Aerosol delivery of nebulised budesonide in young children with asthma

Summary 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...

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Veröffentlicht in:Respiratory medicine 2009-11, Vol.103 (11), p.1738-1745
Hauptverfasser: Schueepp, Karen G, Devadason, Sunalene G, Roller, Christina, Minocchieri, Stefan, Moeller, Alexander, Hamacher, Jürg, Wildhaber, Johannes H
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container_end_page 1745
container_issue 11
container_start_page 1738
container_title Respiratory medicine
container_volume 103
creator Schueepp, Karen G
Devadason, Sunalene G
Roller, Christina
Minocchieri, Stefan
Moeller, Alexander
Hamacher, Jürg
Wildhaber, Johannes H
description Summary 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 2.6 μm) 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.
doi_str_mv 10.1016/j.rmed.2009.04.029
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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 2.6 μm) 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.</description><identifier>ISSN: 0954-6111</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1016/j.rmed.2009.04.029</identifier><identifier>PMID: 19540100</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Administration, Inhalation ; Aerosols ; Age Factors ; Asthma ; Asthma - diagnostic imaging ; Asthma - drug therapy ; Atoms &amp; subatomic particles ; Biological and medical sciences ; Bronchodilator Agents - administration &amp; dosage ; Bronchodilator Agents - analysis ; Budesonide - administration &amp; dosage ; Budesonide - analysis ; Child, Preschool ; Childhood asthma ; Children &amp; youth ; Chronic obstructive pulmonary disease, asthma ; Delivery. Postpartum. Lactation ; Drug dosages ; Efficiency ; Female ; Gynecology. Andrology. 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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 2.6 μm) 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. 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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 2.6 μm) 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.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>19540100</pmid><doi>10.1016/j.rmed.2009.04.029</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Inhalation
Aerosols
Age Factors
Asthma
Asthma - diagnostic imaging
Asthma - drug therapy
Atoms & subatomic particles
Biological and medical sciences
Bronchodilator Agents - administration & dosage
Bronchodilator Agents - analysis
Budesonide - administration & dosage
Budesonide - analysis
Child, Preschool
Childhood asthma
Children & youth
Chronic obstructive pulmonary disease, asthma
Delivery. Postpartum. Lactation
Drug dosages
Efficiency
Female
Gynecology. Andrology. Obstetrics
Humans
Infant
Infants
Inhalation therapy
Lung - chemistry
Lung - diagnostic imaging
Lungs
Male
Medical sciences
Nebuliser
Nebulizers and Vaporizers
Oropharynx - chemistry
Oropharynx - diagnostic imaging
Particle Size
Pneumology
Pulmonary/Respiratory
Radiolabelled aerosols
Radionuclide Imaging
Studies
Treatment Outcome
title Aerosol delivery of nebulised budesonide in young children with asthma
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