Bronchopulmonary dysplasia (BPD) remains a clinical problem in survivo
rs of neonatal intensive care despite recent advances which include su
rfactant replacement. Oxygen toxicity may well be a component in the p
athogenesis of BPD and disturbance of the oxidant-antioxidant balance
constitutes a biochemical problem which should be addressed in the man
agement of preterm babies. Preterm babies appear to have inadequate an
tioxidant potential and yet when delivered may experience considerable
oxidant stress. This imbalance may be ameliorated by antenatal steroi
d therapy which augments pulmonary antioxidants as well as surfactant
production. Augmentation of antioxidants by administration of exogenou
s enzymes such as superoxide dismutase and catalase is possible in ani
mal models but the clinical use of such therapies awaits further resea
rch.