Effects of dapagliflozin on heart failure hospitalizations according to severity of inpatient course: Insights from DELIVER and DAPA‐HF

Author:

Chatur Safia1,Kondo Toru23,Claggett Brian L.1,Docherty Kieran2,Miao Zi Michael1,Desai Akshay S.1,Jhund Pardeep S.2,de Boer Rudolf A.4,Hernandez Adrian F.5,Inzucchi Silvio E.6,Kosiborod Mikhail N.7,Lam Carolyn S.P.8,Martinez Felipe A.9,Shah Sanjiv J.10,Petersson Magnus11,Langkilde Anna Maria11,McMurray John J.V.2,Solomon Scott D.1,Vaduganathan Muthiah1

Affiliation:

1. Cardiovascular Division Brigham and Women's Hospital, Harvard Medical School Boston MA USA

2. BHF Cardiovascular Research Centre University of Glasgow Glasgow UK

3. Department of Cardiology Nagoya University Graduate School of Medicine Nagoya Japan

4. Department of Cardiology Erasmus MC Rotterdam The Netherlands

5. Duke University Medical Center Durham NC USA

6. Yale School of Medicine New Haven CT USA

7. Saint Luke's Mid America Heart Institute and University of Missouri‐Kansas City Kansas City MO USA

8. National Heart Centre Singapore & Duke‐National University of Singapore Singapore Singapore

9. Universidad Nacional de Córdoba Córdoba Argentina

10. Northwestern University Feinberg School of Medicine Chicago IL USA

11. Late‐Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D Gothenburg Sweden

Abstract

AbstractAimsDapagliflozin resulted in significant and sustained reductions in first and recurrent heart failure (HF) hospitalizations among patients with HF across the spectrum of ejection fraction. How treatment with dapagliflozin differentially impacts hospitalization for HF of varying complexity is not well studied.Methods and resultsIn the DELIVER and DAPA‐HF trials, we examined the effects of dapagliflozin on adjudicated HF hospitalizations of varying complexity and hospital length of stay (LOS). HF hospitalizations requiring intensive care unit stay, intravenous vasoactive therapies, invasive/non‐invasive ventilation, mechanical fluid removal or mechanical circulatory support were categorized as complicated. The balance was classified as uncomplicated. Of the total 1209 HF hospitalizations reported in DELIVER, 854 (71%) were uncomplicated and 355 (29%) were complicated. Of the total 799 HF hospitalizations reported in DAPA‐HF, 453 (57%) were uncomplicated and 346 (43%) were complicated. Relative to patients experiencing a first uncomplicated HF hospitalization, those with complicated HF hospitalizations had a significantly higher in‐hospital mortality both in DELIVER (16.7% vs. 2.3%, p < 0.001) and DAPA‐HF (15.1% vs. 3.8%, p < 0.001). Dapagliflozin similarly reduced total ‘uncomplicated’ (DELIVER: rate ratio [RR] 0.67, 95% confidence interval [CI] 0.55–0.82 and DAPA‐HF: RR 0.69, 95% CI 0.54–0.87) and ‘complicated’ HF hospitalizations (DELIVER: RR 0.82, 95% CI 0.63–1.06 and DAPA‐HF: RR 0.75, 95% CI 0.58–0.97). Dapagliflozin consistently reduced hospitalizations irrespective of their LOS: <5 days (DELIVER: RR 0.76, 95% CI 0.58–0.99 and DAPA‐HF: RR 0.58, 95% CI 0.42–0.80) or ≥5 days (DELIVER: RR 0.71, 95% CI 0.58–0.86 and DAPA‐HF: RR 0.77, 95% CI 0.62–0.94).ConclusionA substantial proportion of hospitalizations (∼30–40%) among patients with HF irrespective of ejection fraction required intensification of treatment beyond standard intravenous diuretics. Such patients experienced significantly higher in‐hospital mortality. Treatment with dapagliflozin consistently reduced HF hospitalizations regardless of severity of inpatient course or LOS.Clinical Trial Registration: ClinicalTrials.gov, DELIVER (NCT03619213) and DAPA‐HF (NCT03036124).

Funder

AstraZeneca

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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