Division of Cardiology, University of Perugia School of Medicine, Perugia, Italy.
Heart. 2011 Feb;97(3):209-14. doi: 10.1136/hrt.2010.207365. Epub 2010 Dec 6.
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.
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.
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.
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.
本研究是对β受体阻滞剂奈必洛尔干预心力衰竭老年人结局和住院治疗的研究(SENIORS)的亚组分析,旨在探讨奈必洛尔(一种具有一氧化氮释放特性的β受体阻滞剂)除了对心力衰竭(HF)的作用之外,是否还能通过降低缺血性病因心力衰竭患者的心脏缺血事件提供额外的益处。
一项针对 2128 例老年(≥70 岁)HF 患者的奈必洛尔双盲、随机、安慰剂对照、多中心试验。
本分析提取了 2128 例老年(≥70 岁)HF 患者(其中 68.2%患者的冠状动脉疾病(CAD)为潜在病因)的资料,这些患者的冠状动脉疾病(CAD)为潜在病因(68.2%;717 例安慰剂治疗患者和 735 例奈必洛尔治疗患者)。
主要终点是 2 年随访时的心脏缺血事件复合终点:死亡/因心肌梗死、不稳定型心绞痛或猝死住院,如原始病例报告表中所确定的。
随访时,奈必洛尔治疗组缺血事件风险降低了三分之一,安慰剂组和奈必洛尔治疗组的复合终点发生率分别为 15.9%和 10.7%(HR 0.68;95%CI 0.51 至 0.90;p=0.008)。这种作用独立于年龄、性别和射血分数。在非缺血病因亚组中,未观察到该复合终点存在差异。
奈必洛尔可有效降低缺血性病因心力衰竭患者的心脏缺血事件。在基础 CAD 的 HF 患者中,β受体阻滞剂的预防缺血事件可能是其额外的有益作用。