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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:免疫球蛋白联合泼尼松龙预防严重川崎病中冠状动脉异常的功效(RAISE研究):一项随机,开放标签,无盲点试验

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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:背景证据表明,皮质类固醇疗法可能对重度川崎病的初步治疗有益。我们评估了将强的松龙与阿司匹林一起加入静脉注射免疫球蛋白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日至2010年12月2日之间,在日本74家医院进行了一项多中心,前瞻性,随机,开放标签,盲点试验。重度川崎病患者采用最小化方法随机分配以接受静脉注射免疫球蛋白(每天2 g / kg,每天24小时阿司匹林和30 mg / kg阿司匹林)或静脉注射免疫球蛋白加泼尼松龙(与静脉注射免疫球蛋白组加泼尼松龙相同的静脉注射免疫球蛋白方案,每天两次,每次15 mg) C反应蛋白标准化)。患者和主治医生没有受到小组分配的限制。主要终点是研究期间冠状动脉异常的发生率。分析是按意向进行的。该试验已在大学医院医学信息网络临床试验注册中心注册,编号为UMIN000000940。结果我们随机将125例患者分配给静脉免疫球蛋白加泼尼松龙组,将123例患者分配给静脉免疫球蛋白组。在研究期间,静脉注射免疫球蛋白加泼尼松龙组的冠状动脉异常发生率显着低于静脉注射免疫球蛋白组(4例[3%] vs 28例[23%];风险差异0 20、95%CI 0 12 -0 28,p <0 0001)。两组之间的严重不良事件相似:静脉注射免疫球蛋白加泼尼松龙组的两名患者总胆固醇高,中性粒细胞减少,静脉注射免疫球蛋白组的总胆固醇高,另一名非阻塞性血栓。解释在日本重度川崎病患者中,将泼尼松龙添加到静脉免疫球蛋白的标准治疗方案中可改善冠状动脉预后。有必要对混合种族人群中的这种疾病加强一级治疗的进一步研究。资助日本厚生劳动省。

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