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频发或反复室性早搏患者心肌梗死后转归的随机试验:CAMIAT。加拿大胺碘酮心肌梗死心律失常试验研究者。

Randomised trial of outcome after myocardial infarction in patients with frequent or repetitive ventricular premature depolarisations: CAMIAT. Canadian Amiodarone Myocardial Infarction Arrhythmia Trial Investigators.

作者信息

Cairns J A, Connolly S J, Roberts R, Gent M

机构信息

Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Lancet. 1997 Mar 8;349(9053):675-82. doi: 10.1016/s0140-6736(96)08171-8.

Abstract

BACKGROUND

Survivors of acute myocardial infarction with frequent or repetitive ventricular premature depolarisations (VPDs) have higher mortality 1-2 years after the event than those without VPDs. Although there is no therapy of proven efficacy for such patients, previous studies of amiodarone have been encouraging. CAMIAT was a randomised double-blind placebo-controlled trial designed to assess the effect of amiodarone on the risk of resuscitated ventricular fibrillation or arrhythmic death among survivors of myocardial infarction with frequent or repetitive VPDs (> or = 10 VPDs per h or > or = 1 run of ventricular tachycardia).

METHODS

Patients from 36 Canadian hospitals were randomly assigned amiodarone or placebo; a loading dose of 10 mg/kg daily for 2 weeks, a maintenance dose of 300-400 mg daily for 3.5 months, 200-300 mg daily for 4 months, and 200 mg for 5-7 days per week for 16 months. Patients were followed up for 2 years. The primary outcome was the composite of resuscitated ventricular fibrillation or arrhythmic death.

FINDINGS

We recruited 1202 patients (606 in the amiodarone group and 596 in the placebo group). The mean follow-up was 1.79 years (SD 0.44). In the efficacy analysis, resuscitated ventricular fibrillation or arrhythmic death occurred in 39 (6.9%) [corrected] patients in the placebo group and in 25 (4.5%) [corrected] in the amiodarone group (relative-risk reduction 48.5% [95% CI 4.5 to 72.2], p = 0.016). In the intention-to-treat analysis, primary outcome events occurred in 24 (6.9%) patients in the placebo group and in 15 (4.5%) in the amiodarone group (38.2% [95% CI -2.1 to 62.6], p = 0.029). The absolute-risk reductions were greatest among patients with congestive heart failure or a history of myocardial infarction.

INTERPRETATION

Amiodarone reduces the incidence of ventricular fibrillation or arrhythmic death among survivors of acute myocardial infarction with frequent or repetitive VPDs. Treatment decisions for individual survivors should require an assessment of their baseline risk factors and judgments based on the synthesis of our findings with those of related trials.

摘要

背景

急性心肌梗死幸存者中,伴有频繁或反复室性早搏(VPDs)者在事件发生后1至2年的死亡率高于无VPDs者。尽管尚无已证实对此类患者有效的治疗方法,但既往有关胺碘酮的研究令人鼓舞。心肌梗死存活者胺碘酮心律失常试验(CAMIAT)是一项随机双盲安慰剂对照试验,旨在评估胺碘酮对伴有频繁或反复VPDs(每小时≥10次VPDs或≥1阵室性心动过速)的心肌梗死幸存者发生心脏复苏的室颤或心律失常性死亡风险的影响。

方法

来自36家加拿大医院的患者被随机分配接受胺碘酮或安慰剂治疗;负荷剂量为每日10mg/kg,持续2周,维持剂量为每日300 - 400mg,持续3.5个月,每日200 - 300mg,持续4个月,每周5 -

7天服用200mg,持续16个月。对患者随访2年。主要结局为心脏复苏的室颤或心律失常性死亡的复合终点。

结果

我们招募了1202例患者(胺碘酮组606例,安慰剂组596例)。平均随访时间为1.79年(标准差0.44)。在疗效分析中,安慰剂组39例(6.9%)[校正后]患者发生心脏复苏的室颤或心律失常性死亡,胺碘酮组为25例(4.5%)[校正后](相对风险降低48.5%[95%CI 4.5至72.2],p = 0.016)。在意向性分析中,安慰剂组24例(6.9%)患者发生主要结局事件,胺碘酮组为15例(4.5%)(38.2%[95%CI - 2.1至62.6],p = 0.029)。绝对风险降低在充血性心力衰竭或有心肌梗死病史的患者中最为显著。

解读

胺碘酮可降低伴有频繁或反复VPDs的急性心肌梗死幸存者发生室颤或心律失常性死亡的发生率。对于个体幸存者的治疗决策应要求评估其基线风险因素,并根据我们的研究结果与相关试验结果的综合分析做出判断。

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