Heart failure with reduced ejection fraction (HFrEF) remains a formidable clinical challenge, necessitating innovative pharmacological interventions to mitigate morbidity and mortality. Vericiguat, a novel oral soluble guanylate cyclase (sGC) stimulator, has emerged as a promising therapeutic agent, targeting the nitric oxide (NO)-sGC-cyclic guanosine monophosphate (cGMP) pathway to enhance myocardial and vascular function. The pivotal VICTORIA (Vericiguat Global Study in Subjects with Heart Failure with Reduced Ejection Fraction) trial demonstrated a significant reduction in the composite endpoint of cardiovascular death or heart failure hospitalization in high-risk HFrEF patients when vericiguat was added to standard guideline-directed medical therapy (GDMT). This article comprehensively reviews the pharmacodynamic and pharmacokinetic properties of vericiguat, its mechanistic role in HFrEF pathophysiology, and the critical findings from the VICTORIA trial. Furthermore, we discuss the clinical implications of vericiguat in contemporary HFrEF management, including its potential integration into existing therapeutic algorithms and its impact on patient-centered outcomes.
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David López
Universidad de Las Palmas de Gran Canaria
Suellen Marinho Andrade
Memorial University of Newfoundland
Érica Vieira de Andrade
Universidade Federal do Triângulo Mineiro
International Journal of Medical Science and Clinical Research Studies
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López et al. (Sat,) studied this question.
synapsesocial.com/papers/68af59d7ad7bf08b1eade458 — DOI: https://doi.org/10.47191/ijmscrs/v5-i08-11
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