β-blockade with nebivolol for prevention of acute ischaemic events in elderly patients with heart failure

奈比洛尔 医学 心脏病学 内科学 心力衰竭 射血分数 心肌梗塞 安慰剂 临床终点 不稳定型心绞痛 冠状动脉疾病 病因学 心绞痛 随机对照试验 血压 替代医学 病理
作者
G. Ambrosio,Marcus Flather,Michael Böhm,Andrew J.S. Coats,Luigi Tavazzi,Dirk J. van Veldhuisen,M. Conti,G. Spinucci,F. Mascagni,Adriano Murrone,Alain Cohen‐Solal
出处
期刊:Cardiovascular Therapy and Prevention 卷期号:10 (4): 69-76
标识
DOI:10.15829/1728-8800-2011-4-69-76
摘要

Aim. This subanalysis of the Study of the Effects of Nebivolol Intervention on Outcomes and Hospitalisation in Seniors with Heart Failure (SENIORS) investigates whether treatment with nebivolol, a β-blocker with nitric oxide-releasing properties, can provide additional benefits besides its effects on heart failure (HF), by reducing cardiac ischaemic events in patients with HF of ischaemic aetiology. Material and methods. A double-blind, randomised, placebo-controlled, multicentre trial of nebivolol in 2128 elderly patients. For this analysis, data were extracted for 2128 elderly (≥70 years) HF patients in whom coronary artery disease (CAD) was the underlying aetiology (68,2 %; 717 placebo-treated patients and 735 assigned to nebivolol). The main endpoint was the composite of cardiac ischaemic events at 2 year follow-up: death/hospitalisation for myocardial infarction, unstable angina or sudden death, as originally identified in the case report form. Results . At follow-up, nebivolol treatment was associated with a one-third reduction in the risk of ischaemic events, the composite endpoint occurring in 15,9 % of placebo and 10,7 % of nebivolol-treated patients (HR 0,68; 95 % CI 0,51 to 0,90; p =0,008). This effect was independent of age, gender and ejection fraction. No difference in this composite endpoint was observed in the subgroup of patients of non-ischaemic aetiology. Conclusion. Nebivolol was effective in reducing cardiac ischaemic events in patients with HF of ischaemic aetiology. The prevention of ischaemic events can be an additional beneficial effect of β-blockade in HF patients with underlying CAD.
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