Purpose: We investigated the effect of pregnancy on the kinetics of la
motrigine (LTG), passage of LTG over the placenta and the excretion of
the drug in breast milk. Methods: We used high-performance liquid chr
omatography to determine concentrations of LTG in plasma and in breast
milk in a woman who was treated with LTG monotherapy during pregnancy
and lactation. Results: Plasma levels of LTG decreased as pregancy pr
ogressed. The ratio of dose to plasma concentration was 5.8 times high
er at delivery and 3.6 times higher in late pregnancy as compared with
5 months postpartum, suggesting enhanced clearance of LTG during preg
nancy. The concentration ratio of umbilical cord to mother's plasma wa
s 1.2 indicating extensive passage of LTG over the placenta. The LTG p
lasma concentration in the newborn was still 48 h after birth similar
to the plasma levels of the mother at delivery and in the umbilical co
rd. The ratio of milk to plasma concentration was 0.6 2 weeks after de
livery and the plasma concentration in the breastfed child was 25% of
the mother's plasma levels. No adverse effects were observed in the ne
wborn. Conclusions: The kinetics of LTG may be influenced by pregnancy
to such a degree that dose adjustments may be indicated. Due to an ex
tensive passage of LTG into breast milk, and a slow elimination in the
newborn, LTG concentrations in the nursed infant may reach levels at
which pharmacological effects can be expected.