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F T Ageev1, A G Ovchinnikov

  • 1FSBO National Medical research center of cardiology of the Ministry of healthcare of the Russian Federation. fake@neicon.ru.

Kardiologiia
|January 10, 2019
PubMed

Insights

Patients with mid-range ejection fraction (EF) heart failure (HF) respond well to beta-blockers and RAAS inhibitors, unlike those with preserved EF. A new HF classification should include clinical phenotype for better treatment guidance.

Area of Science:

  • Cardiology
  • Heart Failure Research

Background:

  • Heart failure (HF) classification traditionally categorizes patients based on left ventricular ejection fraction (LVEF) into reduced (<40%), mid-range (40-49%), and preserved (≥50%) groups.
  • Patients with mid-range LVEF exhibit heterogeneous clinical and demographic characteristics, often occupying an intermediate position between reduced and preserved LVEF groups.

Purpose of the Study:

  • To evaluate the clinical expediency of a separate classification subgroup for heart failure patients with mid-range ejection fraction (40-49%).
  • To analyze the treatment response and etiological differences within the mid-range LVEF subgroup compared to reduced and preserved LVEF groups.
  • To advocate for a revised HF classification incorporating clinical phenotype alongside LVEF.

Main Methods:

  • Analysis of studies published between 2017-2018 focusing on patients with mid-range LVEF.
  • Comparison of clinical and demographic parameters, treatment responses (beta-blockers, RAAS inhibitors), and etiological factors (ischemic vs. non-ischemic phenotypes) across different LVEF groups.

Main Results:

  • Patients with mid-range LVEF demonstrate a positive response to beta-blocker and RAAS inhibitor therapy, similar to patients with reduced LVEF.
  • This therapeutic response differs significantly from patients with preserved LVEF, who typically do not benefit from these treatments.
  • Etiology plays a key role, with ischemic heart disease prevalent in reduced and mid-range LVEF, while non-cardiac causes are more common in preserved LVEF.

Conclusions:

  • The mid-range LVEF subgroup is clinically distinct and warrants separate consideration.
  • The positive response to specific therapies in mid-range LVEF suggests a pathogenesis more aligned with reduced LVEF, primarily linked to ischemic heart disease.
  • A comprehensive HF classification should integrate clinical phenotype (e.g., ischemic vs. non-ischemic) with LVEF, especially for the heterogeneous mid-range group, to guide therapeutic strategies.

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