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美托洛尔缓释片/控释片治疗慢性心力衰竭的效果:美托洛尔缓释片/控释片充血性心力衰竭随机干预试验(MERIT-HF)

Effect of metoprolol CR/XL in chronic heart failure: Metoprolol CR/XL Randomised Intervention Trial in Congestive Heart Failure (MERIT-HF).

出版信息

Lancet. 1999 Jun 12;353(9169):2001-7.

Abstract

BACKGROUND

Metoprolol can improve haemodynamics in chronic heart failure, but survival benefit has not been proven. We investigated whether metoprolol controlled release/extended release (CR/XL) once daily, in addition to standard therapy, would lower mortality in patients with decreased ejection fraction and symptoms of heart failure.

METHODS

We enrolled 3991 patients with chronic heart failure in New York Heart Association (NYHA) functional class II-IV and with ejection fraction of 0.40 or less, stabilised with optimum standard therapy, in a double-blind randomised controlled study. Randomisation was preceded by a 2-week single-blind placebo run-in period. 1990 patients were randomly assigned metoprolol CR/XL 12.5 mg (NYHA III-IV) or 25.0 mg once daily (NYHA II) and 2001 were assigned placebo. The target dose was 200 mg once daily and doses were up-titrated over 8 weeks. Our primary endpoint was all-cause mortality, analysed by intention to treat.

FINDINGS

The study was stopped early on the recommendation of the independent safety committee. Mean follow-up time was 1 year. All-cause mortality was lower in the metoprolol CR/XL group than in the placebo group (145 [7.2%, per patient-year of follow-up]) vs 217 deaths [11.0%], relative risk 0.66 [95% CI 0.53-0.81]; p=0.00009 or adjusted for interim analyses p=0.0062). There were fewer sudden deaths in the metoprolol CR/XL group than in the placebo group (79 vs 132, 0.59 [0.45-0.78]; p=0.0002) and deaths from worsening heart failure (30 vs 58, 0.51 [0.33-0.79]; p=0.0023).

INTERPRETATION

Metoprolol CR/XL once daily in addition to optimum standard therapy improved survival. The drug was well tolerated.

摘要

背景

美托洛尔可改善慢性心力衰竭患者的血流动力学,但尚未证实其对生存率有改善作用。我们研究了在标准治疗基础上,每日一次服用美托洛尔控释/缓释片(CR/XL)是否能降低射血分数降低且有心力衰竭症状患者的死亡率。

方法

在一项双盲随机对照研究中,我们纳入了3991例纽约心脏病协会(NYHA)心功能II-IV级、射血分数为0.40或更低且经最佳标准治疗病情稳定的慢性心力衰竭患者。随机分组前有为期2周的单盲安慰剂导入期。1990例患者被随机分配接受美托洛尔CR/XL 12.5mg(NYHA III-IV级)或25.0mg每日一次(NYHA II级),2001例患者被分配接受安慰剂。目标剂量为每日一次200mg,剂量在8周内逐步滴定。我们的主要终点是全因死亡率,采用意向性分析。

结果

根据独立安全委员会的建议,研究提前终止。平均随访时间为1年。美托洛尔CR/XL组的全因死亡率低于安慰剂组(145例[7.2%,每患者年随访])对比217例死亡[11.0%],相对风险0.66[95%CI 0.53-0.81];p=0.00009或经中期分析调整后p=0.0062)。美托洛尔CR/XL组的猝死病例少于安慰剂组(79例对比132例,0.59[0.45-0.78];p=0.0002),因心力衰竭恶化导致的死亡也较少(30例对比58例,0.51[0.33-0.79];p=0.0023)。

结论

在最佳标准治疗基础上,每日一次服用美托洛尔CR/XL可提高生存率。该药物耐受性良好。

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