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抗心律失常药物对早期室性早搏的疗效。

The effectiveness of antiarrhythmic agents on early-cycle premature ventricular complexes.

作者信息

Krone R J, Miller J P, Kleiger R E, Clark K W, Oliver G C

出版信息

Circulation. 1981 Mar;63(3):664-9. doi: 10.1161/01.cir.63.3.664.

Abstract

Twelve patients completed a double-blind, crossover antiarrhythmic drug trial in which 300 mg of quinidine, 500 mg of procainamide, 100 mg of phenytoin, or placebo was given four times daily on subsequent weeks. Analysis of 24-hour Holter tapes with a computerized analysis system (Argus/H) permitted accurate counting of premature ventricular complexes (PVCs) subclassified according to coupling interval. No antiarrhythmic agent demonstrated a significant overall reduction in the number of PVCs, but both quinidine and procainamide showed a statistically significant (p less than 0.05) reduction of PVCs with coupling intervals less than 400 msec. This effect was noted both in isolated PVCs (quinidine only) and in PVCs that were part of a couplet or run (both drugs). These findings demonstrate that clinically important effects of procainamide and quinidine can occur in the absence of an overall reduction in the number of PVCs.

摘要

12名患者完成了一项双盲交叉抗心律失常药物试验,在随后的几周里,每天4次给予300毫克奎尼丁、500毫克普鲁卡因胺、100毫克苯妥英或安慰剂。使用计算机分析系统(Argus/H)对24小时动态心电图进行分析,能够准确计数根据联律间期分类的室性早搏(PVC)。没有一种抗心律失常药物显示出PVC数量的显著总体减少,但奎尼丁和普鲁卡因胺均显示,联律间期小于400毫秒的PVC数量有统计学意义的减少(p<0.05)。在孤立的PVC(仅奎尼丁)以及成对或成串出现的PVC(两种药物均有此效果)中均观察到了这种效应。这些发现表明,在PVC数量没有总体减少的情况下,普鲁卡因胺和奎尼丁也可能产生临床上重要的效果。

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