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Impact of Renal Impairment on Beta-Blocker Efficacy in Patients With Heart Failure.

Kotecha, D; Gill, SK; Flather, MD; Holmes, J; Packer, M; Rosano, G; Böhm, M; McMurray, JJV; Wikstrand, J; Anker, SD; et al. Kotecha, D; Gill, SK; Flather, MD; Holmes, J; Packer, M; Rosano, G; Böhm, M; McMurray, JJV; Wikstrand, J; Anker, SD; van Veldhuisen, DJ; Manzano, L; von Lueder, TG; Rigby, AS; Andersson, B; Kjekshus, J; Wedel, H; Ruschitzka, F; Cleland, JGF; Damman, K; Redon, J; Coats, AJS; Beta-Blockers in Heart Failure Collaborative Group (2019) Impact of Renal Impairment on Beta-Blocker Efficacy in Patients With Heart Failure. J Am Coll Cardiol, 74 (23). pp. 2893-2904. ISSN 1558-3597 https://doi.org/10.1016/j.jacc.2019.09.059
SGUL Authors: Rosano, Giuseppe Massimo Claudio

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Abstract

BACKGROUND: Moderate and moderately severe renal impairment are common in patients with heart failure and reduced ejection fraction, but whether beta-blockers are effective is unclear, leading to underuse of life-saving therapy. OBJECTIVES: This study sought to investigate patient prognosis and the efficacy of beta-blockers according to renal function using estimated glomerular filtration rate (eGFR). METHODS: Analysis of 16,740 individual patients with left ventricular ejection fraction <50% from 10 double-blind, placebo-controlled trials was performed. The authors report all-cause mortality on an intention-to-treat basis, adjusted for baseline covariates and stratified by heart rhythm. RESULTS: Median eGFR at baseline was 63 (interquartile range: 50 to 77) ml/min/1.73 m2; 4,584 patients (27.4%) had eGFR 45 to 59 ml/min/1.73 m2, and 2,286 (13.7%) 30 to 44 ml/min/1.73 m2. Over a median follow-up of 1.3 years, eGFR was independently associated with mortality, with a 12% higher risk of death for every 10 ml/min/1.73 m2 lower eGFR (95% confidence interval [CI]: 10% to 15%; p < 0.001). In 13,861 patients in sinus rhythm, beta-blockers reduced mortality versus placebo; adjusted hazard ratio (HR): 0.73 for eGFR 45 to 59 ml/min/1.73 m2 (95% CI: 0.62 to 0.86; p < 0.001) and 0.71 for eGFR 30 to 44 ml/min/1.73 m2 (95% CI: 0.58 to 0.87; p = 0.001). The authors observed no deterioration in renal function over time in patients with moderate or moderately severe renal impairment, no difference in adverse events comparing beta-blockers with placebo, and higher mortality in patients with worsening renal function on follow-up. Due to exclusion criteria, there were insufficient patients with severe renal dysfunction (eGFR <30 ml/min/1.73 m2) to draw conclusions. In 2,879 patients with atrial fibrillation, there was no reduction in mortality with beta-blockers at any level of eGFR. CONCLUSIONS: Patients with heart failure, left ventricular ejection fraction <50% and sinus rhythm should receive beta-blocker therapy even with moderate or moderately severe renal dysfunction.

Item Type: Article
Additional Information: Correction available at https://doi.org/10.1016/j.jacc.2020.02.037 © 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: beta-blockers, heart failure, mortality, renal impairment, Beta-Blockers in Heart Failure Collaborative Group, Cardiovascular System & Hematology, 1102 Cardiorespiratory Medicine and Haematology, 1117 Public Health and Health Services
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: J Am Coll Cardiol
ISSN: 1558-3597
Language: eng
Dates:
DateEvent
10 December 2019Published
2 December 2019Published Online
16 September 2019Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
AA/18/2/34218British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
CDF-2015-08-074National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PG/17/55/33087British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
116074EU Innovative Medicines InitiativeUNSPECIFIED
RE/18/6/34217British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
PubMed ID: 31806133
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/111561
Publisher's version: https://doi.org/10.1016/j.jacc.2019.09.059

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