Evidence map›Paper›PMID 35458532›Full record

ArticleViruses2022

Incidence and Risk Factors of COVID-19 Vaccine Breakthrough Infections: A Prospective Cohort Study in Belgium.

Veerle Stouten, Pierre Hubin, Freek Haarhuis, Joris A F van Loenhout, Matthieu Billuart, Ruben Brondeel, Toon Braeye, Herman Van Oyen, Chloé Wyndham-Thomas, Lucy Catteau

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 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

10 authors at 1 institution in 1 country.

Veerle StoutenDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.ORCID 0000-0002-0162-2202
Pierre HubinDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Freek HaarhuisDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Joris A F van LoenhoutDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Matthieu BilluartDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.ORCID 0000-0002-4805-9242
Ruben BrondeelDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.ORCID 0000-0002-9876-4150
Toon BraeyeDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Herman Van OyenDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Chloé Wyndham-ThomasDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Lucy CatteauDepartment of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Sciensano (Belgium) · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to investigate the incidence and risk factors associated with COVID-19 vaccine breakthrough infections. We included all persons ≥18 years that had been fully vaccinated against COVID-19 for ≥14 days, between 1 February 2021 and 5 December 2021, in Belgium. The incidence of breakthrough infections (laboratory confirmed SARS-CoV-2-infections) was determined. Factors associated with breakthrough infections were analyzed using COX proportional hazard models. Among 8,062,600 fully vaccinated adults, we identified 373,070 breakthrough infections with an incidence of 11.2 (95%CI 11.2-11.3)/100 person years. Vaccination with Ad26.COV2.S (HR1.54, 95%CI 1.52-1.56) or ChAdOx1 (HR1.68, 95%CI 1.66-1.69) was associated with a higher risk of a breakthrough infection compared to BNT162b2, while mRNA-1273 was associated with a lower risk (HR0.68, 95%CI 0.67-0.69). A prior COVID-19-infection was protective against a breakthrough infection (HR0.23, 95%CI 0.23-0.24), as was an mRNA booster (HR0.44, 95%CI 0.43-0.45). During a breakthrough infection, those who had a prior COVID-19 infection were less likely to have COVID-19 symptoms of almost all types than naïve persons. We identified risk factors associated with breakthrough infections, such as vaccination with adenoviral-vector vaccines, which could help inform future decisions on booster vaccination strategies. A prior COVID-19 infection lowered the risk of breakthrough infections and of having symptoms, highlighting the protective effect of hybrid immunity.

Indexed as

COVID-19COVID-19 VaccinesAd26COVS1AdultBelgiumBNT162 VaccineBreakthrough InfectionsHumansIncidenceProspective StudiesRisk FactorsSARS-CoV-2Ad26COVS1BNT162 VaccineCOVID-19 Vaccinesbreakthrough infectionCOVID-19hybrid immunitymRNA booster vaccinemRNA vaccinesSARS-CoV-2symptomsvaccinationviral vector vaccines

Identifiers

PMID35458532
PMCPMC9029338
OpenAlexW4223972323

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.