首页> 外文期刊>Catheterization and cardiovascular interventions: Official journal of the Society for Cardiac Angiography & Interventions >Comparison of in vivo acute stent recoil between the bioabsorbable everolimus-eluting coronary stent and the everolimus-eluting cobalt chromium coronary stent: Insights from the ABSORB and SPIRIT trials.
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Comparison of in vivo acute stent recoil between the bioabsorbable everolimus-eluting coronary stent and the everolimus-eluting cobalt chromium coronary stent: Insights from the ABSORB and SPIRIT trials.

机译:可生物吸收的依维莫司洗脱冠状动脉支架与依维莫司洗脱钴铬冠状动脉支架之间的体内急性支架后坐力比较:来自ABSORB和SPIRIT试验的见解。

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OBJECTIVES: This study sought to evaluate and compare in vivo acute stent recoil of a novel bioabsorbable stent and a metallic stent. BACKGROUND: The bioabsorbable everolimus-eluting coronary stent (BVS) is composed of a poly-L-lactic acid backbone, coated with a bioabsorbable polymer containing the antiproliferative drug, everolimus, and expected to be totally metabolized and absorbed in the human body. Because the BVS is made from polymer, it may have more acute recoil than metallic stents in vivo. METHODS: A total of 54 patients, who underwent elective stent implantation for single de novo native coronary artery lesions, were enrolled: 27 patients treated with the BVS and 27 patients treated with the everolimus-eluting cobalt chromium stent (EES). Acute absolute recoil, assessed by quantitative coronary angiography, was defined as the difference between mean diameter of the last inflated balloon at the highest pressure (X) and mean lumen diameter of the stent immediately after the last balloon deflation (Y). Acute percent recoil was defined as (X - Y)/X and expressed as a percentage. RESULTS: Acute absolute recoil of the BVS and EES was 0.20 +/- 0.21 mm and 0.13 +/- 0.21 mm, respectively (P = 0.32). Acute percent recoil was 6.9% +/- 7.0% in the BVS group and 4.3% +/- 7.1% in the EES group (P = 0.25). CONCLUSIONS: In vivo acute stent recoil of the BVS is slightly larger but insignificantly different from that of the EES, implying that the BVS may have good radial strength similar to the metallic stent.
机译:目的:本研究旨在评估和比较新型生物可吸收支架和金属支架在体内的急性支架后坐力。背景:生物可吸收的依维莫司洗脱冠状动脉支架(BVS)由聚L-乳酸骨架组成,涂有含有抗增殖药物依维莫司的生物可吸收聚合物,并有望在人体中完全代谢和吸收。由于BVS由聚合物制成,因此在体内它可能比金属支架具有更大的后坐力。方法:共有54例患者接受了从头开始的原生冠状动脉病变的选择性支架植入术:27例接受BVS治疗的患者和27例依维莫司洗脱钴铬支架(EES)治疗的患者。通过定量冠状动脉造影术评估的急性绝对后坐力定义为最高压力下的最后一个膨胀球囊的平均直径(X)与最后一个球囊放气后的支架的平均内腔直径之间的差(Y)。急性后座力百分比定义为(X-Y)/ X,并以百分比表示。结果:BVS和EES的急性绝对后坐力分别为0.20 +/- 0.21毫米和0.13 +/- 0.21毫米(P = 0.32)。 BVS组的急性后座力百分比为6.9%+/- 7.0%,EES组的急性后座力百分比为4.3%+/- 7.1%(P = 0.25)。结论:BVS的体内急性支架后坐力稍大,但与EES的后坐力无显着差异,这意味着BVS可能具有与金属支架相似的良好径向强度。

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