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Updated: Mar 13, 2026

Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Evolving therapies for the management of chronic and acute decompensated heart failure
Jennifer C Cook1, Richard H Tran2, J Herbert Patterson2
1Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC.
Insights
New pharmacologic agents offer improved outcomes for heart failure (HF) management, reducing mortality and hospitalizations. Careful patient selection and optimization of existing therapies are crucial for integrating these advancements in HF treatment.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Therapeutics
Background:
- Heart failure (HF) remains a significant health burden with high mortality and hospitalization rates despite traditional therapies.
- Existing guideline-directed medical therapies (GDMT) include ACE inhibitors, ARBs, beta-blockers, and ARNIs, yet outcomes are suboptimal.
- There is a critical need for novel pharmacologic agents to improve management of chronic and acute decompensated heart failure (ADHF).
Purpose of the Study:
- To describe the pharmacology, clinical efficacy, and safety profiles of emerging therapies for HF and ADHF.
- To review recently approved and investigational drugs for heart failure.
- To emphasize the importance of patient selection and integration of new therapies with existing GDMT.
Main Methods:
- Review of clinical trial data and FDA-approved/under-review therapeutic compounds.
- Analysis of efficacy and safety data for novel heart failure medications.
- Discussion of ongoing research and future directions in pharmacologic HF management.
Main Results:
- Sacubitril-valsartan has shown significant benefits in reducing cardiovascular mortality and HF hospitalizations.
- Ivabradine and ferric carboxymaltose have demonstrated efficacy in reducing HF-related hospitalizations.
- Serelaxin is under investigation for ADHF, with other agents like bucindolol hydrochloride and omecamtiv mecarbil also in development.
Conclusions:
- New agents like sacubitril-valsartan, ivabradine, and ferric carboxymaltose represent advancements in HF treatment.
- Optimizing current GDMT alongside careful patient selection is essential for maximizing benefits of new therapies.
- Continuous monitoring of emerging literature and clinical trial results is vital for optimal application of novel HF therapies.
Purpose:
The pharmacology, clinical efficacy, and safety profiles of evolving therapies for the management of chronic heart failure (HF) and acute decompensated heart failure (ADHF) are described.
Summary:
HF confers a significant financial burden despite the widespread use of traditional guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, β-blockers, and aldosterone receptor antagonists, and the rates of HF-related mortality and hospitalization have remained unacceptably high. In response to a demand for novel pharmacologic agents, several therapeutic compounds have recently gained approval or are currently under review by the Food and Drug Administration. Sacubitril-valsartan has demonstrated benefit in reducing cardiovascular mortality and HF-related hospitalizations in clinical trials, while ivabradine and ferric carboxymaltose have proven efficacious in reducing HF-related hospitalizations. Lastly, the role of serelaxin in ADHF is currently under investigation in an ongoing Phase III study. While large, outcome-driven clinical trials are fundamental in informing the clinical application of these therapeutic agents, careful patient selection is imperative to ensuring similar outcomes postmarketing. In addition, optimization of current guideline-directed medical therapy remains essential as new therapies emerge and are incorporated into guideline recommendations. Additional therapeutic agents currently undergoing investigation include bucindolol hydrochloride, cimaglermin alfa, nitroxyl, omecamtiv mecarbil, TRV027, and ularitide. Clinical practitioners should remain abreast of emerging literature so that new therapeutic entities are optimally applied and positive patient outcomes are achieved.
Conclusion:
Recently introduced agents for the treatment of patients with HF include sacubitril-valsartan, ivabradine, and ferric carboxymaltose. Additional agents worthy of attention include serelaxin and other therapies currently under investigation.
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