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Etiology and outcome of bronchiectasis in children: a study of 41 patients
Olfa Bouyahia1, Leila Essadem, Nadia Matoussi
1Paediatric Department C, Paediatric Hospital of Tunis, Tunisia.
Insights
Delayed diagnosis of pediatric bronchiectasis is common in developing nations. Congenital causes are frequent, leading to a poor prognosis with significant chronic respiratory failure.
Area of Science:
- Pediatric Pulmonology
- Epidemiology
- Medical Diagnostics
Background:
- Bronchiectasis is a significant cause of chronic suppurative lung disease in developing countries.
- Understanding its characteristics in pediatric populations is crucial for effective management.
Purpose of the Study:
- To describe the epidemiological profile, clinical presentation, underlying causes, and outcomes of pediatric bronchiectasis.
- To highlight diagnostic challenges and long-term prognosis in a Tunisian pediatric hospital.
Main Methods:
- Retrospective study of 41 children diagnosed with bronchiectasis between 1994 and 2006.
- Diagnosis confirmed by chest X-ray and/or high-resolution computed tomography (HRCT).
Main Results:
- Mean age at diagnosis was 5 years 9 months; common symptoms included persistent cough and bronchorrhea.
- Underlying causes identified in 52%, with cystic fibrosis, prior pneumonia, primary ciliary dyskinesia, and immunodeficiency being most frequent.
- Significant reduction in lower respiratory infection rates post-diagnosis, but 21.9% developed chronic respiratory failure.
Conclusions:
- Delayed diagnosis of pediatric bronchiectasis is a persistent issue in the region.
- Congenital and indeterminate etiologies are prevalent, contributing to a poor prognosis.
- High rates of chronic respiratory failure necessitate improved diagnostic strategies and early intervention.
Background:
Bronchiectasis remains an important cause of chronic suppurative lung disease in the developing world. The aim of this study is to describe the epidemiological characteristics, clinical features, underlying aetiologies and outcome of bronchiectasis in the paediatric hospital of Tunis.
Methods:
A retrospective study of 41 children with bronchiectasis was conducted between January 1994 and December 2006. Diagnosis was made in patients with clinical suspicion of bronchiectasis associated with abnormalities on chest X ray (n=37) and/or on high resolution computed tomography (HRCT) (n=36).
Results:
Mean age at diagnosis was 5 years 9 months; (range: 6 months-14 years). Persistent cough and bronchorrhea were the most common symptoms. Fourteen patients (34%) had dyspnoea on first presentation, 11 of them (26.8%) had chest deformation and/or finger clubbing. Haemoptysis was noted in only two cases. Mean time to diagnosis from symptom onset was 2.7 years (range: 2 months-4 years). The underlying aetiologies were identified in 52% of patients. Cystic fibrosis (17%), previous pneumonic illness (9.7%), primary ciliary dyskinesia (9.7%) and immunodeficiency (9.7%) were the most common causes. After a mean follow-up of 6.6 years, the annual lower respiratory infection rate decreased from 7.2 +/- 3 to 3.1 +/- 2.6 (p<0.05), Twenty one point nine per cent of patients had chronic respiratory failure and five patients required surgery.
Conclusions:
Delays diagnosis of bronchiectasis remains important in our country. Congenital and indeterminate aetiologies are the most common forms. Prognosis is poor with a high prevalence of chronic respiratory failure.
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