Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial

Author:

Chatur Safia1ORCID,Vaduganathan Muthiah1ORCID,Claggett Brian1,Vardeny Orly2ORCID,Desai Akshay S1ORCID,Jhund Pardeep S3,de Boer Rudolf A4,Lam Carolyn S P5,Kosiborod Mikhail N6,Shah Sanjiv J7,Martinez Felipe8,Inzucchi Silvio E9,Hernandez Adrian F10,Haddad Tariq11,Mitter Sumeet S12,Miao Zi Michael1ORCID,Petersson Magnus13,Maria Langkilde Anna13,McMurray John J V3,Solomon Scott D1ORCID

Affiliation:

1. Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School , 75 Francis Street, Boston, MA 02115 , USA

2. Minneapolis VA Center for Care Delivery and Outcomes Research, University of Minnesota , Minneapolis, MN , USA

3. BHF Cardiovascular Research Centre, University of Glasgow , Glasgow , UK

4. Department of Cardiology, Erasmus Medical Center , Rotterdam , the Netherlands

5. National Heart Centre Singapore & Duke-National University of Singapore , Singapore , Singapore

6. Saint Luke’s Mid America Heart Institute and University of Missouri-Kansas City , Kansas City, MO , USA

7. Northwestern University Feinberg School of Medicine , Chicago, IL , USA

8. Universidad Nacional de Córdoba , Córdoba , Argentina

9. Yale School of Medicine , New Haven, CT , USA

10. Duke University Medical Center , Durham, NC , USA

11. Department of Cardiology, Virginia Heart , Falls Church, VA , USA

12. Icahn School of Medicine at Mount Sinai , New York, NY , USA

13. Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca , Gothenburg , Sweden

Abstract

Abstract Aims Dapagliflozin reduced the combined risk of worsening heart failure or cardiovascular death among patients with heart failure with mildly reduced or preserved ejection fraction. In this study, the safety and efficacy of dapagliflozin according to background diuretic therapy and the influence of dapagliflozin on longitudinal diuretic use were evaluated. Methods and results In this pre-specified analysis of the Dapagliflozin Evaluation to Improve the LIVEs of Patients With Preserved Ejection Fraction Heart Failure (DELIVER) trial, the effects of dapagliflozin vs. placebo were assessed in the following subgroups: no diuretic, non-loop diuretic, and loop diuretic furosemide equivalent doses of <40, 40, and >40 mg, respectively. Of the 6263 randomized patients, 683 (10.9%) were on no diuretic, 769 (12.3%) were on a non-loop diuretic, and 4811 (76.8%) were on a loop diuretic at baseline. Treatment benefits of dapagliflozin on the primary composite outcome were consistent by diuretic use categories (P  interaction = 0.64) or loop diuretic dose (P  interaction = 0.57). Serious adverse events were similar between dapagliflozin and placebo arms, irrespective of diuretic use or dosing. Dapagliflozin reduced new initiation of loop diuretics by 32% [hazard ratio (HR) 0.68; 95% confidence interval (CI): 0.55–0.84, P < 0.001] but did not influence discontinuations/disruptions (HR 0.98; 95% CI: 0.86–1.13, P = 0.83) in follow-up. First sustained loop diuretic dose increases were less frequent, and sustained dose decreases were more frequent in patients treated with dapagliflozin: net difference of −6.5% (95% CI: −9.4 to −3.6; P < 0.001). The mean dose of loop diuretic increased over time in the placebo arm, a longitudinal increase that was significantly attenuated with treatment with dapagliflozin (placebo-corrected treatment effect of −2.5 mg/year; 95% CI: −1.5, −3.7, P < 0.001). Conclusion In patients with heart failure with mildly reduced or preserved ejection fraction, the clinical benefits of dapagliflozin relative to placebo were consistent across a wide range of diuretic categories and doses with a similar safety profile. Treatment with dapagliflozin significantly reduced new loop diuretic requirement over time.

Funder

AstraZeneca

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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