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Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
Structural Lung Disease in Children and Adolescents With Severe Neurological Disorders
Daniel A F Bernard1, Cathrin Dahl1, Luca Salhöfer2
1Pediatric Pulmonology and Sleep Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, North Rhine-Westphalia, Germany.
Insights
Children with severe neurological disorders often have lung structure changes. Chest CT scans revealed common abnormalities and identified distinct patient phenotypes, guiding management changes.
Area of Science:
- Pediatric Pulmonology
- Radiology
- Neurology
Background:
- Children with severe neurological disorders face high risks of respiratory complications.
- Data on structural lung changes in this population are limited.
Purpose of the Study:
- To investigate structural lung abnormalities in children with severe neurological disorders using chest CT.
- To identify distinct clinical phenotypes and their association with lung changes.
Main Methods:
- Retrospective analysis of chest CT scans in 34 children with severe neurological disorders.
- Exploratory hierarchical clustering to define clinical phenotypes based on etiology, respiratory support, dysphagia, and mobility.
Main Results:
- Structural lung abnormalities were frequent, including lobar consolidation (76%) and bronchial wall thickening (62%).
- Three phenotypes were identified: stable neuromuscular, advanced neuromuscular-dysphagic (high bronchiectasis), and neurologic-dysphagic (high consolidation/ground-glass opacities).
- Chest CT prompted management changes in 91% of patients, with many findings not visible on prior radiographs.
Conclusions:
- Structural lung abnormalities are common in children with severe neurological disorders, even without primary lung disease.
- Clinical phenotyping may help identify patients benefiting from chest CT.
- Further prospective studies are needed to confirm CT-based strategies.
Background And Objective:
Children with severe neurological disorders are at risk of secondary respiratory morbidity due to impaired airway clearance and dysphagia, but systematic data on structural lung changes remain scarce.
Methods:
We retrospectively analyzed all clinically indicated chest CT examinations at a tertiary care center (2015-2025) in 34 children with severe neurological disorders (median age 10 years), excluding those with primary lung disease. Exploratory hierarchical clustering identified clinical phenotypes based on disease etiology, respiratory support, dysphagia, and mobility.
Results:
Structural abnormalities were common. Lobar consolidation (76%) and bronchial wall thickening (62%) were the most frequent CT findings. Cluster analysis identified three phenotypes: a stable neuromuscular phenotype without bronchiectasis or Pseudomonas aeruginosa colonization, an advanced neuromuscular-dysphagic phenotype with the highest bronchiectasis prevalence (64%, p = 0.005), and a neurologic-dysphagic phenotype characterized by frequent consolidations (86%) and ground-glass opacities (36%). Although most scans were elective (76%), CT prompted management changes in 91% of patients, mainly intensified airway clearance, antibiotic treatment, and escalated respiratory support. Among CT abnormalities associated with subsequent management change, 60% were not clearly identifiable on retrospectively reviewed preceding chest radiographs.
Conclusion:
In this selective cohort of children with severe neurological disorders undergoing clinically indicated chest CT, structural lung abnormalities were common despite the absence of a primary pulmonary diagnosis. Exploratory clinical phenotyping suggested distinct risk patterns linked to dysphagia, impaired airway clearance, and microbial colonization, and may help identify patients in whom CT provides clinically relevant additional information. Prospective studies are warranted before broader CT-based strategies can be recommended.
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