Evidence map›Paper›PMID 35773122›Full record

ArticleVaccine2022

Relative effectiveness of booster vs. 2-dose mRNA Covid-19 vaccination in the Veterans Health Administration: Self-controlled risk interval analysis.

Caroline Korves, Hector S Izurieta, Jeremy Smith, Gabrielle M Zwain, Ethan I Powell, Abirami Balajee, Kathryn M Ryder, Yinong Young-Xu

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 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

8 authors at 3 institutions in 1 country.

Caroline KorvesWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA. Electronic address: caroline.korves@va.gov.
Hector S IzurietaOffice of Vaccines Research and Review, Center for Biologics Evaluation and Research, United States Food and Drug Administration, White Oak, MD USA. Electronic address: hector.izurieta@fda.hhs.gov.
Jeremy SmithWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA. Electronic address: jeremy.smith5@va.gov.
Gabrielle M ZwainWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA. Electronic address: gabrielle.zwain@va.gov.
Ethan I PowellWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA. Electronic address: ethan.powell@va.gov.
Abirami BalajeeWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA. Electronic address: abriami.balajee@va.gov.
Kathryn M RyderVeterans Affairs Pacific Island Health Care, Honolulu, HI USA. Electronic address: kathryn.ryder@va.gov.
Yinong Young-XuWhite River Junction Veterans Affairs Medical Center, White River Junction, VT USA; Geisel School of Medicine at Dartmouth, Hanover, NH USA. Electronic address: yinong.young-xu@va.gov.
White River Junction VA Medical Center · USUnited States Food and Drug Administration · USVA Pacific Islands Health Care System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo estimate relative effectiveness of the booster mRNA Covid-19 vaccination versus the 2-dose primary series for both Delta and Omicron variants with self-controlled study design.

methodsWe used the Veterans Health Administration (VHA) Corporate Data Warehouse to identify U.S. Veterans who received the 2-dose primary mRNA Covid-19 vaccine series and a mRNA Covid-19 booster, and who had a positive SARS-CoV-2 test during the Delta (9/23/2021-11/30/2021) or Omicron (1/1/22-3/19/22) predominant period. Among them, we conducted a self-controlled risk interval (SCRI) analysis to compare odds of SARS-CoV-2 infection during a booster exposure interval versus a control interval. Exposures were a control interval (days 4-6 post-booster vaccination, presumably prior to gain of booster immunity), and booster exposure interval (days 14-16 post-booster vaccination, presumably following gain of booster immunity). Cases had a positive PCR or antigen SARS-CoV-2 test. Separately for Delta and Omicron periods, we used conditional logistic regression to calculate odds ratios (OR) of a positive test for the booster versus control interval and calculated relative effectiveness of booster versus 2-dose primary series as (1-OR)*100. The SCRI approach implicitly controlled for time-fixed confounders.

resultsWe found 42 individuals with a positive SARS-CoV-2 test in the control interval and 14 in the booster exposure interval during the Delta period, and 141 and 70, respectively, in the Omicron period. For the booster versus 2-dose primary series, the odds of infection were 70% (95 %CI: 42%, 84%) lower during the Delta period and 54% (95 %CI: 38%, 66%) lower during Omicron. In sensitivity analyses among those with prior Covid-19 history, and age stratification, ORs were similar to the main analysis.

conclusionsBooster vaccination was more effective relative to a 2-dose primary series during the Delta and Omicron predominant periods, and the relative effectiveness was consistent across age groups.

Indexed as

COVID-19COVID-19 VaccinesHumansImmunization, SecondaryRNA, MessengerSARS-CoV-2VaccinationVeterans HealthCOVID-19 VaccinesRNA, Messenger(Maximum 6): Covid-19SARS-CoV-2Self-controlled case seriesVaccine effectiveness

Identifiers

PMID35773122
PMCPMC9212417
OpenAlexW4283213568

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.