TY - JOUR
T1 - Postnatal corticosteroids to treat or prevent chronic lung disease in preterm infants
AU - Jefferies, Ann L.
AU - Lacaze-Masmonteil, Thierry
AU - Newhook, Leigh Anne
AU - Peliowski, Abraham
AU - Sorokan, S. Todd
AU - Stanwick, Richard
AU - Whyte, Hilary E.A.
AU - Dunn, Michael S.
AU - Dunn, Sandra
AU - Gagnon, Andrée
AU - Gagnon, Robert
AU - León, Juan Andrés
AU - Ng, Eugene H.
AU - O'Flaherty, Patricia A.
AU - Papile, Lu Ann
AU - Whyte, Robin K.
PY - 2012/12
Y1 - 2012/12
N2 - Postnatal corticosteroids have been used for prevention and treatment of neonatal chronic lung disease (CLD) (also know as bronchopulmonary dysplasia), a significant cause of mortality and morbidity in preterm infants. As both dexamethasone and hydrocortisone administration within the first seven days of life is associated with an increased risk of cerebral palsy, early postnatal corticosteroid therapy is not recommended to prevent CLD. After seven days of life, dexamethasone has been shown to decrease the rate of CLD at 36 weeks' postmenstrual age with less impact on neurodevelopmental outcome. No trials have examined whether the benefits of corticosteroids outweigh the adverse effects for infants at high risk of, or with, severe CLD. While routine dexamethasone therapy of all ventilated infants is not recommended, clinicians may consider a short course of low-dose dexamethasone for individual infants at high risk of or with severe CLD. There is no evidence that hydrocortisone is an effective or safe alternative to dexamethasone and little evidence to support routine use of inhaled corticosteroids for prevention or treatment. Inhaled corticosteroids may be considered as an alternative to dexamethasone for treating individual infants with severe CLD. This revision replaces a statement published jointly with the American Academy of Pediatrics in 2002.
AB - Postnatal corticosteroids have been used for prevention and treatment of neonatal chronic lung disease (CLD) (also know as bronchopulmonary dysplasia), a significant cause of mortality and morbidity in preterm infants. As both dexamethasone and hydrocortisone administration within the first seven days of life is associated with an increased risk of cerebral palsy, early postnatal corticosteroid therapy is not recommended to prevent CLD. After seven days of life, dexamethasone has been shown to decrease the rate of CLD at 36 weeks' postmenstrual age with less impact on neurodevelopmental outcome. No trials have examined whether the benefits of corticosteroids outweigh the adverse effects for infants at high risk of, or with, severe CLD. While routine dexamethasone therapy of all ventilated infants is not recommended, clinicians may consider a short course of low-dose dexamethasone for individual infants at high risk of or with severe CLD. There is no evidence that hydrocortisone is an effective or safe alternative to dexamethasone and little evidence to support routine use of inhaled corticosteroids for prevention or treatment. Inhaled corticosteroids may be considered as an alternative to dexamethasone for treating individual infants with severe CLD. This revision replaces a statement published jointly with the American Academy of Pediatrics in 2002.
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U2 - 10.1093/pch/17.10.573
DO - 10.1093/pch/17.10.573
M3 - Review article
AN - SCOPUS:84872673026
SN - 1205-7088
VL - 17
SP - 573
JO - Paediatrics and Child Health
JF - Paediatrics and Child Health
IS - 10
ER -