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Initiation of eplerenone vs. spironolactone and all-cause mortality in HFrEF: linked database study
Henrik Svanström1,2, Anders Hviid1,3, Björn Pasternak1,2
1Department of Data Science and AI in Health, Statens Serum Institut, Artillerivej 5, Copenhagen S 2300, Denmark.
Aims:
Mineralocorticoid receptor antagonists are recommended as part of guideline-directed medical therapy for heart failure with reduced ejection fraction (HFrEF). The comparative effectiveness of spironolactone and eplerenone, however, remains uncertain.
Methods And Results:
This was a non-interventional database study using nationwide Danish health registries, 1 January 2020 to 30 June 2025. Patients aged ≥45 years with HFrEF (ejection fraction ≤40%) initiating eplerenone or spironolactone were included. An active-comparator, new-user design and inverse-probability-of-treatment weighting based on propensity scores was used. The primary outcome was all-cause mortality. Secondary outcomes included cardiovascular mortality, heart failure hospitalization, and their composite. Weighted hazard ratios (wHRs) were estimated using Cox proportional hazards models. A total of 4550 patients initiating eplerenone and 6651 initiating spironolactone were included. Median follow-up was 2.3 years. There were 571 deaths in the eplerenone group (5.0 per 100 person-years) and 1168 in the spironolactone group (7.0 per 100 person-years). A lower risk of death was observed with eplerenone [wHR, 0.83; 95% confidence interval (CI), 0.75-0.93], corresponding to an absolute rate difference of -1.10 per 100 person-years (95% CI, -0.50 to -1.70). For secondary outcomes, wHRs were 0.89 (95% CI, 0.81-0.98) for cardiovascular death or heart failure hospitalization, 0.79 (95% CI, 0.67-0.92) for cardiovascular death, and 0.97 (95% CI, 0.87-1.09) for heart failure hospitalization. Effect estimates were attenuated in per-protocol analyses.
Conclusion:
In this large nationwide study, initiation of eplerenone was associated with lower risks of all-cause and cardiovascular mortality compared with spironolactone, with findings suggesting a contribution of better treatment persistence.
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