HealthDay News — Everolimus-eluting bioresorbable vascular scaffolds (BVSs) are associated with increased odds of scaffold thrombosis and other thrombotic events compared with everolimus-eluting metallic stents (EESs), according to a review published online October 16 in the Annals of Internal Medicine

Xin-Lin Zhang, MD, from the Nanjing University School of Medicine in China, and colleagues compared the safety and efficacy of everolimus-eluting BVSs with that of EESs using data from 7 randomized trials and 38 observational studies involving adults with coronary artery disease who underwent percutaneous coronary intervention.  

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The researchers found that at a median follow-up of 1 year and beyond 1 year, the pooled incidence of definite or probable scaffold thrombosis after BVS implantation was 1.8 and 0.8%, respectively. In 7 trials involving 5,578 patients that directly compared BVSs with EESs, the risk of definite or probable scaffold thrombosis was increased with BVSs at a median follow-up of 25 months (odds ratio, 3.4). Increased risks were seen at early, late, and very late stages; the odds were almost double for beyond 1 year versus within 1 year. BVSs were correlated with increased risks for myocardial infarction, target lesion revascularization, and target lesion failure (odds ratios, 1.63, 1.31, and 1.37, respectively); over time, there were increases in the odds for these end points.

“Compared with EESs, BVSs increased the risks for scaffold thrombosis and other thrombotic events at mid- and long-term follow-up, and risks increased over time,” the authors write.

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