Evidence map›Paper›PMID 38341293›Full record

ArticleVaccine2024

COVID-19 Vaccine Safety Technical (VaST) Work Group: Enhancing vaccine safety monitoring during the pandemic.

Lauri E Markowitz, Robert H Hopkins, Karen R Broder, Grace M Lee, Kathryn M Edwards, Matthew F Daley, Lisa A Jackson, Jennifer C Nelson, Laura E Riley, Veronica V McNally and 18 more

Abstract read
In one paragraph

Article in Vaccine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

28 authors.

Lauri E MarkowitzNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA. Electronic address: lem2@cdc.gov.
Robert H HopkinsNational Vaccine Advisory Committee, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Karen R BroderImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Grace M LeeStanford University School of Medicine, Stanford, CA, USA.
Kathryn M EdwardsVanderbilt University School of Medicine, Nashville, TN, USA.
Matthew F DaleyInstitute for Health Research, Kaiser Permanente Colorado, Denver, CO, USA.
Lisa A JacksonKaiser Permanente Washington Health Research Institute, Seattle, WA, USA.
Jennifer C NelsonKaiser Permanente Washington Health Research Institute, Seattle, WA, USA.
Laura E RileyWeill Cornell School of Medicine, New York, NY, USA.
Veronica V McNallyFranny Strong Foundation, West Bloomfield, MI, USA.
Robert SchechterAssociation of Immunization Managers, California Department of Public Health, Richmond, CA, USA.
Patricia N Whitley-WilliamsRutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Francesca CunninghamDepartment of Veterans Affairs, Veterans Affairs Center for Medication Safety - Pharmacy Benefit Management Services, Hines, IL, USA.
Matthew ClarkIndian Health Service (IHS), IHS National Pharmacy & Therapeutics Committee, Anchorage, AK, USA.
Margaret RyanDefense Health Agency, Immunization Healthcare Division, San Diego, CA, USA.
Karen M FarizoOffice of Vaccines Research and Review, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.
Hui-Lee WongOffice of Biostatistics and Pharmacovigilance, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.
Jeffery KelmanCenters for Medicare & Medicaid Services, Baltimore, MD, USA.
Tatiana BeresnevNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Valerie MarshallOffice of the Assistant Secretary for Health, Department of Health and Human Services, Washington, DC, USA.
David K ShayImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Julianne GeeImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Jared WooImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Michael M McNeilImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
John R SuImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Tom T ShimabukuroImmunization Safety Office, National Center for Emerging Zoonotic Infectious Diseases, CDC, Atlanta, GA, USA.
Melinda WhartonNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.
H Keipp TalbotVanderbilt University School of Medicine, Nashville, TN, USA.

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

During the COVID-19 pandemic, candidate COVID-19 vaccines were being developed for potential use in the United States on an unprecedented, accelerated schedule. It was anticipated that once available, under U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA) or FDA approval, COVID-19 vaccines would be broadly used and potentially administered to millions of individuals in a short period of time. Intensive monitoring in the post-EUA/licensure period would be necessary for timely detection and assessment of potential safety concerns. To address this, the Centers for Disease Control and Prevention (CDC) convened an Advisory Committee on Immunization Practices (ACIP) work group focused solely on COVID-19 vaccine safety, consisting of independent vaccine safety experts and representatives from federal agencies - the ACIP COVID-19 Vaccine Safety Technical Work Group (VaST). This report provides an overview of the organization and activities of VaST, summarizes data reviewed as part of the comprehensive effort to monitor vaccine safety during the COVID-19 pandemic, and highlights selected actions taken by CDC, ACIP, and FDA in response to accumulating post-authorization safety data. VaST convened regular meetings over the course of 29 months, from November 2020 through April 2023; through March 2023 FDA issued EUAs for six COVID-19 vaccines from four different manufacturers and subsequently licensed two of these COVID-19 vaccines. The independent vaccine safety experts collaborated with federal agencies to ensure timely assessment of vaccine safety data during this time. VaST worked closely with the ACIP COVID-19 Vaccines Work Group; that work group used safety data and VaST's assessments for benefit-risk assessments and guidance for COVID-19 vaccination policy. Safety topics reviewed by VaST included those identified in safety monitoring systems and other topics of scientific or public interest. VaST provided guidance to CDC's COVID-19 vaccine safety monitoring efforts, provided a forum for review of data from several U.S. government vaccine safety systems, and assured that a diverse group of scientists and clinicians, external to the federal government, promptly reviewed vaccine safety data. In the event of a future pandemic or other biological public health emergency, the VaST model could be used to strengthen vaccine safety monitoring, enhance public confidence, and increase transparency through incorporation of independent, non-government safety experts into the monitoring process, and through strong collaboration among federal and other partners.

Indexed as

Centers for Disease Control and Prevention, U.S.COVID-19COVID-19 VaccinesAdvisory CommitteesHumansPandemicsUnited StatesUnited States Food and Drug AdministrationCOVID-19 VaccinesCOVID-19 vaccinesEmergency Use AuthorizationVaccine safety

Identifiers

PMID38341293
PMCPMC11310362

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.