Epidemiology and Clinical Outcomes of Refractory Kawasaki Disease in South Korea

Jong-Won Choi, G. Kim
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Abstract

Refractory Kawasaki disease (KD) is defined as KD resistant to initial intravenous immunoglobulin (IVIG) therapy. The proportion of refractory KD is reported to be 10%−20%, and the risk of coronary arterial aneurysm (CAA) is increased in refractory KD. We analyzed data of Korean nationwide surveys on KD to know the epidemiology, treatment modalities, and clinical outcomes of refractory KD in South Korea. We analyzed the data of three triennial Korean nationwide surveys on KD from 2009 to 2017, and selected patients with refractory KD who had persistent or recrudescent fever at least 36 hours after completion of initial IVIG therapy. Among a total of 42,705 KD patients from 2009 through 2017, 5,581 (13.1%) had refractory KD. The annual proportions of refractory KD were between 10.1% and 18.7%, which showed significant changes with the nadir in 2013 and increased proportions in 2015−2017 (P < 0.05). Treatment modalities for refractory KD were second IVIG in 86.2%, third or more IVIG in 3.8%, corticosteroids in 34.4%, infliximab in 3.7%, methotrexate in 1.0%, plasmapheresis in 0.1%, and cyclosporine in 0.02%. The use of third or more IVIG showed a decreasing trend, and the use of corticosteroids and infliximab showed an increasing trend. The incidence of CAA was significantly higher in refractory KD patients than in total KD patients (5.5% vs 1.8%; P < 0.05). The overall proportion of refractory KD was 13.1% from 2009 through 2017 in South Korea. The annual proportions of refractory KD showed significant changes with increased proportions in recent years. Treatment modalities for refractory KD showed a decreasing trend in the use of third or more IVIG and an increasing trend in the use of corticosteroids and infliximab. The incidence of CAA was significantly higher in refractory KD patients than in total KD patients.
韩国难治性川崎病的流行病学和临床结果
难治性川崎病(KD)被定义为对初始静脉注射免疫球蛋白(IVIG)治疗有耐药性的川崎病。据报道,难治性KD的比例为10% ~ 20%,难治性KD发生冠状动脉动脉瘤(CAA)的风险增加。我们分析了韩国全国性的KD调查数据,以了解韩国难治性KD的流行病学、治疗方式和临床结果。我们分析了2009年至2017年三次三年一次的韩国全国性KD调查的数据,并选择了在完成初始IVIG治疗后至少36小时出现持续或复发发热的难治性KD患者。在2009年至2017年的42705例KD患者中,5581例(13.1%)患有难治性KD。难治性KD的年占比在10.1% ~ 18.7%之间,2013年呈显著变化,2015 ~ 2017年呈上升趋势(P < 0.05)。难治性KD的治疗方式为第二次IVIG占86.2%,第三次或更多次IVIG占3.8%,皮质类固醇占34.4%,英夫利昔单抗占3.7%,甲氨蝶呤占1.0%,血浆置换占0.1%,环孢素占0.02%。第三次及以上IVIG的使用呈下降趋势,糖皮质激素和英夫利昔单抗的使用呈上升趋势。难治性KD患者的CAA发生率显著高于全部KD患者(5.5% vs 1.8%;P < 0.05)。从2009年到2017年,韩国难治性KD的总体比例为13.1%。近年来,难治性KD的年度比例呈显著变化,比例有所增加。难治性KD的治疗方式显示第三次或更多次IVIG的使用呈下降趋势,而皮质类固醇和英夫利昔单抗的使用呈上升趋势。难治性KD患者中CAA的发生率明显高于全部KD患者。
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