Evidence map›Paper›PMID 39757926›Full record

ArticleEpidemiology and infection2025

Case-only analysis of routine surveillance data: detection of increased vaccine breakthrough infections with SARS-CoV-2 variants in Europe.

Jeremy Brown, Piers Mook, Maarten Vanhaverbeke, Amy Gimma, José Hagan, Isaac Singini, Mária Avdičová, Gillian Cullen, Liidia Dotsenko, Joël Mossong and 4 more

Abstract read
In one paragraph

Article in Epidemiology and infection, 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

14 authors.

Jeremy BrownWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.ORCID 0000-0002-9941-7759
Piers MookWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.
Maarten VanhaverbekeWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.
Amy GimmaWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.
José HaganWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.
Isaac SinginiWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.
Mária AvdičováThe Regional Authority of Public Health in Banska Bystrica, Public Health Authority of the Slovak Republic.
Gillian CullenHealth Protection Surveillance Centre, Dublin, Republic of Ireland.
Liidia DotsenkoHealth Board, Tallinn, Republic of Estonia.
Joël MossongHealth Directorate, Luxembourg, Luxembourg.
Malgorzata Sadkowska-TodysNational Institute of Public Health NIH - National Research Institute, Warsaw, Poland.
Heelene SuijaHealth Board, Tallinn, Republic of Estonia.
Nick BundleEuropean Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.
Richard PebodyWorld Health Organization (WHO) Regional Office for Europe, Copenhagen, Denmark.

Funding

CDC HHS NU511P000936-02-020World Health Organization 001
6 · The paper itself

Abstract

With the ongoing emergence of SARS-CoV-2 variants, there is a need for standard approaches to characterize the risk of vaccine breakthrough. We aimed to estimate the association between variant and vaccination status in case-only surveillance data. Included cases were symptomatic adult laboratory-confirmed COVID-19 cases, with onset between January 2021 and April 2022, reported by five European countries (Estonia, Ireland, Luxembourg, Poland, and Slovakia) to The European Surveillance System. Associations between variant and vaccination status were estimated using conditional logistic regression, within strata of country and calendar date, and adjusting for age and sex. We included 80,143 cases including 20,244 Alpha (B.1.1.7), 152 Beta (B.1.351), 39,900 Delta (B.1.617.2), 361 Gamma (P.1), 10,014 Omicron BA.1, and 9,472 Omicron BA.2. Partially vaccinated cases were more likely than unvaccinated cases to be Beta than Alpha (adjusted odds ratio [aOR] 2.48, 95% CI 1.29-4.74), and Delta than Alpha (aOR 1.75, 1.31-2.34). Fully vaccinated cases were relative to unvaccinated cases more frequently Beta than Alpha (aOR 4.61, 1.89-11.21), Delta than Alpha (aOR 2.30, 1.55-3.39), and Omicron BA.1 than Delta (aOR 1.91, 1.60-2.28). We found signals of increased breakthrough infections for Delta and Beta relative to Alpha, and Omicron BA.1 relative to Delta.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2AdolescentAdultAgedAged, 80 and overBreakthrough InfectionsEuropeFemaleHumansMaleMiddle AgedVaccinationYoung AdultCOVID-19 Vaccines

Identifiers

PMID39757926
PMCPMC11748014

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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.