Wikstrand John, Ghali Jalal K, Goldstein Sydney
Sahlgrenska University Hospital, SE 413 45 Göteborg, Sweden.
Postgrad Med. 2002 Nov;112(5 Suppl Unanswered):16-23. doi: 10.3810/pgm.11.2002.suppl22.116.
Several recently completed survival trials, including Metoprolol CR/XL Randomized Intervention Trial in Congestive Heart Failure (MERIT-HF), Cardiac Insufficiency Bisoprolol Study II (CIBIS-II), and the Carvedilol Prospective Randomized Cumulative Survival (COPERNICUS) trial have examined the effects of ss-blockers on survival and the need for hospitalization. The results from these trials are remarkably consistent regarding reduction of both mortality and hospitalizations for worsening heart failure. MERIT-HF investigated the effect of the lipophilic ss-blocker extended-release metoprolol succinate given once daily in addition to optimum standard therapy in patients with New York Heart Association (NYHA) functional classes II through IV chronic heart failure and ejection fractions of 40% or below. The aim of this article is to review the consistency of ss-blocker effect across various predefined risk groups as well as some post hoc subgroups in MERIT-HF.
最近完成的几项生存试验,包括美托洛尔缓释片治疗充血性心力衰竭随机干预试验(MERIT-HF)、比索洛尔治疗心力衰竭研究II(CIBIS-II)以及卡维地洛前瞻性随机累积生存试验(COPERNICUS),均研究了β受体阻滞剂对生存及住院需求的影响。这些试验结果在降低死亡率和因心力衰竭恶化导致的住院率方面显著一致。MERIT-HF研究了在纽约心脏协会(NYHA)心功能II至IV级的慢性心力衰竭且射血分数为40%或更低的患者中,除最佳标准治疗外,每日一次给予亲脂性β受体阻滞剂琥珀酸美托洛尔缓释片的效果。本文旨在回顾MERIT-HF中不同预定义风险组以及一些事后亚组中β受体阻滞剂效果的一致性。