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      1935. COVID-19 mRNA Vaccination Reduces the Occurrence of Post-COVID Conditions in U.S. Children Aged 5-17 Years Following Omicron SARS-CoV-2 Infection, July 2021-September 2022

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          Abstract

          Background

          An estimated 1-3% of children with SARS-CoV-2 infection will develop Post-COVID Conditions (PCC). This study evaluates mRNA COVID-19 vaccine impact on likelihood of PCC in children.

          Methods

          A multi-site cohort of children enrolled 7/21/2021-9/1/2022 underwent weekly SARS-CoV-2 screening tests and were surveyed via self- or parental report 12/1/2022-5/31/2023 regarding PCC (defined as ≥1 new or on-going symptoms lasting ≥ 1 month after infection). Multivariable logistic regression was performed to estimate the occurrence of PCC by vaccination status among children aged 5–17 years whose first PCR-confirmed SARS-CoV-2 infection occurred in-study with Omicron variant, who completed the survey >60 days from infection, and who were vaccine age-eligible at time of infection per ACIP recommendations. Vaccination status was categorized as vaccinated (at least primary series completed >14 days before infection) and unvaccinated (no vaccine doses before infection). Vaccination status was verified through vaccine registry and/or medical records.

          Results

          Of 622 participants surveyed, 5% (n=28) had PCC (Table 1) and 67% (n=474) were vaccinated (Table 2). Surveys were completed a median (IQR) of 203.7 days (119.0–293.0) after infection. Children with non-Hispanic Black race/ethnicity and good/fair/poor self-rated baseline health were more likely to report PCC. Children aged 12-18 years, Non-Hispanic Asian and White children, those reporting symptomatic SARS-CoV-2 infection, and those with excellent/very good self-rated baseline health were more likely to report vaccination When comparing children with and without PCC symptoms, COVID-19 mRNA vaccination was associated with a decreased likelihood of >1 PCC symptom (aOR 0.66, 95% CI 0.43-0.99), >2 PCC symptoms (aOR 0.52, 95% 0.32-0.83), and respiratory PCC symptoms (aOR 0.53, 95% CI 0.33-0.87) (Table 3).

          Figure 1.

          Relative Risk of Post-COVID Conditions among Patients who Received Paxlovid, Ages ≥50 (N=564,303)

          Figure 2.

          Relative Risk of Post-COVID Conditions among Patients who Received Paxlovid, Ages 18-49 (N=292,818)

          Figure 3.

          Relative Risk of Post-COVID Conditions among Patients who Received Paxlovid, Ages 12-17 (N=17,178)

          Conclusion

          In this study, mRNA COVID-19 vaccination appeared to be protective against PCC in children following Omicron SARS-CoV-2 infection. The adjusted ORs correspond to an estimated 34%, 48%, and 47% reduced likelihood of >1, >2, and respiratory PCC symptoms among vaccinated children, respectively. These findings support COVID-19 vaccination for children and may encourage increased pediatric vaccine uptake.

          Disclosures

          Lisa Gwynn, MBA, MSPH, Merck: Honoraria

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          Author and article information

          Contributors
          Journal
          Open Forum Infect Dis
          Open Forum Infect Dis
          ofid
          Open Forum Infectious Diseases
          Oxford University Press (US )
          2328-8957
          December 2023
          27 November 2023
          27 November 2023
          : 10
          : Suppl 2 , IDWeek 2023 Abstracts
          : ofad500.2466
          Affiliations
          Centers for Disease Control and Prevention , Atlanta, GA
          Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention , Atlanta, Georgia
          Miller School of Medicine, University of Miami , Miami, Florida
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Abt Associates , Rockville, Maryland
          Centers for Disease Control and Prevention , Atlanta, GA
          Baylor Scott & White Health , Temple, TX
          University of Utah School of Medicine , Salt Lake City, Utah
          U.Utah , SLC, Utah
          University of Arizona , Tucson, Arizona
          Centers for Disease Control and Prevention , Atlanta, GA
          Centers for Disease Control and Prevention , Atlanta, GA
          Centers for Disease Control and Prevention , Atlanta, GA
          Centers for Disease Control and Prevention , Atlanta, GA
          Author notes

          Session: 176. Late Breaking Abstracts: COVID-19 & Friends

          Friday, October 13, 2023: 1:57 PM

          Article
          ofad500.2466
          10.1093/ofid/ofad500.2466
          10678185
          f5259538-64e6-42ef-a77c-802be0a9ff14
          © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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          AcademicSubjects/MED00290

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