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The burden of disease in pediatric non-cystic fibrosis bronchiectasis
Nitin Kapur1, I Brent Masters2, Peter Newcombe3
1Department of Respiratory Medicine and the Queensland Children's Medical Research Institute, Royal Children's Hospital, Herston, QLD, Australia; Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Insights
Children with non-CF bronchiectasis face significant burdens, particularly during exacerbations. Managing these events is key to improving quality of life and parental mental health in pediatric bronchiectasis patients.
Area of Science:
- Pediatric Pulmonology
- Child Health Outcomes
- Respiratory Medicine
Background:
- The disease burden in children with non-cystic fibrosis (non-CF) bronchiectasis remains largely unknown.
- Quality of life (QOL) and parental mental health are critical aspects of managing pediatric chronic respiratory conditions.
Purpose of the Study:
- To identify factors influencing QOL and parental mental health in children with non-CF bronchiectasis.
- To assess the impact of disease exacerbations on these parameters in pediatric patients.
Main Methods:
- Prospective study involving parents of 69 children with non-CF bronchiectasis.
- Utilized parent-proxy cough-specific QOL (PC-QOL) and Depression, Anxiety, and Stress Scale (DASS) questionnaires during stable and exacerbation states.
- Collected clinical, investigational, and lung function data.
Main Results:
- Younger age correlated with worse QOL in stable states; other factors like lung function or cause did not significantly impact QOL.
- Exacerbations led to significant worsening of PC-QOL scores and DASS scores, indicating increased parental stress and anxiety.
- During exacerbations, 38% reported elevated anxiety and 54% abnormal depression/stress scores.
Conclusions:
- Children with non-CF bronchiectasis experience a substantial disease burden, especially during exacerbations.
- Parental mental health is significantly affected during exacerbations.
- Effective prevention, early detection, and treatment of exacerbations are crucial for reducing psychologic morbidity in affected families.
Background:
The burden of disease in children with non-cystic fibrosis (non-CF) bronchiectasis is unknown. Our study aimed to identify the determinants of quality of life (QOL) and parental mental health in this group of patients and their parents and to evaluate the effect of exacerbations on these parameters.
Methods:
Parents of 69 children (median age 7 years) with non-CF bronchiectasis prospectively completed two questionnaires (parent-proxy cough-specific quality of life [PC-QOL] and the Depression, Anxiety, and Stress Scale [DASS]) at stable and exacerbation states. Data on clinical, investigational, and lung function parameters were also collected.
Results:
During the stable state, the median interquartile range (IQR) PC-QOL score was 6.5 (5.3-6.9) and the DASS 21-item questionnaire score was 6 (0-20). Being of a young age correlated with a worse QOL (r(5) = 0.242, P = .04) but radiologic extent, lung function, underlying cause, environmental tobacco smoke exposure, and chronic upper-airway disease did not influence these scores. Exacerbations caused significant worsening in the PC-QOL scores (median [IQR], 4.6 [3.8-5.4]; P = .001) and DASS scores (median [IQR], 22 [9-42]; P < .001; 38% with elevated anxiety, 54% with abnormal depression/stress scores during exacerbation). The presence of viral infection, hypoxia, and hospitalization did not influence the exacerbation PC-QOL and DASS scores.
Conclusions:
There is a significant burden of disease, especially during exacerbation, on parents of children with bronchiectasis. Prevention, early detection, and appropriate treatment of exacerbations are likely to reduce psychologic morbidity in this group.
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