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.
J Clin Immunol. 2024 Nov 30;45(1):51. doi: 10.1007/s10875-024-01845-z.
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.
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.
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.
The incidence of MIS-C was low in Japan. The clinical features distinctively exhibited a more KD-like phenotype, with less severe clinical features.
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。
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。
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。
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。