Mitchell L B, Wyse D G, Gillis A M, Duff H J
Department of Medicine, Foothills General Hospital, Calgary, Alberta, Canada.
Circulation. 1989 Jul;80(1):34-42. doi: 10.1161/01.cir.80.1.34.
The time courses of onset of the electrophysiologic and antiarrhythmic effects of amiodarone were determined with serial electrophysiologic studies in 34 patients with inducible ventricular tachycardia. A standardized oral loading dosage was used for all patients (1,200 mg/day for 14 days; 800 mg/day for 7 days; and 400 mg/day thereafter). Eleven patients had the studies performed at baseline and after 2, 6, 10, and 20 weeks. Subsequently, 23 patients had studies at baseline and after 2 and 10 weeks. Changes in atrial, sinus, and atrioventricular nodal properties and in conduction intervals were maximal within 2 weeks (early effects). For example, atrioventricular nodal Wenckebach cycle length increased between baseline (369 +/- 80 msec) and 2 weeks (498 +/- 78 msec) (p less than 0.001) but did not change further after 10 weeks (500 +/- 89 msec). However, ventricular Class III effects required 10 weeks to become maximal (late effects). For example, the QT interval during atrial pacing increased between baseline (355 +/- 36 msec) and 2 weeks (406 +/- 37 msec) (p less than 0.001) and increased further after 10 weeks (436 +/- 45 msec) (p less than 0.001). Antiarrhythmic effects also followed different time courses of onset. Suppression of ventricular premature beats was maximal within 2 weeks. However, suppression of ventricular tachycardia inducibility and slowing of ventricular tachycardia rate was not maximal for 10 weeks. Correlations between serum desethylamiodarone concentrations and some late effects suggest that the mechanism of the time delay to maximal ventricular Class III effects may involve desethylamiodarone.(ABSTRACT TRUNCATED AT 250 WORDS)
在34例可诱发室性心动过速的患者中,通过系列电生理研究确定了胺碘酮电生理及抗心律失常作用的起效时间过程。所有患者均采用标准化口服负荷剂量(14天内每天1200毫克;7天内每天800毫克;此后每天400毫克)。11例患者在基线时以及2、6、10和20周后进行了研究。随后,23例患者在基线时以及2和10周后进行了研究。心房、窦房结和房室结特性以及传导间期的变化在2周内达到最大(早期效应)。例如,房室结文氏周期长度在基线时(369±80毫秒)到2周时(498±78毫秒)增加(p<0.001),但在10周后(500±89毫秒)没有进一步变化。然而,心室Ⅲ类效应需要10周才能达到最大(晚期效应)。例如,心房起搏时的QT间期在基线时(355±36毫秒)到2周时(406±37毫秒)增加(p<0.001),并在10周后进一步增加(436±45毫秒)(p<0.001)。抗心律失常作用也遵循不同的起效时间过程。室性早搏的抑制在2周内达到最大。然而,室性心动过速诱发的抑制和室性心动过速速率的减慢在10周内并非最大。血清去乙基胺碘酮浓度与一些晚期效应之间的相关性表明,心室Ⅲ类效应达到最大延迟的机制可能涉及去乙基胺碘酮。(摘要截短于250字)