BNT162b2 mRNA Vaccination Against Coronavirus Disease 2019 is Associated With a Decreased Likelihood of Multisystem Inflammatory Syndrome in Children Aged 5–18 Years—United States, July 2021 – April 2022. (20th August 2022)
- Record Type:
- Journal Article
- Title:
- BNT162b2 mRNA Vaccination Against Coronavirus Disease 2019 is Associated With a Decreased Likelihood of Multisystem Inflammatory Syndrome in Children Aged 5–18 Years—United States, July 2021 – April 2022. (20th August 2022)
- Main Title:
- BNT162b2 mRNA Vaccination Against Coronavirus Disease 2019 is Associated With a Decreased Likelihood of Multisystem Inflammatory Syndrome in Children Aged 5–18 Years—United States, July 2021 – April 2022
- Authors:
- Zambrano, Laura D
Newhams, Margaret M
Olson, Samantha M
Halasa, Natasha B
Price, Ashley M
Orzel, Amber O
Young, Cameron C
Boom, Julie A
Sahni, Leila C
Maddux, Aline B
Bline, Katherine E
Kamidani, Satoshi
Tarquinio, Keiko M
Chiotos, Kathleen
Schuster, Jennifer E
Cullimore, Melissa L
Heidemann, Sabrina M
Hobbs, Charlotte V
Nofziger, Ryan A
Pannaraj, Pia S
Cameron, Melissa A
Walker, Tracie C
Schwartz, Stephanie P
Michelson, Kelly N
Coates, Bria M
Flori, Heidi R
Mack, Elizabeth H
Smallcomb, Laura
Gertz, Shira J
Bhumbra, Samina S
Bradford, Tamara T
Levy, Emily R
Kong, Michele
Irby, Katherine
Cvijanovich, Natalie Z
Zinter, Matt S
Bowens, Cindy
Crandall, Hillary
Hume, Janet R
Patel, Manish M
Campbell, Angela P
Randolph, Adrienne G
… (more) - Abstract:
- Abstract: Background: Multisystem inflammatory syndrome in children (MIS-C), linked to antecedent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, is associated with considerable morbidity. Prevention of SARS-CoV-2 infection or coronavirus disease 2019 (COVID-19) by vaccination might also decrease MIS-C likelihood. Methods: In a multicenter, case-control, public health investigation of children ages 5–18 years hospitalized from 1 July 2021 to 7 April 2022, we compared the odds of being fully vaccinated (2 doses of BNT162b2 vaccine ≥28 days before hospital admission) between MIS-C case-patients and hospital-based controls who tested negative for SARS-CoV-2. These associations were examined by age group, timing of vaccination, and periods of Delta and Omicron variant predominance using multivariable logistic regression. Results: We compared 304 MIS-C case-patients (280 [92%] unvaccinated) with 502 controls (346 [69%] unvaccinated). MIS-C was associated with decreased likelihood of vaccination (adjusted OR [aOR]: .16; 95% CI: .10–.26), including among children ages 5–11 years (aOR: .22; 95% CI: .10–.52), ages 12–18 years (aOR: .10; 95% CI: .05–.19), and during the Delta (aOR: .06; 95% CI: .02–.15) and Omicron (aOR: .22; 95% CI: .11–.42) variant-predominant periods. This association persisted beyond 120 days after the second dose (aOR: .08; 95% CI: .03–.22) in 12–18-year-olds. Among all MIS-C case-patients, 187 (62%) required intensive care unit admissionAbstract: Background: Multisystem inflammatory syndrome in children (MIS-C), linked to antecedent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, is associated with considerable morbidity. Prevention of SARS-CoV-2 infection or coronavirus disease 2019 (COVID-19) by vaccination might also decrease MIS-C likelihood. Methods: In a multicenter, case-control, public health investigation of children ages 5–18 years hospitalized from 1 July 2021 to 7 April 2022, we compared the odds of being fully vaccinated (2 doses of BNT162b2 vaccine ≥28 days before hospital admission) between MIS-C case-patients and hospital-based controls who tested negative for SARS-CoV-2. These associations were examined by age group, timing of vaccination, and periods of Delta and Omicron variant predominance using multivariable logistic regression. Results: We compared 304 MIS-C case-patients (280 [92%] unvaccinated) with 502 controls (346 [69%] unvaccinated). MIS-C was associated with decreased likelihood of vaccination (adjusted OR [aOR]: .16; 95% CI: .10–.26), including among children ages 5–11 years (aOR: .22; 95% CI: .10–.52), ages 12–18 years (aOR: .10; 95% CI: .05–.19), and during the Delta (aOR: .06; 95% CI: .02–.15) and Omicron (aOR: .22; 95% CI: .11–.42) variant-predominant periods. This association persisted beyond 120 days after the second dose (aOR: .08; 95% CI: .03–.22) in 12–18-year-olds. Among all MIS-C case-patients, 187 (62%) required intensive care unit admission and 280 (92%) vaccine-eligible case-patients were unvaccinated. Conclusions: Vaccination with 2 doses of BNT162b2 is associated with reduced likelihood of MIS-C in children ages 5–18 years. Most vaccine-eligible hospitalized patients with MIS-C were unvaccinated. Abstract : We conducted a multicenter public health investigation of hospitalized vaccine-eligible US patients ages 5–18 years comparing 304 MIS-C patients with 502 SARS-CoV-2–negative controls. BNT162b2 vaccination was associated with a decreased likelihood of MIS-C across periods of Delta and Omicron predominance. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 76:Number 3(2023)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 76:Number 3(2023)
- Issue Display:
- Volume 76, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 76
- Issue:
- 3
- Issue Sort Value:
- 2023-0076-0003-0000
- Page Start:
- e90
- Page End:
- e100
- Publication Date:
- 2022-08-20
- Subjects:
- MIS-C -- vaccine effectiveness -- Pfizer (BioNTech) -- COVID-19 -- children
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciac637 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
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