Pediatric pulmonology · 2026
Bronchodilator Responsiveness in Preterm-Born Children With Chronic Lung Disease: Importance of Individualized Testing.
СтатьяРандомизированное исследованиеНазвание и аннотация: Перевод в очереди
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Ophir Yotam, Tukova Jana
Аннотация
BACKGROUND: Children born preterm with chronic lung disease of Immaturity (CLDI) frequently present with obstructive lung function, yet optimal bronchodilator therapy remains uncertain. Previous studies focused on β2-agonists, while evidence for muscarinic antagonist therapy is limited.
METHODS: We conducted a prospectively planned cross-sectional study of preterm-born children (< 35 weeks) with CLDI and obstructive spirometry (FEV1 z-score < -1.64). Of 73 screened, 64 were enrolled, and 55 completed the protocol. Each attended three randomized crossover visits with salbutamol, ipratropium bromide, or fenoterol/ipratropium combination. Spirometry was performed before and after administration.
RESULTS: Overall, 48 children demonstrated bronchodilator responsiveness to at least one agent. Response rates were 56.4% for salbutamol (95% CI 43-70), 58.2% for ipratropium (95% CI 45-71), and 65.5% for the combination (95% CI 53-78), with no significant differences (McNemar's test, p = 0.45). Exclusive responses were observed in 9.1% to salbutamol (95% CI 3.0-20.0), 5.5% to ipratropium (95% CI 1.1-15.1), and 9.1% to the combination (95% CI 3.0-20.0). Among children with reversibility, repeated-measures ANOVA showed no significant difference in the effect of drugs (F = 0.1, p = 0.9), phenotype (F = 2.46, p = 0.12), or their interaction (F = 1.1, p = 0.34).
CONCLUSIONS: In our cohort, 87% of preterm-born children with CLDI exhibit reversible bronchial obstruction, with a substantial subset responding exclusively to a single bronchodilator. Due to the fact that single-drug testing may underestimate reversibility, individualized bronchodilator testing should be incorporated into care, and its long-term implications merit further study.
METHODS: We conducted a prospectively planned cross-sectional study of preterm-born children (< 35 weeks) with CLDI and obstructive spirometry (FEV1 z-score < -1.64). Of 73 screened, 64 were enrolled, and 55 completed the protocol. Each attended three randomized crossover visits with salbutamol, ipratropium bromide, or fenoterol/ipratropium combination. Spirometry was performed before and after administration.
RESULTS: Overall, 48 children demonstrated bronchodilator responsiveness to at least one agent. Response rates were 56.4% for salbutamol (95% CI 43-70), 58.2% for ipratropium (95% CI 45-71), and 65.5% for the combination (95% CI 53-78), with no significant differences (McNemar's test, p = 0.45). Exclusive responses were observed in 9.1% to salbutamol (95% CI 3.0-20.0), 5.5% to ipratropium (95% CI 1.1-15.1), and 9.1% to the combination (95% CI 3.0-20.0). Among children with reversibility, repeated-measures ANOVA showed no significant difference in the effect of drugs (F = 0.1, p = 0.9), phenotype (F = 2.46, p = 0.12), or their interaction (F = 1.1, p = 0.34).
CONCLUSIONS: In our cohort, 87% of preterm-born children with CLDI exhibit reversible bronchial obstruction, with a substantial subset responding exclusively to a single bronchodilator. Due to the fact that single-drug testing may underestimate reversibility, individualized bronchodilator testing should be incorporated into care, and its long-term implications merit further study.