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Clinical potential of nicorandil to inhibit major cardiac events in hemodialysis patients with suspected myocardial ischemia.

机译:尼可地尔抑制可疑心肌缺血的血液透析患者的主要心脏事件的临床潜力。

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摘要

BACKGROUND/AIMS: We examined whether nicorandil, which is a hybrid of an adenosine triphosphate-sensitive potassium channel opener and a nitrate, could inhibit major adverse cardiac events (MACE) in maintenance hemodialysis patients with suspected myocardial ischemia. METHODS: We enrolled 148 asymptomatic patients on maintenance hemodialysis, who had exhibited potential myocardial ischemia as assessed by myocardial fatty acid imaging. The end-point was MACE including cardiac death and non-fatal acute myocardial infarction. A propensity-matched analysis was performed. RESULTS: Over a mean duration of follow-up of 2.8 +/- 1.6 years in the 82 propensity-matched patients (41 in the nicorandil group and 41 in the non-nicorandil group), we observed 17 cardiac deaths and 12 cases of nonfatal myocardial infarction. The incidence of MACE was lower (p = 0.0365) in the nicorandil group (10/41, 24.4%) than in the non-nicorandil group (19/41, 46.3%). On stepwise Cox hazard analysis, MACE was significantly inhibited by administration of nicorandil (hazard risk, 0.387; 95% CI 0.178-0.842; p = 0.0168). Kaplan-Meier survival estimates revealed that MACE-free survival rates at 3 years were 80.5 and 58.5% in patients with and without nicorandil, respectively. CONCLUSIONS: Oral administration of nicorandil may offer new potential for the inhibition of MACE in hemodialysis patients.
机译:背景/目的:我们检查了尼可地尔(一种对三磷酸腺苷敏感的钾通道开放剂和硝酸盐的混合物)是否可以抑制可疑心肌缺血的维持性血液透析患者的主要不良心脏事件(MACE)。方法:我们招募了148例无症状的维持性血液透析患者,这些患者通过心肌脂肪酸成像评估表现出潜在的心肌缺血。终点是MACE,包括心源性死亡和非致命性急性心肌梗死。进行了倾向匹配分析。结果:在82名倾向匹配患者中平均随访时间为2.8 +/- 1。6年(尼可地尔组41例,非尼可地尔组41例),我们观察到17例心脏死亡和12例非致命性死亡。心肌梗塞。尼可地尔组(10/41,24.4%)的MACE发生率较低(p = 0.0365),而非尼可地尔组(19/41,46.3%)更低。在逐步Cox危害分析中,尼可地尔的给药显着抑制了MACE(危害风险0.387; 95%CI 0.178-0.842; p = 0.0168)。 Kaplan-Meier生存估计显示,有或没有尼古地尔的患者3年无MACE生存率分别为80.5和58.5%。结论:口服尼可地尔可能为抑制血液透析患者的MACE提供新的潜力。

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