首页> 外文期刊>中华医学杂志(英文版) >Nine-month angiographic and two-year clinical follow-up of polymer-free sirolimus-eluting stent versus durable-polymer sirolimus-eluting stent for coronary artery disease: the Nano randomized trial
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Nine-month angiographic and two-year clinical follow-up of polymer-free sirolimus-eluting stent versus durable-polymer sirolimus-eluting stent for coronary artery disease: the Nano randomized trial

机译:九个月的无聚合物西罗莫司洗脱支架与耐用聚合物西罗莫司洗脱支架对冠状动脉疾病的血管造影和两年临床随访:Nano随机试验

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Background First generation drug-eluting stents (DES) were associated with a high incidence of late stent thrombosis (ST),mainly due to delayed healing and re-endothelization by the durable polymer coating.This study sought to assess the safety and efficacy of the Nano polymer-free sirolimus-eluting stent (SES) in the treatment of patients with de novo coronary artery lesions.Methods The Nano trial is the first randomized trial designed to compare the safety and efficacy of the Nano polymer-free SES and Partner durable-polymer SES (Lepu Medical Technology,Beijing,China) in the treatment of patients with de novo native coronary lesions.The primary endpoint was in-stent late lumen loss (LLL) at 9-month follow-up.The secondary endpoint was major adverse cardiac events (MACE),a composite of cardiac death,myocardial infarction or target lesion revascularization.Results A total of 291 patients (Nano group:n=143,Partner group:n=148) were enrolled in this trial from 19 Chinese centers.The Nano polymer-free SES was non-inferior to the Partner durable-polymer DES at the primary endpoint of 9 months (P <0.001).The 9-month in-segment LLL of the polymer-free Nano SES was comparable to the Partner SES (0.34±0.42) mm vs.(0.30±0.48) mm,P=0.21).The incidence of MACE in the Nano group were 7.6% compared to the Partner group of 5.9% (P=0.75) at 2 years follow-up.The frequency of cardiac death and stent thrombosis was low for both Nano and Partner SES (0.8% vs.0.7%,0.8% vs.1.5%,both P=1.00).Conclusions In this multicenter randomized Nano trial,the Nano polymer-free SES showed similar safety and efficacy compared with the Partner SES in the treatment of patients with de novo coronary artery lesions.Trials in patients with complex lesions and longer term follow-up are necessary to confirm the clinical performance of this novel Nano polymer-free SES.
机译:背景技术第一代药物洗脱支架(DES)与晚期支架内血栓形成(ST)的发生率高有关,主要是由于耐用的聚合物涂层延缓了愈合和重新内皮化。本研究旨在评估支架的安全性和有效性。方法使用无纳米聚合物的西罗莫司洗脱支架(SES)治疗从头冠状动脉病变的患者。方法纳米试验是第一个随机试验,旨在比较无纳米聚合物SES和合作伙伴耐久的安全性和有效性。聚合物SES(北京乐普医疗技术有限公司)治疗从头开始的原发性冠状动脉病变。主要终点是术后9个月的支架内晚期腔内丢失(LLL),次要终点是严重不良反应结果:心脏事件(MACE)是由心脏死亡,心肌梗塞或目标病变血运重建引起的。结果本研究共纳入了来自19个中国中心的291例患者(纳诺组:n = 143,伙伴组:n = 148)。纳米在9个月的主要终点时,不含聚合物的SES不亚于合作伙伴耐久聚合物DES(P <0.001)。不含聚合物的Nano SES的9个月段内LLL与合作伙伴SES相当( 0.34±0.42)mm vs.(0.30±0.48)mm,P = 0.21)。在两年的随访中,纳米组的MACE发生率为7.6%,而伴侣组为5.9%(P = 0.75)。 Nano和合作伙伴SES的心源性死亡和支架血栓形成频率均较低(0.8%vs.0.7%,0.8%vs.1.5%,均为P = 1.00)。结论在该多中心随机Nano试验中,不含Nano聚合物与伴侣SES相比,SES在从头冠状动脉病变的治疗中显示出相似的安全性和有效性,因此需要对具有复杂病变和长期随访的患者进行试验,以确认这种新型无纳米聚合物的SES的临床表现。

著录项

  • 来源
    《中华医学杂志(英文版)》 |2014年第11期|2153-2158|共6页
  • 作者单位

    Department of Cardiology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China;

    Thoraxcenter, Erasmus Medical Center, Rotterdam, 3015CE, The Netherlands;

    Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China;

    Thoraxcenter, Erasmus Medical Center, Rotterdam, 3015CE, The Netherlands;

    Department of Cardiology, Beijing Fuwai Hospital, Beijing 100037, China;

    Department of Cardiology, Liaoning Provincial People's Hospital, Shenyang, Liaoning 110016, China;

    Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China;

    Department of Cardiology, Beijing Hospital, Beijing 100730, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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