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2081. COVID-19 mRNA Vaccine Effectiveness against Hospitalizations among U.S. Children and Adolescents During Omicron Variant Predominance

BACKGROUND: SARS-CoV-2 Omicron variants have increased vaccine-induced immune evasion and their emergence coincided with waning COVID-19 vaccine effectiveness (VE). The duration of immunity from the primary series and VE of booster doses against pediatric COVID-19 (Omicron)-associated hospitalizatio...

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Detalles Bibliográficos
Autores principales: Zambrano, Laura D, Newhams, Margaret M, Wu, Michael J, Simeone, Regina, Orzel, Amber, Halasa, Natasha B, Fleming-Dutra, Katherine E, Campbell, Angela P, Randolph, Adrienne G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679226/
http://dx.doi.org/10.1093/ofid/ofad500.151
Descripción
Sumario:BACKGROUND: SARS-CoV-2 Omicron variants have increased vaccine-induced immune evasion and their emergence coincided with waning COVID-19 vaccine effectiveness (VE). The duration of immunity from the primary series and VE of booster doses against pediatric COVID-19 (Omicron)-associated hospitalizations has not been characterized in the United States. METHODS: Using a case-control design, we examined VE against laboratory-confirmed COVID-19-associated hospitalizations, enrolling case-patients hospitalized for COVID-19 and SARS-CoV-2 test-negative controls with COVID-like illness from 31 hospitals in 23 states. VE was estimated through multivariable logistic regression by comparing the odds of antecedent primary series or booster COVID-19 mRNA vaccination within and beyond 60 days prior to hospitalization. Results were analyzed by age group (5–11 and 12–18 years) among patients admitted December 19, 2021–March 30, 2023. RESULTS: We enrolled 1,242 case-patients (972 [78%] of whom were unvaccinated, 164 [13%] of whom received life support, and 11 of whom died) and 1,309 controls. Among children aged 5-18 years, VE of 2 mRNA doses (complete primary series) against pediatric COVID-19 hospitalization was 64% (95% confidence interval [CI]: 44–76%) at 14-60 days after dose 2 (median time since dose 2, 38 days); VE waned to 38% (95% CI: 23–50%) at ≥60 days (median time since vaccination, 213 days). Within 60 days of a monovalent booster dose, VE was 52% (95% CI: -3–77%); among children aged 5-11 years, VE of a bivalent booster dose was 79% (95% CI: 25-94%). Among case-patients who required life support or died, 122/164 (74%) were unvaccinated and only 3 (2%) had received a bivalent booster dose. [Figure: see text] VE estimates were only plotted if confidence interval width was <200. Adjusted models included ≥1 underlying medical condition (yes/no), age in years, census region, biweekly date of hospital admission, and social vulnerability index (SVI) score. Sex and race/ethnicity were tested as confounders in the full model but were dropped for absence of evidence of confounding. [Figure: see text] Abbreviations: ICU, intensive care unit; ECMO, extracorporeal membrane oxygenation CONCLUSION: COVID-19 mRNA vaccination reduced the likelihood of pediatric COVID-19 hospitalization by >60%; VE waned but remained protective, even at a median of 213 days after dose 2. Although not reaching statistical significance due to limited power, monovalent boosters appeared to temporarily restore protection, and bivalent booster doses among 5–11-year-olds were nearly 80% protective against hospitalization. Nearly three quarters of children requiring life support or who died were unvaccinated. DISCLOSURES: Regina Simeone, PhD, Pfizer: Stocks/Bonds Natasha B. Halasa, MD, MPH, Merck: Grant/Research Support|Quidell: Grant/Research Support|Quidell: donation of kits|Sanofi: Grant/Research Support|Sanofi: vaccine support