Inhaled budesonide and beclomethasone for the prevention and treatment of bronchopulmonary dysplasia in very preterm infants: a prospective randomized controlled trial - Report - MDSpire
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Inhaled budesonide and beclomethasone for the prevention and treatment of bronchopulmonary dysplasia in very preterm infants: a prospective randomized controlled trial
Clinical Report: Efficacy of Inhaled Budesonide and Beclomethasone in BPD
Overview
Inhaled budesonide and beclomethasone significantly shorten the duration of respiratory support in very preterm infants at high risk of bronchopulmonary dysplasia (BPD) without increasing adverse outcomes. However, these treatments do not demonstrate significant advantages in reducing the incidence or severity of BPD.
Background
Bronchopulmonary dysplasia (BPD) is a prevalent and serious complication in very preterm infants, leading to long-term respiratory issues. Despite advancements in neonatal care, the incidence of BPD remains high, necessitating effective preventive and therapeutic strategies. Corticosteroids, such as inhaled budesonide and beclomethasone, are commonly used due to their anti-inflammatory properties, yet their efficacy in this context requires further investigation.
Data Highlights
Group
Total Duration of Respiratory Support (days)
Length of Hospital Stay (days)
Control
43.5 ± 13.5
50.4 ± 8.5
Budesonide
36.4 ± 14.9
39.5 ± 10.1
Beclomethasone
35.6 ± 15.1
39.8 ± 11.0
Key Findings
Inhaled budesonide and beclomethasone reduced the total duration of respiratory support compared to control.
No significant differences in the incidence of BPD or its severity among the treatment groups.
Both treatment groups showed lower interleukin-8 and higher interleukin-10 levels compared to the control group on day 14 post-treatment initiation.
Younger gestational age and lower birth weight were identified as independent risk factors for BPD.
Inhaled corticosteroids did not increase the incidence of adverse outcomes.
Clinical Implications
The findings suggest that inhaled budesonide and beclomethasone can be safely used to reduce the duration of respiratory support in very preterm infants at risk for BPD. However, clinicians should be aware that these treatments do not significantly impact the overall incidence or severity of BPD.
Conclusion
Inhaled budesonide and beclomethasone are effective in shortening respiratory support duration in very preterm infants without increasing adverse outcomes, but they do not significantly reduce BPD incidence or severity.