Distinguishing Incomplete Kawasaki and Nonsevere Multisystem Inflammatory Syndrome in Children

Author:

Fan Lucie K.1,Bai Shasha2,Du Chenxi2,Bass Marissa3,Jones Kaitlin3,Sherry Whitney3,Morris Claudia R.34,Oster Matthew E.3,Shane Andi L.56,Jaggi Preeti56

Affiliation:

1. aDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia

2. bPediatric Biostatistics Core, Department of Pediatrics, Emory University, Atlanta, Georgia

3. cDepartment of Pediatrics, Children’s Healthcare of Atlanta, Atlanta, Georgia

4. dDivisions of Pediatric Emergency Medicine

5. ePediatric Infectious Disease

6. fDivision of Pediatric Infectious Disease

Abstract

OBJECTIVES Characterizing inflammatory syndromes during the coronavirus disease 2019 pandemic was complicated by recognition of multisystem inflammatory syndrome in children (MIS-C), contemporaneous with episodes of Kawasaki disease. We hypothesized a substantial overlap between the 2 and assessed the performance of an MIS-C likelihood score in differentiating inpatients with nonsevere MIS-C from prepandemic incomplete Kawasaki disease (iKD) without coronary involvement. METHODS A retrospective review of inpatient records was conducted; the nonsevere MIS-C cohort (March 2020–February 2021) met the 2023 definition for MIS-C; the iKD cohort (January 2018–January 2019) met the American Heart Association criteria for iKD without coronary involvement. We applied the likelihood score to both cohorts. We estimated the percent of children with iKD who could have met the clinical criteria of the MIS-C, had they presented in 2023. RESULTS The 68 children in the nonsevere MIS-C cohort were older (8 vs 4 years, P < .001) than the 28 children in the iKD cohort. Those in the nonsevere MIS-C cohort had higher rates of thrombocytopenia (P < .001) and lymphopenia (P = .021); those in the iKD cohort had higher rates of pyuria (P < .001). Twenty-four (86%) children in the iKD cohort met the 2023 MIS-C definition. The scoring system correctly predicted 71% to 74% children with their respective clinical diagnoses. CONCLUSIONS Though there was considerable clinical overlap, thrombocytopenia, lymphopenia, and the absence of pyuria were the most helpful parameters to distinguish children with nonsevere MIS-C from those with iKD.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics,General Medicine,Pediatrics, Perinatology and Child Health

Reference18 articles.

1. Multisystem inflammatory syndrome in children-United States, February 2020-July 2021;Miller;Clin Infect Dis,2022

2. Centers for Disease Control and Prevention. Multisystem inflammatory syndrome in children (MIS-C) associated with coronavirus disease 2019 (COVID-19). Available at: https://emergency.cdc.gov/han/2020/han00432.asp. Accessed December 22, 2022

3. Seroprevalence of infection-induced SARS-CoV-2 antibodies - United States, September 2021 – February 2022;Clarke;MMWR Morb Mortal Wkly Rep,2022

4. Distinguishing multisystem inflammatory syndrome in children from COVID-19, Kawasaki disease and toxic shock syndrome;Godfred-Cato;Pediatr Infect Dis J,2022

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