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Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
CCS/CHFS Heart Failure Guidelines: Clinical Trial Update on Functional Mitral Regurgitation, SGLT2 Inhibitors, ARNI
Eileen O'Meara1, Michael McDonald2, Michael Chan3
1Institut de Cardiologie de Montréal, Université de Montréal, Montréal, Québec, Canada.
Insights
New heart failure (HF) therapies show promise. Transcatheter mitral valve repair, transthyretin amyloidosis treatment, and sodium-glucose cotransport inhibitors offer improved outcomes for HF patients. Further research is needed for angiotensin receptor-neprilysin inhibitors in HF with preserved ejection fraction.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Heart failure (HF) management requires updated clinical guidance based on recent evidence.
- Key therapeutic areas include valvular heart disease, cardiac amyloidosis, and HF with preserved and reduced ejection fraction.
- Guideline-directed medical therapy and multidisciplinary approaches are crucial for optimal patient care.
Purpose of the Study:
- To review recent clinical trials (post-2017) on selected HF therapies.
- To provide evidence-based recommendations for managing patients considered for novel HF treatments.
- To offer practical tips for healthcare providers treating diverse HF populations.
Main Methods:
- Systematic review of clinical trials published after 2017 focusing on specific HF interventions.
- Analysis of evidence for transcatheter mitral valve repair, transthyretin cardiac amyloidosis treatment, ARNI therapy in HFpEF, and SGLT inhibitors in HF.
- Emphasis on guideline-directed medical therapy and multidisciplinary team roles.
Main Results:
- Transcatheter mitral valve repair requires optimal guideline-directed medical therapy and multidisciplinary evaluation.
- Tafamidis is the first agent to demonstrate outcome improvement in transthyretin cardiac amyloidosis.
- Sacubitril/valsartan may benefit subgroups of HFpEF patients, but further data are needed.
- Sodium-glucose cotransport inhibitors (e.g., dapagliflozin) reduce HF risk, hospitalizations, and cardiovascular death in patients with and without type 2 diabetes, including those with HF with reduced ejection fraction.
Conclusions:
- Healthcare providers should consider cardiac amyloidosis in patients with suggestive clinical signs.
- Tafamidis offers a new therapeutic option for transthyretin cardiac amyloidosis.
- The role of sacubitril/valsartan in HFpEF requires further investigation.
- Sodium-glucose cotransport inhibitors are beneficial for HF prevention and treatment across various patient groups, including those with HF with reduced ejection fraction.
Abstract:
In this update, we focus on selected topics of high clinical relevance for health care providers who treat patients with heart failure (HF), on the basis of clinical trials published after 2017. Our objective was to review the evidence, and provide recommendations and practical tips regarding the management of candidates for the following HF therapies: (1) transcatheter mitral valve repair in HF with reduced ejection fraction; (2) a novel treatment for transthyretin amyloidosis or transthyretin cardiac amyloidosis; (3) angiotensin receptor-neprilysin inhibition in patients with HF and preserved ejection fraction (HFpEF); and (4) sodium glucose cotransport inhibitors for the prevention and treatment of HF in patients with and without type 2 diabetes. We emphasize the roles of optimal guideline-directed medical therapy and of multidisciplinary teams when considering transcatheter mitral valve repair, to ensure excellent evaluation and care of those patients. In the presence of suggestive clinical indices, health care providers should consider the possibility of cardiac amyloidosis and proceed with proper investigation. Tafamidis is the first agent shown in a prospective study to alter outcomes in patients with transthyretin cardiac amyloidosis. Patient subgroups with HFpEF might benefit from use of sacubitril/valsartan, however, further data are needed to clarify the effect of this therapy in patients with HFpEF. Sodium glucose cotransport inhibitors reduce the risk of incident HF, HF-related hospitalizations, and cardiovascular death in patients with type 2 diabetes and cardiovascular disease. A large clinical trial recently showed that dapagliflozin provides significant outcome benefits in well treated patients with HF with reduced ejection fraction (left ventricular ejection fraction ≤ 40%), with or without type 2 diabetes.
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