- Journal
- LANCET REGIONAL HEALTH-EUROPE
- Année
- 2025
- Volume
- 55
- Article
- 101348
- Mois
- AUG
- DOI
- 10.1016/j.lanepe.2025.101348
Abstract
Background The SECURE trial (NCT02596126) demonstrated the efficacy of the cardiovascular polypill (''CV-Polypill''-acetyl salicylic acid, atorvastatin and ramipril) in reducing the risk of recurrent major cardiovascular events compared with standard care when initiated within six months of a myocardial infarction. This analysis aimed to estimate the cost-effectiveness of the CV-Polypill from the Spanish healthcare perspective using SECURE trial data. Methods A decision analytic Markov modelling approach was conducted to compare the CV-Polypill with standard care over a lifetime time horizon. Six parametric distributions were fitted to SECURE trial data on time to reinfarction, stroke or death (cardiovascular or non-cardiovascular). Cost and utility data were sourced from literature. Respective model outputs were discounted at 3%. The model captured direct medical costs associated with treatment acquisition and acute/ongoing cardiovascular events. Probabilistic sensitivity analyses (PSA) and scenario analyses were conducted. Findings The CV-Polypill is dominant (improves health outcomes and reduces costs) in 84.8% of PSA iterations (848/1000 iterations), and cost effective in 89.3% of PSA iterations (893/1000 iterations) at a