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Published on: March 17, 2014
Outcomes of protracted bacterial bronchitis in children: A 5-year prospective cohort study
Tom J C Ruffles1,2, Julie M Marchant1, Ian B Masters1
1Department of Respiratory and Sleep Medicine, Queensland Children's Hospital, Centre for Children's Health Research, Queensland University of Technology, Brisbane, QLD, Australia.
Insights
Many children with pneumonia with biphasic Беларусі (PBB) experience ongoing symptoms, including bronchiectasis and asthma, 5 years later. Recurrent PBB and Haemophilus influenzae infection predict bronchiectasis, while allergies predict asthma.
Area of Science:
- Pediatric Respiratory Medicine
- Clinical Outcomes Research
- Chronic Lung Disease
Background:
- Persistent Pulmonary Bleeding (PBB) in children necessitates long-term outcome research.
- Identifying chronic respiratory diseases and their risk factors following PBB is a priority.
Purpose of the Study:
- To describe the 5-year outcomes for children diagnosed with PBB.
- To identify risk factors for chronic respiratory diseases such as bronchiectasis and asthma post-PBB.
Main Methods:
- A prospective cohort study involving 166 children with PBB and 28 controls.
- Monthly monitoring, clinical reviews, spirometry, and CT scans were utilized.
- Follow-up duration was a median of 59 months.
Main Results:
- 67.5% of children experienced ongoing symptoms; 9.6% developed bronchiectasis.
- Recurrent PBB and Haemophilus influenzae in bronchoalveolar lavage (BAL) predicted bronchiectasis.
- Asthma was diagnosed in 27.1% of children with PBB, predicted by positive allergen-specific IgE and bronchomalacia.
Conclusions:
- A significant proportion of children with PBB have persistent symptoms, bronchiectasis, and asthma at 5 years.
- Close clinical follow-up is essential for these children.
- Further research into biomarkers, endotypes, and mechanisms is needed to understand diverse outcomes.
Background And Objective:
Long-term data on children with PBB has been identified as a research priority. We describe the 5-year outcomes for children with PBB to ascertain the presence of chronic respiratory disease (bronchiectasis, recurrent PBB and asthma) and identify the risk factors for these.
Methods:
Prospective cohort study was undertaken at the Queensland Children's Hospital, Brisbane, Australia, of 166 children with PBB and 28 controls (undergoing bronchoscopy for symptoms other than chronic wet cough). Monitoring was by monthly contact via research staff. Clinical review, spirometry and CT chest were performed as clinically indicated.
Results:
A total of 194 children were included in the analysis. Median duration of follow-up was 59 months (IQR: 50-71 months) post-index PBB episode, 67.5% had ongoing symptoms and 9.6% had bronchiectasis. Significant predictors of bronchiectasis were recurrent PBB in year 1 of follow-up (ORadj = 9.6, 95% CI: 1.8-50.1) and the presence of Haemophilus influenzae in the BAL (ORadj = 5.1, 95% CI: 1.4-19.1). Clinician-diagnosed asthma at final follow-up was present in 27.1% of children with PBB. A significant BDR (FEV1 improvement >12%) was obtained in 63.5% of the children who underwent reversibility testing. Positive allergen-specific IgE (ORadj = 14.8, 95% CI: 2.2-100.8) at baseline and bronchomalacia (ORadj = 5.9, 95% CI: 1.2-29.7) were significant predictors of asthma diagnosis. Spirometry parameters were in the normal range.
Conclusion:
As a significant proportion of children with PBB have ongoing symptoms at 5 years, and outcomes include bronchiectasis and asthma, they should be carefully followed up clinically. Defining biomarkers, endotypes and mechanistic studies elucidating the different outcomes are now required.
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