Nebivolol had a similar effect on all-cause mortality or cardiovascular hospitalizations in elderly heart failure patients with impaired (HR 0.86) and preserved (HR 0.81) ejection fraction (P=0.720 for interaction).
RCT (n=2,111)
Estimación del efecto: HR 0.86 (impaired EF); HR 0.81 (preserved EF) (95% CI 0.72-1.04 (impaired EF); 0.63-1.04 (preserved EF))
valor p: p=0.720 for subgroup interaction
OBJECTIVES: In this pre-specified subanalysis of the SENIORS (Study of Effects of Nebivolol Intervention on Outcomes and Rehospitalization in Seniors With Heart Failure) trial, which examined the effects of nebivolol in elderly heart failure (HF) patients, we explored the effects of left ventricular ejection fraction (EF) on outcomes, including the subgroups impaired EF (35%). BACKGROUND: Beta-blockers are established drugs in patients with HF and impaired EF, but their value in preserved EF is unclear. METHODS: We studied 2,111 patients; 1,359 (64%) had impaired (35%) EF (mean 49.2%). The effect of nebivolol was investigated in these 2 groups, and it was compared to explore the interaction of EF with outcome. Follow-up was 21 months; the primary end point was all-cause mortality or cardiovascular hospitalizations. RESULTS: Patients with preserved EF were more often women (49.9% vs. 29.8%) and had less advanced HF, more hypertension, and fewer prior myocardial infarctions (all p < 0.001). During follow-up, the primary end point occurred in 465 patients (34.2%) with impaired EF and in 235 patients (31.2%) with preserved EF. The effect of nebivolol on the primary end point (hazard ratio HR of nebivolol vs. placebo) was 0.86 (95% confidence interval: 0.72 to 1.04) in patients with impaired EF and 0.81 (95% confidence interval: 0.63 to 1.04) in preserved EF (p = 0.720 for subgroup interaction). Effects on all secondary end points were similar between groups (HR for all-cause mortality 0.84 and 0.91, respectively), and no p value for interaction was <0.48. CONCLUSIONS: The effect of beta-blockade with nebivolol in elderly patients with HF in this study was similar in those with preserved and impaired EF.
“There isn't that level of recommendation for beta-blockers in preserved heart failure with ejection fraction because it's not shown to improve those hard clinical outcomes in trials. In fact, we have some data that coming off of beta-blockers can help patients feel and function better.”
Veldhuisen et al. (Mon,) conducted a rct in Heart failure (n=2,111). Nebivolol vs. Placebo was evaluated on all-cause mortality or cardiovascular hospitalizations (HR 0.86 (impaired EF); HR 0.81 (preserved EF), 95% CI 0.72-1.04 (impaired EF); 0.63-1.04 (preserved EF), p=0.720 for subgroup interaction). Nebivolol had a similar effect on all-cause mortality or cardiovascular hospitalizations in elderly heart failure patients with impaired (HR 0.86) and preserved (HR 0.81) ejection fraction (P=0.720 for interaction).
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