Evidence map›Paper›PMID 35511586›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant.

Adeel A Butt, Victor B Talisa, Obaid S Shaikh, Saad B Omer, Florian B Mayr

Open access · hybridAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 3 pooled it
4.7field-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

29 citing papers in PubMed, 3 syntheses or guidelines pooled it, 48 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Adeel A ButtVA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-1118-1826
Victor B TalisaVA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA.
Obaid S ShaikhVA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA.
Saad B OmerYale Institute for Global Health, Yale University, New Haven, Connecticut, USA.
Florian B MayrVA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · USCornell University · USYale University · US

Funding

A precision medicine framework to improve long-term outcomes in Sepsis SurvivorsK23GM132688 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MAYR, FLORIAN · 2019 to 2022
$749k
NIGMS NIH HHS K23 GM132688
6 · The paper itself

Abstract

backgroundThe current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may be less effective against the Omicron variant than against earlier variants. With recent resurgence of SARS-CoV-2 cases, the role of booster doses of the vaccine needs to be highlighted.

methodsUsing a retrospective cohort study design emulating a target trial, we determined the relative vaccine effectiveness (RVE) of a homologous booster dose of a SARS-CoV-2 messenger RNA (mRNA) vaccine compared with the primary vaccine series alone in preventing infection, hospitalization, and intensive care unit admission, and death in the Department of Veterans Affairs healthcare system in the United States. Among infection-free survivors who received 2 doses of a mRNA vaccine before 30 April 2021, we identified those who received a booster between 22 September and 25 December 2021 and matched them 1:1 with individuals who did not receive a booster.

resultsAmong 2 384 272 previously uninfected persons with 2 doses of an mRNA vaccine by 30 April 2021, we identified 462 950 booster recipients between 22 September and 25 December 2021, who were matched 1:1 with non-booster recipients. The RVE (95% confidence interval) was 19% (17%-22%) for confirmed infection, 52% (46%-57%) for hospitalization, and 83% (65%-92%) for intensive care unit admission or death. Recipients of the mRNA-1273 vaccine had a lower cumulative incidence of infections and hospitalizations than recipients of the BNT162b2 vaccine (log-rank P <.001 for both comparisons).

conclusionsWhile the RVE of SARS-CoV-2 mRNA booster vaccine dose in preventing infection against the Omicron variant is low, it is substantial in preventing hospitalization and high in preventing the most severe/critical disease.

Indexed as

COVID-19Vaccines2019-nCoV Vaccine mRNA-1273BNT162 VaccineCOVID-19 VaccinesHumansRetrospective StudiesRNARNA, MessengerSARS-CoV-2Vaccine Efficacy2019-nCoV Vaccine mRNA-1273BNT162 VaccineCOVID-19 VaccinesRNARNA, MessengerVaccinesboosterDelta variantOmicron variantSARS-CoV-2vaccine effectiveness

Identifiers

PMID35511586
PMCPMC11487159
OpenAlexW4226307229

What OpenQuestion holds

Textmetadata
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.