Evidence map›Paper›PMID 41801614›Full record

ArticleJournal of epidemiology and global health2026

Changing Prevalence of Immunocompromising Conditions in Patients Hospitalized with Severe Acute Respiratory Infection in Europe: Insights from the COVIDRIVE Study.

Wilhelmine Meeraus, Ivana Prokić, J Gabrielle Breugelmans, Konstantina Chatzikonstantinidou, Eduardo Conde-Sousa, Irma Casas, Wendy Hartig-Merkel, Gerrit Luit Ten Kate, Sandra Manzanares-Laya, Charlotte Martin and 6 more

Abstract read
In one paragraph

Article in Journal of epidemiology and global health, 2026. 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

16 authors.

Wilhelmine MeerausMedical Evidence, Vaccines & Immune Therapies, AstraZeneca, Cambridge, UK. wilhelmine.meeraus@astrazeneca.com.
Ivana ProkićP95 Clinical and Epidemiology Services, Leuven, Belgium.
J Gabrielle BreugelmansCoalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
Konstantina ChatzikonstantinidouP95 Clinical and Epidemiology Services, Leuven, Belgium.
Eduardo Conde-SousaP95 Clinical and Epidemiology Services, Leuven, Belgium.
Irma CasasServicio de Medicina Preventiva, German Trias i Pujol University Hospital, Barcelona, Spain.
Wendy Hartig-MerkelP95 Clinical and Epidemiology Services, Leuven, Belgium.
Gerrit Luit Ten KateDepartment of infectious diseases and internal medicine, University Hospital Antwerp, Edegem, Belgium.
Sandra Manzanares-LayaP95 Clinical and Epidemiology Services, Leuven, Belgium.
Charlotte MartinInfectious Diseases Department, Université Libre de Bruxelles, Centre Hospitalier Universitaire Saint-Pierre, Brussels, Belgium.
Andrea OrsiInteruniversity Research Center on Influenza and Other Transmissible Infections (CIRI- IT), Genoa, Italy.
Susana Otero RomeroServicio de Medicina Preventiva y Epidemiología, Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Campus Hospitalari, Barcelona, Spain.
Sudhir VenkatesanBPM Evidence Statistics, Biopharmaceuticals Medical, AstraZeneca, Cambridge, UK. sudhir.venkatesan@astrazeneca.com.
Marc-Alain WiddowsonInstitute Of Tropical Medicine, Antwerp, Belgium.
Kaatje BollaertsP95 Clinical and Epidemiology Services, Leuven, Belgium.
Sylvia TaylorMedical Evidence, Vaccines & Immune Therapies, AstraZeneca, Cambridge, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunocompromised individuals are at substantially increased risk of severe acute respiratory infection (SARI), often compounded by inadequate response to vaccination. We assessed the prevalence of immunocompromising conditions (ICs) among hospitalized SARI patients, overall and by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) status, focusing on temporal trends during the coronavirus disease 2019 (COVID-19) pandemic. We hypothesized that IC prevalence among SARS-CoV-2-positive SARI patients may have increased over time due to increasing background rates of SARS-CoV-2 exposure and differential vaccination coverage and efficacy among those with IC.

methodsWe conducted a secondary data analysis of 5280 adults (≥ 18 years) hospitalized with SARI, enrolled in the COVIDRIVE study from five hospitals in Belgium, Italy, and Spain (June 2021-May 2023) and tested for SARS-CoV-2 by reverse transcription-polymerase chain reaction (RT-PCR). IC prevalence (including 95% confidence intervals [CIs)] was assessed using two definitions (main and alternative), excluding and including cancer patients. Changes in IC prevalence over time were assessed using linear trend analysis.

resultsAmong the 5280 SARI cases, IC prevalence by main definition was 13.9% (95% CI: 12.9–14.8) overall, increasing from 8.3% (95% CI: 3.7–15.8) to a peak of 22.0% (95% CI: 17.9–26.4) in Q3 2022; by alternative definition, IC prevalence was 28.8% (95% CI: 27.6–30.0) overall, increasing from 18.8% (95% CI: 11.5–28.0) to a peak of 38.5% (95% CI: 32.7–44.5) in Q2 2023. Among the 1924 SARS-CoV-2-positive cases, IC prevalence by main definition was 14.2% (95% CI: 12.7–15.9) overall, increasing from 3.4% (95% CI: 0.1–17.8) to a peak of 23.8% (95% CI: 17.4–31.1) in Q3 2022; by alternative definition, IC prevalence was 29.6% (95% CI: 27.6–31.7) overall, increasing from 3.4% (95% CI: 0.1–17.8) to a peak of 46.8% (95% CI: 32.1–61.9) in Q2 2023. The larger observed increase in IC prevalence (by both definitions) over time among SARS-CoV-2-positives, relative to SARI patients without SARS-CoV-2, was statistically significant.

conclusionsImmunocompromised individuals represent a high proportion of hospitalized SARI cases, with results suggesting IC prevalence was higher during later periods of the COVID-19 pandemic. As immunocompromised individuals often respond inadequately to vaccination, alternative strategies are needed to better protect this vulnerable group.

Indexed as

COVID-19HospitalizationImmunocompromised HostSevere Acute Respiratory SyndromeAdultAgedEuropeFemaleHumansMaleMiddle AgedPrevalenceSARS-CoV-2ComorbidityCOVID-19HospitalizationImmunocompromised hostPrevalenceSARS-CoV-2Severe acute respiratory infection

Identifiers

PMID41801614
PMCPMC12976257

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.