Therapeutic Consequences and Prognostic Impact of Multimorbidity in Heart Failure: Time to Act

Fanni Bánfi-Bacsárdi1,2, Ádám Kazay1, Tamás G Gergely1

  • 1Department of Adult Cardiology, Gottsegen National Cardiovascular Center, 1096 Budapest, Hungary.

PubMed

Insights

Patients with heart failure with reduced ejection fraction (HFrEF) and multiple comorbidities face worse outcomes. However, guideline-directed medical therapy (GDMT) significantly improves prognosis even in these complex cases.

Area of Science:

  • Cardiology
  • Internal Medicine
  • Pharmacology

Background:

  • Comorbidities (CMs) significantly impact heart failure with reduced ejection fraction (HFrEF) management and outcomes.
  • Early diagnosis and treatment of CMs are crucial for HFrEF patients.

Purpose of the Study:

  • To assess CM prevalence in hospitalized HFrEF patients.
  • To investigate the effect of CMs on guideline-directed medical therapy (GDMT) implementation.
  • To analyze the impact of CMs on all-cause mortality (ACM) in HFrEF.

Main Methods:

  • Retrospective analysis of 388 consecutive HFrEF patients hospitalized between 2021-2024.
  • Evaluation of 16 comorbidities (CV and non-CV) and categorization into 0-3, 4-6, and ≥7 CMs.
  • Comparison of GDMT at discharge and 1-year ACM across CM categories.

Main Results:

  • Higher comorbidity burden correlated with reduced application of renin-angiotensin system inhibitors (RASi) and beta-blockers (βB).
  • Triple therapy (TT) implementation decreased with increased CMs, while quadruple therapy (QT) remained stable.
  • One-year all-cause mortality (ACM) was significantly higher in patients with ≥7 CMs (25%) compared to those with 0-3 CMs (9%).

Conclusions:

  • Increased comorbidity burden in HFrEF patients is associated with poorer prognosis.
  • Modern GDMT, including TT/QT, can be effectively implemented in multimorbid HFrEF patients, significantly improving outcomes.
  • Early and consistent application of GDMT is vital for improving prognosis in HFrEF patients with multiple comorbidities.

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