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Patient Characteristics, Outcomes, and Effects of Dapagliflozin According to the Duration of Heart Failure: A Prespecified Analysis of the DELIVER Trial

  • Toru Kondo
  • , Karola S. Jering
  • , C. Jan Willem Borleffs
  • , Rudolf A. De Boer
  • , Brian L. Claggett
  • , Akshay S. Desai
  • , Dan Dobreanu
  • , Silvio E. Inzucchi
  • , Adrian F. Hernandez
  • , Stefan P. Janssens
  • , Pardeep S. Jhund
  • , Mikhail N. Kosiborod
  • , Carolyn S.P. Lam
  • , Anna Maria Langkilde
  • , Felipe A. Martinez
  • , Magnus Petersson
  • , Pham Nguyen Vinh
  • , Muthiah Vaduganathan
  • , Scott D. Solomon
  • , John J.V. McMurray*
  • *Corresponding author for this work
  • Glasgow Cardiovascular Research Centre
  • Nagoya University Graduate School of Medicine
  • Hebrew SeniorLife
  • Haga Ziekenhuis
  • George Emil Palade University of Medicine, Pharmacy, Science and Technology of Targu Mures
  • Yale New Haven Health System
  • Duke University
  • University Hospitals Leuven
  • University of Missouri at Kansas City
  • National Heart Centre Singapore
  • AstraZeneca
  • University of Córdoba
  • Tan Tao University

Research output: Contribution to journal › Article › Academic › peer-review

8 Citations (Scopus)
20 Downloads (Pure)

Abstract

Background: How patient characteristics and outcomes vary according to the duration of heart failure (HF) is unknown in individuals with mildly reduced or preserved ejection fraction. We compared these, and the efficacy and safety of dapagliflozin, according to the time from diagnosis of HF in a prespecified analysis of the DELIVER trial (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure). Methods: HF duration was categorized as ≤6 months, >6 to 12 months, >1 to 2 years, >2 to 5 years, or >5 years. The primary outcome was the composite of worsening HF or cardiovascular death. The effect of treatment was examined by HF duration category. Results: The number of patients in each category was as follows: 1160 (≤6 months), 842 (>6 to 12 months), 995 (>1 to 2 years), 1569 (>2 to 5 years), and 1692 (>5 years). Patients with longer-duration HF were older and had more comorbidities with worse symptoms. The rate of the primary outcome (per 100 person-years) increased with HF duration: ≤6 months, 7.3 (95% CI, 6.3 to 8.4); >6 to 12 months, 7.1 (6.0 to 8.5); >1 to 2 years, 8.4 (7.2 to 9.7); >2 to 5 years, 8.9 (7.9 to 9.9); and >5 years, 10.6 (9.5 to 11.7). Similar trends were seen for other outcomes. The benefit of dapagliflozin was consistent across HF duration category: the hazard ratio for the primary outcome in the ≤6-month group was 0.67 (95% CI, 0.50 to 0.91); >6 to 12 months, 0.78 (0.55 to 1.12); >1 to 2 years, 0.81 (0.60 to 1.09); >2 to 5 years, 0.97 (0.77 to 1.22); and >5 years, 0.78 (0.64 to 0.96; Pinteraction=0.41). The absolute benefit was greatest in longest-duration HF; the number needed to treat for HF >5 years was 24 versus 32 for ≤6 months. Conclusions: Patients with longer-duration HF were older, had more comorbidities and symptoms, and had higher rates of worsening HF and death. The benefits of dapagliflozin were consistent across HF duration. Even patients with long-standing HF and generally mild symptoms are not stable, and it is not too late for such patients to benefit from a sodium-glucose cotransporter 2 inhibitor. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03619213.

Original languageEnglish
Pages (from-to)1067-1078
Number of pages12
JournalCirculation
Volume147
Issue number14
DOIs
Publication statusPublished - 4 Apr 2023

Bibliographical note

Funding Information:
DELIVER (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure) was funded by AstraZeneca. Drs Jhund and McMurray are supported by British Heart Foundation Centre of Research Excellence grant RE/18/6/34217 and the Vera Melrose Heart Failure Research Fund.

Publisher Copyright:
© 2023 Lippincott Williams and Wilkins. All rights reserved.

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