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Contemporary Use and Implications of Beta-Blockers in Patients With HFmrEF or HFpEF: The DELIVER Trial

  • Alexander Peikert
  • , Bradley A. Bart
  • , Muthiah Vaduganathan
  • , Brian L. Claggett
  • , Ian J. Kulac
  • , Mikhail N. Kosiborod
  • , Akshay S. Desai
  • , Pardeep S. Jhund
  • , Carolyn S.P. Lam
  • , Silvio E. Inzucchi
  • , Felipe A. Martinez
  • , Rudolf A. de Boer
  • , Adrian F. Hernandez
  • , Sanjiv J. Shah
  • , Magnus Petersson
  • , Anna Maria Langkilde
  • , John J.V. McMurray
  • , Scott D. Solomon
  • , Orly Vardeny

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Although beta-blockers are not recommended for the treatment of heart failure with preserved ejection fraction (HFpEF) according to the latest European Society of Cardiology and American Heart Association/American College of Cardiology/Heart Failure Society of America guidelines, these therapies remain commonly used for comorbidity management. There has been concern that beta-blockers may adversely influence clinical outcomes by limiting chronotropic response in HFpEF. Objectives: This study sought to examine the contemporary use and implications of beta-blockers in patients with heart failure with mildly reduced ejection fraction (HFmrEF) or HFpEF. Methods: In the DELIVER (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure) trial, a total of 6,263 patients with symptomatic heart failure (HF) with a left ventricular ejection fraction (LVEF) >40% were randomized to dapagliflozin or placebo across 20 countries. In this prespecified analysis, efficacy and safety outcomes were examined according to beta-blocker use at randomization. The primary outcome was cardiovascular death or worsening HF. Results: Overall, beta-blockers were used in 5,177 patients (83%), with wide variation by geographic region. Beta-blocker use was associated with a lower risk of the primary outcome in covariate-adjusted models (HR: 0.70; 95% CI: 0.60-0.83). Dapagliflozin consistently reduced the risk of the primary outcome in patients taking beta-blockers (HR: 0.82; 95% CI: 0.72-0.94) and in patients not taking beta-blockers (HR: 0.79; 95% CI: 0.61-1.03; Pinteraction = 0.85), with similar findings for key secondary endpoints. Adverse events were balanced between patients randomized to dapagliflozin and placebo, regardless of background beta-blocker use. Conclusions: In patients with HFmrEF or HFpEF who were enrolled in DELIVER, 4 out of 5 participants were treated with a beta-blocker. Beta-blocker use was not associated with a higher risk of worsening HF or cardiovascular death. Dapagliflozin consistently and safely reduced clinical events, irrespective of background beta-blocker use.

Original languageEnglish (US)
Pages (from-to)631-644
Number of pages14
JournalJACC: Heart Failure
Volume12
Issue number4
DOIs
StatePublished - Apr 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors

Keywords

  • SGLT2 inhibitors
  • beta-blockers
  • heart failure with mildly reduced ejection fraction
  • heart failure with preserved ejection fraction

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