Кардиоваскулярная терапия и профилактика (Aug 2011)

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

  • G. Ambrosio,
  • M. D. Flather,
  • M. Böhm,
  • A. J.S. Coats,
  • L. Tavazzi,
  • D. J. van Veldhuisen,
  • M. G. Conti,
  • G. Spinucci,
  • F. Mascagni,
  • A. Murrone,
  • A. Cohen-Solal

DOI
https://doi.org/10.15829/1728-8800-2011-4-69-76
Journal volume & issue
Vol. 10, no. 4
pp. 69 – 76

Abstract

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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.