Carbamazepine is a standard anticonvulsant in children and adults. Until no
w there is only little information available on its use in neonates. We inv
estigated the oral administration of carbamazepine in refractory neonatal s
eizures treated with phenobarbital. Ten preterm infants (gestational age 23
+ 6 - 34 + 6 weeks, birth weight 640 g-3080 g) with neonatal seizures were
refractory to a primary therapy with phenobarbital. All patients subsequen
tly received carbamazepine exclusively as a second choice anticonvulsant. A
daily dose of 7-23 mg/kg carbamazepine was administered orally in two to t
hree aliquots. All patients reached therapeutic plasma drug levels (3-12 mg
/l; 13-50 mu mol/l). In nine out of ten patients (complete group of small p
reterms with gestational age under 30 weeks and weight less than 1000 g), t
herapeutic success was excellent. Carbamazepine was continued for 1-5 month
s. After termination of therapy no further seizures occurred, also on EEG r
ecordings. Finally, no carbamazepine-induced adverse effects were observed.
Conclusion This is the first report on the use of carbamazepine in small pr
eterm infants. Carbamazepine may provide a useful and effective oral mainte
nance therapy in the management of neonatal seizures in these patients.