2010
DOI: 10.1016/j.eplepsyres.2010.09.004
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Vigabatrin-induced peripheral visual field defects in patients with refractory partial epilepsy

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Cited by 16 publications
(9 citation statements)
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“…VGB‐induced retinal damage (VGB‐RD) was first reported in 1997 and is characterized by permanent, bilateral constriction of the peripheral visual fields . This visual field loss is asymptomatic for most patients; thus, periodic ophthalmologic testing is required to detect it .…”
Section: Clinical Use Of Vigabatrinmentioning
confidence: 99%
See 1 more Smart Citation
“…VGB‐induced retinal damage (VGB‐RD) was first reported in 1997 and is characterized by permanent, bilateral constriction of the peripheral visual fields . This visual field loss is asymptomatic for most patients; thus, periodic ophthalmologic testing is required to detect it .…”
Section: Clinical Use Of Vigabatrinmentioning
confidence: 99%
“…In a recent prospective study, Sergott et al. evaluated visual field impairment by Goldmann perimetry in 258 VGB‐treated patients with refractory partial epilepsy. Fifty‐three percent of patients were classified as having mild visual field defects (60–80 ° monocular temporal field retained), 17% had moderate defects (30–60 ° temporal field retained), and 2% had severe defects (<30 ° temporal field retained).…”
Section: Clinical Use Of Vigabatrinmentioning
confidence: 99%
“…28 The most discussed side effect of vigabatrin involves peripheral vision defects (mainly bilateral nasal defects) with central vision sparing which is often mild to moderate. The incidence ranges between 14% and 92% of patients 29 and can be permanent. The FDA mandated that children have vision screening at baseline, every 3 months for 18 months, then every 6 months thereafter, while receiving treatment.…”
Section: New Advances In Drug Therapymentioning
confidence: 99%
“…Unfortunately, vigabatrin can cause direct retinal toxicity leading to constriction of peripheral visual fields, a difficult complication to monitor in non-verbal and pre-verbal children. This impairment occurs in 16-44% of testable patients treated long term, but often remains asymptomatic [12,13]. In the United States, the Food and Drug Administration (FDA) mandates patient counseling, consent, and monitoring of ongoing ophthalmological follow-up.…”
Section: Box 154 American Academy Of Neurology (Aan) and Child Neuromentioning
confidence: 99%