4.5 Article

Visual field defects after vigabatrin treatment during infancy: retrospective population-based study

Journal

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
Volume 64, Issue 5, Pages 641-648

Publisher

WILEY
DOI: 10.1111/dmcn.15099

Keywords

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Funding

  1. Foundation for Pediatric Research

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This study investigated the prevalence of vigabatrin-attributed visual field defect (VAVFD) in infantile spasms and the utility of optical coherence tomography (OCT) in detecting vigabatrin-related damage. The study found that the overall prevalence of VAVFD is lower after exposure in infancy compared to adulthood, and the risk increases with longer treatment duration. OCT showed concomitant attenuated RNFL in some children with VAVFD. Further studies should aim to identify infants particularly susceptible to VAVFD and clarify the role of OCT.
Aim To investigate the prevalence of vigabatrin-attributed visual field defect (VAVFD) in infantile spasms and the utility of optical coherence tomography (OCT) in detecting vigabatrin-related damage. Method We examined visual fields by Goldmann or Octopus perimetry and the thickness of peripapillary retinal nerve fiber layer (RNFL) with spectral-domain OCT at school age or adolescence. Results Out of 88 patients (38 females, mean age at study 15y, SD 4y 3mo, range 6y 4mo-23y 3mo [n=65] or deceased [n=21] or moved abroad [n=2]) exposed to vigabatrin in infancy, 28 were able to perform formal visual field testing. Two had visual field defect from structural causes. We found mild VAVFD in four patients and severe VAVFD in one patient. Median vigabatrin treatment duration for those with normal visual field was 11 months compared to 19 months for those with VAVFD (p=0.04). OCT showed concomitant attenuated RNFL in three children with VAVFD, and was normal in one. The temporal half of the peripapillary RNFL was significantly thinner in the VAVFD group compared to the normal visual field group. Interpretation The overall prevalence of VAVFD is lower after exposure in infancy compared to 52% which has been reported after exposure in adulthood. The risk increases with longer treatment duration. Further studies should identify infants particularly susceptible to VAVFD and clarify the role of OCT.

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