Epilepsy is a common disorder and approximately 20% of persons with epileps
y are of childbearing potential. The goals of treatment are to gain the bes
t control of seizures with the least adverse effects for both mother and of
fspring. Diagnosing the correct epilepsy syndrome is the most important ste
p in selecting the proper treatment, because it has been established that s
pecific syndromes, such as juvenile myoclonic epilepsy, respond well to val
proic acid (sodium valproate) and possibly lamotrigine, but not to phenytoi
n or carbamazepine. Conversely, valproic acid should not generally be used
in women with symptomatic epilepsy because of the risk for spina bifida tha
t is associated with the use of this drug.
Anticonvulsant drugs may alter hormone levels and influence sexuality and r
eproduction. Anticonvulsants which induce liver metabolism decrease the eff
ectiveness of hormone contraceptives, and their use should be modified by i
ncreasing drug doses or the frequency of administration.
Pregnancy alters the pharmacokinetics of anticonvulsants by increasing thei
r clearance or altering their binding. These effects are most prominent for
phenytoin and valproic acid but may have little effect on a renally cleare
d, unbound anticonvulsant such as gabapentin.
Both animal and human teratogenic effects have been reported for all of the
standard anticonvulsants. Animal studies have shown gabapentin, tiagabine
and lamotrigine to have little association with malformations, but studies
in humans have thus far been limited.
Pre-pregnancy evaluation and counselling are essential. The correct syndrom
e must be diagnosed and the appropriate anticonvulsant started before pregn
ancy. Folic acid supplementation should be used at all times, because some
anticonvulsants deplete this vitamin. Anticonvulsant blood concentrations s
hould be monitored, especially when toxicity is apparent or seizures occur.