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SARS-CoV-2 Serostatus and COVID-19 Illness Characteristics by Variant Time Period in Non-Hospitalized Children and Adolescents.
Messiah, Sarah E; Swartz, Michael D; Abbas, Rhiana A; Talebi, Yashar; Kohl, Harold W; Valerio-Shewmaker, Melissa; DeSantis, Stacia M; Yaseen, Ashraf; Kelder, Steven H; Ross, Jessica A; Padilla, Lindsay N; Gonzalez, Michael O; Wu, Leqing; Lakey, David; Shuford, Jennifer A; Pont, Stephen J; Boerwinkle, Eric.
Afiliación
  • Messiah SE; Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health in Dallas, The University of Texas (UT) Health Science Center at Houston, Dallas, TX 77030, USA.
  • Swartz MD; Center for Pediatric Population Health, UTHealth School of Public Health, Dallas, TX 75207, USA.
  • Abbas RA; Department of Pediatrics, McGovern Medical School, Houston, TX 77030, USA.
  • Talebi Y; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Kohl HW; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Valerio-Shewmaker M; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • DeSantis SM; School of Public Health in Austin, The University of Texas Health Science Center at Houston, Austin, TX 78701, USA.
  • Yaseen A; Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas at Austin, Austin, TX 78705, USA.
  • Kelder SH; School of Public Health in Brownville, The University of Texas Health Science Center at Houston, Brownsville, TX 78520, USA.
  • Ross JA; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Padilla LN; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Gonzalez MO; School of Public Health in Austin, The University of Texas Health Science Center at Houston, Austin, TX 78701, USA.
  • Wu L; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Lakey D; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Shuford JA; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Pont SJ; Department of Biostatistics and Data Sciences, School of Public Health in Houston, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Boerwinkle E; Administration Division, University of Texas System, Austin, TX 78701, USA.
Children (Basel) ; 10(5)2023 Apr 30.
Article en En | MEDLINE | ID: mdl-37238366
ABSTRACT

OBJECTIVE:

To describe COVID-19 illness characteristics, risk factors, and SARS-CoV-2 serostatus by variant time period in a large community-based pediatric sample.

DESIGN:

Data were collected prospectively over four timepoints between October 2020 and November 2022 from a population-based cohort ages 5 to 19 years old.

SETTING:

State of Texas, USA.

PARTICIPANTS:

Participants ages 5 to 19 years were recruited from large pediatric healthcare systems, Federally Qualified Healthcare Centers, urban and rural clinical practices, health insurance providers, and a social media campaign. EXPOSURE SARS-CoV-2 infection. MAIN OUTCOME(S) AND MEASURE(S) SARS-CoV-2 antibody status was assessed by the Roche Elecsys® Anti-SARS-CoV-2 Immunoassay for detection of antibodies to the SARS-CoV-2 nucleocapsid protein (Roche N-test). Self-reported antigen or PCR COVID-19 test results and symptom status were also collected.

RESULTS:

Over half (57.2%) of the sample (N = 3911) was antibody positive. Symptomatic infection increased over time from 47.09% during the pre-Delta variant time period, to 76.95% during Delta, to 84.73% during Omicron, and to 94.79% during the Omicron BA.2. Those who were not vaccinated were more likely (OR 1.71, 95% CI 1.47, 2.00) to be infected versus those fully vaccinated.

CONCLUSIONS:

Results show an increase in symptomatic COVID-19 infection among non-hospitalized children with each progressive variant over the past two years. Findings here support the public health guidance that eligible children should remain up to date with COVID-19 vaccinations.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline / Risk_factors_studies Idioma: En Revista: Children (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline / Risk_factors_studies Idioma: En Revista: Children (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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