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恩卡胺治疗房室结折返性心动过速:异丙肾上腺素逆转药物作用。

Treatment of atrioventricular node reentrant tachycardia with encainide: reversal of drug effect with isoproterenol.

作者信息

Niazi I, Naccarelli G, Dougherty A, Rinkenberger R, Tchou P, Akhtar M

机构信息

Natalie and Norman Soref and Family Electrophysiology Laboratory, University of Wisconsin-Milwaukee Clinical Campus, Sinai Samaritan Medical Center.

出版信息

J Am Coll Cardiol. 1989 Mar 15;13(4):904-10. doi: 10.1016/0735-1097(89)90234-9.

Abstract

To determine the efficacy of encainide in the treatment of atrioventricular (AV) node reentrant tachycardia, Holter electrocardiographic (ECG) monitoring, exercise treadmill testing and programmed electrical stimulation were performed in 16 patients while they were taking no medication and after steady state levels were reached during treatment with encainide (75 to 200 mg/day; mean 117 +/- 47). In addition, to study the possible reversal of drug effects by sympathetic stimulation, AV node conduction and tachycardia induction were reassessed during isoproterenol infusion (1 to 3 micrograms/min), a dose calculated to increase the rest heart rate by 25 +/- 10%. Sustained AV node reentrant tachycardia could be initiated in all 16 patients in the control state, in 2 patients after encainide and in 10 patients during isoproterenol infusion. The shortest mean atrial paced cycle length sustaining 1:1 AV conduction was 358 +/- 57 ms during the control study, which increased to 409 +/- 59 ms with encainide (p less than 0.01 versus control) and decreased to 313 +/- 31 ms during isoproterenol infusion (p less than 0.01 versus control and encainide). The shortest mean ventricular paced cycle length with 1:1 ventriculoatrial conduction was 337 +/- 56 ms in the control study, 551 + 124 ms with encainide infusion (p less than 0.01 versus control) and 354 +/- 72 ms during isoproterenol infusion in the encainide-loaded state (p less than 0.01 versus both control and encainide). During a mean follow-up period of 19 +/- 10 months, significant clinical recurrences occurred in 4 of the 10 patients in whom tachycardia could still be initiated with encainide (with or without isoproterenol).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为确定恩卡胺治疗房室结折返性心动过速的疗效,对16例患者在未服用任何药物时以及达到恩卡胺(75至200毫克/天;平均117±47)治疗稳态水平后进行了动态心电图监测、运动平板试验和程控电刺激。此外,为研究交感神经刺激对药物作用的可能逆转,在静脉输注异丙肾上腺素(1至3微克/分钟)期间重新评估房室结传导和心动过速诱发情况,该剂量经计算可使静息心率增加25±10%。在对照状态下,所有16例患者均可诱发持续性房室结折返性心动过速,服用恩卡胺后2例患者可诱发,静脉输注异丙肾上腺素期间10例患者可诱发。对照研究期间维持1:1房室传导的最短平均心房起搏周期长度为358±57毫秒,服用恩卡胺后增至409±59毫秒(与对照相比,P<0.01),静脉输注异丙肾上腺素期间降至313±31毫秒(与对照和恩卡胺相比,P<0.01)。对照研究中1:1室房传导的最短平均心室起搏周期长度为337±56毫秒,输注恩卡胺时为551 + 124毫秒(与对照相比,P<0.01),在服用恩卡胺状态下静脉输注异丙肾上腺素期间为354±72毫秒(与对照和恩卡胺相比,P<0.01)。在平均19±10个月的随访期内,10例服用恩卡胺(无论有无异丙肾上腺素)仍可诱发心动过速的患者中有4例出现明显的临床复发。(摘要截短至250字)

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