Objective: To assess early visual impairment related to vigabatrin prospect
ively in patients with and without visual symptoms. Background: Vigabatrin
acts as an inhibitor of gamma-aminobutyric acid (GABA) transaminase. GABA-i
nduced ion transport changes in the retinal pigment epithelium have been de
scribed. The electro-oculogram (EOG) is a clinical test that reflects photo
receptor and pigment epithelium function. Patients and methods: Of the 22 c
onsecutive patients presenting with a history of partial seizures currently
treated with vigabatrin, 20 were included in the study. A complete clinica
l ophthalmologic and neurologic examination was performed, including static
100-point perimetry, EGG, and electroretinogram (ERG). Results: In 14 of 2
0 patients, the light/dark ratio (Arden ratio) of the standard EOG was redu
ced in at least one eye. The a- and b-wave amplitudes and implicit time of
the ERG were within the normal range in all patients; however, ERG oscillat
ory potentials could not be recorded in 10 patients. Twelve patients had vi
sual field constriction; five complained of visual symptoms. The most sever
e visual impairment was observed in patients treated with both vigabatrin a
nd valproate. Conclusions: There is some evidence of outer retinal dysfunct
ion in the patients treated with vigabatrin. EGG, a more sensitive diagnost
ic tool than ERG for screening vigabatrin-treated patients, also appears to
be more specific.