Evidence map›Paper›PMID 38656578›Full record

ArticleJAMA network open2024

Safety of Ancestral Monovalent BNT162b2, mRNA-1273, and NVX-CoV2373 COVID-19 Vaccines in US Children Aged 6 Months to 17 Years.

Mao Hu, Azadeh Shoaibi, Yuhui Feng, Patricia C Lloyd, Hui Lee Wong, Elizabeth R Smith, Kandace L Amend, Annemarie Kline, Daniel C Beachler, Joann F Gruber and 16 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 7 institutions in 1 country.

Mao HuAcumen LLC, Burlingame, California.
Azadeh ShoaibiUS Food and Drug Administration, Silver Spring, Maryland.
Yuhui FengAcumen LLC, Burlingame, California.
Patricia C LloydUS Food and Drug Administration, Silver Spring, Maryland.
Hui Lee WongUS Food and Drug Administration, Silver Spring, Maryland.
Elizabeth R SmithAcumen LLC, Burlingame, California.
Kandace L AmendOptum Epidemiology, Boston, Massachusetts.
Annemarie KlineCVS Health/Aetna, Blue Bell, Pennsylvania.
Daniel C BeachlerCarelon Research, Wilmington, Delaware.
Joann F GruberUS Food and Drug Administration, Silver Spring, Maryland.
Mahasweta MitraAcumen LLC, Burlingame, California.
John D SeegerOptum Epidemiology, Boston, Massachusetts.
Charlalynn HarrisCVS Health/Aetna, Blue Bell, Pennsylvania.
Alex SecoraIQVIA, Falls Church, Virginia.
Joyce ObidiUS Food and Drug Administration, Silver Spring, Maryland.
Jing WangAcumen LLC, Burlingame, California.
Jennifer SongOptum Epidemiology, Boston, Massachusetts.
Cheryl N McMahill-WalravenCVS Health/Aetna, Blue Bell, Pennsylvania.
Christian ReichIQVIA, Falls Church, Virginia.
Rowan McEvoyAcumen LLC, Burlingame, California.
Rose DoAcumen LLC, Burlingame, California.
Yoganand ChillarigeAcumen LLC, Burlingame, California.
Robin CliffordOptum Epidemiology, Boston, Massachusetts.
Danielle D CooperCVS Health/Aetna, Blue Bell, Pennsylvania.
Richard A ForsheeUS Food and Drug Administration, Silver Spring, Maryland.
Steven A AndersonUS Food and Drug Administration, Silver Spring, Maryland.
Acumen (United States) · USUnited States Food and Drug Administration · USAetna (United States) · USOptum (United States) · USIQVIA (United States) · USNew England College of Optometry · USWilmington University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Active monitoring of health outcomes after COVID-19 vaccination provides early detection of rare outcomes that may not be identified in prelicensure trials. Objective: To conduct near-real-time monitoring of health outcomes after COVID-19 vaccination in the US pediatric population. Design, Setting, and Participants: This cohort study evaluated 21 prespecified health outcomes after exposure before early 2023 to BNT162b2, mRNA-1273, or NVX-CoV2373 ancestral monovalent COVID-19 vaccines in children aged 6 months to 17 years by applying a near-real-time monitoring framework using health care data from 3 commercial claims databases in the US (Optum [through April 2023], Carelon Research [through March 2023], and CVS Health [through February 2023]). Increased rates of each outcome after vaccination were compared with annual historical rates from January 1 to December 31, 2019, and January 1 to December 31, 2020, as well as between April 1 and December 31, 2020. Exposure: Receipt of an ancestral monovalent BNT162b2, mRNA-1273, or NVX-CoV2373 COVID-19 vaccine dose identified through administrative claims data linked with Immunization Information Systems data. Main Outcomes and Measures: Twenty-one prespecified health outcomes, of which 15 underwent sequential testing and 6 were only monitored descriptively due to lack of historical rates. Results: Among 4 102 016 vaccinated enrollees aged 6 months to 17 years, 2 058 142 (50.2%) were male and 3 901 370 (95.1%) lived in an urban area. Thirteen of 15 sequentially tested outcomes did not meet the threshold for a statistical signal. Statistical signals were detected for myocarditis or pericarditis after BNT162b2 vaccination in children aged 12 to 17 years and seizure after vaccination with BNT162b2 and mRNA-1273 in children aged 2 to 4 or 5 years. However, in post hoc sensitivity analyses, a statistical signal for seizure was observed only after mRNA-1273 when 2019 background rates were selected; no statistical signal was observed when 2022 rates were selected. Conclusions and Relevance: In this cohort study of pediatric enrollees across 3 commercial health insurance databases, statistical signals detected for myocarditis or pericarditis after BNT162b2 (ages 12-17 years) were consistent with previous reports, and seizures after BNT162b2 (ages 2-4 years) and mRNA-1273 vaccinations (ages 2-5 years) should be further investigated in a robust epidemiologic study with confounding adjustment. The US Food and Drug Administration concludes that the known and potential benefits of COVID-19 vaccination outweigh the known and potential risks of COVID-19 infection.

Indexed as

2019-nCoV Vaccine mRNA-1273BNT162 VaccineCOVID-19COVID-19 VaccinesSARS-CoV-2AdolescentChildChild, PreschoolCohort StudiesFemaleHumansInfantMaleUnited StatesVaccination2019-nCoV Vaccine mRNA-1273BNT162 VaccineCOVID-19 Vaccines

Identifiers

PMID38656578
PMCPMC11043896
OpenAlexW4395071639

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.