Romano S, Fattore L, Toscano G, Corsini F, Coppo A, Catanzaro M, Romano A, Martone A, Caccavale F, Iodice E, Di Maggio O, Corsini G
Dipartimento di Cardiologia, Azienda Ospedaliera Ospedale Civile, Caserta.
Ital Heart J Suppl. 2001 Jan;2(1):41-5.
The authors report their experience in recent-onset atrial fibrillation treated with intravenous flecainide and propafenone, in comparison with the placebo group.
We randomized 352 (138 in the flecainide group, 164 in the propafenone group and 50 in the control group) consecutive patients (167 males, 185 females, mean age 59 +/- 12 years) with recent-onset atrial fibrillation. The electrocardiogram of all patients was monitored for at least 24 hours.
The restoration of sinus rhythm occurred in 72.5, 80.4, 86.2 and 89.8% of patients in the flecainide group; in 54.3, 68.3, 75 and 92.1% in the propafenone group; in 22.2, 27.8, 35.2 and 46.3% in the control group, at 1, 3, 6 and 24 hours respectively. The occurrence of side effects was the same in all treatment groups, and occurred in about 10% of patients in the flecainide and propafenone groups, and in 4% in the control group. In our study population the treatment of recent-onset atrial fibrillation with flecainide was faster in converting the arrhythmia to sinus rhythm (p < 0.005 at 1 hour, p < 0.05 at 3 hours, p = 0.05 at 6 hours). However within 24 hours the efficacy of either flecainide or propafenone was the same (p = NS at 24 hours).
Side effects were similar in both treatment groups. In particular malignant arrhythmias did not occur in the treatment groups and in the control group.
作者报告了他们使用静脉注射氟卡尼和普罗帕酮治疗近期发生的心房颤动的经验,并与安慰剂组进行了比较。
我们将352例近期发生心房颤动的连续患者(167例男性,185例女性,平均年龄59±12岁)随机分组(氟卡尼组138例,普罗帕酮组164例,对照组50例)。对所有患者的心电图进行至少24小时监测。
氟卡尼组患者在1、3、6和24小时时窦性心律恢复率分别为72.5%、80.4%、86.2%和89.8%;普罗帕酮组分别为54.3%、68.3%、75%和92.1%;对照组分别为22.2%、27.8%、35.2%和46.3%。所有治疗组的副作用发生率相同,氟卡尼组和普罗帕酮组约10%的患者出现副作用,对照组为%。在我们的研究人群中,用氟卡尼治疗近期发生的心房颤动使心律失常转为窦性心律的速度更快(1小时时p<0.005,3小时时p<0.05,6小时时p=0.05)。然而,在24小时内,氟卡尼或普罗帕酮的疗效相同(24小时时p=无显著性差异)。
两个治疗组的副作用相似。特别是治疗组和对照组均未发生恶性心律失常。