Randomised clinical trials show that two injections of corticosteroid into
the mother before preterm delivery reduce respiratory distress syndrome, ne
onatal mortality, and intraventricular haemorrhage. However, repeated cours
es of antenatal steroid are not backed by such evidence of safety and effic
acy. Animal studies have shown that maternal corticosteroid delays myelinat
ion and reduces the growth of all fetal brain areas particularly the hippoc
ampus. Corticosteroids may reduce or enhance hypoxic-ischaemic injury to th
e developing brain depending on timing and dosage. Clinical trials of mater
nally administered corticosteroid show no evidence of increased disability
on follow up but numbers are small. Postnatal trials of dexamethasone when
brain maturity is still preterm show a significant increase in later disabi
lity in the dexamethasone treated groups. There is evidence from randomised
trials, retrospective data, experiments on pregnant mice, and the chemical
make up of the preparations that betamethasone may be safer and more prote
ctive of the immature brain than dexamethasone. Single course corticosteroi
d treatment before preterm delivery must still be recommended as a life sav
ing and cost effective intervention, but clinicians may wish to change from
using dexamethasone to betamethasone. In view of the animal and postnatal
data, clinicians should be cautious with repeated courses of antenatal cort
icosteroids and repetition may be unnecessary for lung maturity.