首页> 外文期刊>IJC Heart & Vasculature >Effects of high dose atorvastatin before elective percutaneous coronary intervention on highly sensitive troponin T and one year major cardiovascular events; a randomized clinical trial
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Effects of high dose atorvastatin before elective percutaneous coronary intervention on highly sensitive troponin T and one year major cardiovascular events; a randomized clinical trial

机译:选择性经皮冠状动脉介入治疗前大剂量阿托伐他汀对高敏感性肌钙蛋白T和一年主要心血管事件的影响;一项随机临床试验

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IntroductionSome studies have demonstrated that post-PCI elevated cardiac enzymes are associated with worse outcomes. In this study, we aimed to determine if high-dose treatment with atorvastatin before planned elective PCI reduces PMI or MACE at 1-year median follow-up.Material and methodsEligible participants were randomly allocated to group A (80?mg atorvastatin 12?h and 40?mg 2?h before PCI) and group B (40?mg atorvastatin daily). Blood samples were obtained before and at 24?h after PCI to measure hsTnT. All patients were followed regarding MACE (combination of death, re-hospitalizations for ACS, and unplanned coronary revascularization) during one year after PCI.Results207 patients randomly assigned to Group A (n?=?97) or group B (n?=?110). The rate of PMI was lower in group A (5.2%) compared to group B (10.9%); despite near to 50% lower rate of PMI in group A, binary logistic regression showed no significant association between atorvastatin recapture and PMI. The occurrence of MACE in 97 patients of group A was 11 (11.3%), higher than 11 (10%) cases of 110 patients in group B. Cox proportional hazards regression model shows no significant difference in MACE of study groups.ConclusionPretreatment of patients with stable angina who were planned to undergo an elective PCI with 120?mg of atorvastatin before the procedure confer them the same benefit in terms of PMI and MACE as 40?mg routine daily dosage of this statin does.
机译:简介一些研究表明,PCI后心脏酶升高与预后差有关。在这项研究中,我们的目的是确定在计划的择期PCI前大剂量的阿托伐他汀治疗在中位随访1年后是否能降低PMI或MACE。材料和方法将符合条件的参与者随机分配到A组(80 mg阿托伐他汀12 h在PCI前2小时服用40?mg和B组(每天40?mg阿托伐他汀)。在PCI之前和之后24小时采集血样以测量hsTnT。所有患者均在PCI后一年内接受MACE(死亡,ACS再次住院和计划外的冠状动脉血运重建)的随访。结果207例患者随机分为A组(n = 97)或B组(n = 90)。 110)。 A组(5.2%)的PMI率低于B组(10.9%);尽管A组中PMI的发生率降低了近50%,但二元Logistic回归显示阿托伐他汀再摄取与PMI之间无显着关联。 A组97例患者发生MACE的发生率为11(11.3%),高于B组110例患者中发生MACE的11(10%)。Cox比例风险回归模型显示研究组的MACE差异无统计学意义。稳定型心绞痛的患者计划在该过程之前使用120mg的阿托伐他汀进行选择性PCI,从而在PMI和MACE方面获得与他汀类药物常规每日40mg相同的益处。

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