On‐treatment analysis of torsemide versus furosemide for patients hospitalized for heart failure: A post‐hoc analysis of TRANSFORM‐HF

Author:

Kittipibul Veraprapas12,Mentz Robert J.12,Clare Robert M.1,Wojdyla Daniel M.1,Anstrom Kevin J.3,Eisenstein Eric L.1,Ambrosy Andrew P.4,Goyal Parag5,Skopicki Hal A.6,Ketema Fassil7,Kim Dong‐Yun8,Desvigne‐Nickens Patrice7,Pitt Bertram9,Velazquez Eric J.10,Greene Stephen J.12

Affiliation:

1. Duke Clinical Research Institute Durham NC USA

2. Division of Cardiology Duke University School of Medicine Durham NC USA

3. Gillings School of Global Public Health University of North Carolina Chapel Hill NC USA

4. Division of Research Kaiser Permanente Northern California Oakland CA USA

5. Department of Medicine Weill Cornell Medical College, Cornell University New York NY USA

6. Division of Cardiology Stony Brook University Stony Brook NY USA

7. Division of Cardiovascular Sciences National Heart, Lung, and Blood Institute Bethesda MD USA

8. Division of Intramural Research National Heart, Lung, and Blood Institute Bethesda MD USA

9. Division of Cardiology, Department of Medicine University of Michigan Ann Arbor MI USA

10. Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine New Haven CT USA

Abstract

ABSTRACTAimThe TRANSFORM‐HF trial demonstrated no significant outcome differences between torsemide and furosemide following hospitalization for heart failure (HF), but may have been impacted by non‐adherence to the randomized diuretic. The current study sought to determine the treatment effect of torsemide versus furosemide using an on‐treatment analysis inclusive of all randomized patients except those confirmed non‐adherent to study diuretic.Methods and resultsTRANSFORM‐HF was an open‐label, pragmatic randomized trial of 2859 patients hospitalized for HF from June 2018 through March 2022. Patients were randomized to a loop diuretic strategy of torsemide versus furosemide with investigator‐selected dosage. This post‐hoc on‐treatment analysis included all patients alive with either known or unknown diuretic status, and excluded patients confirmed to be non‐adherent to study diuretic. This modified on‐treatment definition was applied separately at time of hospital discharge and 30‐day follow‐up. All‐cause mortality and hospitalization outcomes were assessed over 12 months. Overall, 2570 (89.9%) and 2374 (83.0%) patients were included in on‐treatment analyses at discharge and 30‐day follow‐up, respectively. There was no significant difference in all‐cause mortality between torsemide and furosemide in patients on‐treatment at discharge (17.5% vs. 17.8%; hazard ratio [HR] 1.01 [95% confidence interval [CI] 0.83–1.22], p = 0.96) and at 30‐day follow‐up (14.5% vs. 15.0%; HR 1.02 [95% CI 0.81–1.27], p = 0.90). All‐cause mortality or all‐cause hospitalization was similar between torsemide and furosemide in patients who were on‐treatment at discharge (58.3% vs. 61.3%; HR 0.92 [95% CI 0.82–1.03]) and 30‐day follow‐up (60.9% vs. 64.4%; HR 0.93 [95% CI 0.82–1.05]). In patients who were on‐treatment at 30‐day follow‐up, there were 677 total hospitalizations in the torsemide group and 686 total hospitalizations in the furosemide group (rate ratio 0.99 [95% CI 0.86–1.14], p = 0.87).ConclusionsIn TRANSFORM‐HF, a post‐hoc on‐treatment analysis did not meaningfully differ from the original trial results. Among those deemed compliant with the assigned diuretic, there remained no significant difference in mortality or hospitalization after HF hospitalization with a strategy of torsemide versus furosemide.Clinical Trail Registration: ClinicalTrials.gov Identifier: NCT03296813.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

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