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抗心律失常药物能否根据作用机制来选择?

Can antiarrhythmic agents be selected based on mechanism of action?

作者信息

Lau W, Newman D, Dorian P

机构信息

St Michael's Hospital, Toronto, Ontario, Canada.

出版信息

Drugs. 2000 Dec;60(6):1315-28. doi: 10.2165/00003495-200060060-00006.

Abstract

When selecting an antiarrhythmic agent the clinician needs to be able to accurately predict the probability that a particular drug will serve its intended purpose in a given patient. This is difficult because of the complexity of variables which govern the relationship between drug administration and clinical outcome. The efficacy of a drug may potentially be predicted from its mechanism of action. At least two classifications of antiarrhythmic agents based on mechanism of action have been proposed. The Vaughan Williams classification is based on the predominant electrophysiological effects of a drug on the action potential. In the Sicilian Gambit approach, a number of potential targets ('vulnerable parameters') for drug action are identified and antiarrhythmic drugs or substances that affect cardiac electrophysiology are characterised by their actions on each of these. The usefulness of these classification systems in predicting antiarrhythmic drug efficacy are limited. Furthermore, in the Vaughan Williams classification not all drugs in the same class have identical effects, whereas some drugs in different classes have overlapping actions. The Sicilian Gambit requires in-depth knowledge regarding cellular and molecular targets of antiarrhythmic agents which may make it intimidating or simply impractical for regular clinical use. Surrogate measures such as 24-hour Holter monitoring and programmed electrical stimulation have been used to predict anti-arrhythmic drug efficacy. However, studies such the Cardiac Arrhythmia Suppression Trial (CAST) have shown that suppression of ventricular ectopy on Holter monitoring does not necessarily correlate with improved survival and may in fact be dangerous. Conversely, studies using programmed electrical stimulation to assess drug effect on variables such as tachycardia inducibility, refractory period and ventricular tachycardia cycle length show that suppression of tachycardia inducibility, prolongation of refractory period and prolongation of ventricular tachycardia cycle length, are all associated with reduced recurrence of tachycardia and possibly improved survival. The most practical use of the current classification systems applied to antiarrhythmic agents may be in their ability to predict with reasonable accuracy, the risk and type of proarrhythmia based on the mechanism of action of an agent.

摘要

在选择抗心律失常药物时,临床医生需要能够准确预测某种特定药物在特定患者中达到预期效果的可能性。这很困难,因为决定药物给药与临床结果之间关系的变量非常复杂。一种药物的疗效可能可以从其作用机制中预测出来。基于作用机制,至少已提出了两种抗心律失常药物分类方法。 Vaughan Williams分类法是基于药物对动作电位的主要电生理效应。在西西里策略方法中,确定了许多药物作用的潜在靶点(“易损参数”),影响心脏电生理的抗心律失常药物或物质通过它们对每个靶点的作用来表征。这些分类系统在预测抗心律失常药物疗效方面的作用有限。此外,在Vaughan Williams分类法中,同一类中的并非所有药物都具有相同的作用,而不同类中的一些药物具有重叠作用。西西里策略需要对抗心律失常药物的细胞和分子靶点有深入了解,这可能使其在常规临床应用中令人望而却步或根本不实用。诸如24小时动态心电图监测和程控电刺激等替代措施已被用于预测抗心律失常药物的疗效。然而,像心律失常抑制试验(CAST)这样的研究表明,动态心电图监测上室性早搏的抑制并不一定与生存率提高相关,实际上可能是危险的。相反,使用程控电刺激评估药物对诸如心动过速诱发率、不应期和室性心动过速周期长度等变量的影响的研究表明,心动过速诱发率的抑制、不应期的延长和室性心动过速周期长度的延长,都与心动过速复发减少以及可能的生存率提高相关。应用于抗心律失常药物的当前分类系统最实际的用途可能在于它们能够基于药物的作用机制,以合理的准确性预测致心律失常的风险和类型。

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