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Published on: May 4, 2020
Optimal postnatal corticosteroid regimens to prevent bronchopulmonary dysplasia with minimal adverse effects
1Department of Pediatrics, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Insights
Postnatal corticosteroids aid ventilator weaning and prevent bronchopulmonary dysplasia (BPD) in preterm infants. However, cautious, selective use is advised due to unclear guidelines and potential neurodevelopmental risks.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Pharmacology
Background:
- Postnatal corticosteroids are frequently used for extremely preterm infants to prevent or treat bronchopulmonary dysplasia (BPD).
- Current clinical practice lacks clear guidelines regarding optimal timing, dosage, type, route, and indications for corticosteroid use in BPD.
- Early dexamethasone administration in the first week of life is linked to adverse neurodevelopmental outcomes.
Purpose of the Study:
- To review the current evidence on the use of postnatal corticosteroids in preterm infants with BPD.
- To highlight the complexities and uncertainties surrounding corticosteroid therapy for BPD.
- To emphasize the need for individualized, risk-based decision-making in corticosteroid administration.
Main Methods:
- Systematic review of existing literature on postnatal corticosteroid use in BPD.
- Analysis of studies comparing different corticosteroid types (dexamethasone, hydrocortisone) and administration routes (systemic, inhaled, intratracheal).
- Evaluation of evidence regarding timing, dosage, and neurodevelopmental outcomes.
Main Results:
- Early systemic dexamethasone is not recommended due to neurodevelopmental risks.
- Dexamethasone may benefit high-risk infants for cerebral palsy-free survival but harm low-risk infants.
- Optimal dosing and long-term safety data for various administration routes (inhaled, intratracheal) remain limited or inconclusive.
Conclusions:
- Postnatal corticosteroids should be used cautiously and selectively in ventilator-dependent infants with severe BPD.
- Individualized risk assessment is crucial for guiding corticosteroid therapy.
- Further high-quality trials are necessary to determine optimal strategies and long-term safety, particularly concerning neurodevelopmental outcomes.
Abstract:
Postnatal corticosteroids can facilitate ventilator weaning and reduce the risk of bronchopulmonary dysplasia (BPD); therefore, they are commonly used to prevent or treat BPD in preterm infants, particularly those born extremely preterm. Despite their frequent use in high-risk infants with severe BPD, no clear guidelines have been established for the optimal timing of administration, dosage, corticosteroid type, route of delivery, and indication based on the infant's baseline risk of BPD. Early systemic corticosteroid administration, particularly dexamethasone within the first week of life, appears to be associated with adverse neurodevelopmental outcomes and is generally not recommended. Dexamethasone and hydrocortisone exhibit distinct biological and clinical effects, yet evidence from direct comparative studies is limited. Dexamethasone may improve cerebral palsy-free survival of infants at high risk of BPD but poses potential harm in those at low risk, highlighting the need for individualized risk-based decision-making. Optimal dosing remains unclear: lower doses may reduce systemic side effects despite the uncertainty of their neurodevelopmental safety, whereas higher doses may be more effective in selected high-risk infants. Inhaled corticosteroids have inconclusive benefits compared with systemic therapy. The intratracheal administration of corticosteroids with surfactant improves distal airway delivery and reduces death or BPD rates; however, short- and long-term safety data remain limited. Overall, postnatal corticosteroids should be used cautiously and selectively in high-risk, ventilator-dependent infants with severe BPD. Future high-quality trials are needed to evaluate long-term survival free of neurodevelopmental impairments.
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