Evidence map›Paper›PMID 42334917›Full record

ArticleJAMA network open2026

Interim Estimated Effectiveness of 2025-2026 COVID-19 Vaccines in Adults Using a Test-Negative Design.

Ryan E Wiegand, Sean Chickery, Duck-Hye Yang, Sarah W Ball, Malini B DeSilva, Kristin Dascomb, Stephanie A Irving, Karthik Natarajan, Nicola P Klein, Shaun J Grannis and 27 more

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

37 authors.

Ryan E WiegandNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Sean ChickeryWestat, Bethesda, Maryland.
Duck-Hye YangWestat, Bethesda, Maryland.
Sarah W BallWestat, Bethesda, Maryland.
Malini B DeSilvaHealthPartners Institute, Minneapolis, Minnesota.
Kristin DascombDivision of Infectious Diseases and Clinical Epidemiology, Intermountain Health, Salt Lake City, Utah.
Stephanie A IrvingKaiser Permanente Center for Health Research, Portland, Oregon.
Karthik NatarajanDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York.
Nicola P KleinKaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
Shaun J GrannisCenter for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
Toan C OngSchool of Medicine, University of Colorado Anschutz Medical Campus, Aurora.
Elizabeth A K RowleyWestat, Bethesda, Maryland.
Adam YatesWestat, Bethesda, Maryland.
Yan ZhuangWestat, Bethesda, Maryland.
Sarah WilsonWestat, Bethesda, Maryland.
Charlene E McEvoyHealthPartners Institute, Minneapolis, Minnesota.
Inih J EssienHealthPartners Institute, Minneapolis, Minnesota.
Omobosola O AkinseteHealthPartners Institute, Minneapolis, Minnesota.
Allison L NalewayKaiser Permanente Center for Health Research, Portland, Oregon.
Padma KoppoluKaiser Permanente Center for Health Research, Portland, Oregon.
Ousseny ZerboKaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
John R HansenKaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
Karen B JacobsonKaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
Lawrence BlockKaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
Brian E DixonCenter for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
Thomas DuszynskiCenter for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
Colin RogersonCenter for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
Michelle A BarronSchool of Medicine, University of Colorado Anschutz Medical Campus, Aurora.
Catia ChavezSchool of Medicine, University of Colorado Anschutz Medical Campus, Aurora.
Josephine MakNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Allison Avrich CieslaNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Monica GodfreyNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Amber KautzNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Morgan NajdowskiNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Ruth Link-GellesNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jennifer DeCuirNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Amanda B PayneNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The 2025-2026 COVID-19 vaccine, targeting JN.1 and JN.1-derived sublineages, became available in the US in September 2025. Objective: To assess the estimated interim effectiveness of 2025-2026 COVID-19 vaccines against medically attended COVID-19 among immunocompetent adults aged 18 years or older in the US. Design, Setting, and Participants: This case-control study used a test-negative design to investigate patient encounters captured in the Virtual SARS-CoV-2, Influenza, and Other Respiratory Viruses Network, an electronic medical record-based network of health care systems (253 emergency departments/urgent cares [ED/UCs] and 179 hospitals in 7 states) from September 3, 2025, to December 31, 2025. Patient encounters with COVID-19-like illness and a molecular or antigen SARS-CoV-2 test 10 days before to 3 days after the encounter date were included. Exposure: 2025-2026 COVID-19 vaccination regardless of prior COVID-19 vaccination. Main Outcomes and Measures: The main outcomes were COVID-19-associated ED/UC encounters and COVID-19-associated hospitalizations. Cases were defined as encounters with a positive molecular or antigen SARS-CoV-2 test and controls as encounters with a negative molecular SARS-CoV-2 test. The odds of 2025-2026 COVID-19 vaccination among cases and controls, adjusting for confounders, were compared and used to estimate vaccine effectiveness (VE) as (1 - adjusted odds ratio) × 100%. Results: In 85 725 ED/UC encounters among adults aged 18 years and older (51 841 [60%] aged 18-64 years; 51 775 female [60%]), 206 of 3941 cases (5%) and 9453 of 81 784 controls (12%) received a 2025-2026 COVID-19 vaccination. Estimated VE against COVID-19-associated ED/UC encounters was 50% (95% CI, 42%-57%; median [IQR] time since 2025-2026 COVID-19 vaccine dose receipt, 47 [27-69] days). In 26 073 hospitalizations with a COVID-19-like illness (17 530 [67%] aged ≥65 years; 13 985 female [54%]), 60 of 1022 cases (6%) received a 2025-2026 COVID-19 vaccination compared with 3080 of 25 051 controls (12%). Estimated VE against COVID-19-associated hospitalization was 55% (95% CI, 41%-66%; median [IQR] time since 2025-2026 COVID-19 vaccine dose receipt, 46 [26-68] days). Among patients aged 65 years or older, estimated VE against ED/UC encounters was 48% (95% CI, 37%-56%; median [IQR] time since dose receipt, 48 [27-69] days; 33 884 encounters) and against hospitalization was 53% (95% CI, 37%-65%; median [IQR] time since dose receipt, 46 [26-69] days; 17 530 hospitalizations). Conclusions and Relevance: In this study, receipt of 2025-2026 COVID-19 vaccination was associated with additional protection beyond existing immunity in adults against medically attended COVID-19, including ED/UC encounters and hospitalizations, compared with no receipt of a 2025-2026 vaccine dose. These findings suggest that adults can reduce their likelihood of severe COVID-19-associated outcomes by obtaining a 2025-2026 COVID-19 vaccination.

Indexed as

COVID-19COVID-19 VaccinesVaccine EfficacyAdolescentAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedSARS-CoV-2United StatesYoung AdultCOVID-19 Vaccines

Identifiers

PMID42334917
PMCPMC13291846

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.