# Respiratory assessment and management of newborns and children with congenital lung diseases: a cohort study

**Authors:** Federica Porcaro, Antonella Coretti, Valerio Pardi, Ivan Pietro Aloi, Andrea Conforti, Francesca Petreschi, Renato Cutrera

PMC · DOI: 10.1186/s13052-025-01918-8 · 2025-03-11

## TL;DR

This study examines the diagnosis and treatment of congenital lung diseases in children, finding that early surgical or endoscopic interventions improve symptoms more quickly.

## Contribution

The study provides insights into the management of congenital lung diseases through a long-term cohort analysis and highlights the benefits of early intervention.

## Key findings

- Children with congenital lung diseases often experience symptoms like wheezing and respiratory infections.
- Surgical or endoscopic treatment leads to faster symptom improvement compared to medical treatment alone.
- No malignant transformation was observed in patients with specific lung malformations during follow-up.

## Abstract

Children with congenital lung disease (CLD) may suffer from long-term complications, such as impairments in lung growth, decreased total lung volume, recurrent lower respiratory tract infections and, in some cases, malignant transformation.

we described retrospective data on diagnostic process, clinical and functional data regarding a cohort of symptomatic and asymptomatic children with CLD followed in a single third level center in the last twenty years.

91 children were included in the study. Five classes of disease were examined. Bronchial tree and pulmonary abnormalities represent the most common anomalies. Despite the improved resolution of prenatal diagnosis, most of patients underwent chest CT scan to confirm the initial diagnostic suspicion. The most reported symptoms were wheezing, recurrent respiratory infections and acute respiratory failure. According to malformation type, patients underwent to surgery, endoscopic and/or medical treatment. Improvement of symptoms occurred faster in patients surgically and endoscopically treated. No statistical difference in the number of exacerbations before and after treatment was recorded, as well as no differences in spirometry values were observed among surgically and non-surgically treated children. No malignant transformation was observed in two patients with intra-lobar sequestration and hybrid lesion during the follow up period.

the clinical presentation of congenital airway and lung disorders varies significantly depending on the type of malformation, making it challenging to standardize treatment strategies and follow-up programs. Based on our experience, prompt surgical or endoscopic intervention in early symptomatic children leads to faster symptom improvement and normal lung function in the follow-up period. However, further prospective studies are needed to better define optimal treatment strategies for these rare conditions, particularly for asymptomatic patients, for whom management approaches remain poorly established.

The online version contains supplementary material available at 10.1186/s13052-025-01918-8.

## Full-text entities

- **Diseases:** respiratory infections (MESH:D012141), CLD (MESH:D008171), congenital airway and lung disorders (MESH:C562992), wheezing (MESH:D012135), acute respiratory failure (MESH:D012131), impairments in lung growth (MESH:D006130)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC11899023