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首页> 外文期刊>Vascular Health and Risk Management >Real-World Use Of Ultrathin-Strut Biodegradable Polymer–Coated Sirolimus-Eluting Stents In Patients With Coronary Artery Disease: 6-Month Clinical Outcomes
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Real-World Use Of Ultrathin-Strut Biodegradable Polymer–Coated Sirolimus-Eluting Stents In Patients With Coronary Artery Disease: 6-Month Clinical Outcomes

机译:冠状动脉疾病患者超薄支杆可生物降解聚合物涂层西罗莫司洗脱支架的实际应用:6个月的临床结果

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Background: Although a number of drug-eluting stents have been developed with different design, composition, and polymers, the search for an ideal drug-eluting stent is ongoing. The Tetriflex (Sahajanand Medical Technology, Surat, India) is a newer-generation, ultrathin (60 μm) biodegradable polymer–coated sirolimus-eluting stent (SES) designed with a unique long dual Z-link on a cobalt–chromium alloy. The present registry aimed to evaluate the safety and clinical outcomes of the Tetriflex SES at 6-month post-implantation. Methods: This was an investigator-initiated, retrospective, multicenter, single-arm, observational registry conducted at five tertiary-care centers in India. A total of 1,269 consecutive patients with coronary artery disease who underwent implantation of at least one Tetriflex SES between March 2017 and March 2018 were included. The primary outcome was considered a composite of cardiac death, myocardial infarction and target-lesion revascularization (TLR) at 6-month follow-up. Stent thrombosis was evaluated as a safety outcome at 6-month follow-up. Results: The mean age of patients was 54.99±10.80 years. Among 1,515 lesions treated with 1,682 Tetriflex SES, 58.3% were type C lesions. Six-month follow-up was done for 1,245 of 1,269 (98.1%) patients. At 6 months, composite events had occurred in 31 (2.5%) patients, consisting of ten (0.8%) cardiac deaths, 16 (1.3%) myocardial infarctions, and five (0.4%) TLRs. Stent thrombosis was observed in seven (0.56%) cases at 6 months. A subgroup analysis between diabetic and nondiabetic patients did not reveal any statistically significant difference for clinical outcomes at 6-month follow-up. Conclusion: The results of the current registry outline the safety and effectiveness of the Tetriflex SES in real-world patients, as it displayed favorable clinical outcomes at 6-month follow-up, with low incidence of TLR and stent thrombosis.
机译:背景:尽管已经开发出许多具有不同设计,组成和聚合物的药物洗脱支架,但仍在寻找理想的药物洗脱支架。 Tetriflex(印度苏拉特Sahajanand医疗技术公司)是新一代的超薄(60μm)可生物降解聚合物涂层的西罗莫司洗脱支架(SES),在钴铬合金上设计有独特的长双Z键。本注册表旨在评估植入后6个月内Tetriflex SES的安全性和临床结果。方法:这是由研究人员发起的,回顾性,多中心,单臂,观察性登记系统,在印度的五个三级医疗中心进行。在2017年3月至2018年3月期间,总共纳入了1,269例连续的冠状动脉疾病患者,这些患者接受了至少一种Tetriflex SES的植入。主要结果被认为是在6个月的随访中心脏死亡,心肌梗死和靶病变血运重建(TLR)的综合结果。在6个月的随访中,将支架血栓形成作为安全性评估结果。结果:患者的平均年龄为54.99±10.80岁。在用1,682种Tetriflex SES治疗的1,515个病变中,有58.3%是C型病变。对1,269名患者中的1,245名(98.1%)进行了六个月的随访。在6个月时,发生了31例(2.5%)患者的复合事件,包括10例(0.8%)心脏死亡,16例(1.3%)心肌梗死和5例(0.4%)TLR。 6个月时有7例(0.56%)出现支架血栓形成。糖尿病和非糖尿病患者之间的亚组分析在6个月的随访中没有发现临床结局有任何统计学上的显着差异。结论:当前注册表的结果概述了Tetriflex SES在现实世界患者中的安全性和有效性,因为它在6个月的随访中显示出良好的临床效果,TLR和支架血栓形成的发生率较低。

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