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Factors Differentiating Multisystem Inflammatory Syndrome in Children (MIS-C) From Severe/Critical COVID-19 Infection
1Division 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. neha_gupta_2008@hotmail.com.
Insights
Distinguishing multisystem inflammatory syndrome in children (MIS-C) from severe coronavirus disease 2019 (COVID-19) is crucial. Elevated C-reactive protein (CRP), low platelet counts, and mucocutaneous symptoms aid in this differentiation.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Critical Care Medicine
Background:
- Differentiating multisystem inflammatory syndrome in children (MIS-C) from severe coronavirus disease 2019 (COVID-19) is clinically challenging.
- Both conditions can present with overlapping symptoms, necessitating accurate diagnostic markers.
Purpose of the Study:
- To identify key clinical and laboratory features that differentiate MIS-C from severe/critical COVID-19 in pediatric patients.
- To develop a predictive model for MIS-C diagnosis.
Main Methods:
- A single-center chart review compared characteristics of children diagnosed with MIS-C versus severe/critical COVID-19.
- Multivariate logistic regression analysis was employed to build predictive models.
Main Results:
- MIS-C patients exhibited higher rates of fever, mucocutaneous, cardiac, and gastrointestinal involvement, with fewer respiratory symptoms compared to COVID-19 patients.
- Key differentiating factors identified included elevated C-reactive protein (CRP), thrombocytopenia (low platelet count), mucocutaneous involvement, and absence of respiratory symptoms.
- A predictive model incorporating CRP, platelet count, gastrointestinal/mucocutaneous involvement, and lack of respiratory symptoms achieved a performance of 0.94.
Conclusions:
- Elevated CRP levels, thrombocytopenia, and mucocutaneous involvement are significant indicators for differentiating MIS-C from severe COVID-19 in children.
- A diagnostic approach utilizing CRP, platelet count, and specific symptom patterns demonstrates high specificity for MIS-C.
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.
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