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高剂量阿托伐他汀未能重新获得冠状动脉旁路移植术的心脏保护作用:一项随机对照试验。

Failure to recapture cardioprotection with high-dose atorvastatin in coronary artery bypass surgery: a randomised controlled trial.

机构信息

The Hatter Cardiovascular Institute, University College London Hospital, 67 Chenies Mews, London WC1E 6HX, UK.

出版信息

Basic Res Cardiol. 2011 Nov;106(6):1387-95. doi: 10.1007/s00395-011-0209-5. Epub 2011 Aug 11.

Abstract

The acute administration of atorvastatin has been reported to reduce myocardial infarct size in animal studies. However, this cardioprotective effect is lost with the chronic administration of atorvastatin, although it can be recaptured by administering an acute high-dose of atorvastatin. We hypothesised that pre-treatment with high-dose atorvastatin, on a background of chronic standard 'statin' therapy, would reduce myocardial injury in patients undergoing elective coronary artery bypass graft (CABG) surgery. One hundred and one consenting patients undergoing elective CABG surgery at a single tertiary cardiac centre were recruited into two randomised controlled, single-blinded clinical studies. Study 1: 45 patients were randomised to receive either 160 mg of atorvastatin 2 h preoperatively and 24 h following surgery or their standard statin therapy. Study 2: 56 patients were randomised to receive either 160 mg of atorvastatin 12 h preoperatively and 24 h following surgery or their standard statin therapy. Blood samples for troponin T and creatine kinase were taken prior to surgery and then at 6, 12, 24, 48 and 72 h post-surgery. Cardiac enzyme levels at each time point and the total area-under curve (AUC) were calculated. The group characteristics and surgical methods were well matched. High-dose atorvastatin was not associated with any significant side effects. There was no significant difference in serum troponin T or creatine kinase in either study at each time point or over 72 h. Study 1: AUC, troponin T: atorvastatin 29.6 ± 34.8 μg/L versus control 25.0 ± 22.0 μg/L:P > 0.05. Creatine kinase: atorvastatin 33,544 ± 20,063 IU/L versus control 30,620 ± 10,776 IU/L:P > 0.05. Study 2: AUC, troponin T: atorvastatin 21.8 ± 14.3 μg/L versus control 20.9 ± 8.7 μg/L:P > 0.05. Creatine kinase: atorvastatin 36,262 ± 28,821 IU/L versus control 33,448 ± 14,984:P > 0.05. There were no differences in postoperative outcomes. We report that the administration of high-dose atorvastatin to low risk patients undergoing elective CABG surgery, who are already on standard dose 'statin' therapy is safe, but does not further reduce perioperative myocardial injury.

摘要

阿托伐他汀的急性给药已被报道可减少动物研究中的心肌梗死面积。然而,这种心脏保护作用在阿托伐他汀的慢性给药中丢失,尽管通过给予急性高剂量阿托伐他汀可以重新获得。我们假设,在慢性标准“他汀类”治疗的基础上,预先给予高剂量阿托伐他汀治疗,将减少接受择期冠状动脉旁路移植术(CABG)的患者的心肌损伤。在一家单一的三级心脏中心,有 101 名同意接受择期 CABG 手术的患者被纳入两项随机对照、单盲临床试验中。研究 1:45 名患者随机分为术前 2 小时和术后 24 小时接受 160mg 阿托伐他汀治疗组或接受标准他汀类药物治疗组。研究 2:56 名患者随机分为术前 12 小时和术后 24 小时接受 160mg 阿托伐他汀治疗组或接受标准他汀类药物治疗组。在手术前和手术后 6、12、24、48 和 72 小时采集肌钙蛋白 T 和肌酸激酶血样。计算每个时间点的心肌酶水平和总曲线下面积(AUC)。组特征和手术方法均匹配良好。高剂量阿托伐他汀无明显副作用。在每个时间点或 72 小时内,两项研究中的血清肌钙蛋白 T 或肌酸激酶均无显著差异。研究 1:AUC,肌钙蛋白 T:阿托伐他汀 29.6±34.8μg/L 与对照组 25.0±22.0μg/L:P>0.05。肌酸激酶:阿托伐他汀 33544±20063IU/L 与对照组 30620±10776IU/L:P>0.05。研究 2:AUC,肌钙蛋白 T:阿托伐他汀 21.8±14.3μg/L 与对照组 20.9±8.7μg/L:P>0.05。肌酸激酶:阿托伐他汀 36262±28821IU/L 与对照组 33448±14984IU/L:P>0.05。术后结局无差异。我们报告称,在已经接受标准剂量“他汀类”药物治疗的低危择期 CABG 手术患者中,给予高剂量阿托伐他汀是安全的,但不能进一步减少围手术期心肌损伤。

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