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慢性肾脏病患者经冠状动脉介入治疗后,氯吡格雷反应低下会增加风险。

Low responsiveness to clopidogrel increases risk among CKD patients undergoing coronary intervention.

机构信息

Medizinische Klinik III, Kardiologie und Kreislauferkrankungen, Universitätsklinikum der Eberhard-Karls-Universität Tübingen, Otfried-Müller-Strasse 10, 72076 Tübingen, Germany.

出版信息

J Am Soc Nephrol. 2011 Apr;22(4):627-33. doi: 10.1681/ASN.2010020220. Epub 2011 Jan 27.

Abstract

Patients with CKD are at higher risk for major events after percutaneous coronary intervention (PCI) compared with subjects with normal renal function. The aims of this study were to evaluate responsiveness to clopidogrel in patients with CKD and to examine the effect of antiplatelet drug response on post-PCI outcome. We retrospectively evaluated a consecutive cohort of 1567 patients with symptomatic coronary artery disease undergoing PCI, 648 (41%) of whom had stage 3 to 5 CKD. We assessed responsiveness to clopidogrel by ADP-induced platelet aggregation after oral administration of a 600-mg clopidogrel loading dose and 100 mg of aspirin. In a multivariate survival analysis that included 1335 (85%) of the cohort, stage 3 to 5 CKD and low response to clopidogrel were independent predictors of the primary end point (composite of myocardial infarction, ischemic stroke, and death within 1 year). In summary, a low response to clopidogrel might be an additional risk factor for the poorer outcomes in patients with stage 3 to 5 CKD compared with patients with better renal function.

摘要

与肾功能正常的患者相比,慢性肾脏病(CKD)患者经皮冠状动脉介入治疗(PCI)后发生重大事件的风险更高。本研究旨在评估 CKD 患者对氯吡格雷的反应性,并研究抗血小板药物反应对 PCI 术后结果的影响。我们回顾性评估了连续 1567 例有症状的冠心病患者行 PCI 的队列,其中 648 例(41%)患有 3 至 5 期 CKD。我们通过口服 600mg 氯吡格雷负荷剂量和 100mg 阿司匹林后 ADP 诱导的血小板聚集来评估氯吡格雷的反应性。在一项包含 1335 例(85%)队列的多变量生存分析中,3 至 5 期 CKD 和氯吡格雷低反应是主要终点(包括 1 年内心肌梗死、缺血性卒中和死亡的复合终点)的独立预测因素。总之,与肾功能较好的患者相比,氯吡格雷低反应可能是 3 至 5 期 CKD 患者预后较差的另一个危险因素。

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