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. 2022 Oct 25:jiac423. doi: 10.1093/infdis/jiac423

Pediatric Infection-Induced SARS-CoV-2 Seroprevalence Increases and Seroprevalence by Type of Clinical Care—September 2021-February 2022

Kristie E N Clarke 1,, Yun Kim 2, Jefferson Jones 3,, Adam Lee 4, Yangyang Deng 5, Elise Nycz 6,7, Ronaldo Iachan 8, Adi V Gundlapalli 9, Adam MacNeil 10, Aron Hall 11
PMCID: PMC9620360  PMID: 36281757

Abstract

Background and Objectives

Trends in estimates of US pediatric SARS-CoV-2 infection-induced seroprevalence from commercial laboratory specimens may overrepresent children with frequent healthcare needs. We examined seroprevalence trends and compared seroprevalence estimates by testing type and diagnostic coding.

Methods

Cross-sectional convenience samples of residual sera between September 2021 and February 2022 from 52 U.S. jurisdictions were assayed for infection-induced SARS-CoV-2 antibodies; monthly seroprevalence estimates were calculated by age group. Multivariate logistic analyses compared seroprevalence estimates for specimens associated with ICD-10 codes and laboratory orders indicating well-child care with estimates for other pediatric specimens.

Results

Infection-induced SARS-CoV-2 seroprevalence increased in each age group; from 30% to 68% (1-4 years), 38% to 77% (5-11 years), and 40% to 74% (12-17 years). On multivariate analysis, patients with well-child ICD-10 codes were seropositive more often than other patients aged 1-17 years (adjusted prevalence ratio [aPR] 1.04; 95% CI 1.02-1.07); children aged 9-11 years receiving standard lipid screening were seropositive more often than those receiving other laboratory tests (1.05; 1.02-1.08).

Conclusions

Infection-induced seroprevalence more than doubled among children under 12 between September 2021 and February 2022, and increased 85% in adolescents. Differences in seroprevalence by care type did not substantially impact US pediatric seroprevalence estimates.

Keywords: COVID-19, SARS-CoV-2, seroprevalence, serosurveillance, antibody, immunology

Contributor Information

Kristie E N Clarke, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Yun Kim, ICF, Rockville, Maryland, USA.

Jefferson Jones, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Adam Lee, ICF, Rockville, Maryland, USA.

Yangyang Deng, ICF, Rockville, Maryland, USA.

Elise Nycz, Centers for Disease Control and Prevention, Atlanta, Georgia, USA; Abt Associates, Rockville, Maryland, USA.

Ronaldo Iachan, ICF, Rockville, Maryland, USA.

Adi V Gundlapalli, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Adam MacNeil, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Aron Hall, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Supplementary Material

jiac423_Supplementary_Data

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

jiac423_Supplementary_Data

Articles from The Journal of Infectious Diseases are provided here courtesy of Oxford University Press

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