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在心电图监测下,使用妥卡尼对Curschmann-Steinert型强直性肌营养不良进行抗强直治疗。

Antimyotonic therapy with tocainide under ECG control in the myotonic dystrophy of Curschmann-Steinert.

作者信息

Mielke U, Haass A, Sen S, Schmidt W

出版信息

J Neurol. 1985;232(5):271-4. doi: 10.1007/BF00313863.

Abstract

Ten patients suffering from advanced myotonic dystrophy with severe myotonic symptoms were treated with 800-1200 mg/day of the anti-arrhythmic drug tocainide (Xylotocan). All patients reported a marked subjective improvement of myotonia, which was confirmed by objective tests. Except for a slight QT-prolongation in one patient, the ECG was not significantly altered by the treatment. Twenty-four-hour ECG after treatment disclosed that pre-existing ventricular arrhythmia disappeared in three cases. The occurrence of complex ventricular arrhythmia in two patients under treatment was not necessarily due to specific effects of the drug but might be explained by the high spontaneous variability of rhythm disorders. In these patients suffering from myotonic dystrophy with typical cardiomyopathy no deleterious effects of the drug were observed, especially no cardiac arrhythmias which would have necessitated interruption of treatment. Therefore, the authors recommend symptomatic therapy with tocainide for myotonia and paramyotonia congenita, as well as in myotonic dystrophy patients suffering from marked myotonic stiffness. ECG and 24-h ECG should be carefully recorded as necessary in any treatment with anti-arrhythmic drugs.

摘要

十名患有晚期强直性肌营养不良且伴有严重肌强直症状的患者,接受了每日800 - 1200毫克抗心律失常药物妥卡尼(Xylotocan)的治疗。所有患者均报告肌强直主观症状有显著改善,客观测试也证实了这一点。除一名患者出现轻微QT间期延长外,治疗对心电图无明显改变。治疗后的24小时心电图显示,三名患者原有的室性心律失常消失。两名正在接受治疗的患者出现复杂性室性心律失常,不一定是药物的特定作用所致,可能是由于节律紊乱的高自发变异性。在这些患有强直性肌营养不良并伴有典型心肌病的患者中,未观察到该药物的有害作用,尤其是没有出现需要中断治疗的心律失常。因此,作者建议用妥卡尼对肌强直和先天性副肌强直进行对症治疗,以及用于患有明显肌强直僵硬的强直性肌营养不良患者。在使用抗心律失常药物进行任何治疗时,如有必要,应仔细记录心电图和24小时心电图。

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