Prevalence and Determinants of Wheezing and Bronchodilatation in Children With Cystic Fibrosis: A Retrospective

Francois Galodé1, O Ladipo2, A Andrieux1

  • 1Paediatric Cystic Fibrosis Reference Center, Hôpital Pellegrin-Enfants, CHU de Bordeaux, Bordeaux, France.

Insights

Wheezing and bronchodilatory response are common in children with cystic fibrosis (CF). Current wheezing at age six is linked to poorer lung function, suggesting "CF-asthma" is a misnomer.

Area of Science:

  • Pediatric Pulmonology
  • Cystic Fibrosis Research
  • Respiratory Medicine

Background:

  • Wheezing is frequently observed in pediatric cystic fibrosis (CF) patients, often leading to a misdiagnosis of CF-asthma.
  • Understanding the underlying causes of wheezing in CF is crucial for effective treatment and to avoid unnecessary therapies.

Purpose of the Study:

  • To determine the prevalence and characteristics of wheezing and positive bronchodilatory response (BDR) in children with CF.
  • To identify predictive markers for wheezing and BDR and assess their impact on lung function.

Main Methods:

  • A retrospective single-center study analyzed data from children with CF.
  • Wheezing was assessed in patients under 6 years, and BDR in those aged 6-17 years.
  • Data included anthropometric, lung function, genetic, laboratory, and microbiological information.

Main Results:

  • 71.2% of preschool CF patients experienced wheezing; 37.9% had persistent wheezing.
  • Positive BDR prevalence varied by age group (73.5% in 6-8 years, 48.5% in 10-12 years, 52.9% in 15-17 years).
  • Current wheezing at age 6 correlated with lower FEV1 and FVC; allergic factors and early Pseudomonas aeruginosa infection were not predictive.

Conclusions:

  • Wheezing and BDR are highly prevalent in pediatric CF patients.
  • Persistent wheezing in early childhood is associated with diminished lung function.
  • The term "CF-asthma" is misleading; wheezing in CF has distinct determinants compared to asthma.
Abstract

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