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ABSTRACT: Background
This study evaluated the safety and efficacy of BioMime sirolimus-eluting stent (SES) system, with an ultra-low strut thickness (65 µm), in real-world all-comers population with coronary artery stenosis (CAD).Methods
This was a post-marketing, multicenter, single-arm, observational clinical registry among patients undergoing intervention for CAD. Patients were clinically followed up at 1, 9, 12, and 24 months after the index percutaneous coronary intervention. Four major indications, namely long stents of > 30 mm, stents with diameters of 4 and 4.5 mm, bifurcation subgroup, and chronic total occlusion (CTO) were evaluated as pre-specified subsets.Results
A total of 771 patients (1,079 treated lesions) from 23 sites were included in this study. The mean le
SUBMITTER: Hudec M
PROVIDER: S-EPMC11650571 | biostudies-literature | 2024 Dec
REPOSITORIES: biostudies-literature