Key result
Nebivolol significantly reduced the risk of cardiac ischaemic events compared to placebo in elderly heart failure patients with ischaemic aetiology (10.7% vs 15.9%; HR 0.68; 95% CI 0.51-0.90; p=0.008).
RCT (n=1,452)
Double-blind
randomised
Yes
Effect estimate: HR 0.68 (95% CI 0.51 to 0.90)
Absolute Event Rate: 10.7% vs 15.9%
p-value: p=0.008
Nebivolol reduces ischaemic events in elderly ischaemic HF; extends beta-blocker evidence to this aetiology subgroup.
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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Ambrosio et al. (2011) conducted an RCT in Heart failure of ischaemic aetiology (n=1,452). Nebivolol vs. Placebo was evaluated on Composite of cardiac ischaemic events: death/hospitalisation for myocardial infarction, unstable angina or sudden death (HR 0.68, 95% CI 0.51 to 0.90, p=0.008). Nebivolol significantly reduced the risk of cardiac ischaemic events compared to placebo in elderly heart failure patients with ischaemic aetiology (10.7% vs 15.9%; HR 0.68; 95% CI 0.51-0.90; p=0.008).
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