The idea of replacing 17 beta -oestradiol (E2) and progesterone (P) in pret
erm infants is based on the observation that during pregnancy E2 and P plas
ma concentrations rise in the mother and the fetus by a factor of 100. Disr
uption of the placental supply of these hormones is a physiological event f
or an infant delivered at term. A preterm infant is deprived from this supp
ly at an earlier developmental stage. In vitro and ill vivo data are discus
sed, and they highlights the potential benefit of E2 and P on the developme
nt of different organ systems. The postnatal replacement of E2 and P has th
e aim of maintaining in utero plasma concentrations. In the first randomize
d clinical study in 30 extremely preterm infants, E2 and P were replaced po
stnatally for a total of 6 weeks. With a median intravenous replacement of
8.4 mu mol/kg/day of E2 (4.2-22.9) and 67.4 mu mol/kg/day of P (35.7-87.0),
plasma levels of E2 and P were maintained within the intrauterine referenc
e values of 7.3-22.0 nmol/L and 0.95-1.9 mu mol/L, respectively. Three- to
sixfold higher dosages were needed via the transepidermal route. Trends tow
ards an improved postnatal bone mineral accretion and a reduced incidence o
f chronic lung disease were found. Further studies are warranted to clarify
the potentially important role of E2 and P for the postnatal development o
f an extremely preterm infant.