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首页> 外文期刊>International Journal of Cardiology >Predictors and clinical implications of stent thrombosis in patients with ST-segment elevation myocardial infarction: Insights from the EXAMINATION trial
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Predictors and clinical implications of stent thrombosis in patients with ST-segment elevation myocardial infarction: Insights from the EXAMINATION trial

机译:ST段抬高型心肌梗死患者支架内血栓形成的预测因素及其临床意义:EXAMINATION试验的启示

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Background Few data are available about safety of second generation drug eluting stents in an all-comer ST elevation myocardial infarction (STEMI) population. We sought to investigate the predictors and clinical implications of 1-year stent thrombosis (ST) in patients with STEMI, included in the EXAMINATION trial. Methods and results The EXAMINATION trial is an all-comer prospective, randomized 1:1 controlled trial, testing everolimus-eluting stent (EES) vs. cobalt chromium bare metal stent (BMS) in STEMI patients. It included 1498 patients, randomized to EES (n = 751) or BMS (n = 747). At 1 year, definite/probable stent thrombosis, defined according to ARC criteria, occurred in 26 patients (1.73%), including 18 definite and 8 probable events. The incidence of ST was lower in patients treated with EES than in those treated with BMS (HR 0.16, 95% CI 0.03-0.29, p = 0.017). Patients with ST have higher 1-year rates of cardiac death (30.8% vs. 2.5%, p < 0.001), myocardial infarction (30.8% vs. 0.5%, p < 0.001) and target vessel revascularization (65.4% vs. 4.2%, p < 0.001) compared with those without. Independent predictors of 1-year definite/probable ST were BMS implantation at the index procedure (HR 3.41, 95% CI 1.35-8.60), ST segment resolution of at least 70% in the EKG post-PCI (HR 0.30, 95% CI 0.13-0.70) and Killip class on admission (HR 2.57, 95% CI 1.70-3.90). Conclusions ST had low frequency in the first year after implantation of EES/BMS in STEMI patients, but it is associated with adverse events. BMS implantation, lack of ST-segment resolution and high Killip class on admission were independent predictors of 1-year ST.
机译:背景:关于第二代药物洗脱支架在全ST段抬高型心肌梗死(STEMI)人群中的安全性尚无数据。我们试图调查包括在EXAMINATION试验中的STEMI患者1年支架血栓形成(ST)的预测因素和临床意义。方法和结果EXAMINATION试验是一项前瞻性随机对照1:1对照试验,在STEMI患者中测试依维莫司洗脱支架(EES)与钴铬裸金属支架(BMS)。它包括1498名患者,随机分为EES(n = 751)或BMS(n = 747)。在1年时,根据ARC标准定义的明确/可能的支架血栓形成发生在26例患者中(1.73%),包括18例明确的事件和8例可能的事件。 EES患者的ST发生率低于BMS患者(HR 0.16,95%CI 0.03-0.29,p = 0.017)。 ST患者的1年心死率(30.8%vs. 2.5%,p <0.001),心肌梗塞(30.8%vs. 0.5%,p <0.001)和目标血管血运重建率更高(65.4%vs. 4.2%) ,p <0.001)与没有的相比。 1年明确/可能发生ST的独立预测因素是指数手术时BMS植入(HR 3.41,95%CI 1.35-8.60),PCI后心电图ST段分辨率至少70%(HR 0.30,95%CI 0.13-0.70)和入院时的Killip类别(HR 2.57,95%CI 1.70-3.90)。结论STEMI患者EES / BMS植入后第一年ST发生率较低,但与不良事件相关。 BMS植入,缺乏ST段分辨率和入院时Killip等级高是1年ST的独立预测因素。

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