THERAPY FOR EPILEPSY
SAFETY OF ANTICONVULSANTS
Avoid
The following agents are
strongly porphyrinogenic, have been associated
with acute attacks and should be avoided:
- phenobarbital
- primidone
- phenytoin
- mephenytoin
- ethosuximde
- methosuximide.
Use with only
extreme caution
The following agents are
of contentious safety, and are best avoided:
- carbamazepine
- valproic acid
- topiramate
- vigabatrin
Carbamazepine is of contentious
safety. Some authors have described patients
who tolerated it well whereas they had
reacted poorly to other anticonvulsants.
However, there are also a number of reports
detailing clinical and biochemical deterioration
in porphyria on carbamazepine; it is also
porphyrinogenic in experimental systems
and in human volunteers. We suggest that
it be avoided.
Several lists have suggested
that valproic acid is safe. However, review
of the literature reveals a number of
reports of clinical deterioration following
valproic acid therapy or of failure to
resolve until it was discontinued; it
is also porphyrinogenic in both experimental
systems and in normal human volunteers.
We suggest that it be avoided.
Topiramate is a CYP inducer
and should therefore be avoided, although
there are no data on its clinical use.
Use
The following agents appear
to be the safest for use in porphyria:
- clonazepam
- gabapentin
- lamotrigine
Clonazepam is weakly porphyrinogenic
in experimental systems, and there are
isolated reports of a rise in urine precursors
on clonazepam therapy. However, several
authors report that patients whose porphyria
had deteriorated on agents such as phenytoin
and carbamazepine were maintained in complete
safety on clonazepam. It has been used
safely on both a short- and a long-term
basis in Cape Town for patients with active
porphyria, and we regard it as a safe
agent.
Gabapentin appears safe.
Several patients in Cape Town have successfully
used gabapentin for chronic control of
epilepsy.
Lamotrigine is very little
metabolised, and one would predict it
is safe, though data are lacking .
IMMEDIATE CONTROL
OF SEIZURES
There is no evidence
that a single injection of
a benzodiazepine such as diazepam
is dangerous; we suggest diazepam
or preferably clonazepam for
the termination of seizures.
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