Evidence map›Paper›PMID 39405261›Full record

ArticleThe Journal of infectious diseases2025

Effectiveness of the Original Monovalent Messenger RNA Coronavirus Disease 2019 (COVID-19) Vaccination Series Against Hospitalization for COVID-19-Associated Venous Thromboembolism.

David N Hager, Yuwei Zhu, Ine Sohn, William B Stubblefield, Michael B Streiff, Manjusha Gaglani, Jay S Steingrub, Abhijit Duggal, Jamie R Felzer, Mary O'Rourke and 14 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

David N HagerDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-5148-4872
Yuwei ZhuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Ine SohnDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0009-0001-0702-1416
William B StubblefieldDepartment of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0003-3817-1414
Michael B StreiffDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Manjusha GaglaniBaylor Scott and White Health, Baylor College of Medicine-Temple, Texas A&M University College of Medicine, Temple, Texas, USA.ORCID 0000-0002-3952-9230
Jay S SteingrubDepartment of Medicine, Baystate Medical Center, Springfield, Massachusetts, USA.
Abhijit DuggalDepartment of Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Jamie R FelzerDepartment of Medicine, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-9317-950X
Mary O'RourkeDepartment of Emergency Medicine and Medicine, Hennepin County Medical Center, Minneapolis, Minnesota, USA.ORCID 0009-0004-2379-0743
Ithan D PeltanDepartment of Medicine, Intermountain Medical Center, Murray, Utah, USA.ORCID 0000-0003-1730-234X
Amira MohamedDepartment of Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0009-0002-8381-1265
Robin StillerDivision of Pulmonary, Allergy and Critical Care Medicine, Oregon Health and Sciences University, Portland, Oregon, USA.ORCID 0000-0002-7896-1608
Jennifer G WilsonDepartment of Emergency Medicine, Stanford University School of Medicine, Stanford, California, USA.ORCID 0000-0002-4254-8475
Nida QadirDepartment of Medicine, University of California-Los Angeles, Los Angeles, California, USA.ORCID 0000-0001-7791-049X
Adit A GindeDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA.
Anne E ZepeskiDepartment of Emergency Medicine, University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0001-6309-6554
Christopher MallowDepartment of Medicine, University of Miami, Miami, Florida, USA.ORCID 0000-0002-8211-7629
Adam S LauringDepartments of Internal Medicine and Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-2906-8335
Nicholas J JohnsonDepartment of Emergency Medicine and Division of Pulmonary, Critical Care and Sleep Medicine, University of Washington, Seattle, Washington, USA.
Kevin W GibbsDepartment of Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0002-5272-2289
Jennie H KwonDepartment of Medicine, Washington University, St. Louis, Missouri, USA.ORCID 0009-0007-9774-6835
Wesley H SelfDepartment of Emergency Medicine and Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-9300-3045
Investigating Respiratory Viruses in the Acutely Ill (IVY) Network

Funding

Clinical and Translational Training Program in Pulmonary MedicineT32HL087738 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lorraine B Ware · 2007 to 2026
$7.0M
Measuring and Learning from Care Variation in SepsisR35GM151147 · NIGMS · IHC HEALTH SERVICES, INC. · PI Ithan Daniel Peltan · 2023 to 2026
$1.5M
NHLBI NIH HHS T32 HL087738NIGMS NIH HHS R35 GM151147US Centers for Disease Control and Prevention 75D30119C05670
6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19) is a strong risk factor for venous thromboembolism (VTE). Few studies have evaluated the effectiveness of COVID-19 vaccination in preventing hospitalization for COVID-19 with VTE.

methodsAdults hospitalized at 21 sites between March 2021 and October 2022 with symptoms of acute respiratory illness were assessed for COVID-19, completion of the original monovalent messenger RNA (mRNA) COVID-19 vaccination series, and VTE. Prevalence of VTE was compared between unvaccinated and vaccinated patients with COVID-19. The vaccine effectiveness (VE) in preventing COVID-19 hospitalization with VTE was calculated using a test-negative design. The VE was also stratified by predominant circulating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant.

resultsAmong 18 811 patients (median age [interquartile range], 63 [50-73] years; 49% women; 59% non-Hispanic white, 20% non-Hispanic black, and 14% Hispanic; and median of 2 comorbid conditions [interquartile range, 1-3]), 9792 were admitted with COVID-19 (44% vaccinated), and 9019 were test-negative controls (73% vaccinated). Among patients with COVID-19, 601 had VTE diagnosed by hospital day 28, of whom 170 were vaccinated. VTE was more common among unvaccinated than vaccinated patients with COVID-19 (7.8% vs 4.0%; P = .001). The VE against COVID-19 hospitalization with VTE was 84% overall (95% confidence interval, 80%-87%), and VE stratified by predominant circulating variant was 88% (73%-95%) for Alpha, 93% (90%-95%) for Delta, and 68% (58%-76%) for Omicron variants.

conclusionsVaccination with the original monovalent mRNA series was associated with a decrease in COVID-19 hospitalization with VTE, though data detailing prior history of VTE and use of anticoagulation were not available. These findings will inform risk-benefit considerations for those considering vaccination.

Indexed as

COVID-19COVID-19 VaccinesHospitalizationVaccine EfficacyVenous ThromboembolismAgedFemaleHumansMaleMiddle AgedSARS-CoV-2VaccinationCOVID-19 VaccinesCOVID-19SARS-CoV-2vaccinevenous thromboembolism

Identifiers

PMID39405261
PMCPMC12063076

What OpenQuestion holds

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Registered trials

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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.