کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5962213 | 1176186 | 2012 | 6 صفحه PDF | دانلود رایگان |
IntroductionDespite considerable benefits associated with current drug-eluting stents, continued attention to the safety, efficacy, and deliverability of available drug-eluting stent has led to the development of newer stent.MethodsThis study was a single-centre, prospective, non-randomized, first-in-man study which included clinical follow-up data was collected at 1, 8 and 12 months after the procedure. The study included 105 patients with de novo native coronary artery lesions including multi-vessel disease treated with Supralimus-Core® stent. Repeat angiography was performed 8 months post-stent implantation.ResultsAt quantitative coronary angiography 8-month luminal late loss was 0.39 ± 0.33 mm in-stent and 0.33 ± 0.35 mm in-segment. The incidence of any major adverse cardiac event at 30 days, 8 months and 12 months was 1 (1%), 6 (6%) and 7 (7%) respectively.ConclusionThis study demonstrates that the Supralimus-Core® SES is a safe and effective treatment for patients with obstructive coronary artery disease.ClinicalTrials.gov ID: NCT00811616.
Journal: Indian Heart Journal - Volume 64, Issue 6, NovemberâDecember 2012, Pages 547-552