Abstract
Introduction. We present a case series diagnosed with cortical developments disorders on vigabatrin treatment. Objetive. The study aims to evaluate the effectiveness in terms of crisis control these patients, according to histological findings and functional disorders caused by tuberous sclerosis..
Materials and methods. We reviewed records of patients diagnosed with cortical developmental disorder treated with Vigabatrin, in the period between 2005 to 2008 at the Liga central contra la epilepsia Bogotá, Colombia. Data about type of disturbance of cortical development, classification of epilepsy, treatment before and after treatment with vigabatrin and presence of adverse effects.
Results. We reviewed 14 records, being 57.11% males, aged between 4 and 28 years. The most common form of epilepsy was the focal of a different location and type of cortical malformation was the most common focal cortical dysplasia.
The response obtained in terms of seizure control in 50% of the patients was over 90% with respect to seizure frequency prior to the start of vigabatrin. Only one patient showed clinically decreased visual field and improved with the cessation of treatment.
Conclusion. Vigabatrin is an effective and safe treatment for the management of patients with epilepsy secondary to cortical development disorders. Should closely monitor the possible occurrence of adverse effects.
References
Ben-Menachem E. Vigabatrin. En E. Wyllie, editor, The treatment of epilepsy principles and practice. Philadelphia: Lippincot Williams & Wilkins, 2001:961-968.
Appleton RE, Peters AC, Mumford JP et al. Randomised, placebo-controlled study of Vigabatrin as first-line treatment of infantile spasms. Epilepsia 1999; 40: 1627-1633.
Camposano S, Major P, Halpern E, Thiele E. Vigabatrin in the treatment of childhood epilepsy: A retrospective chart review of efficacy and safety profile. Epilepsia 2008; 49(7): 1186-1191.
Mitchell W, Shah N. Vigabatrin for Infantil Spasm. Pediatr Neurol 2002; 27: 161-164.
Curatolo P, Verdecchia M, Bombarderi R. Vigabatrin for Tuberous Sclerosis Complex. Brain & Development 2001; 23: 649-653.
Cepeda C, André V, Levine M, Salamon N, Miyata H, Vinters H, Mathern G. Epileptogenesis in Pediatric Cortical Dysplasia: The Dysmature Cerebral Developmental Hypothesis. Epilepsy and Behavior 2006; 9: 219-235.
Pang T, Atefy R, Sheen V. Malformations of Cortical Development. The Neurologist 2008; 14: 181-191.
Guerrini R, Sicca F, Parmeggiani L. Epilepsy and Malformations of the Cerebral Cortex. Epileptic Disord 2003; 5 (suppl 2): S9-S26.
Lortie A, Plouin P, Chiron C, Delande O, Dulac O. Characteristics of Epilepsy in Focal Cortical Dysplasia in Infancy. Epilepsy Research 2002; 51: 133-145.
Chau V, Karvelas G, Jacob P, Carmant L. Early Treatment of Aicardi Syndrome with Vigabatrin can Improve Outcome. Neurology 2004; 63: 1756-1757.
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformations of cortical development. Update 2001. Neurology 2001; 57: 2168-78.
Eslava J. Epilepsias refractarias en adultos, capítulo 10. Guía neurológica, No. 2. Bogotá: Asociación Colombiana de Neurología; 2000: 137-150.
Mc Donald D, Najam Y, Keegan M, Whooley M, Madden D. The Use of Lamotrigine, Vigabatrin and Gabapentin as Add-on therapy in Intractable Epilepsy of Childhood. Seizure 2005; 14:112-116.
Jambaque I, Chiron C, Dumas C et al. Mental and behavioural outcome of infantile epilepsy treated by Vigabatrin in tuberous sclerosis patients. Epilepsy Res 2000; 38: 151-160.
Guzzeta F, Cioni G, Mercuri E, Fazzi E, Biagioni E, Veggiotti P et al. Neurodevelopmental Evolution of West Syndrome: A two year Prospective Study. European Journal of Paediatric Neurology 2008; (12): 387-397.
Gaily E, Jonsson H, Lappi M. Visual Field at School – age in children treated with v igabatrin in infancy. Epilepsia 2009; 50(2): 206-219.
Werth R, Schädler G. Visual Field Loss in Young Children and Mentally Handicapped Adolescents Receiving Vigabatrin. Invest Ophtalmol Vis Sci 2006; 47: 3028-3035.

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