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Postnatal corticosteroids to prevent or treat bronchopulmonary dysplasia in preterm infants
Brigitte Lemyre1, Michael Dunn1, Bernard Thebaud1
1Canadian Paediatric Society, Fetus and Newborn Committee, Ottawa, Ontario.
Insights
New evidence suggests prophylactic hydrocortisone may improve survival without bronchopulmonary dysplasia (BPD) in preterm infants. Dexamethasone is not recommended for prevention, but may be considered after the first week for high-risk infants.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Pharmacology
Background:
- Bronchopulmonary dysplasia (BPD) is a major cause of morbidity and mortality in preterm infants.
- Historically, postnatal corticosteroids like dexamethasone have been used to prevent and treat BPD.
- Concerns exist regarding neurodevelopmental risks and mortality associated with early corticosteroid use.
Purpose of the Study:
- To evaluate the efficacy and safety of prophylactic hydrocortisone for preventing BPD in preterm infants.
- To assess the neurodevelopmental outcomes at 2 years of age.
- To provide updated recommendations on the use of corticosteroids for BPD prevention and treatment.
Main Methods:
- A review of current evidence on postnatal corticosteroid use for BPD.
- Analysis of studies investigating prophylactic hydrocortisone initiated within 48 hours post-birth.
- Examination of data on dexamethasone use after the first week post-birth and inhaled corticosteroids.
Main Results:
- Prophylactic physiological-dose hydrocortisone, initiated early and without indomethacin, improves survival without BPD and shows no adverse neurodevelopmental effects at 2 years.
- Routine early dexamethasone for BPD prevention is not recommended due to increased risks of cerebral palsy.
- Low-dose dexamethasone may be considered after the first week for high-risk infants with evolving BPD; hydrocortisone is not proven for treating established BPD.
Conclusions:
- Early prophylactic hydrocortisone is a potential therapeutic option for preterm infants at high risk for BPD.
- Dexamethasone use should be restricted, with specific considerations for late-stage intervention in select cases.
- Inhaled corticosteroids are not supported for BPD treatment based on current evidence.
Abstract:
Historically, postnatal corticosteroids have been used to prevent and treat bronchopulmonary dysplasia (BPD), a significant cause of morbidity and mortality in preterm infants. Administering dexamethasone to prevent BPD in the first 7 days post-birth has been associated with increasing risk for cerebral palsy, while early inhaled corticosteroids appear to be associated with an increased risk of mortality. Neither medication is presently recommended to prevent BPD. New evidence suggests that prophylactic hydrocortisone, when initiated in the first 48 hours post-birth, at a physiological dose, and in the absence of indomethacin, improves survival without BPD, with no adverse neurodevelopmental effects at 2 years. This therapy may be considered by clinicians for infants at highest risk for BPD. Routine dexamethasone therapy for all ventilator-dependent infants is not recommended, but after the first week post-birth, clinicians may consider a short course of low-dose dexamethasone (0.15 mg/kg/day to 0.2 mg/kg/day) for individual infants at high risk for, or with evolving, BPD. There is no evidence that hydrocortisone is an effective or safe alternative to dexamethasone for treating evolving or established BPD. Current evidence does not support inhaled corticosteroids for the treatment of BPD.
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