The association of beta-blocker use with mortality in elderly patients with congestive heart failure and advanced chronic kidney disease

Author:

Molnar Amber O123,Petrcich William2,Weir Matthew A245,Garg Amit X245,Walsh Michael136,Sood Manish M278

Affiliation:

1. Division of Nephrology, Department of Medicine, McMaster University, Hamilton, ON, Canada

2. Institute for Clinical Evaluative Sciences, Toronto, ON, Canada

3. Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada

4. Division of Nephrology, Department of Medicine, Western University, London, ON, Canada

5. Department of Epidemiology, Western University, London, ON, Canada

6. Population Heath Research Institute, McMaster University/Hamilton Health Sciences, Hamilton, ON, Canada

7. Division of Nephrology, Department of Medicine, University of Ottawa, Ottawa, ON, Canada

8. Epidemiology, Ottawa Hospital Research Institute, Ottawa, ON, Canada

Abstract

Abstract Background Whether the survival benefit of β-blockers in congestive heart failure (CHF) from randomized trials extends to patients with advanced chronic kidney disease (CKD) [estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 m2 but not receiving dialysis] is uncertain. Methods This was a retrospective cohort study using administrative datasets. Older adults from Ontario, Canada, with incident CHF (median age 79 years) from April 2002 to March 2014 were included. We matched new users of β-blockers to nonusers on age, sex, eGFR categories (>60, 30–60, <30), CHF diagnosis date and a high-dimensional propensity score. Using Cox proportional hazards models, we examined the association of β-blocker use versus nonuse with all-cause mortality. Results We matched 5862 incident β-blocker users (eGFR >60, n = 3136; eGFR 30–60, n = 2368; eGFR <30, n = 358). There were 2361 mortality events during follow-up. β-Blocker use was associated with reduced all-cause mortality [adjusted hazard ratio (HR) 0.58, 95% confidence interval (CI) 0.54–0.64]. This result was consistent across all eGFR categories (>60: adjusted HR 0.55, 95% CI 0.49–0.62; 30–60: adjusted HR 0.63, 95% CI 0.55–0.71; <30: adjusted HR 0.55, 95% CI 0.41–0.73; interaction term, P = 0.30). The results were consistent in an intention-to-treat analysis and with β-blocker use treated as a time-varying exposure. Conclusions β-Blocker use is associated with reduced all-cause mortality in elderly patients with CHF and CKD, including those with an eGFR <30. Randomized trials that examine β-blockers in patients with CHF and advanced CKD are needed.

Funder

Institute for Clinical Evaluative Sciences

ICES

Ontario Ministry of Health and Long-Term Care

MOHLTC

Academic Medical Organization of Southwestern Ontario

AMOSO

Schulich School of Medicine and Dentistry

SSMD

Western University and the Lawson Health Research Institute

LHRI

Canadian Institutes of Health Research

CIHR

KRESCENT Foundation

McMaster Department of Medicine

Kidney Foundation of Canada

St Joseph’s Research Institute Hamilton

Jindal Research Chair

Prevention of Kidney Disease

Dr Adam Linton Chair in Kidney Health Analytics

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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