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首页> 外文期刊>The American Journal of Cardiology >Efficacy of high-dose clopidogrel treatment (600 mg) less than two hours before percutaneous coronary intervention in patients with non-ST-segment elevation acute coronary syndromes.
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Efficacy of high-dose clopidogrel treatment (600 mg) less than two hours before percutaneous coronary intervention in patients with non-ST-segment elevation acute coronary syndromes.

机译:在非ST段抬高的急性冠脉综合征患者中,在经皮冠状动脉介入治疗之前不到两小时,大剂量氯吡格雷治疗(600 mg)的疗效。

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Current guidelines recommend pretreatment with a loading dose of clopidogrel before percutaneous coronary intervention (PCI) to reduce the incidence of periprocedural myocardial infarctions in patients undergoing PCI. However, because of concerns about postoperative bleeding, clopidogrel loading is frequently administered either immediately before or after PCI. Using the 2004/2005 Cornell Angioplasty Registry, we analyzed 1,041 consecutive patients undergoing urgent PCI for non-ST-elevation acute coronary syndrome. The patients were divided into 2 groups. The first group was the "preangiography clopidogrel therapy" group for those receiving chronic 75-mg clopidogrel therapy or receiving a clopidogrel loading dose (300 mg > or = 12 hours or 600 mg > or = 2 hours) before angiography according to the guidelines. The second group was the in-laboratory 600-mg clopidogrel loading the clopidogrel loading dose <2 hours before PCI (immediately before or after PCI). The mean clinical follow-up was 23.8 + or - 7.6 months. Of the 1,041 study patients, 467 (44.9%) received clopidogrel before angiography and 574 (55.1%) received in-laboratory loading. The incidence of in-hospital death (0.4% vs 0.5%, respectively; p = 1.000), myocardial infarction (7.7% vs 6.8%, respectively; p = 0.630), and major adverse cardiovascular events (8.4% vs 7.1%, respectively; p = 0.484) were similar between the 2 groups. The Kaplan-Meier long-term survival rates were similar in the 2 groups (93.4% vs 95.8%, p log-rank = 0.152). After multivariate Cox regression analysis, administration of a 600-mg clopidogrel loading dose <2 hours before PCI did not have a significant effect on long-term mortality (hazard ratio 0.97, 95% confidence interval 0.54 to 1.75, p = 0.927). In conclusion, treatment with a 600-mg loading dose <2 hours before PCI is associated with similar short-term ischemic outcomes and long-term mortality compared to the currently recommended clopidogrel pretreatment regimen.
机译:当前的指南建议在经皮冠状动脉介入治疗(PCI)之前进行负荷剂量的氯吡格雷预处理,以减少接受PCI的患者围手术期心肌梗死的发生率。但是,由于担心术后出血,因此在PCI之前或之后经常进行氯吡格雷负荷治疗。使用2004/2005康奈尔血管成形术注册中心,我们分析了1,041例因非ST段抬高的急性冠脉综合征而接受紧急PCI的连续患者。将患者分为两组。第一组是“血管造影术前氯吡格雷治疗”组,针对那些按照指南在血管造影之前接受慢性75 mg氯吡格雷治疗或接受氯吡格雷负荷剂量(300 mg≥12小时或600 mg≥2小时)的患者。第二组为实验室内600 mg氯吡格雷负荷,在PCI前2小时(PCI之前或之后)负荷氯吡格雷。平均临床随访时间为23.8 +或-7.6个月。在1,041名研究患者中,有467名(44.9%)接受了血管造影前的氯吡格雷治疗,有574名(55.1%)接受了实验室负荷。院内死亡发生率(分别为0.4%和0.5%; p = 1.000),心肌梗塞(分别为7.7%和6.8%; p = 0.630)和主要的不良心血管事件(分别为8.4%和7.1%) ; p = 0.484)在两组之间相似。两组的Kaplan-Meier长期存活率相似(93.4%vs 95.8%,p log-rank = 0.152)。经过多因素Cox回归分析后,在PCI前2小时内服用600 mg氯吡格雷负荷剂量对长期死亡率无明显影响(危险比0.97,95%置信区间0.54至1.75,p = 0.927)。总之,与目前推荐的氯吡格雷预处理方案相比,PCI前2小时以600毫克负荷剂量进行治疗具有相似的短期缺血性结果和长期死亡率。

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