来自印度东部的一项单中心经验,描述了第一波和第二波新冠肺炎后与严重急性呼吸系统综合征冠状病毒2型相关的儿童多系统炎症综合征(MISC)的流行病学和表型变异19

Mimi Ganguly, P. Giri, S. Basu
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引用次数: 1

摘要

与SARS-CoV-2相关的儿童多系统炎症综合征(MIS-C)在世界范围内引起了重大的健康问题。在我们中心,从2020年6月到2021年1月,我们经历了第一波misc,而从2021年4月到2021年8月,第二波misc激增。在这项研究中,我们对这两个波中不同表型的MIS-C进行了比较分析。对象和方法:这是一项单中心观察性研究,符合世卫组织misc标准的儿童被纳入研究。记录临床和实验室结果、病程、治疗和结果,并对患者进行随访。根据不同的表现,将病例分为四种不同的表型(1型:与急性COVID-19重叠的misc, 2型:与休克/ misc合并多器官功能障碍综合征(MODS)的misc, 3型:misc川asaki病表型,4型:轻度misc /发热性炎症状态),并在两波中对这些表型进行比较分析。结果:第一波发病7个月86例,第二波发病5个月102例。临床表现和实验室结果比较,2型表型的比例增加,需要更多的儿科重症监护病房入院。在第二波中观察到死亡率,而在我们的队列中在第一波中没有。结论:MIS-C具有典型的疾病表现谱,从轻度发热炎症状态到全面MODS。早期表型分化和基于表型的靶向免疫调节治疗已被证明是有用的。
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A single-center experience from Eastern India depicting the epidemiology and phenotypic variations of Multisystem inflammatory syndrome in children (MISC) associated with SARS-CoV2 seen after first wave and second wave of COVID 19
Introduction: Multisystem inflammatory syndrome in children (MIS-C) associated with SARS-CoV-2 caused significant health concerns worldwide. In our center, we had encountered the first wave of MIS-C from June 2020 to January 2021, whereas the second wave surged up from April 2021 to August 2021. In this study, we have done a comparative analysis of different phenotypes of MIS-C seen during these two waves. Subjects and Methods: This was a single-center observational study where the children fulfilled the WHO criteria for MIS-C were included in the study. Clinical and laboratory findings, course of the illness, treatment, and outcome were noted down, and the patients were followed up. Depending on the presentations, cases were classified in four different phenotypes (Type 1: MIS-C overlapping with acute COVID-19, Type 2: MIS-C with shock/MIS-C with multiple organ dysfunction syndrome (MODS), Type 3: MIS-C Kawasaki disease phenotype, Type 4: Mild MIS-C/Febrile inflammatory state), and a comparative analysis of these phenotypes in the two waves was done. Results: There were 86 cases in 7 months during the first wave, whereas 102 cases in 5-month duration during the second wave. The clinical manifestations and laboratory findings were compared, type 2 phenotypes increased in proportion requiring more pediatric intensive care unit admissions. Mortality was seen during the 2nd wave which was absent in our cohort during the first wave. Conclusions: MIS-C typically showed a spectrum of disease manifestations starting from a mild febrile inflammatory state to full-blown MODS. Early phenotypic differentiation and targeted immunomodulatory therapy depending on the phenotype had shown to be useful.
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