首页> 外文期刊>American journal of therapeutics >Effect of High-Dose Allopurinol Pretreatment on Cardiac Biomarkers of Patients Undergoing Elective Percutaneous Coronary Intervention: A Randomized Clinical Trial
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Effect of High-Dose Allopurinol Pretreatment on Cardiac Biomarkers of Patients Undergoing Elective Percutaneous Coronary Intervention: A Randomized Clinical Trial

机译:高剂量Allopurinol预处理对接受经皮冠状动脉介入的患者心脏生物标志物的影响:随机临床试验

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Background:Increased accumulation of reactive oxygen species contributes to pathophysiologic states such as endothelial dysfunction, metabolic and functional impairment, inflammatory activation, and other features of cardiovascular pathophysiology. Allopurinol acts as a xanthine oxidase inhibitor that reduces the amount of free radicals after reactive oxygen species generation.Methods and Results:In this placebo-controlled randomized clinical trial, all patients admitted with coronary artery disease who are candidates for elective percutaneous coronary intervention (PCI) were included. The 254 patients were randomly divided into 2 groups. Blood samples for cardiac biomarkers (creatine kinase [CK]-MB and troponin T [cTnT]) were collected from all patients after admission (the day before PCI), and also 8 and 16 hours after intervention. In group 1 (133 patients), 600 mg allopurinol was orally administered on the day before PCI, and another same dose on the day of PCI, and the elective PCI was performed. In group 2 (121 patients), elective PCI was performed without pretreatment with allopurinol. In an unadjusted model, the serum levels of both CK-MB and cTnT, 16 hours after PCI were higher in the placebo group as compared with the allopurinol group, although it was statistically insignificant. We compared the maximum levels of CK-MB and cTnT (8 or 16 hours after PCI) and their maximum changes in both groups. After adjustment for confounders, use of allopurinol did not have any statistically significant association with the rise of cardiac-spec-fic enzymes.Conclusions:Allopurinol could not be effective significantly, in patients undergoing elective PCI, to decrease cardiac-specific enzymes, and seems not to be of use before PCI.
机译:背景:增加反应性氧物种的积累有助于病理物理学状态,例如内皮功能障碍,代谢和功能障碍,炎症激活和心血管病理学生理学的其他特征。 Allopurinol作为黄嘌呤氧化酶抑制剂,可减少反应性氧物种生成后的自由基量。方法和结果:在这种安慰剂对照的随机临床试验中,所有患者患有冠心病患者的患者,患者是选择经皮冠状动脉介入的候选者(PCI )包括在内。将254名患者随机分为2组。在入院(PCI前一天)后,从所有患者收集心脏生物标志物的血液样品(肌酸激酶[CK] -MB和肌钙蛋白T [CTNT]),并在干预后8和16小时。在第1组(133名患者)中,在PCI前一天口服600毫克Allopurinol,并在PCI的当天进行另一种剂量,并且进行了选择性PCI。在第2组(121名患者)中,在没有预处理的情况下进行选择性PCI,而不预处理含有Allopurinol。在不调整的模型中,与Allopurinol基团相比,PCI在PCI中PCI患者血清CK-MB和CTNT的血清水平较高,尽管它是统计学上微不足道的。我们比较了CK-MB和CTNT的最大水平(PCI后8小时或16小时)及其两组的最大变化。在对混凝剂进行调整后,使用Allopurinol与心脏抑制酶的兴观没有任何统计学上显着的关联。结论:在接受选修PCI的患者中,Allopurinol无法显着有效,以减少心脏特异性酶,似乎在PCI之前不要使用。

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