# Pathogen and Patient Characteristics and the Severity of Viral Respiratory Infections in Children

**Authors:** Cristina Moracas, Marco Poeta, Elisabetta Venturini, Amelia Licari, Valeria Garbo, Marta Stracuzzi, Ester Del Tufo, Laura Petrarca, Marco Maglione, Claudio Cafagno, Agnese Tamborino, Sofia Sgubbi, Andrea Lo Vecchio, Claudia Colomba, Vania Giacomet, Luisa Galli, Gian Luigi Marseglia, Alfredo Guarino

PMC · DOI: 10.1001/jamanetworkopen.2026.0129 · JAMA Network Open · 2026-02-26

## TL;DR

The study finds that respiratory syncytial virus and influenza infections, along with chronic conditions, are linked to more severe respiratory infections in children.

## Contribution

The study identifies specific pathogens and comorbidities associated with severe outcomes in pediatric viral respiratory infections.

## Key findings

- Respiratory syncytial virus and influenza infections are significantly associated with severe disease in children.
- Chronic comorbidities increase the risk of severe outcomes in hospitalized children with respiratory infections.
- The INF-ACT network provides a scalable model for real-time monitoring of pediatric infectious diseases.

## Abstract

How are pathogens, age, comorbidities, and coinfections associated with the severity of viral respiratory infections in children?

In this cohort study of 516 children, respiratory syncytial virus infections, influenza infections, and the presence of preexisting chronic conditions were associated with significantly worse clinical outcomes, including clinical severity score, length of hospital stay, intensive care unit admission, and the need for oxygen therapy.

These results underscore the importance of targeted surveillance and preventive measures, including vaccination and early intervention, particularly for vulnerable pediatric subgroups.

This cohort study examines the association of risk factors and clinical outcomes with several viral respiratory infections among hospitalized children in a multicenter pediatric health care system in Italy.

Respiratory infections are a leading cause of pediatric hospitalization and impose a significant burden on health care systems.

To evaluate clinical outcomes and risk factors for severe disease in hospitalized children with viral respiratory infections, focusing on the role of etiologies, comorbidities, age, and coinfections.

This multicenter observational cohort study is part of an active pediatric surveillance system established in September 2023, within the framework of the European Union–funded National Recovery and Resilience Plan. The One Health Basic and Translational Actions Addressing Unmet Needs on Emerging Infectious Diseases (INF-ACT) network, which includes 12 pediatric infectious disease referral centers across Italy, is designed to enable early detection of emerging infectious threats in children. The network is based on 3 pillars: monthly online meetings, a register of cases of unusual severity or induced by unusual pathogens, and a sample repository to investigate microbiology or host-related risk factors. Hospitalized children with respiratory symptoms and confirmed or suspected viral infection between September 2023 and December 2024 were eligible.

Type of respiratory virus, viral or bacterial coinfections, and presence of chronic comorbidities.

Severity was assessed using a clinical severity score (CSS), with a score greater than 3 indicating severe disease. The CSS considered mechanical ventilator support, hospital admission, length of hospital stay, oxygen saturation level, and use of supplemental oxygen. Length of hospital stay, intensive care unit admission, and the need for oxygen therapy were also considered as individual outcomes.

Of 516 children hospitalized with respiratory symptoms (median [IQR] age, 13.3 [4.0-43.0] months; 288 male [55.8%]), 34 (6.6%) had severe disease (CSS >3). In multivariable analysis, among patients with respiratory symptoms, infection with respiratory syncytial virus (10 of 67 [14.9%]; adjusted odds ratio [AOR], 4.26 [95% CI, 1.80-10.10]) or influenza (14 of 104 [13.5%]; AOR, 4.13 [95% CI, 1.88-9.04]) and the presence of cardiac or pulmonary diseases (4 of 18 [22.2%]; AOR, 5.25 [95% CI, 1.47-18.78]) or congenital malformations (3 of 14 [21.4%]; AOR, 4.94 [95% CI, 1.23-19.93]) were associated with increased risk of severe infection. A higher ICU admission rate was observed in children with influenza infection (12 of 104 [11.5%] vs 9 of 412 [2.2%]; P < .001) and preexisting comorbidities (9 of 69 [13.0%] vs 12 of 447 [2.7%]; P < .001). Age and coinfections were not significantly associated with worse outcomes.

In this cohort study of hospitalized children, respiratory syncytial virus and influenza infections, as well as the presence of chronic comorbidities, were significantly associated with severe disease. These findings support the need for targeted prevention and vaccination strategies, as well as early identification of children at risk for severe disease. The INF-ACT network offered a scalable model for real-time infectious disease monitoring in pediatric populations.

## Linked entities

- **Diseases:** influenza (MONDO:0005812), cardiac disease (MONDO:0005267), pulmonary disease (MONDO:0005275)

## Full-text entities

- **Diseases:** bacterial (MESH:D001424), premature (MESH:C536271), cardiac disease (MESH:D006331), human immunodeficiency virus infection (MESH:D015658), bronchiolitis (MESH:D001988), chromosomal disorders (MESH:D025063), pertussis (MESH:D014917), chronic (MESH:D002908), Infectious Diseases (MESH:D003141), epilepsy (MESH:D004827), CRS (MESH:D012818), death (MESH:D003643), immunodeficiency (MESH:D007153), Viral infections (MESH:D014777), ERV infection (MESH:D007239), gastrointestinal disorders (MESH:D005767), COVID-19 (MESH:D000086382), endocrine and metabolic diseases (MESH:D004700), dehydration (MESH:D003681), congenital heart diseases (MESH:D006330), parvovirus B19 infection (MESH:D016731), respiratory (MESH:D012131), immune or autoimmune diseases (MESH:D001327), cytomegalovirus (MESH:D003586), myocarditis (MESH:D009205), deficit of enzymes (MESH:D009461), endocrine and inherited metabolic diseases (MESH:D030342), fever (MESH:D005334), respiratory distress (MESH:D012128), Respiratory infections (MESH:D012141), neurological conditions (MESH:D019636), Diseases (MESH:D004194), cerebral palsy (MESH:D002547), Influenza (MESH:D007251), respiratory disease (MESH:D012140), congenital malformations (OMIM:163000), acute gastroenteritis (MESH:D005759), RSV (MESH:D018357), hormone glands disfunctions (MESH:D057215), lung disease (MESH:D008171), asthma (MESH:D001249)
- **Chemicals:** steroid (MESH:D013256), nirsevimab (MESH:C000709769), oxygen (MESH:D010100)
- **Species:** Respiratory syncytial virus (no rank) [taxon 12814], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Homo sapiens (human, species) [taxon 9606], Human bocavirus (species) [taxon 329641], herpes virus [taxon 39059], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Human adenovirus sp. (species) [taxon 1907210], human metapneumovirus (no rank) [taxon 162145], Coxsackievirus (species) [taxon 12066], Erysiphe sp. RV (species) [taxon 662690], Human rhinovirus sp. (species) [taxon 169066], Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Orthocoronavirinae (subfamily) [taxon 2501931], Chlamydia pneumoniae (species) [taxon 83558]

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947030/full.md

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Source: https://tomesphere.com/paper/PMC12947030