首页> 外文期刊>European Heart Journal: The Journal of the European Society of Cardiology >Clopidogrel pre-treatment in stable angina: for all patients > 6 h before elective coronary angiography or only for angiographically selected patients a few minutes before PCI? A randomized multicentre trial PRAGUE-8.
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Clopidogrel pre-treatment in stable angina: for all patients > 6 h before elective coronary angiography or only for angiographically selected patients a few minutes before PCI? A randomized multicentre trial PRAGUE-8.

机译:氯吡格雷在稳定型心绞痛中的预处理:适用于所有在选择性冠状动脉造影之前> 6小时的患者,或者仅适用于在PCI前几分钟进行血管造影选择的患者?一项随机的多中心试验PRAGUE-8。

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AIMS: To compare two different clopidogrel regimens on the outcomes of patients undergoing elective coronary angiography (CAG)+/-ad hoc percutaneous coronary intervention (PCI). METHODS AND RESULTS: Open-trial randomized 1028 patients with stable angina to group A ('non-selective'-clopidogrel 600 mg > 6 h before CAG; n 513) or group B ('selective'-clopidogrel 600 mg in the cath-lab after CAG, only in case of PCI; n = 515). Combined primary endpoint was death/periprocedural myocardial infarction (MI)/stroke/re-intervention within 7 days. Secondary endpoints were troponin elevation and bleeding complications. Primary endpoint occurred in 0.8% group A patients vs. 1% group B (P = 0.749; 90% CI for the percentage difference -1.2-0.8). Periprocedural troponin elevation (> 3 x ULN) was detected in 2.6% group A vs. 3.3% group B (P = 0.475; 90% CI -2.5-1.0). Bleeding complications occurred in 3.5% group A patients vs. 1.4% group B (P = 0.025). After adjustment for covariates and factors that may influence the bleeding risk, patients in group A were shown to have more likely bleeding complications when compared with group B (OR = 3.03; 95% CI 1.14-8.10; P = 0.027). CONCLUSION: High (600 mg) loading dose of clopidogrel before elective CAG increased the risk of minor bleeding complications, while the benefit on periprocedural infarction was not significant. Clopidogrel can be given safely in the catheterization laboratory between CAG and PCI in chronic stable angina patients.
机译:目的:比较两种不同的氯吡格雷方案对择期冠状动脉造影(CAG)+/-特设经皮冠状动脉介入治疗(PCI)患者的预后。方法和结果:1028例稳定型心绞痛患者接受开放试验,随机分为A组(“非选择性”-氯吡格雷600 mg,CAG前6小时; n 513)或B组(“选择性”-氯吡格雷600 mg,导管中)。 CAG之后的实验,仅在PCI情况下; n = 515)。合并的主要终点是7天之内死亡/围手术期心肌梗死(MI)/中风/再次干预。次要终点是肌钙蛋白升高和出血并发症。主要终点发生在0.8%的A组患者与1%的B组之间(P = 0.749; 90%CI为百分率-1.2-0.8)。在2.6%的A组和3.3%的B组中检测到围手术期肌钙蛋白升高(> 3 x ULN)(P = 0.475; 90%CI -2.5-1.0)。 A组3.5%的患者发生出血并发症,而B组1.4%的患者发生出血并发症(P = 0.025)。在校正可能影响出血风险的协变量和因素之后,与B组相比,A组患者显示出更多的出血并发症(OR = 3.03; 95%CI 1.14-8.10; P = 0.027)。结论:选择性CAG之前高剂量(600毫克)的氯吡格雷可增加轻微出血并发症的风险,而对围手术期梗塞的益处并不显着。对于慢性稳定型心绞痛患者,可以在CAG和PCI之间的导管实验室中安全地给予氯吡格雷。

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