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Randomized Controlled Trial
. 2024 Feb 1;9(2):182-188.
doi: 10.1001/jamacardio.2023.4776.

Torsemide vs Furosemide Among Patients With New-Onset vs Worsening Chronic Heart Failure: A Substudy of the TRANSFORM-HF Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Torsemide vs Furosemide Among Patients With New-Onset vs Worsening Chronic Heart Failure: A Substudy of the TRANSFORM-HF Randomized Clinical Trial

Selim R Krim et al. JAMA Cardiol. .

Abstract

Importance: Differences in clinical profiles, outcomes, and diuretic treatment effects may exist between patients with de novo heart failure (HF) and worsening chronic HF (WHF).

Objectives: To compare clinical characteristics and treatment outcomes of torsemide vs furosemide in patients hospitalized with de novo HF vs WHF.

Design, setting, and participants: All patients with a documented ejection fraction who were randomized in the Torsemide Comparison With Furosemide for Management of Heart Failure (TRANSFORM-HF) trial, conducted from June 18 through March 2022, were included in this post hoc analysis. Study data were analyzed March to May 2023.

Exposure: Patients were categorized by HF type and further divided by loop diuretic strategy.

Main outcomes and measures: End points included all-cause mortality and hospitalization outcomes over 12 months, as well as change from baseline in the Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS).

Results: Among 2858 patients (mean [SD] age, 64.5 [14.0] years; 1803 male [63.1%]), 838 patients (29.3%) had de novo HF, and 2020 patients (70.7%) had WHF. Patients with de novo HF were younger (mean [SD] age, 60.6 [14.5] years vs 66.1 [13.5] years), had a higher glomerular filtration rate (mean [SD], 68.6 [24.9] vs 57.0 [24.0]), lower levels of natriuretic peptides (median [IQR], brain-type natriuretic peptide, 855.0 [423.0-1555.0] pg/mL vs 1022.0 [500.0-1927.0] pg/mL), and tended to be discharged on lower doses of loop diuretic (mean [SD], 50.3 [46.2] mg vs 63.8 [52.4] mg). De novo HF was associated with lower all-cause mortality at 12 months (de novo, 65 of 838 [9.1%] vs WHF, 408 of 2020 [25.4%]; adjusted hazard ratio [aHR], 0.50; 95% CI, 0.38-0.66; P < .001). Similarly, lower all-cause first rehospitalization at 12 months and greater improvement from baseline in KCCQ-CSS at 12 months were noted among patients with de novo HF (median [IQR]: de novo, 29.94 [27.35-32.54] vs WHF, 23.68 [21.62-25.74]; adjusted estimated difference in means: 6.26; 95% CI, 3.72-8.81; P < .001). There was no significant difference in mortality with torsemide vs furosemide in either de novo (No. of events [rate per 100 patient-years]: torsemide, 27 [7.4%] vs furosemide, 38 [10.9%]; aHR, 0.70; 95% CI, 0.40-1.14; P = .15) or WHF (torsemide 212 [26.8%] vs furosemide, 196 [24.0%]; aHR, 1.08; 95% CI, 0.89-1.32; P = .42; P for interaction = .10), In addition, no significant differences in hospitalizations, first all-cause hospitalization, or total hospitalizations at 12 months were noted with a strategy of torsemide vs furosemide in either de novo HF or WHF.

Conclusions and relevance: Among patients discharged after hospitalization for HF, de novo HF was associated with better clinical and patient-reported outcomes when compared with WHF. Regardless of HF type, there was no significant difference between torsemide and furosemide with respect to 12-month clinical or patient-reported outcomes.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Krim reported receiving research support from Abbott and CareDx. Dr Greene reported receiving research support from the Duke University Department of Medicine Chair’s Research Award, American Heart Association, National Heart Lung and Blood Institute, Amgen, AstraZeneca, Bristol Myers Squibb, Cytokinetics, Merck, Novartis, Pfizer, and Sanofi; serving on advisory boards for Amgen, AstraZeneca, Boehringer Ingelheim/Lilly, Bristol Myers Squibb, Cytokinetics, Roche Diagnostics, and Sanofi; serving as a consultant for Amgen, Bayer, Bristol Myers Squibb, Boehringer Ingelheim/Lilly, Corteria, CSL Vifor, Lexicon, Merck, PharmaIN, Roche Diagnostics, Sanofi, scPharmaceuticals, Tricog Health, Urovant Pharmaceuticals; and receiving speaker fees from Bayer, Boehringer Ingelheim, Cytokinetics, Lexicon, and Roche Diagnostics. Dr Herre reported serving as a consultant for Medtronic, nonexecutive chair, LifeNet Health (a not-for-profit Organ Procurement Organization and tissue bank). Dr Eisenstein reported receiving grants from the National Heart, Lung, and Blood Institute during the conduct of the study. Dr Anstrom reported receiving research support from Merck, Bayer, Pfizer, the National Institutes of Health, and Patient-Centered Oucomes Research Institute. Dr Pitt reported receiving personal fees from Bayer, scPharmaceuticals, Sqinnovation, Boehringer Ingelheim, Vifor, AstraZeneca, G3 Pharmaceuticals, Sarfez, Cereno Scientific, Phasebio, KPB Biosciences, Protonintel, Brainstorm Medical; having a patent for US 9931413 issued, site-specific delivery of eplerenone to the myocardium, and having a patent for US 63/045,783 pending, histone modulating agents for the prevention and protection from organ injury. Dr Velazquez reported receiving grants from the National Heart, Lung, and Blood Institute to Yale University as principal investigator of the clinical coordinating center during the conduct of the study and personal fees from Novartis and consultant fees from Abiomed to Yale University and from Baim Institute to Yale University outside the submitted work. Dr Mentz reported receiving research support and honoraria from Abbott outside the submitted work. No other disclosures were reported.

Figures

Figure.
Figure.. Treatment Effect of Torsemide vs Furosemide Among Patients With De Novo vs Worsening Chronic Heart Failure.
Forest plot of hazard ratio (HR)/rate ratio (RR) comparing randomized diuretic treatments (torsemide vs furosemide) for all end points among patients with de novo heart failure and patients with worsening chronic heart failure (WHF). aFirst event rates per 100 patient-years are reported for all-cause mortality, all-cause mortality or hospitalization, and all-cause hospitalization. bFor total hospitalizations, the total event rates per 100 patient-years are reported.

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