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

**Authors:** 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, Andrea Orsi, Susana Otero Romero, Sudhir Venkatesan, Marc-Alain Widdowson, Kaatje Bollaerts, Sylvia Taylor

PMC · DOI: 10.1007/s44197-025-00503-w · 2026-03-09

## TL;DR

The study found that the proportion of hospitalized patients with severe respiratory infections who are immunocompromised increased during the later stages of the COVID-19 pandemic in Europe.

## Contribution

This study provides new insights into how the prevalence of immunocompromising conditions changed over time among hospitalized SARI patients during the pandemic.

## Key findings

- Immunocompromising conditions increased from 8.3% to 22.0% among hospitalized SARI patients by mid-2022.
- Among SARS-CoV-2-positive patients, immunocompromising conditions rose from 3.4% to 23.8% during the same period.
- The increase in immunocompromised patients was significantly higher among SARS-CoV-2-positive cases compared to those without the virus.

## Abstract

Immunocompromised 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.

We 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.

Among 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.

Immunocompromised 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.

The online version contains supplementary material available at 10.1007/s44197-025-00503-w.

## Linked entities

- **Diseases:** coronavirus disease 2019 (MONDO:0100096), SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** infection (MESH:D007239), cardiovascular disease (MESH:D002318), end stage-kidney disease (MESH:D007676), COVID-19 (MESH:D000086382), Cough (MESH:D003371), death (MESH:D003643), immunodeficiencies (MESH:D007153), hypertension (MESH:D006973), pneumococcal disease (MESH:D011008), cardiovascular and respiratory comorbidities (MESH:D018376), Problems (MESH:D019973), HIV (MESH:D015658), Basal cell carcinomas (MESH:D002280), nasal obstruction (MESH:D015508), infectious diseases (MESH:D003141), SARI (MESH:D045169), deficiency of humoral and/or cellular immunity (MESH:C567115), lymphoid malignancies (MESH:D008223), orthopedic injury (MESH:D009140), type 2 diabetes (MESH:D003924), renal disease (MESH:D007674), ageusia (MESH:D000370), shortness of breath (MESH:D004417), RSV infection (MESH:D018357), Benign and in situ neoplasms (MESH:D009369), lung disease (MESH:D008171), chronic kidney disease (MESH:D051436), IC (MESH:C537984), asthma (MESH:D001249), ICs (MESH:D020763), liver disease (MESH:D008107), acute respiratory infection (MESH:D012141), Diseases (MESH:D004194), influenza (MESH:D007251), dysgeusia (MESH:D004408), Fever (MESH:D005334), Anosmia (MESH:D000857), autoimmune conditions (MESH:D001327), pneumonia (MESH:D011014), pneumococcal pneumonia (MESH:D011018), nasal septum deviation (MESH:D061270)
- **Chemicals:** pneumococcal conjugate (-), prednisolone (MESH:D011239), tacrolimus (MESH:D016559), ciclosporin (MESH:D016572), azathioprine (MESH:D001379), mycophenolate (MESH:D009173), methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606], Respiratory syncytial virus (no rank) [taxon 12814], Human immunodeficiency virus (species) [taxon 12721], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976257/full.md

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Source: https://tomesphere.com/paper/PMC12976257