Related Experiment Video
Updated: Aug 16, 2026

Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Personalizing Modern Heart Failure Therapy in HFrEF: Bridging Evidence, Clinical Practice, and Future Perspectives
Ehsan Shahverdi1, Amin Shahverdi2, Sendooran Shahi1
1Department of Cardiology, Rhythmology, Angiology and Intensive Care Medicine, Klinikum Osnabrück, Osnabrück, Germany.
Guideline-directed medical therapy (GDMT) for heart failure with reduced ejection fraction (HFrEF) is effective but underutilized. Optimizing implementation through phenotype-based strategies is key for better patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Heart failure with reduced ejection fraction (HFrEF) significantly impacts morbidity and mortality globally.
- Despite advances, four foundational pharmacologic therapies (renin-angiotensin system inhibition/angiotensin receptor-neprilysin inhibition, beta-blockers, mineralocorticoid receptor antagonists, SGLT2 inhibitors) are underused in real-world settings.
Purpose of the Study:
- To review current evidence for guideline-directed medical therapy (GDMT) in HFrEF.
- To examine challenges in GDMT sequencing and optimization.
- To propose a phenotype-based framework for individualized treatment decisions.
Main Methods:
- A structured narrative review of literature from January 2000 to February 2026.
- Searches included PubMed/MEDLINE, Embase, and Google Scholar.
- Prioritized randomized controlled trials, guidelines, meta-analyses, and registries on GDMT initiation, sequencing, and implementation.
Main Results:
- Early, combined use of the four GDMT classes significantly reduces mortality and hospitalizations.
- Rapid initiation and uptitration are favored over sequential strategies.
- Barriers include hypotension, renal dysfunction, hyperkalemia, frailty, polypharmacy, and access issues.
Conclusions:
- The main challenge in HFrEF management is suboptimal delivery of proven therapies.
- Future progress relies on optimizing implementation via phenotype-informed, patient-centered strategies rather than new drug classes.
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