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Comparative neuropsychological effects of carbamazepine and eslicarbazepine acetate.
Meador, Kimford J; Seliger, Jordan; Boyd, Alan; Razavi, Babak; Falco-Walter, Jessica; Le, Scheherazade; Loring, David W.
Afiliação
  • Meador KJ; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. Electronic address: kmeador@stanford.edu.
  • Seliger J; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. Electronic address: jseliger@stanford.edu.
  • Boyd A; CNS Vital Signs, Morrisville, NC, USA. Electronic address: aboyd@cnsvs.com.
  • Razavi B; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. Electronic address: Brazavi@stanford.edu.
  • Falco-Walter J; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. Electronic address: jessica.walter@stanford.edu.
  • Le S; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. Electronic address: schele@stanford.edu.
  • Loring DW; Department of Neurology, Emory University, Atlanta, GA, USA. Electronic address: dloring@emory.edu.
Epilepsy Behav ; 94: 151-157, 2019 05.
Article em En | MEDLINE | ID: mdl-30939410
ABSTRACT
People with epilepsy are at increased risk for neuropsychological dysfunction due to multiple factors, of which the most amendable are antiseizure medications (ASMs). Antiseizure medication effectiveness is frequently determined by tolerability. In this study, we compared the neuropsychological effects of eslicarbazepine acetate (ESL) and carbamazepine immediate-release (CBZ) using a randomized, double-blind, crossover design in healthy volunteers with a 2-week titration and 4-week maintenance phase in each treatment arm (CBZ = 400 mg BID and ESL = 800 mg qAM). Neuropsychological testing was performed at the initial visit, repeated at 1st baseline nondrug condition, end treatment #1, 2nd nondrug condition one month after treatment #1, end treatment #2, and 3rd nondrug condition one month after treatment #2. Neuropsychological testing was conducted 2 h after morning dose and included computer (i.e., dual task test, selective attention test, symbol digit, verbal memory, visuospatial memory, and 1- & 2-back continuous performance) and noncomputer tasks (i.e., Medical College of Georgia (MCG) paragraph memory, Stroop, Symbol Digit Modalities Test, Profile of Mood States). z-Scores calculated from nondrug conditions were used to compare ESL and CBZ for the 23 completers. Follow-up analyses included individual test scores and distribution of individual raw means. Mean blood levels on test day were CBZ = 8.9 µg/ml and ESL = 15.3 µg/ml. Omnibus z-score was significantly better for ESL (p = .0001). For individual measures, executive function and selective attention tests were statistically significantly better for ESL. Individual test raw means favored ESL over CBZ on 22 of 30 measures (p = .016, 2-tailed sign test). Eslicarbazepine acetate demonstrated less adverse neuropsychological effects than CBZ.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbamazepina / Dibenzazepinas / Epilepsia / Anticonvulsivantes Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsy Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbamazepina / Dibenzazepinas / Epilepsia / Anticonvulsivantes Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsy Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article