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儿童多系统炎症综合征(MIS-C)与儿童严重/危重症 COVID-19 感染的鉴别因素。

Factors Differentiating Multisystem Inflammatory Syndrome in Children (MIS-C) From Severe/Critical COVID-19 Infection in Children.

机构信息

Division of Critical Care Medicine, Department of Pediatrics, OU College of Medicine, Oklahoma City, USA. Correspondence to: Dr Neha Gupta, 1200 Everette Drive, Suite 8305, Oklahoma City, OK 73104, USA.

Division of Gastroenterology, Department of Pediatrics, OU College of Medicine, Oklahoma City, USA.

出版信息

Indian Pediatr. 2022 Feb 15;59(2):120-124. doi: 10.1007/s13312-022-2442-4. Epub 2021 Sep 22.

Abstract

OBJECTIVE

To differentiate severe/critical coronavirus disease 2019 (COVID-19) infection from multisystem inflammatory syndrome in children (MIS-C).

METHODS

Single-center chart review comparing characteristics of children with MIS-C and 'severe/critical' COVID-19 infection. Multivariate logistic regression was performed to create predictive models for predicting MIS-C.

RESULTS

Of 68 patients, 28 (41.2%) had MIS-C while 40 (58.8%) had severe/critical COVID-19 infection. MIS-C patients had a higher prevalence of fever, mucocutaneous, cardiac and gastrointestinal involvement and a lower prevalence of respiratory symptoms (P<0.05). Significantly lower hemoglobin, platelet count, serum electrolytes, and significantly elevated inflammatory and coagulation markers were observed in MIS-C cohort. Upon multivariate logistic regression, the best model included C-reactive protein (CRP), platelet count, gastrointestinal and mucocutaneus involvement and absence of respiratory involvement (performance of 0.94). CRP>40 mg/L with either platelet count <150x109 or mucocutaneous involvement had specificity of 97.5% to diagnose MIS-C.

CONCLUSION

Elevated CRP, thrombocytopenia and mucocutaneous involvement at presentation are helpful in differentiating MIS-C from severe COVID-19.

摘要

目的

区分严重/危重新冠病毒病 2019(COVID-19)感染与儿童多系统炎症综合征(MIS-C)。

方法

单中心图表回顾比较了 MIS-C 患儿和“严重/危重症”COVID-19 感染患儿的特征。采用多变量逻辑回归建立预测 MIS-C 的预测模型。

结果

68 例患儿中,28 例(41.2%)为 MIS-C,40 例(58.8%)为严重/危重症 COVID-19 感染。MIS-C 患儿发热、黏膜皮肤、心脏和胃肠道受累的发生率较高,呼吸道症状的发生率较低(P<0.05)。MIS-C 组的血红蛋白、血小板计数、血清电解质明显较低,炎症和凝血标志物明显升高。多变量逻辑回归后,最佳模型包括 C 反应蛋白(CRP)、血小板计数、胃肠道和黏膜皮肤受累以及无呼吸道受累(效能为 0.94)。CRP>40mg/L 伴血小板计数<150x109 或黏膜皮肤受累具有诊断 MIS-C 的特异性 97.5%。

结论

发病时 CRP 升高、血小板减少和黏膜皮肤受累有助于区分 MIS-C 与严重 COVID-19。

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