Your browser doesn't support javascript.
loading
Adaptive behaviour in adolescents and adults with Dravet syndrome.
Lo Barco, Tommaso; Offredi, Francesca; Castino, Eva; Proietti, Jacopo; Cossu, Alberto; Fiorini, Elena; Fontana, Elena; Cantalupo, Gaetano; Dalla Bernardina, Bernardo; Darra, Francesca.
Afiliação
  • Lo Barco T; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Offredi F; Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, Modena, Italy.
  • Castino E; Research Center for Pediatric Epilepsies Verona, Verona, Italy.
  • Proietti J; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Cossu A; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Fiorini E; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Fontana E; Research Center for Pediatric Epilepsies Verona, Verona, Italy.
  • Cantalupo G; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Dalla Bernardina B; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
  • Darra F; Child Neuropsychiatry Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
Dev Med Child Neurol ; 65(6): 838-846, 2023 06.
Article em En | MEDLINE | ID: mdl-36316303
AIM: To explore the feasibility of using an adaptive behaviour profile (ABP) assessment generated from a well-known measure-the Vineland Adaptive Behavior Scales, Second Edition (VABS-II)-as an instrument for outcome measures in adolescents and adults with Dravet syndrome. METHOD: We administered the VABS-II to 35 adolescents and adults with Dravet syndrome (15 males; mean age 24 years, SD 8 years, range: 12-46 years) and collected epilepsy history and neurological features at the time of assessment. We conducted a cross-sectional analysis of VABS-II raw scores and performed cluster analysis to identify different subgroups. We then explored possible relationships between clinical and epilepsy features, ABPs, and age. RESULTS: Most participants obtained the minimum standard scores in the various VABS-II subdomains, while the raw score analysis outlined interindividual and intraindividual differences among skills. We found two subpopulations: one with a 'lower' ABP and one with a 'higher' ABP, corresponding respectively to individuals in whom myoclonic seizures or generalized spike-and-wave activity were present ('complete phenotype') or absent ('incomplete phenotype') on electroencephalography. INTERPRETATION: This study further delineates the natural history of Dravet syndrome. The assessment of an ABP through the VABS-II raw score analysis provides a means by which to illustrate profiles of adaptive behaviour in adolescents and adults with Dravet syndrome but shows limitations related to poor sensitivity in measuring fine clinical details. There is a need for new and more specific tools to monitor patients with developmental and epileptic encephalopathies. WHAT THIS PAPER ADDS: Most adults with Dravet syndrome obtained the minimum standard scores in the Vineland Adaptive Behavior Scales, Second Edition (VABS-II) subdomains. The VABS-II raw score analysis showed interindividual and intraindividual variability. Individuals with myoclonic seizures and/or generalized spike-and-wave activity on electroencephalography showed a worse adaptive behaviour profile.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Epilepsia Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Epilepsia Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália