首页> 外文期刊>Cardiology Journal >Comparison of short-term clinical outcomes between Resolute Onyx zotarolimus-eluting stents and everolimus-eluting stent in patients with acute myocardial infarction: Results from the Korea Acute Myocardial infarction Registry (KAMIR)
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Comparison of short-term clinical outcomes between Resolute Onyx zotarolimus-eluting stents and everolimus-eluting stent in patients with acute myocardial infarction: Results from the Korea Acute Myocardial infarction Registry (KAMIR)

机译:急性心肌梗死患者使用Resolute Onyx玛瑙左唑莫司洗脱支架和依维莫司洗脱支架的近期临床疗效比较:韩国急性心肌梗死注册中心(KAMIR)的结果

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Background: There are few studies which compare the efficacy and safety of the Resolute Onyx zotarolimus-eluting stent (O-ZES) and everolimus-eluting stent (EES) in patients with acute myocardial infarction (AMI). Therefore, the present study aimed to compare clinical outcomes of O-ZES and EES in patients with AMI undergoing successful percutaneous coronary intervention (PCI). Methods: From January 2016 to December 2016, the Korea Acute Myocardial Infarction Registry (KAMIR) enrolled 3,364 consecutive patients. Among them, O-ZES was used in 402 patients and EES was used in 1,084 patients. The primary endpoint was target lesion failure (TLF), as defined by composite of cardiac death, target vessel myocardial infarction (TV-MI), and ischemic driven-target lesion revascularization (ID-TLR) at 6 month clinical follow-up. Results: At 6 months, the incidence of TLF was not significantly different between O-ZES and EES group (4.0% vs. 3.9%, adjusted hazard ratio [HR] 1.17, 95% confidential interval [CI] 0.58–2.35, p = 0.665). O-ZES also showed similar results of cardiac death (3.7% vs. 3.4%, adjusted HR 1.25, 95% CI 0.59–2.63, p = 0.560), TV-MI (0.2% vs. 0.6%, adjusted HR 0.56, 95% CI 0.07–4.85, p = 0.600), ID-TLR (0.0% vs. 0.3%, p = 0.524), and definite or probable stent thrombosis (0.2% vs. 0.3%, adjusted HR 0.63, 95% CI 0.06–6.41, p = 0.696) when compared with EES. Conclusions: The present study shows that implantation of O-ZES or EES provided similar clinical outcomes with similar risk at 6-month of TLF and definite/probable ST in patients with AMI undergoing successful PCI.
机译:背景:很少有研究比较Resolute Onyx玛瑙唑酮洗脱支架(O-ZES)和依维莫司洗脱支架(EES)在急性心肌梗死(AMI)患者中的疗效和安全性。因此,本研究旨在比较O-ZES和EES在成功进行经皮冠状动脉介入治疗(PCI)的AMI患者中的临床结局。方法:从2016年1月至2016年12月,韩国急性心肌梗塞登记处(KAMIR)连续招募了3,364名患者。其中,O-ZES用于402例患者,EES用于1,084例患者。主要终点为目标病灶衰竭(TLF),定义为心脏死亡,目标血管心肌梗死(TV-MI)和缺血性驱动的目标病灶血运重建(ID-TLR)的复合,在6个月的临床随访中。结果:在6个月时,O-ZES和EES组之间的TLF发生率无显着差异(4.0%比3.9%,调整后的危险比[HR] 1.17,95%机密间隔[CI] 0.58–2.35,p = 0.665)。 O-ZES也显示​​出相似的心源性死亡结果(3.7%vs. 3.4%,调整后的HR 1.25,95%CI 0.59–2.63,p = 0.560),TV-MI(0.2%vs. 0.6%,调整后的HR 0.56,95) %CI 0.07–4.85,p = 0.600),ID-TLR(0.0%vs. 0.3%,p = 0.524)以及明确或可能的支架血栓形成(0.2%vs. 0.3%,调整后的HR 0.63,95%CI 0.06–与EES相比为6.41,p = 0.696)。结论:本研究表明,在成功接受PCI的AMI患者中,植入O-ZES或EES可以在6个月的TLF和明确的/可能的ST中提供相似的临床结局,具有相似的风险。

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