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Updated: Aug 1, 2025

Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Heart failure therapy: the fifth card
Giulio Balestrieri1, Edoardo Sciatti1, Salvatore D'isa1
1Cardiovascular Department, Pope John XXIII Hospital, Bergamo, Italy.
Insights
New heart failure (HF) guidelines recommend four drug classes for all eligible patients. Vericiguat, a novel therapy, shows promise in reducing cardiovascular death and HF hospitalizations in high-risk populations.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- The 2021 European Society of Cardiology guidelines shift from sequential to a four-drug class approach for heart failure (HF) management.
- This new strategy involves initiating and titrating angiotensin receptor-neprilysin inhibitors, beta-blockers, mineralocorticoid receptor antagonists, and sodium-glucose cotransporter-2 inhibitors for patients with reduced ejection fraction (<35%).
- Advantages include rapid initiation, improved tolerability, and earlier reassessment of treatment efficacy.
Purpose of the Study:
- To evaluate the efficacy and safety of vericiguat, a soluble guanylate cyclase activator, in patients with heart failure.
- To assess vericiguat's impact on cardiovascular death and HF hospitalizations in a high-risk population, as demonstrated in the VICTORIA study.
- To investigate vericiguat's role in patients with HF on optimized therapy without recent stabilization events, as explored in the ongoing VICTOR trial.
Main Methods:
- The VICTORIA study assessed vericiguat's effect on a composite outcome of cardiovascular death and HF hospitalization.
- The VICTOR trial is a randomized clinical trial evaluating vericiguat in HF patients receiving optimized therapy.
- These studies involve high-risk populations and patients with specific HF characteristics.
Main Results:
- The VICTORIA study demonstrated that vericiguat significantly reduced the composite outcome of cardiovascular death and first HF hospitalization in a high-risk population.
- Vericiguat's mechanism as a soluble guanylate cyclase activator offers a novel therapeutic pathway for HF management.
Conclusions:
- The updated HF guidelines promote a comprehensive, multi-drug approach for optimal patient management.
- Vericiguat represents a promising therapeutic option for reducing adverse cardiovascular events in specific HF populations.
- Ongoing research, including the VICTOR trial, will further elucidate vericiguat's role in diverse HF patient profiles.
Abstract:
The 2021 European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure (HF) have abandoned the sequential approach for optimal drug therapy and propose four drug classes (enzyme inhibitors conversion agents, angiotensin receptor antagonists, beta-blockers, and sodium-glucose cotransporter inhibitors 2) to be initiated and titrated in all patients with an ejection fraction <35%. This new approach offers advantages such as rapid introduction and titration, better tolerability, and early instrumental re-evaluation. In the VICTORIA study, the molecule vericiguat, a soluble guanylate cyclase activator, was shown to reduce the composite outcome of death from cardiovascular causes and first hospitalization for HF in a high-risk population. An additional randomized clinical trial (VICTOR) is ongoing to evaluate the efficacy and safety of vericiguat in a population with HF on optimized therapy and with no recent episodes of stabilization.
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