Evidence map›Paper›PMID 36851257›Full record

ArticleVaccines2023

Homologous and Heterologous Prime-Boost Vaccination: Impact on Clinical Severity of SARS-CoV-2 Omicron Infection among Hospitalized COVID-19 Patients in Belgium.

Marjan Meurisse, Lucy Catteau, Joris A F van Loenhout, Toon Braeye, Laurane De Mot, Ben Serrien, Koen Blot, Emilie Cauët, Herman Van Oyen, Lize Cuypers and 4 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

14 authors at 4 institutions in 1 country.

Marjan MeurisseDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.ORCID 0000-0002-4409-0664
Lucy CatteauDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Joris A F van LoenhoutDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Toon BraeyeDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Laurane De MotDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Ben SerrienDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Koen BlotDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Emilie CauëtDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.
Herman Van OyenDepartment of Public Health and Primary Care, Ghent University, 9000 Ghent, Belgium.
Lize CuypersDepartment of Laboratory Medicine, National Reference Center for Respiratory Pathogens, University Hospitals Leuven, 3000 Leuven, Belgium.ORCID 0000-0002-9433-8752
Belgian Collaborative Group On Covid-Hospital Surveillance
Covid-Genomics Belgium Consortium
Annie RobertDepartment of Epidemiology and Biostatistics, Institut de Recherche Expérimentale et Clinique, Faculty of Public Health, Université Catholique de Louvain, 1200 Woluwe-Saint-Lambert, Belgium.ORCID 0000-0003-3720-7331
Nina Van GoethemDepartment of Epidemiology and public health, Sciensano, 1070 Brussels, Belgium.ORCID 0000-0001-7316-6990
Sciensano (Belgium) · BEGhent University · BEKU Leuven · BEUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated effectiveness of (1) mRNA booster vaccination versus primary vaccination only and (2) heterologous (viral vector-mRNA) versus homologous (mRNA-mRNA) prime-boost vaccination against severe outcomes of BA.1, BA.2, BA.4 or BA.5 Omicron infection (confirmed by whole genome sequencing) among hospitalized COVID-19 patients using observational data from national COVID-19 registries. In addition, it was investigated whether the difference between the heterologous and homologous prime-boost vaccination was homogenous across Omicron sub-lineages. Regression standardization (parametric g-formula) was used to estimate counterfactual risks for severe COVID-19 (combination of severity indicators), intensive care unit (ICU) admission, and in-hospital mortality under exposure to different vaccination schedules. The estimated risk for severe COVID-19 and in-hospital mortality was significantly lower with an mRNA booster vaccination as compared to only a primary vaccination schedule (RR = 0.59 [0.33; 0.85] and RR = 0.47 [0.15; 0.79], respectively). No significance difference was observed in the estimated risk for severe COVID-19, ICU admission and in-hospital mortality with a heterologous compared to a homologous prime-boost vaccination schedule, and this difference was not significantly modified by the Omicron sub-lineage. Our results support evidence that mRNA booster vaccination reduced the risk of severe COVID-19 disease during the Omicron-predominant period.

Indexed as

clinical severityCOVID-19 vaccinationSARS-CoV-2 variants

Identifiers

PMID36851257
PMCPMC9961733
OpenAlexW4319598679

What Socratic 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 Socratic graph.