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Heart failure with reduced, mildly reduced, and preserved ejection fraction: outcomes and predictors of prognosis
Tomasz M Rywik1, Anna Wiśniewska2, Urszula Cegłowska2
1Department of Heart Failure and Transplantology, National Institute of Cardiology, Warsaw, Poland. trywik@ikard.pl
Insights
Survival in heart failure with reduced ejection fraction (HFrEF) is significantly worse than in mildly reduced (HFmrEF) and preserved (HFpEF) phenotypes, where outcomes are similar. Treatment with ACE inhibitors improved survival across all heart failure types.
Area of Science:
- Cardiology
- Internal Medicine
- Clinical Research
Background:
- Heart failure (HF) classification has evolved with new phenotypes based on ejection fraction (EF).
- Limited data exists on long-term survival trends for individual HF phenotypes.
- Previous research primarily focused on HF with reduced ejection fraction (HFrEF).
Purpose of the Study:
- To evaluate survival rates across different HF phenotypes: HFrEF, HFmrEF, and HFpEF.
- To identify predictors of mortality in HF patients.
- To compare long-term survival trends among HF subtypes.
Main Methods:
- Analysis of 2601 patients hospitalized for HF between 2014 and 2019.
- HF phenotyping based on EF: HFrEF (<40%), HFmrEF (40%-49%), HFpEF (≥50%).
- Median follow-up of 2.43 years to assess survival and mortality predictors.
Main Results:
- HFrEF patients (62%) had a 61% higher risk of death compared to HFpEF patients (25%).
- Survival rates at 1 and 5 years were lower for HFrEF (81%, 47%) versus HFmrEF (84%, 61%) and HFpEF (84%, 59%).
- Inotrope use increased mortality risk, while ACE inhibitor use decreased it, independent of HF phenotype.
Conclusions:
- Survival outcomes are significantly worse in HFrEF compared to HFmrEF and HFpEF, which have similar survival rates.
- HF phenotypes exhibit distinct prognostic parameters.
- ACE inhibitors demonstrate a survival benefit across all HF phenotypes.
Introduction:
Recently, a stratification of the heart failure (HF) phenotypes, which classifies HF into 3 subtypes based on ejection fraction, has been introduced. Before that, clinical trials and registries have been mainly devoted to HF with reduced ejection fraction (HFrEF). As a result, data on long‑term survival trends for individual HF phenotypes are scarce.
Objectives:
The study aimed to evaluate survival according to the HF phenotype and to identify predictors of mortality.
Patients And Methods:
Patients hospitalized for HF in our referral center between January 2014 and May 2019 were included in the analysis. HF phenotyping was based on EF: reduced (HFrEF with EF <40%), mildly reduced (HFmrEF with EF = 40%-49%), and preserved (HFpEF with EF ≥50%).
Results:
Of 2601 patients included in the study, 1608 individuals (62%) presented with HFrEF, 331 patients with HFmrEF (13%), and 662 patients with HFpEF (25%). The median follow‑up was 2.43 years (interquartile range, 1.56-3.49). The risk of death was 61% higher in HFrEF than in HFpEF (P <0.001), while in HFmrEF and HFpEF it was similar. Survival rates at 1 and 5 years in HFrEF, HFmrEF, and HFpEF were 81%, 84%, 84%, and 47%, 61%, and 59%, respectively. The HF phenotypes differed in most of the parameters that affect prognosis. Only the use of inotropes, which was linked to an increased risk of death, and the use of angiotensin‑converting enzyme inhibitors, which reduced this risk, were independent of the HF phenotype.
Conclusions:
Survival in HFrEF is worse as compared with HFmrEF and HFpEF, where it is similar. The HF phenotypes differ in most of the parameters that affect survival.
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