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首页> 外文期刊>Cardiovascular revascularization medicine: including molecular interventions >Safety and efficacy of everolimus-eluting stents compared with first-generation drug-eluting stents in patients undergoing primary percutaneous coronary intervention
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Safety and efficacy of everolimus-eluting stents compared with first-generation drug-eluting stents in patients undergoing primary percutaneous coronary intervention

机译:在进行首次经皮冠状动脉介入治疗的患者中,依维莫司洗脱支架与第一代药物洗脱支架相比的安全性和有效性

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Objective: To assess the safety and efficacy everolimus-eluting stents (EES) compared with first-generation drug-eluting stents (DES) in patients with acute myocardial infarction (MI) undergoing primary percutaneous coronary intervention (PCI). Background: EES have been associated with improved clinical outcomes compared to paclitaxel-eluting stents (PES) and with similar outcomes compared to sirolimus-eluting stents (SES). Methods: A total of 520 patients who presented with ST-elevation myocardial infarction (STEMI) from 2003 to 2013, who underwent primary PCI with DES, were retrospectively analyzed. Of these, 247 received SES, 136 PES, and 137 EES. Patients were followed up to 2 years for major adverse cardiac events (MACE). Univariate and multivariate models detected correlates to outcome. Results: EES implantation, compared with PES and SES, resulted in comparable rates of MACE (8.8% vs. 16.2%, p = 0.06 and 8.8% vs. 12.6%, respectively, p = 0.26), stent thrombosis, MI, and target lesion revascularization. Patients who received EES had lower rates of all-cause mortality (3.7% vs. 12.6% vs. 9.4%, p = 0.03) at 1-year follow up. However, in the univariate and multivariate analyses, stent type was not independently associated with the primary outcome or with all-cause mortality. Diabetes mellitus and number of stents implanted were independently associated with the primary outcome. Conclusion: While EES seem to be associated with better outcome when compared to PES, the main correlates of STEMI patients are the presence of diabetes and number of stents implanted, and not the type of stent used for intervention.
机译:目的:评估在第一阶段经皮冠状动脉介入治疗(PCI)的急性心肌梗死(MI)患者中,依维莫司洗脱支架(EES)与第一代药物洗脱支架(DES)的安全性和有效性。背景:与紫杉醇洗脱支架(PES)相比,EES与改善临床疗效相关,与西罗莫司洗脱支架(SES)相比具有相似的疗效。方法:回顾性分析2003年至2013年间共520例ST段抬高性心肌梗死(STEMI)患者,并对其进行了DES原发PCI。其中,有247个获得了SES,136个PES和137个EES。对患者进行了长达2年的严重不良心脏事件(MACE)随访。检测到的单变量和多变量模型与结果相关。结果:与PES和SES相比,EES植入导致MACE发生率,支架血栓形成,心梗和靶标发生率相当(分别为8.8%vs. 16.2%,p = 0.06和8.8%vs. 12.6%,p = 0.26)。病变血运重建。在1年的随访中,接受EES的患者的全因死亡率较低(3.7%对12.6%对9.4%,p = 0.03)。然而,在单因素和多因素分析中,支架类型并非与主要结局或全因死亡率无关。糖尿病和植入支架的数量与主要结局独立相关。结论:尽管与PES相比,EES似乎具有更好的预后,但STEMI患者的主要相关因素是糖尿病的存在和植入支架的数量,而不是用于干预的支架类型。

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