Evidence map›Paper›PMID 39460274›Full record

ArticleVaccines2024

Comparative Effectiveness of the Bivalent (Original/Omicron BA.4/BA.5) mRNA COVID-19 Vaccines mRNA-1273.222 and BNT162b2 Bivalent in Adults with Underlying Medical Conditions in the United States.

Hagit Kopel, Van Hung Nguyen, Alina Bogdanov, Isabelle Winer, Catherine Boileau, Thierry Ducruet, Ni Zeng, Jessamine P Winer-Jones, Daina B Esposito, Mary Bausch-Jurken and 3 more

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  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

13 authors.

Hagit KopelModerna, Inc., Cambridge, MA 02139, USA.
Van Hung NguyenVHN Consulting Inc., Montreal, QC H2V 3L8, Canada.
Alina BogdanovVeradigm, Chicago, IL 60654, USA.
Isabelle WinerVeradigm, Chicago, IL 60654, USA.
Catherine BoileauVHN Consulting Inc., Montreal, QC H2V 3L8, Canada.
Thierry DucruetVHN Consulting Inc., Montreal, QC H2V 3L8, Canada.
Ni ZengVeradigm, Chicago, IL 60654, USA.
Jessamine P Winer-JonesVeradigm, Chicago, IL 60654, USA.ORCID 0000-0002-6412-4139
Daina B EspositoModerna, Inc., Cambridge, MA 02139, USA.
Mary Bausch-JurkenModerna, Inc., Cambridge, MA 02139, USA.
Ekkehard BeckModerna, Inc., Cambridge, MA 02139, USA.ORCID 0000-0002-2022-9190
Machaon BonafedeVeradigm, Chicago, IL 60654, USA.
James A MansiModerna, Inc., Cambridge, MA 02139, USA.ORCID 0000-0001-7650-6778

Funding

Moderna Therapeutics (United States) N/A
6 · The paper itself

Abstract

BACKGROUND/

objectivesThis retrospective cohort study evaluated the relative vaccine effectiveness (rVE) of two bivalent (original/Omicron BA.4/BA.5) vaccines mRNA-1273.222 versus the BNT162b2 Bivalent in preventing COVID-19-related outcomes in adults with underlying medical conditions associated with increased risk for severe COVID-19.

methodsIn a linked electronic health record/claims dataset, US adults (≥18 years) with ≥1 underlying medical condition of interest who received either the bivalent vaccine between 31 August 2022 and 28 February 2023 were identified. The inverse probability of treatment weighting was used to adjust for cohort differences. Cohorts were followed up for COVID-19-related hospitalizations and outpatient encounters until 31 May 2023. Hazard ratios and rVEs were estimated using Cox regression. Subgroup analyses were performed on individuals with pre-specified comorbid conditions.

results757,572 mRNA-1273.222 and 1,204,975 BNT162b2 Bivalent recipients were identified. The adjusted rVE over a median follow-up of 198 days was 10.9% (6.2%-15.2%) against COVID-19-related hospitalization and 3.2% (1.7%-4.7%) against COVID-19-related outpatient encounters. rVE estimates for COVID-19 hospitalizations among subgroups with comorbid conditions were as follows: diabetes 15.1% (8.7%-21.0%), cerebro- and cardiovascular disease 14.7% (9.0%-20.1%), chronic lung disease 11.9% (5.1%-18.2%), immunocompromised 15.0% (7.2%-22.2%), chronic kidney disease 8.4% (0.5%-15.7%).

conclusionsOverall, among adults with underlying medical conditions, mRNA-1273.222 was more effective than BNT162b2 Bivalent, especially in preventing COVID-19-related hospitalizations.

Indexed as

BNT162b2comorbiditiesCOVID-19high riskmRNA-1273rVEvaccine

Identifiers

PMID39460274
PMCPMC11511346

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.