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Published on: May 4, 2020
[Postnatal steroid treatment in preterm infants: risk/benefit ratio]
1Service de Néonatologie et INSERM E9935, Hôpital Robert Debré, 48, boulevard Sérurier, 75019 Paris. olivier.baud@rdb.ap-hop-paris.fr
Insights
Postnatal steroid treatment for preterm infants reduces ventilator use but does not lower mortality. Adverse effects, including neurological impairment and white matter damage, necessitate caution, especially with early dexamethasone use.
Area of Science:
- Neonatal Medicine
- Pediatric Pharmacology
- Neurodevelopmental Biology
Context:
- Preterm infants often require respiratory support, increasing the risk of chronic lung disease.
- Postnatal steroid administration is a common strategy to manage respiratory distress in premature neonates.
- Concerns exist regarding the long-term neurodevelopmental effects of these treatments.
Purpose:
- To review the risk/benefit profile of postnatal steroid therapy in preterm infants.
- To correlate epidemiological data with experimental evidence on steroid impact on brain development.
- To evaluate the association between steroid treatment and neurological outcomes.
Summary:
- Steroid treatment consistently reduced the need for assisted ventilation in preterm infants.
- However, it did not decrease oxygen requirement at term or neonatal mortality.
- Adverse effects include hyperglycemia, hypertension, GI complications, and increased risk of cerebral palsy.
Impact:
- Dexamethasone's impact on brain development, particularly white matter, may link to neurological impairment.
- Sulphiting preservatives in injectable dexamethasone might affect neuronal maturation.
- Early dexamethasone use in preterm infants should be avoided; alternative glucocorticoids require further study.
Abstract:
This review examines the risk/benefit ratio of postnatal steroid treatment in preterm infants and correlates epidemiological data with special emphasis on experimental evidence concening the impact of steroid on brain development. With all regimens, steroid treatment consistently reduced the need for assisted ventilation at 28 days of postnatal age or at term. However, neither oxygen at term nor neonatal mortality has been decreased by this treatment. Conversely, respiratory benefits should be weighed against several adverse effects: hyperglycemia, hypertension, gastrointestinal bleeding or perforation, increased risk of cerebral palsy. The impact of dexamethasone on brain development and risk factors of white matter damage could be involved in the association between postnatal steroid treatment and neurological impairment in treated infants. Injectable preparations of dexamethasone contain sulphiting preservatives which could account for the alterations in neuronal maturation observed in animal models. Early use of dexamethasone should especially be avoided for postnatal steroid treatment in premature infants. Other glucocorticoids as alternatives to dexamethasone need to be evaluated in appropriate and large controlled trials with long term follow up.
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