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Effect of budesonide on pulmonary hyperinflation in young asthmatic children

A Greenough1, J Pool, J G Gleeson

  • 1Paediatric Respiratory Laboratory, King's College Hospital, London.

Thorax
|November 1, 1988
PubMed

Insights

Inhaled budesonide reduced lung hyperinflation in young children with asthma. This treatment also showed a trend toward improving bronchodilator response, suggesting benefits for pediatric asthma management.

Area of Science:

  • Pediatric Pulmonology
  • Respiratory Medicine
  • Clinical Pharmacology

Background:

  • Asthma is a common chronic respiratory disease in children.
  • Hyperinflation, indicated by increased functional residual capacity (FRC), is a common finding in pediatric asthma.
  • Effective management of childhood asthma requires addressing airway inflammation and airflow obstruction.

Purpose of the Study:

  • To evaluate the effect of inhaled budesonide on functional residual capacity (FRC) in young asthmatic children.
  • To assess the impact of budesonide treatment on bronchodilator responsiveness in this age group.
  • To determine if inhaled corticosteroids can reduce lung hyperinflation in early childhood asthma.

Main Methods:

  • A double-blind, randomized crossover trial was conducted.
  • Nineteen children aged 2-6 years with asthma participated.
  • Inhaled budesonide or placebo was administered for six weeks, with assessments of FRC (helium dilution) and bronchodilator response.

Main Results:

  • Functional residual capacity (FRC) was elevated in most children at baseline.
  • Budesonide treatment led to a significant reduction in FRC compared to placebo (median change 9% vs. 0%; p < 0.05).
  • A trend towards improved bronchodilator response was observed after budesonide treatment.

Conclusions:

  • Inhaled budesonide effectively reduces lung hyperinflation in young children with asthma.
  • The findings suggest that inhaled corticosteroids are beneficial in managing hyperinflation in pediatric asthma.
  • Budesonide may also positively influence bronchodilator responsiveness, warranting further investigation.

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