Association Between Vericiguat and Clinical Outcomes Across Patients With Heart Failure: A Systematic Review and Meta-Analysis of Randomized Controlled Trials
Recommended Citation
Nasir YM, Yasmeen J, Shama N, Ang SP, Doshi NA, Deb N, Hamsakutty H, Haris S, Jaiswal V, Mattumpuram J. Association Between Vericiguat and Clinical Outcomes Across Patients With Heart Failure: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Rev Cardiovasc Med. 2026;27(4):49095.
Document Type
Article
Publication Date
4-1-2026
Publication Title
Reviews in cardiovascular medicine
Abstract
BACKGROUND: Heart failure (HF) remains a major global health burden, with mortality continuing to rise despite therapeutic advances. Vericiguat, a soluble guanylate cyclase stimulator, has demonstrated potential benefit in patients with worsening HF with reduced ejection fraction (HFrEF), although results across randomized trials have been inconsistent. METHODS: We conducted a systematic literature search across PubMed, Scopus, and ClinicalTrials.gov for relevant articles from inception through September 30th, 2025. Outcomes were reported as pooled odds ratios (ORs) with corresponding 95% confidence intervals (CIs). Statistical significance was defined as a 95% confidence interval not crossing 1.0 with a two-tailed p-value < 0.05. RESULTS: Five randomized controlled trials (RCTs) with 12,877 patients (6857 in the vericiguat group and 6020 in the placebo group) were included. Vericiguat demonstrated a borderline but non-significant reduction in composite outcome of cardiovascular death (CVD) or hospitalization for HF (OR 0.92, 95% CI 0.85-1.00; p = 0.05), hospitalization for HF (OR 0.93, 95% CI 0.85-1.02; p = 0.14), and all-cause mortality (ACM) (OR 0.91, 95% CI 0.81-1.01; p = 0.07). CONCLUSION: The findings of this study suggest that Vericiguat, when added to guideline-directed medical therapy in patients with heart failure, was associated with a borderline, non-significant reduction in the risk of the composite outcome of cardiovascular death or heart failure hospitalization, as well as all-cause mortality. Further large-scale randomized trials are warranted to better define its clinical benefit.
PubMed ID
42110159
Volume
27
Issue
4
First Page
49095
Last Page
49095
