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Published on: April 6, 2017
Aerosol delivery of nebulised budesonide in young children with asthma
Karen G Schueepp1, Sunalene G Devadason, Christina Roller
1Department of Pediatrics and Respiratory Medicine, University Children's Hospital, Berne, Switzerland. karen.schuepp@insel.ch
Insights
Improving aerosol therapy for young children with asthma is crucial. A modified nebuliser significantly enhanced lung deposition of budesonide, but child cooperation remains a key challenge.
Area of Science:
- Pediatric Pulmonology
- Respiratory Drug Delivery
- Asthma Management
Background:
- Lung deposition of inhaled corticosteroids is suboptimal in young children with asthma due to anatomical, physiological, and cooperation factors.
- Low lung deposition impacts treatment efficacy and increases the risk of systemic side effects.
- Optimizing aerosol delivery is critical for effective anti-inflammatory treatment in pediatric asthma.
Purpose of the Study:
- To evaluate lung deposition and lung-to-oropharyngeal deposition ratio of budesonide using a modified vibrating membrane nebuliser in young children.
- To assess the impact of a small particle size formulation delivered via an age-adjusted device on aerosol deposition.
- To determine the efficacy of a novel delivery system in addressing the challenges of pediatric aerosol therapy.
Main Methods:
- Ten asthmatic children (mean age 20.3 months) inhaled radiolabeled budesonide (MMD 2.6 µm) via a modified vibrating membrane nebuliser (PARI e-Flow).
- Lung deposition was quantified using scintigraphy, measuring the percentage of the emitted dose.
- The ratio of lung deposition to oropharyngeal deposition was calculated to assess drug distribution.
Main Results:
- Mean lung deposition was 48.6% in quietly breathing children and 20.0% when crying.
- The lung-to-oropharyngeal deposition ratio was 1.0 for quiet breathing versus 0.3 when crying.
- The modified device demonstrated significantly higher lung deposition and improved deposition ratios compared to crying conditions.
Conclusions:
- An optimized combination of delivery device and small-particle drug formulation significantly improves lung deposition and lung-to-oropharyngeal deposition ratio in young asthmatic children.
- Despite technological advancements, patient cooperation remains the primary limitation for effective aerosol delivery in this age group.
- This improved delivery system holds promise for enhancing asthma management in pediatric populations.
Background:
Lung deposition of inhaled steroids, likely to be of benefit in the anti-inflammatory treatment of asthma in young children, is low. This is explained by age specific anatomical and physiological characteristics as well as poor cooperation with aerosol therapy. However, total lung deposition and the ratio of lung deposition to oropharyngeal deposition are key determinants of clinical efficacy and of systemic side effects of aerosolized drugs.
Objectives:
The aim of this study was to determine lung deposition and ratio of lung deposition to oropharyngeal deposition using a modified vibrating membrane nebuliser to deliver budesonide with a small particle size, taking into account the needs of young children.
Patients And Methods:
Ten asthmatic children (5 males), mean age 20.3 months (range 6-41 months) inhaled radiolabelled budesonide (MMD 2.6microm) through a modified vibrating membrane nebuliser (modified PARI e-Flow). Lung deposition expressed as a percentage of the emitted dose was measured using scintigraphy and the ratio of lung deposition to oropharyngeal deposition was calculated.
Results:
Mean lung deposition (SD) expressed as percentage of emitted dose and mean lung to oropharyngeal deposition ratio (SD) in quietly breathing children (n=5) and in children crying during inhalation were 48.6% (10.5) versus 20.0% (10.9), and 1.0 (0.3) versus 0.3 (0.2), respectively.
Conclusions:
We have shown that by using an improved age-adjusted complementary combination of delivery device and drug formulation to deliver small particles, lung deposition and ratio of lung deposition to oropharyngeal deposition in young asthmatic children is highly improved. But the main factor limiting aerosol delivery in this age group remains cooperation.
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