was an important cause of exercise related syncope in apparently normal children. TU complex abnormalities can be identified by repeated electrocardiography. beta Blockers are effective in preventing recurrent episodes. The role of amiodarone in this type of ventricular tachycardia needs further evaluation.
机译:目的-强调与运动相关的晕厥中与复极异常相关的室性心动过速的重要性。设计-对1985年至1993年间出现晕厥的儿童的数据进行回顾性分析。PATIENTS--5显然是正常儿童,其反复运动相关的晕厥与心电图异常TU复合物相关。结果--3儿童被诊断为患有长QT综合征和儿茶酚胺敏感型室性心动过速的中间形式,因为异常TU复合物与多形性室性心动过速有关,这不是尖端扭转型室速的典型表现。在所有患者中,运动均诱发心动过速;在一名接受测试的患者中,异丙肾上腺素诱发心动过速。一名患者也有窦房结功能障碍。 1名儿童多发性室性心律失常和间歇性异常TU复合体反复发作,提示复极异常。另一个患有典型的先天性长QT综合征。治疗对三例患者有效;两名患者仅服用了β受体阻滞剂,一名服用了β受体阻滞剂和低剂量的胺碘酮。一名患者突然死亡,死亡与窦房结功能障碍有关。在一名患有持续性室性心律不齐的患者中,使用β受体阻滞剂,胺碘酮或Ic药物治疗无效,并且总是伴有心律失常或晕厥。尽管患有轻度心脏肥大,但他没有得到进一步的治疗并且没有症状。结论:与复极异常有关的室性心动过速是与运动有关的晕厥的一个重要原因,显然是正常儿童。 TU复合体异常可以通过重复心电图检查来识别。 beta阻滞剂可有效预防复发发作。胺碘酮在这种心室性心动过速中的作用需要进一步评估。

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