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日本 2019 冠状病毒病相关儿童多系统炎症综合征的全国性调查。

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

机构信息

Department of Pediatrics, Jichi Medical University, 3311-1 Shimotsuke, Tochigi, 329-0498, Japan.

Division of Public Health, Center for Community Medicine, Jichi Medical University, Tochigi, Japan.

出版信息

J Clin Immunol. 2024 Nov 30;45(1):51. doi: 10.1007/s10875-024-01845-z.

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.

摘要

背景

儿童多系统炎症综合征 (MIS-C) 与川崎病 (KD) 存在一些临床重叠。尽管 KD 在日本很常见,但日本的 MIS-C 临床特征尚不清楚。因此,我们旨在确定日本 MIS-C 的流行病学和临床特征。

方法

使用病例报告表,于 2020 年 11 月至 2023 年 3 月期间在日本全国范围内建立了一个登记处,涉及日本各地的 2080 家医疗机构。我们前瞻性和回顾性地招募了 MIS-C 患儿。主要结局为 MIS-C 患儿的数量和发病率。次要结局包括 KD 表型、器官受累、休克、入住重症监护病房和冠状动脉病变等临床特征。

结果

在注册的 398 名患者中,中心审查确定了 129 例 MIS-C 病例(平均年龄:8.8±3.7 岁)。总体发病率估计为每 100000 例 COVID-19 病例 1.5 例,随着 COVID-19 大流行的进展而下降,从德尔塔前时期的 12.3 例降至奥密克戎时期的 1.3 例;80%的 MIS-C 病例发生在奥密克戎变异株流行期间,72%的 MIS-C 患儿符合 KD 标准。心血管(88%)和胃肠道(90%)受累较为常见。在日本,MIS-C 病例的临床特征相对较轻,休克发生率为 29%,重症监护病房入住率为 12%。15 例(11.6%)存在冠状动脉病变,与是否存在休克无关。未报告死亡病例。

结论

日本 MIS-C 的发病率较低。临床特征明显表现出更类似 KD 的表型,且临床特征较轻。

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