Estes N A, Garan H, Ruskin J N
Am J Cardiol. 1984 Feb 27;53(5):26B-29B. doi: 10.1016/0002-9149(84)90498-3.
Preliminary clinical experience indicates that flecainide is a useful antiarrhythmic agent for the suppression of spontaneous ventricular arrhythmias. The drug also exerts marked effects on accessory atrioventricular (AV) pathway and retrograde fast AV nodal pathway refractoriness, and therefore may be effective in treatment and prevention of reentrant supraventricular tachycardias. Electrophysiologic studies indicate that flecainide slows atrial, AV nodal, His-Purkinje and intraventricular conduction and, to a far lesser degree, prolongs refractory periods in these tissues. The effect of the drug in slowing conduction within the His-Purkinje system is particularly marked and is commonly associated with prolongation of the HV interval beyond the normal range. Flecainide causes a small but significant increase in the QT interval duration, which results largely from prolongation of the QRS interval. Significant prolongation of the sinus node recovery time has been observed in patients with preexisting sinus node dysfunction. Available electrophysiologic data suggest that flecainide should not be administered to patients with advanced disease of the His-Purkinje system or sinus node. The safety of the drug in patients with mild to moderate abnormalities of His-Purkinje conduction or sinus node function awaits further study.
初步临床经验表明,氟卡尼是一种用于抑制自发性室性心律失常的有效抗心律失常药物。该药物对房室旁道和逆向快速房室结道不应期也有显著影响,因此可能对折返性室上性心动过速的治疗和预防有效。电生理研究表明,氟卡尼可减慢心房、房室结、希氏-浦肯野纤维和心室内传导,并且在这些组织中延长不应期的程度要小得多。该药物在减慢希氏-浦肯野系统内传导方面的作用尤为显著,并且通常与HV间期延长至正常范围之外有关。氟卡尼使QT间期时长有小幅但显著的增加,这主要是由QRS间期延长导致的。在已有窦房结功能障碍的患者中观察到窦房结恢复时间显著延长。现有的电生理数据表明,氟卡尼不应给予希氏-浦肯野系统或窦房结严重病变的患者。该药物在希氏-浦肯野传导或窦房结功能轻度至中度异常患者中的安全性有待进一步研究。