Literature DB >> 11440348

Visual function is stable in patients who continue long-term vigabatrin therapy: implications for clinical decision making.

S R Paul1, G L Krauss, N R Miller, M T Medura, T A Miller, M A Johnson.   

Abstract

PURPOSE: Vigabatrin (VGB) has been shown to cause visual field constriction and other forms of mild visual dysfunction. We determined the safety of continuing VGB therapy in patients who had received prolonged treatment (>2 years) with the drug by serially monitoring changes in visual function over a 1-year period of continued therapy. We also followed up patients who discontinued VGB to see whether alternative therapies are effective.
METHODS: Fifteen of 17 patients who continued VGB therapy had visual-function testing (visual acuity, color vision, kinetic and static perimetry) every 3 months for 1 year. Eighteen patients who discontinued VGB were given alternative antiepileptic drugs (AEDs); their seizure responses were measured after > or =3 months of treatment.
RESULTS: Patients continuing VGB showed no worsening of visual acuity, color vision, or visual-field constriction beyond that measured in the initial test. Many patients who discontinued VGB had good seizure control with either newer or previously unsuccessful AEDs.
CONCLUSIONS: For patients who have an excellent response to VGB and only mild visual changes, continued therapy may be safe with close visual monitoring. Patients who do not have a significant reduction in seizures or who experience considerable visual dysfunction with VGB may respond well to alternative therapies.

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Year:  2001        PMID: 11440348     DOI: 10.1046/j.1528-1157.2001.49299.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  7 in total

1.  Evaluating risks for vigabatrin treatment.

Authors:  Gregory L Krauss
Journal:  Epilepsy Curr       Date:  2009 Sep-Oct       Impact factor: 7.500

2.  Electroretinographic (ERG) responses in pediatric patients using vigabatrin.

Authors:  Anne Moskowitz; Ronald M Hansen; Susan E Eklund; Anne B Fulton
Journal:  Doc Ophthalmol       Date:  2012-03-20       Impact factor: 2.379

3.  Sub-chronic low dose gamma-vinyl GABA (vigabatrin) inhibits cocaine-induced increases in nucleus accumbens dopamine.

Authors:  Wynne K Schiffer; Douglas Marsteller; Stephen L Dewey
Journal:  Psychopharmacology (Berl)       Date:  2003-04-09       Impact factor: 4.530

Review 4.  Vigabatrin.

Authors:  James W Wheless; R Eugene Ramsay; Stephen D Collins
Journal:  Neurotherapeutics       Date:  2007-01       Impact factor: 7.620

5.  A controlled study comparing visual function in patients treated with vigabatrin and tiagabine.

Authors:  G L Krauss; M A Johnson; S Sheth; N R Miller
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-03       Impact factor: 10.154

6.  Examining visual field defects in the paediatric population exposed to vigabatrin.

Authors:  E L Spencer; G F A Harding
Journal:  Doc Ophthalmol       Date:  2003-11       Impact factor: 2.379

7.  Relationship between the area of isopters and Vigabatrin dosage during two years of observation.

Authors:  Katarzyna Nowomiejska; Marian Jedrych; Agnieszka Brzozowska; Konrad Rejdak; Tomasz Zarnowski; Michael J Koss; Katarzyna Ksiazek; Piotr Ksiazek; Ryszard Maciejewski; Anselm G Juenemann; Ulrich Schiefer; Robert Rejdak
Journal:  BMC Ophthalmol       Date:  2014-04-30       Impact factor: 2.209

  7 in total

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