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DOI 10.1016/j.arcped.2026.105578

Медицинская библиотека · Archives de pediatrie : organe officiel de la Societe francaise de pediatrie · 2026

Bronchodilator reversibility in children with cystic fibrosis: prevalence and associated factors.

Harvey Astrid, Beydon Nicole, Thouvenin Guillaume, Peulier-Maitre Elora, Taytard Jessica, Corvol Harriet

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Аннотация

BACKGROUND

In cystic fibrosis (CF), respiratory disease is the main determinant of prognosis. However, the prevalence and determinants of bronchodilator reversibility (BDR) in pediatric patients remain poorly characterized.

OBJECTIVE

This study aimed to estimate the prevalence of significant BDR and to identify associated clinical and microbiological factors in children with CF (CwCF).

METHODS AND SETTINGS: We conducted a retrospective study including CwCF under 20 years of age followed at Armand Trousseau Hospital between April 2018 and July 2024. A total of 48 CwCF and 164 pulmonary function tests (PFTs) including a bronchodilator assessment were analyzed. BDR was assessed using spirometric indexes and respiratory resistance measured by the interrupter technique (Rint). Univariate and multivariate logistic regression analyses were performed to identify factors associated with BDR.

RESULTS

Significant BDR (BDR+) was observed in 16 CwCF (33% [95% CI: 20-48]) at least once during follow-up, mainly detected through a significant decrease in Rint (n = 14, 87.5%), and less frequently through spirometric criteria (increase in forced expiratory volumes, n = 6, 37.5%). In multivariate analysis, BDR+ remained independently associated with the presence of an obstructive ventilatory defect (p = 0.007) and with the total number of PFTs performed (p = 0.035). Chronic colonization with Pseudomonas aeruginosa was associated with BDR+ in univariate analysis (p = 0.006) but not after adjustment (p = 0.30). No significant association was found with sex, clinical asthma, or allergic bronchopulmonary aspergillosis.

CONCLUSION

Significant bronchodilator reversibility was present in approximately one-third of CwCF, predominantly detected using respiratory resistance measurements. These findings highlight the importance of comprehensive functional respiratory follow-up in CwCF, including resistance measurements, and support a more individualized and functionally guided use of inhaled therapies.

Для цитирования: Harvey Astrid, Beydon Nicole, Thouvenin Guillaume, Peulier-Maitre Elora, Taytard Jessica, Corvol Harriet. Bronchodilator reversibility in children with cystic fibrosis: prevalence and associated factors.. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 2026. DOI: 10.1016/j.arcped.2026.105578.

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