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I类抗心律失常药物的亚分类:CAST研究后相关性增强

Subclassification of class I antiarrhythmic drugs: enhanced relevance after CAST.

作者信息

Campbell T J

机构信息

Department of Cardiology, St. Vincent's Hospital, Sydney, Australia.

出版信息

Cardiovasc Drugs Ther. 1992 Oct;6(5):519-28. doi: 10.1007/BF00055611.

Abstract

Class I antiarrhythmic drugs are traditionally divided into three subclasses--Ia, Ib, and Ic--on the grounds of differences in kinetics of interaction with the sodium channel and different effects on the duration of the action potential. The CAST study has highlighted our growing awareness of the proarrhythmic potential of this group of agents, particularly the Class Ic subgroup. Class I drugs can cause arrhythmias either by slowing conduction to critical levels, thus enhancing the possibility of reentrant arrhythmias, or in some cases by prolonging action potential duration, leading to early afterdepolarizations, which probably underlie triggered automaticity. Evidence is presented that the Class Ic compounds may be inherently more proarrhythmic than the Ib compounds, because of their lesser ability to depress ischemic myocardium selectively. Arguments are advanced for the continued use of a slightly modified subclassification of Class I antiarrhythmic drugs.

摘要

I类抗心律失常药物传统上根据与钠通道相互作用的动力学差异以及对动作电位持续时间的不同影响分为三个亚类——Ia、Ib和Ic。CAST研究凸显了我们对这类药物致心律失常潜力的日益认识,尤其是Ic亚类。I类药物可通过将传导减慢至临界水平从而增加折返性心律失常的可能性来引发心律失常,或在某些情况下通过延长动作电位持续时间导致早期后除极,这可能是触发自律性的基础。有证据表明,Ic类化合物可能比Ib类化合物在本质上更易致心律失常,因为它们选择性抑制缺血心肌的能力较弱。有人提出应继续使用经过略微修改的I类抗心律失常药物亚分类方法。

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