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Pulmonary function and long-term follow-up of children with tracheobronchomalacia
Peter Moore1, Holly Smith, Ristan M Greer
1School of Medicine, University of Queensland, Brisbane, QLD, Australia.
Insights
Long-term follow-up of primary tracheobronchomalacia (TBM) reveals persistent airway abnormalities. Most children with TBM experience ongoing symptoms, indicating a chronic condition without significant reactive airways disease.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Airway Diseases
Background:
- Primary tracheobronchomalacia (TBM) affects large airways, but long-term outcomes remain understudied.
- Understanding the natural history of TBM is crucial for patient management.
- Investigating concomitant reactive airways disease is important for comprehensive care.
Purpose of the Study:
- To determine the long-term natural history of primary tracheobronchomalacia (TBM) in children.
- To assess the presence of reactive airways disease in TBM patients.
- To correlate clinical symptoms with pulmonary function test results.
Main Methods:
- A cohort of 21 children diagnosed with TBM between 1998-2001 was recruited in 2008 for a follow-up study.
- Parents completed questionnaires on respiratory symptoms; children underwent pulmonary function testing.
- Bronchial provocation tests or spirometry assessed for reactive airways disease.
Main Results:
- Data from 19 children showed persistent symptoms in 15, with significantly reduced mean FEV1, FEV1/FVC, FEF(25-75), and PEF compared to predicted values.
- Only four participants exhibited a classical TBM flow-volume loop.
- Reactive airways disease was identified in only one participant (6.7%).
Conclusions:
- Clinical profiles and pulmonary function suggest persistent mechanical abnormalities in both large and small airways in TBM patients.
- The study indicates a lack of significant reactive airways disease in this TBM cohort.
- These findings highlight the chronic nature of TBM and its impact on airway function.
Background:
Primary tracheobronchomalacia (TBM) is a disease of the large airways. Long-term follow-up studies of TBM patients have not been reported. This study was undertaken to further elicit the natural history of this condition and the presence of concomitant reactive airways disease through clinical profiling and pulmonary function testing.
Methods:
Twenty-one children diagnosed with TBM by bronchoscopy between 1998 and 2001 in Queensland were recruited in 2008. Parents completed a questionnaire detailing their child's respiratory symptoms over the previous 12 months. Children then undertook pulmonary function and flow-volume loop classification. Mannitol bronchial provocation testing or post-bronchodilator spirometry was performed to assess for the confounding presence of reactive airways disease.
Results:
Data from 19 children (12 males) were able to be analyzed. The median age was 9.4 (range 7.6-14.3) years. 15 parents indicated their child's symptoms were unresolved. The mean FEV(1) was 81% predicted with 7 <80% predicted. This was significantly lower than the percent predicted population mean (P = 0.0005). Mean FEV(1) /FVC, FEF(25-75) , and PEF were also significantly reduced (P = < 0.0001). Four participants had a classical TBM flow-volume loop on analysis. One of 15 (6.7%) participants recorded a positive test for reactive airways disease.
Conclusions:
Clinical symptom profiles and pulmonary function indicate persistent functional mechanical abnormalities of the large and small airways in TBM patients, and the absence of reactive airways disease.
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