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法利帕米(AQA - 39)——一种新型的减慢心率药物的电生理特性。

Electrophysiologic properties of falipamil (AQA-39)--a new bradycardiac agent.

作者信息

Lévy S, Mètge M, Hilaire J, Cointe R, Bru P, Eychenne J L, Gérard R

机构信息

Department of Cardiology, University of Aix-Marseille, School of Medicine, France.

出版信息

Eur Heart J. 1987 Nov;8(11):1236-40. doi: 10.1093/oxfordjournals.eurheartj.a062198.

Abstract

Falipamil hydrochloride (AQA 39) is a new antiarrhythmic agent structurally related to verapamil. We evaluated the electrophysiologic properties of intravenous falipamil (1.5 mg kg-1 within 20 minutes) in 12 patients. The spontaneous cycle length was significantly (P less than 0.001) prolonged (+79 +/- 59 ms). Atrioventricular conduction was significantly (P less than 0.001) shorter due to AH interval shortening (-17 +/- 14 ms), most probably related to an anticholinergic effect. Similarly, the anterograde Wenckebach point occurred at a significantly (P less than 0.06) higher rate after falipamil (+10 +/- 7 beats min-1). No statistically significant effect was noted on the refractory periods of the AV node, although there was a trend to shortening. The refractoriness of the right atrium and ventricle was significantly prolonged. It is concluded that falipamil is a bradycardiac agent with electrophysiologic properties quite different from those of verapamil and similar to those of class IA antiarrhythmic agents.

摘要

盐酸法利帕米(AQA 39)是一种结构上与维拉帕米相关的新型抗心律失常药物。我们评估了12例患者静脉注射法利帕米(20分钟内1.5毫克/千克)的电生理特性。自发周期长度显著延长(+79±59毫秒,P<0.001)。由于AH间期缩短(-17±14毫秒),房室传导显著缩短(P<0.001),这很可能与抗胆碱能作用有关。同样,法利帕米给药后,顺行性文氏点显著升高(+10±7次/分钟,P<0.06)。尽管有缩短的趋势,但对房室结不应期未观察到统计学上的显著影响。右心房和心室的不应期显著延长。结论是,法利帕米是一种致心动过缓药物,其电生理特性与维拉帕米有很大不同,与IA类抗心律失常药物相似。

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