Why the study?
Limited evidence guides clinicians regarding the selection between bumetanide and torsemide in patients with heart failure.
Does bumetanide compared to torsemide affect all-cause mortality and clinical outcomes in patients with HFrEF?
Does bumetanide compared to torsemide affect all-cause mortality and clinical outcomes in patients with HFrEF?
In patients with HFrEF, torsemide is associated with lower risks of all-cause mortality, hospitalizations, and adverse renal/electrolyte events compared to bumetanide.
Bumetanide associated with higher mortality than torsemide in HFrEF; hypothesis-generating and should not change practice without RCTs.
Introduction Limited evidence guides clinicians regarding the agent selection between bumetanide and torsemide in patients with heart failure (HF). The present study aimed to compare the efficacy and safety profile of bumetanide and torsemide in patients with HF. Methods Patients aged > 18 years with HF with reduced ejection fraction (HFrEF) receiving either bumetanide or torsemide were included from the TriNetX research network. Patients with end-stage renal disease were excluded from this study. The primary outcome was all-cause mortality, and secondary outcomes included all-cause hospitalization or emergency department visits, acute kidney injury, or hypokalemia over one- year follow-up period. Results After propensity score matching, 16,277 patients in each group were included. The use of bumetanide was significantly associated with a higher risk of all-cause mortality (19.7 vs. 16.0 %; OR 1.28; 95% CI [1,21, 1.36]) compared to the torsemide group. The use of bumetanide was also significantly associated with higher risks of all-cause hospitalization or emergency department visits (53.3 vs. 48.3%; OR 1.22 95% CI [1.17, 1.28]), acute kidney injury (33.4 vs. 27.1 %; OR 1.35; 95% CI [1.29, 1.42]), and hypokalemia (16.6 vs. 13.7%; OR 1.21, 95% CI [1.17, 1.33]) compared to the torsemide group. Conclusion The use of torsemide in patients with HFrEF is associated with lower risks of clinical outcomes than bumetanide. Further investigation of this association is warranted in clinical trials.
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Kido et al. (2025) studied this question.
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