Nationwide Survey of Multisystem Inflammatory Syndrome in Children Associated with Coronavirus Disease 2019 in Japan.

IF 7.2 2区 医学 Q1 IMMUNOLOGY Journal of Clinical Immunology Pub Date : 2024-11-30 DOI:10.1007/s10875-024-01845-z
Daisuke Matsubara, Yuri Matsubara, Mamoru Ayusawa, Hiromichi Hamada, Mitsuru Seki, Hiroyuki Yamagishi, Yoshihide Mitani, Yoshihiro Onouchi, Hiroyuki Moriuchi, Isao Miyairi, Keiko Tanaka-Taya, Tomohiro Katsuta, Hiroshi Kurosawa, Kazunori Aoki, Naoki Shimizu, Yosikazu Nakamura
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Abstract

Background: Multisystem inflammatory syndrome in children (MIS-C) presents some clinical overlap with Kawasaki disease (KD). Although KD is common in Japan, the clinical characteristics of MIS-C in Japan remain unknown. Therefore, we aimed to determine the epidemiological and clinical features of MIS-C in Japan.

Methods: Using a case reporting form, a nationwide registry was created between November 2020 and March 2023, involving 2,080 facilities throughout Japan. We prospectively and retrospectively enrolled patients with MIS-C. The primary outcomes were the number and incidence rates of children with MIS-C. The secondary outcomes included clinical features, such as KD phenotype, organ involvement, shock, intensive care unit admission, and coronary artery lesions.

Results: Among 398 patients registered, central review identified 129 MIS-C cases (mean age: 8·8 ± 3·7 years). The overall incidence rate was estimated to be 1·5 per 100,000 COVID-19 cases, exhibiting a decline as the COVID-19 pandemic progressed, from 12·3 cases (Pre-Delta) to 1·3 cases (Omicron); 80% of MIS-C cases occurred during the Omicron variant predominant period, and 72% of children with MIS-C met the KD criteria. Cardiovascular (88%) and gastrointestinal (90%) involvement were frequent. In Japan, MIS-C cases showed comparatively less severe clinical features, with shock in 29% and admission to the intensive care unit in 12% of cases. Coronary artery lesions were identified in 15 cases (11·6%), irrespective of the presence of shock. No fatalities were reported.

Conclusion: The incidence of MIS-C was low in Japan. The clinical features distinctively exhibited a more KD-like phenotype, with less severe clinical features.

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日本2019冠状病毒病相关儿童多系统炎症综合征全国调查
背景:儿童多系统炎症综合征(MIS-C)与川崎病(KD)有一定的临床重叠。虽然KD在日本很常见,但MIS-C在日本的临床特征尚不清楚。因此,我们旨在确定日本misc的流行病学和临床特征。方法:使用病例报告表,在2020年11月至2023年3月期间创建了一个全国性的登记处,涉及日本各地的2080个设施。我们前瞻性和回顾性地纳入了MIS-C患者。主要结局是MIS-C患儿的数量和发病率。次要结局包括临床特征,如KD表型、器官受累、休克、重症监护病房入院和冠状动脉病变。结果:在登记的398例患者中,中心回顾发现129例misc病例(平均年龄:8.8±3.7岁)。总发病率估计为每10万例COVID-19病例1.5例,随着COVID-19大流行的进展呈现下降趋势,从12.3例(Pre-Delta)降至1.3例(Omicron);80%的MIS-C病例发生在Omicron变异优势期,72%的MIS-C患儿符合KD标准。经常累及心血管(88%)和胃肠道(90%)。在日本,misc病例表现出相对较轻的临床特征,29%的病例出现休克,12%的病例进入重症监护病房。15例(11.6%)发现冠状动脉病变,与有无休克无关。没有人员死亡的报道。结论:MIS-C在日本发病率较低。临床特征明显表现为kd样表型,临床特征较轻。
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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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