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Long-term respiratory outcomes of post-op congenital lung malformations
Alican Dincel1, Cansu Yilmaz Yegit2, Almala Pinar Ergenekon2
1Department of Pediatrics, School of Medicine, Marmara University, Istanbul, Turkey.
Insights
Children who underwent surgery for congenital lung malformations (CLM) show long-term pulmonary function impairment. The Lung Clearance Index (LCI) may detect airway disease earlier than spirometry in these patients.
Area of Science:
- Pediatric Pulmonology
- Thoracic Surgery
- Respiratory Physiology
Background:
- Congenital lung malformations (CLM) are rare conditions requiring surgical intervention.
- Long-term outcomes of surgical treatment for CLM are not fully understood.
- Evaluating post-surgical lung function in pediatric CLM patients is crucial.
Purpose of the Study:
- To assess and compare the long-term pulmonary function of children with CLM after surgery against healthy controls.
- To investigate the utility of spirometry and Lung Clearance Index (LCI) in evaluating lung function in this cohort.
Main Methods:
- A cohort of 16 children with CLM (post-surgery) and 30 healthy controls were enrolled.
- Demographic data were collected for both groups.
- Pulmonary function was assessed using spirometry (FEV1, FVC, FEF25-75) and nitrogen-based Lung Clearance Index (LCI).
Main Results:
- Patients with CLM exhibited significantly lower FEV1, FVC, and FEF25-75 compared to healthy controls.
- The LCI was significantly higher in the CLM group (8.33 ± 1.52) than in controls (7.28 ± 0.80).
- A strong inverse correlation was observed between LCI and FEV1/FVC in patients with CLM.
Conclusions:
- Surgical treatment for CLM is associated with long-term pulmonary function deficits in children.
- The Lung Clearance Index (LCI) shows potential as a more sensitive marker for early airway disease detection in post-surgical CLM patients than traditional spirometry.
Background:
Congenital lung malformations (CLM) are rare disorders and surgical intervention is the definitive treatment. Our aim is to evaluate the long-term lung function of patients with CLM after surgery compared to healthy children.
Methods:
Sixteen children with CLM (M/F: 9/7) and 30 age-matched, healthy controls (M/F: 13/17) were included in the study. Demographic data were recorded and both groups were compared by spirometry and the nitrogen-based Lung Clearance Index (LCI).
Results:
Mean ± SD age of the patients was 12.0 ± 5.4 years. The mean forced expiratory volume in 1 s (FEV1 ), forced vital capacity (FVC), FEV1 /FVC, and forced expiratory flow between 25% and 75% of force expiration (FEF25-75 ) predicted was, 86.68 ± 16.65, 88.00 ± 14.58, 97.44 ± 9.89, and 79.00 ± 26.41, respectively in the patient group. Patients with CLM had significantly lower values in FEV1 , FVC, FEF25-75 than healthy controls (P = 0.002, P 0.007, P 0.045). While the mean LCI2,5% value in patients' group was 8.33 ± 1.52, it was 7.28 ± 0.80 in healthy controls (P = 0.023). Strong inverse correlation between LCI and FEV1 , FEV1 /FVC was detected in the patient group (P = 0.023; r: -0.581, P 0.017; r: -0.606 respectively).
Conclusion:
This study revealed that, in long-term follow-up, patients who had surgery because of CLM have impairment in the pulmonary function compared to healthy children and LCI may be more accurate in detecting airway diseases early than spirometry.
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