首页> 外文期刊>The Lancet >Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): A randomised, open-label, blinded-endpoints trial
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Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): A randomised, open-label, blinded-endpoints trial

机译:免疫球蛋白加上泼尼松酮的功效预防严重川崎病患者冠状动脉异常(提高研究):随机,开放标签,盲终点试验

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摘要

Background Evidence indicates that corticosteroid therapy might be beneficial for the primary treatment of severe Kawasaki disease. We assessed whether addition of prednisolone to intravenous immunoglobulin with aspirin would reduce the incidence of coronary artery abnormalities in patients with severe Kawasaki disease. Methods We did a multicentre, prospective, randomised, open-label, blinded-endpoints trial at 74 hospitals in Japan between Sept 29, 2008, and Dec 2, 2010. Patients with severe Kawasaki disease were randomly assigned by a minimisation method to receive either intravenous immunoglobulin (2 g/kg for 24 h and aspirin 30 mg/kg per day) or intravenous immunoglobulin plus prednisolone (the same intravenous immunoglobulin regimen as the intravenous immunoglobulin group plus prednisolone 2 mg/kg per day given over 15 days after concentrations of C-reactive protein normalised). Patients and treating physicians were unmasked to group allocation. The primary endpoint was incidence of coronary artery abnormalities during the study period. Analysis was by intention to treat. This trial is registered with the University Hospital Medical Information Network clinical trials registry, number UMIN000000940. Findings We randomly assigned 125 patients to the intravenous immunoglobulin plus prednisolone group and 123 to the intravenous immunoglobulin group. Incidence of coronary artery abnormalities was significantly lower in the intravenous immunoglobulin plus prednisolone group than in the intravenous immunoglobulin group during the study period (four patients [3%] vs 28 patients [23%]; risk difference 0 20, 95% CI 0 12-0 28, p<0 0001). Serious adverse events were similar between both groups: two patients had high total cholesterol and one neutropenia in the intravenous immunoglobulin plus prednisolone group, and one had high total cholesterol and another non-occlusive thrombus in the intravenous immunoglobulin group. Interpretation Addition of prednisolone to the standard regimen of intravenous immunoglobulin improves coronary artery outcomes in patients with severe Kawasaki disease in Japan. Further study of intensified primary treatment for this disease in a mixed ethnic population is warranted. Funding Japanese Ministry of Health, Labour and Welfare.
机译:背景技术证据表明皮质类固醇治疗可能对严重川崎病的主要治疗有益。我们评估了对阿司匹林的静脉内免疫球蛋白的添加泼尼松龙是否会降低严重川崎病患者冠状动脉异常的发生率。方法我们在2008年9月29日和2010年12月2日在日本的74家医院做了多中心,前瞻性,随机,开放标签的盲目 - 终点试验,并通过最小化方法随机分配严重的川崎病患者静脉注射免疫球蛋白(2克/千克24小时,阿司匹林每天30毫克/千克)或静脉注射免疫球蛋白加泼尼松龙(相同的静脉内免疫球蛋白治疗方案作为静脉注射免疫球蛋白组加泼尼松龙2毫克/千克的浓度后给予15天以上天C-反应蛋白标准化)。患者和治疗医生未被拆除划分分配。在研究期间,主要终点是冠状动脉异常的发生率。分析是意图治疗。该试验是在大学医院医疗信息网络临床试验登记处注册,编号UMIN0000940。结果我们将125名患者随机分配给静脉内免疫球蛋白加泼尼松组和123次静脉内免疫球蛋白基团。静脉内免疫球蛋白加泼尼松组冠状动脉异常的发生率显着低于研究期间静脉内免疫球蛋白基团(四名患者[3%]患者28例[23%];风险差0 20,95%CI 0 12 -0 28,p <0 0001)。两组之间的严重不良事件是相似的:两名患者在静脉内免疫球蛋白加上的胆固醇中的总胆固醇和一个中性粒细胞素,并且在静脉内免疫球蛋白基团中具有高总胆固醇和另一种非闭塞血栓。解释对静脉内免疫球蛋白的标准方案的解释增加了日本严重川崎疾病患者的冠状动脉结果。有必要进一步研究混合族裔人群中这种疾病的强化初级治疗。资助日本卫生部,劳动力和福利部。

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  • 来源
    《The Lancet》 |2012年第9826期|共8页
  • 作者单位

    Department of Pediatrics Gunma University Graduate School of Medicine Gunma 371-8511 Japan;

    First Department of Pediatrics Toho University Omori Medical Center Tokyo Japan;

    Department of Health Policy National Center for Child Health and Development Tokyo Japan;

    Faculty of Education Saitama University Saitama Japan;

    Clinical Investigation and Research Unit Gunma University Hospital Gunma Japan;

    Department of Pediatrics Gunma University Graduate School of Medicine Gunma 371-8511 Japan;

    Department of Pediatrics Nagoya University Graduate School of Medicine Nagoya Japan;

    Department of Pediatrics Kyusyu University Graduate School of Medical Sciences Fukuoka Japan;

    Department of Pediatric Cardiology and Nephrology Kyoto Prefectural University of Medicine;

    Department of Pediatrics Nippon Medical School Tokyo Japan;

    Department of Cardiology Tokyo Metropolitan Children's Medical Center Tokyo Japan;

    Department of Pediatrics Kagoshima University Graduate School of Medicine and Dental Sciences;

    Department of Pediatrics NTT East Japan Sapporo Hospital Sapporo Japan;

    Department of Pediatrics Toyama University Toyama Japan;

    Department of Cardiology Gunma Children's Medical Center Gunma Japan;

    Department of Pediatrics Nippon Medical School Tokyo Japan Department of Pediatrics Nippon;

    Department of Pediatrics St Luke's International Hospital Tokyo Japan;

    Department of Pediatrics Fukuoka Higashi Medical Center Fukuoka Japan;

    Department of Pediatrics Nagoya Memorial Hospital Nagoya Japan;

    First Department of Pediatrics Toho University Omori Medical Center Tokyo Japan;

    Department of Pediatrics Toyota Memorial Hospital Toyota Japan;

    Department of Pediatrics Gunma University Graduate School of Medicine Gunma 371-8511 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
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