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卡马西平治疗心脏传导系统异常患者神经系统疾病的电生理效应及临床危害。

Electrophysiologic effects and clinical hazards of carbamazepine treatment for neurologic disorders in patients with abnormalities of the cardiac conduction system.

作者信息

Kennebäck G, Bergfeldt L, Vallin H, Tomson T, Edhag O

机构信息

Department of Medicine, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.

出版信息

Am Heart J. 1991 May;121(5):1421-9. doi: 10.1016/0002-8703(91)90148-b.

Abstract

Carbamazepine, a first-line drug for the treatment of epilepsy and neuralgia, may exert hazardous effects on the cardiac conduction system. Standard ECG and long-term ECG monitoring and invasive electrophysiologic testing were carried out in 10 patients who required this drug for neurologic disorders, but in whom its safe use had been questioned because of symptoms of ECG abnormalities. We observed depression of sinus node function and an atrioventricular conduction delay with a significant prolongation of the PQ interval of 16 msec (9%; 95% confidence interval: 1.9% to 16.5%; p less than 0.05), of which the HV interval was significantly prolonged but not the PA and AH intervals. These effects are in accordance with previously shown class 1A properties. However, the lack of effects on QRS, JT, and QT intervals at normal heart rates is a class 1B characteristic. Thus carbamazepine seems to have composite electropharmacologic actions. A cause effect relationship between carbamazepine treatment and significant arrhythmias was established in five patients. Thus the negative chronotropic and dromotropic effects of carbamazepine may, at least in predisposed patients, induce symptoms confusingly similar to the epileptic seizures it is used to prevent.

摘要

卡马西平是治疗癫痫和神经痛的一线药物,可能对心脏传导系统产生有害影响。对10例因神经系统疾病需要使用该药物但因心电图异常症状而对其安全使用存疑的患者进行了标准心电图、长期心电图监测和有创电生理检查。我们观察到窦房结功能抑制和房室传导延迟,PQ间期显著延长16毫秒(9%;95%置信区间:1.9%至16.5%;p<0.05),其中HV间期显著延长,但PA和AH间期未延长。这些效应与先前显示的1A类特性一致。然而,在正常心率下对QRS、JT和QT间期无影响是1B类特征。因此,卡马西平似乎具有复合电药理作用。在5例患者中确立了卡马西平治疗与严重心律失常之间的因果关系。因此,卡马西平的负性变时和变传导作用至少在易感患者中可能诱发与它用于预防的癫痫发作相似的症状。

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