Evidence map›Paper›PMID 42230808›Full record

Observational studyEuropean journal of pediatrics2026

Lung ultrasound combined with C-reactive protein for identifying a bacterial component in children hospitalized with acute lower respiratory tract infections: a prospective observational study.

Jiří Fremuth, Tereza Fremuthová, Michal Huml, Eva Sládková, Veronika Schwarzová, Josef Sýkora, Zuzana Rosolová, Jan Forejt, Stanislav Kormunda, Jana Amlerová and 7 more

Abstract readObservational Study
In one paragraph

Observational study in European journal of pediatrics, 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

17 authors.

Jiří FremuthDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Tereza FremuthováDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Michal HumlDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic. humlm@fnplzen.cz.
Eva SládkováDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Veronika SchwarzováDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Josef SýkoraDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Zuzana RosolováDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Jan ForejtDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Stanislav KormundaDepartments of Pediatrics, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Jana AmlerováDepartment of Microbiology, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Kateřina ChudějováDepartment of Microbiology, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Jindra WindrichováCentral Laboratory of Immunoanalysis, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Renata VondrákováDepartment of Imaging Methods, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Jan BaxaDepartment of Imaging Methods, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Martin PeštaInstitute of Biology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Ondřej TopolčanCentral Laboratory of Immunoanalysis, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Daniel RajdlInstitute of Clinical Biochemistry and Haematology, Faculty Hospital, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lower respiratory tract infections (ALRTIs) remain a major cause of pediatric morbidity and antibiotic use. Early identification of a bacterial component is crucial for rational treatment decisions. We evaluated the diagnostic performance of lung ultrasound (LUS), alone and combined with C-reactive protein (CRP), for identifying a clinically adjudicated bacterial component in children hospitalized with ALRTIs. In this prospective study, 160 children (1 month-19 years) hospitalized with ALRTIs underwent LUS within 24 h of admission. LUS-based presumptive classification (viral, bacterial, combined) was assigned using predefined criteria. Final etiological classification was determined independently by three senior pediatricians blinded to LUS findings, using an adjudicated composite reference standard integrating clinical course, laboratory markers, microbiology, and chest radiography. No prespecified biomarker thresholds were applied. Diagnostic performance for identifying a bacterial component (bacterial or combined vs. viral) was assessed using ROC analysis. Seventy-five children (47%) were classified as viral, 60 (37%) as combined, and 25 (16%) as bacterial/atypical according to the adjudicated composite reference standard. Large consolidations (≥ 20 mm), bronchograms, confluent B-lines, and pleural effusions were associated with a bacterial component, whereas viral cases showed small bilateral subpleural consolidations and non-confluent B-lines. LUS demonstrated good diagnostic accuracy (AUROC 0.89, 95% CI 0.84-0.94; sensitivity 83.5%; specificity 94.6%). CRP ≥ 40 mg/L showed comparable performance (AUROC 0.91, 95% CI 0.87-0.96; sensitivity 75.3%; specificity 94.7%).

conclusionIn children hospitalized with ALRTIs, LUS-particularly alongside CRP-may support early bedside identification of a clinically adjudicated bacterial component and assist treatment decisions. WHAT IS KNOWN: • Clinical exams and chest X-rays (CXR) poorly distinguish bacterial and combined from viral ALRTIs. • Lung ultrasound (LUS) is validated for diagnosing pneumonia, but its role in identifying the etiology is less studied. WHAT IS NEW: • LUS may help identify the presence of a bacterial component in children hospitalized with ALRTIs. • CRP was the laboratory marker most strongly associated with bacterial component, and its combination with LUS may support early bedside etiological assessment and more rational antibiotic decision-making.

Indexed as

C-Reactive ProteinLungRespiratory Tract InfectionsAcute DiseaseAdolescentBiomarkersChildChild, PreschoolFemaleHospitalizationHumansInfantMaleProspective StudiesROC CurveSensitivity and SpecificityBiomarkersC-Reactive ProteinAcute lower respiratory tract infectionChest X-rayChildrenC-reactive proteinLung ultrasoundPneumonia

Identifiers

PMID42230808
PMCPMC13230270

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Registered trials

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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.