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口服苄普地尔治疗稳定型冠状动脉供血不足性室性心律失常的疗效

[Efficacy of oral bepridil in ventricular arrhythmias in stable coronary insufficiency].

作者信息

Rio A, Pasco A, Dupont T, Deroubaix G, Moulinie E, Rossignol B, Pellet J, Brechenmacher C

出版信息

Arch Mal Coeur Vaiss. 1985 Oct;78 Spec No:75-8.

PMID:3938263
Abstract

The electrophysiological properties of bepridil suggest a possible ventricular antiarrhythmic effect. This prospective multicentre trial was undertaken to study the antiarrhythmic efficacy of oral bepridil on ventricular arrhythmias in patients with stable coronary insufficiency and more than 1 000 ventricular extrasystoles per 24 hours or ventricular tachycardia. The patients were divided into 3 groups according to the arrhythmias observed and the dosage used. In group I, the dosage was 300 mg/day and 12 out of 44 patients (27%) responded favourably to two criteria of efficacy (decrease of 84% of the number of ventricular extrasystoles; suppression of complex ventricular extrasystoles). In group II, the dosage was 300 mg/day, and then increased to 500 mg in non responders. Using the same criteria of efficacy, 13 out of 19 positive results were observed (68.4%). Group III comprised all cases of ventricular tachycardia; bepridil was effective in 3 out of 6 cases, associated with amiodarone in 1 case. The results demonstrate an antiarrhythmic effect of bepridil which is modest at 300 mg/day but which becomes more marked at the dosage of 500 mg/day.

摘要

苄普地尔的电生理特性提示其可能具有室性抗心律失常作用。本前瞻性多中心试验旨在研究口服苄普地尔对稳定型冠状动脉功能不全且每24小时室性期前收缩超过1000次或室性心动过速患者室性心律失常的抗心律失常疗效。根据观察到的心律失常和所用剂量,将患者分为3组。在第一组中,剂量为300毫克/天,44例患者中有12例(27%)对两项疗效标准有良好反应(室性期前收缩数量减少84%;复杂性室性期前收缩得到抑制)。在第二组中,剂量为300毫克/天,无反应者随后增至500毫克。采用相同的疗效标准,观察到19例中有13例阳性结果(68.4%)。第三组包括所有室性心动过速病例;苄普地尔在6例中有3例有效,1例与胺碘酮联合使用有效。结果表明,苄普地尔具有抗心律失常作用,300毫克/天的剂量时作用较弱,但500毫克/天的剂量时作用更明显。

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