Role of vericiguat in management of patients with heart failure with reduced ejection fraction after worsening episode

Worsening heart failure (HF) is a vulnerable period in which the patient has a markedly high risk of death or HF hospitalization (up to 10% and 30%, respectively, within the first weeks after episode). The prognosis of HF patients can be improved through a comprehensive approach that considers the d...

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Detalles Bibliográficos
Autores: Olivella, Aleix|||0000-0003-4912-2343, Almenar Bonet, Luis|||0000-0002-7710-361X, Moliner, P.|||0000-0002-5511-8597, Coloma, Emmanuel, Martinez Rubio, Antoni|||0000-0002-2070-4617, Paz Bermejo, Marco, Boixeda, Ramon, Cediel, Germán|||0000-0001-9667-7507, Méndez Fernández, Ana Belén, Facila Rubio, Lorenzo|||0000-0003-1402-4364
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:294994
Acceso en línea:https://ddd.uab.cat/record/294994
https://dx.doi.org/urn:doi:10.1002/ehf2.14647
Access Level:acceso abierto
Palabra clave:Heart failure
Sacubitril-valsartan
SGLT2
Vericiguat
Worsening
Descripción
Sumario:Worsening heart failure (HF) is a vulnerable period in which the patient has a markedly high risk of death or HF hospitalization (up to 10% and 30%, respectively, within the first weeks after episode). The prognosis of HF patients can be improved through a comprehensive approach that considers the different neurohormonal systems, with the early introduction and optimization of the quadruple therapy with sacubitril-valsartan, beta-blockers, mineralocorticoid receptor antagonists, and inhibitors. Despite that, there is a residual risk that is not targeted with these therapies. Currently, it is recognized that the cyclic guanosine monophosphate deficiency has a negative direct impact on the pathogenesis of HF, and vericiguat, an oral stimulator of soluble guanylate cyclase, can restore this pathway. The effect of vericiguat has been explored in the VICTORIA study, the largest chronic HF clinical trial that has mainly focused on patients with recent worsening HF, evidencing a significant 10% risk reduction of the primary composite endpoint of cardiovascular death or HF hospitalization (number needed to treat 24), after adding vericiguat to standard therapy. This benefit was independent of background HF therapy. Therefore, optimization of treatment should be performed as earlier as possible, particularly within vulnerable periods, considering also the use of vericiguat.