Safety of continuing mineralocorticoid receptor antagonist treatment in patients with heart failure with reduced ejection fraction and severe kidney disease: Data from Swedish Heart Failure Registry

Author:

Guidetti Federica1,Lund Lars H.12,Benson Lina1,Hage Camilla1,Musella Francesca13,Stolfo Davide14,Mol Peter G.M.5,Flammer Andreas J.6,Ruschitzka Frank6,Dahlstrom Ulf7,Rosano Giuseppe M.C.8,Braun Oscar Ö.9,Savarese Gianluigi12ORCID

Affiliation:

1. Division of Cardiology, Department of Medicine Karolinska Institutet Stockholm Sweden

2. Heart, Vascular and Neuro Theme Karolinska University Hospital Stockholm Sweden

3. Cardiology Department Santa Maria delle Grazie Hospital Naples Italy

4. Division of Cardiology, Cardiovascular Department Azienda Sanitaria Universitaria Integrata di Trieste (ASUITS) Trieste Italy

5. Department of Clinical Pharmacy and Pharmacology University Medical Center Groningen, University of Groningen Groningen The Netherlands

6. Department of Cardiology University Heart Center, University Hospital Zurich Zurich Switzerland

7. Department of Cardiology and Department of Health Medicine and Caring Sciences Linköping University Linköping Sweden

8. IRCCS San Raffaele Pisana Rome Italy

9. Cardiology, Department of Clinical Sciences Lund University and Skåne University Hospital Lund Sweden

Abstract

ABSTRACTAimsMineralocorticoid receptor antagonists (MRAs) improve outcomes in heart failure with reduced ejection fraction (HFrEF) but remain underused and are often discontinued especially in patients with chronic kidney disease (CKD) due to concerns on renal safety. Therefore, in a real‐world HFrEF population we investigated the safety of MRA use, in terms of risk of renal events, any mortality and any hospitalization, across the estimated glomerular filtration rate (eGFR) spectrum including severe CKD.Methods and resultsWe analysed patients with HFrEF (ejection fraction <40%), not on dialysis, from the Swedish Heart Failure Registry. We performed multivariable logistic regression models to investigate patient characteristics independently associated with MRA use, and univariable and multivariable Cox regression models to assess the associations between MRA use and outcomes. Of 33 942 patients, 17 489 (51%) received MRA, 32%, 45%, 54%, 54% with eGFR <30, 30–44, 45–59 or ≥60 ml/min/1.73 m2, respectively. An eGFR ≥60 ml/min/1.73 m2 and patient characteristics linked with more severe HF were independently associated with more likely MRA use. In multivariable analyses, MRA use was consistently not associated with a higher risk of renal events (i.e. composite of dialysis/renal death/hospitalization for renal failure or hyperkalaemia) (hazard ratio [HR] 1.04, 95% confidence interval [CI] 0.98–1.10), all‐cause death (HR 1.02, 95% CI 0.97–1.08) as well as of all‐cause hospitalization (HR 0.99, 95% CI 0.95–1.02) across the eGFR spectrum including also severe CKD.ConclusionsThe use of MRAs in patients with HFrEF decreased with worse renal function; however their safety profile was demonstrated to be consistent across the entire eGFR spectrum.

Funder

Hjärt-Lungfonden

HORIZON EUROPE Framework Programme

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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