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口服普罗帕酮在慢性心房颤动电复律前给药的效果:一项安慰剂对照研究。

Effects of oral propafenone administration before electrical cardioversion of chronic atrial fibrillation: a placebo-controlled study.

作者信息

Bianconi L, Mennuni M, Lukic V, Castro A, Chieffi M, Santini M

机构信息

Department of Heart Diseases, San Filippo Neri Hospital, Rome, Italy.

出版信息

J Am Coll Cardiol. 1996 Sep;28(3):700-6. doi: 10.1016/0735-1097(96)00230-6.

Abstract

OBJECTIVES

Our aim was to evaluate the benefits and risks of administering propafenone before electrical defibrillation for chronic atrial fibrillation.

BACKGROUND

In this context, an antiarrhythmic drug-although potentially useful in preventing early recurrence of arrhythmia-could adversely affect the defibrillation threshold and reduce the cardioversion success rate.

METHODS

We randomly assigned 100 patients with chronic atrial fibrillation to oral treatment with either placebo (51 patients) or 750 mg/day of propafenone (49 patients) for 48 h before administration of direct current shock. After successful cardioversion, all patients received propafenone therapy and were followed up for 48 h.

RESULTS

Before defibrillation, three patients in the propafenone group (6.1%) had reversion to sinus rhythm and one had sustained ventricular tachycardia. Shock efficacy (82.4% vs. 84.4%) and the cumulative effective energy (395 +/- 258 vs. 421 +/- 236 J) were not different between the placebo and propafenone groups. In the propafenone group, 11 patients had their arrhythmia transformed into atrial flutter and required a lower energy level for arrhythmia conversion than did the other patients with continued atrial fibrillation (245 +/- 197 vs. 493 +/- 215 J, p < 0.01); the latter patients showed a trend (p < 0.10) toward higher energy requirements than that of patients who received placebo. The incidence of asymptomatic bradyarrhythmias was higher in the propafenone group (28.9% vs. 7.1%, p < 0.02), but more patients who received placebo had early recurrence of atrial fibrillation (16.7% vs. 0%, p < 0.02). Two days after cardioversion, more patients given propafenone (73.5% vs. 52.9%, p < 0.05) were discharged from the hospital with sinus rhythm. During the in-hospital stay, propafenone was withdrawn from six patients (6.6%) because of side effects.

CONCLUSIONS

Propafenone, given before electrical cardioversion for chronic atrial fibrillation does not affect the mean defibrillation threshold or the rate of successful arrhythmia conversion. It decreases the recurrence of atrial fibrillation early after shock, thus allowing more patients to be discharged from the hospital with sinus rhythm.

摘要

目的

我们的目的是评估在慢性房颤患者进行电除颤前给予普罗帕酮的益处和风险。

背景

在这种情况下,抗心律失常药物虽然可能有助于预防心律失常的早期复发,但可能会对除颤阈值产生不利影响并降低复律成功率。

方法

我们将100例慢性房颤患者随机分为两组,一组(51例)口服安慰剂,另一组(49例)口服750毫克/天的普罗帕酮,持续48小时,然后进行直流电电击。成功复律后,所有患者均接受普罗帕酮治疗,并随访48小时。

结果

除颤前,普罗帕酮组有3例患者(6.1%)恢复窦性心律,1例发生持续性室性心动过速。安慰剂组和普罗帕酮组的电击成功率(82.4%对84.4%)和累积有效能量(395±258焦耳对421±236焦耳)无差异。在普罗帕酮组中,11例患者的心律失常转变为心房扑动,与其他持续房颤患者相比,其心律失常转复所需能量水平较低(245±197焦耳对493±215焦耳,p<0.01);后者所需能量有高于接受安慰剂患者的趋势(p<0.10)。普罗帕酮组无症状性缓慢性心律失常的发生率较高(28.9%对7.1%,p<0.02),但接受安慰剂的患者房颤早期复发更多(16.7%对0%,p<0.02)。复律两天后,接受普罗帕酮治疗的患者出院时窦性心律的比例更高(73.5%对52.9%,p<0.05)。住院期间,有6例患者(6.6%)因副作用停用普罗帕酮。

结论

在慢性房颤患者进行电复律前给予普罗帕酮,不影响平均除颤阈值或心律失常成功转复率。它可降低电击后早期房颤的复发率,并使更多患者出院时为窦性心律。

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