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Heart failure in the last year: progress and perspective
Daniela Tomasoni1,2, Marianna Adamo1,2, Markus S Anker3,4,5,6
1Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
Insights
Recent heart failure research highlights new treatments for reduced ejection fraction, including sacubitril/valsartan, dapagliflozin, empagliflozin, and vericiguat, improving patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart failure (HF) research has advanced significantly, necessitating an update on recent findings.
- Established treatments for HF with reduced ejection fraction (HFrEF) have been enhanced by new therapeutic options.
Purpose of the Study:
- To review the latest advancements in heart failure management.
- To discuss novel therapeutic strategies and ongoing challenges in HF treatment.
Main Methods:
- Review of landmark clinical trials, including PARADIGM-HF, DAPA-HF, and EMPEROR-Reduced.
- Analysis of recent therapeutic developments such as sacubitril/valsartan, SGLT2 inhibitors (dapagliflozin, empagliflozin), and vericiguat.
Main Results:
- Sacubitril/valsartan demonstrated superiority over enalapril in HFrEF.
- Dapagliflozin and empagliflozin significantly reduced composite endpoints in HFrEF.
- Vericiguat lowered the risk of cardiovascular death or HF hospitalization.
Conclusions:
- New pharmacotherapies offer improved outcomes for HFrEF patients.
- Diagnosis and treatment of HF with preserved ejection fraction (HFpEF) and advanced HF remain challenging.
- Enhanced patient phenotyping and exploration of devices, arrhythmia management, and percutaneous valvular interventions are crucial for future HF care.
Abstract:
Research about heart failure (HF) has made major progress in the last years. We give here an update on the most recent findings. Landmark trials have established new treatments for HF with reduced ejection fraction. Sacubitril/valsartan was superior to enalapril in PARADIGM-HF trial, and its initiation during hospitalization for acute HF or early after discharge can now be considered. More recently, new therapeutic pathways have been developed. In the DAPA-HF and EMPEROR-Reduced trials, dapagliflozin and empagliflozin reduced the risk of the primary composite endpoint, compared with placebo [hazard ratio (HR) 0.74; 95% confidence interval (CI) 0.65-0.85; P < 0.001 and HR 0.75; 95% CI 0.65-0.86; P < 0.001, respectively]. Second, vericiguat, an oral soluble guanylate cyclase stimulator, reduced the composite endpoint of cardiovascular death or HF hospitalization vs. placebo (HR 0.90; 95% CI 0.82-0.98; P = 0.02). On the other hand, both the diagnosis and treatment of HF with preserved ejection fraction, as well as management of advanced HF and acute HF, remain challenging. A better phenotyping of patients with HF would be helpful for prognostic stratification and treatment selection. Further aspects, such as the use of devices, treatment of arrhythmias, and percutaneous treatment of valvular heart disease in patients with HF, are also discussed and reviewed in this article.
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