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Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study.
Toldo, Irene; Brunello, Francesco; Cavasin, Paola; Nosadini, Margherita; Sartori, Stefano; Frigo, Anna Chiara; Mai, Roberto; Pelliccia, Veronica; Mancardi, Maria Margherita; Striano, Pasquale; Severino, Marisavina; Zara, Federico; Rizzi, Romana; Casellato, Susanna; Di Rosa, Gabriella; Mastrangelo, Mario; Spalice, Alberto; Budetta, Mauro; De Palma, Luca; Guerrini, Renzo; Pruna, Dario; Cordelli, Duccio Maria; Sofia, Vito; Papa, Amanda; Chiesa, Valentina; Ragona, Francesca; Parisi, Pasquale; D'Aniello, Alfredo; Veggiotti, Pierangelo; Dainese, Filippo; Giordano, Lucio; Licchetta, Laura; Tinuper, Paolo; D'Orsi, Giuseppe; Cassina, Matteo; Manara, Renzo.
Afiliação
  • Toldo I; Child Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy. Electronic address: irene.toldo@unipd.it.
  • Brunello F; Child Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy.
  • Cavasin P; Child Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy.
  • Nosadini M; Child Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy.
  • Sartori S; Child Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy.
  • Frigo AC; Department of Cardiac, Thoracic and Vascular Sciences, University of Padua, Padua, Italy.
  • Mai R; 'Claudio Munari' Centre for Epilepsy Surgery, ASST GOM Niguarda, Milan, Italy.
  • Pelliccia V; 'Claudio Munari' Centre for Epilepsy Surgery, ASST GOM Niguarda, Milan, Italy.
  • Mancardi MM; Child Neuropsychiatry Unit, Clinical and Surgical Neurosciences Department, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Striano P; Child Neuropsychiatry Unit, Clinical and Surgical Neurosciences Department, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Severino M; Pediatric Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Zara F; Laboratory of Neurogenetics and Neuroscience, IRCCS Istituto G. Gaslini, Genova, Italy.
  • Rizzi R; Neurology Unit, Department of Neuro-Motor Diseases, Azienda Unità Sanitaria Locale IRCCS, Reggio Emilia, Italy.
  • Casellato S; Child Neuropsychiatry Unit, University Hospital of Sassari, Sassari, Italy.
  • Di Rosa G; Child Neuropsychiatry Unit, Department of Human Pathology of the Adult and Developmental Age, University Hospital "G. Martino", Messina, Italy.
  • Mastrangelo M; Unit of Child Neurology and Psychiatry, Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
  • Spalice A; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
  • Budetta M; Pediatric and Child Neurology Unit, Cava de' Tirreni AOU S. Giovanni di Dio e Ruggiero d'Aragona Hospital, Salerno, Italy.
  • De Palma L; Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Guerrini R; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Pruna D; Pediatric Neurology and Epileptology Unit, "Brotzu" Hospital, Cagliari, Italy.
  • Cordelli DM; IRCCS Institute of Neurological Sciences of Bologna, UOC Neuropsychiatry of the Pediatric Age, Bologna, Italy.
  • Sofia V; Department G.F. Ingrassia, Section of Neurosciences, University of Catania, Catania, Italy.
  • Papa A; Department of Child Neurology and Psychiatry, AOU Maggiore della Carità Novara, Novara, Italy.
  • Chiesa V; Epilepsy Centre-Child Neuropsychiatry Unit, ASST Santi Paolo e Carlo, San Paolo Hospital, Milan, Italy.
  • Ragona F; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Parisi P; Child Neurology, Faculty of Medicine & Psychology, NESMOS Department, Sapienza University, Rome, Italy.
  • D'Aniello A; IRCCS "NEUROMED", Pozzilli, Italy.
  • Veggiotti P; Pediatric Neurology Unit, V. Buzzi Hospital, University of Milan, Milan, Italy.
  • Dainese F; Epilepsy Centre, SS. Giovanni e Paolo Hospital, Venice, Italy.
  • Giordano L; Child Neuropsychiatric Division, Spedali Civili, Brescia, Italy.
  • Licchetta L; Department of Biomedical and Neuromotor Sciences, University of Bologna, Milan, Italy.
  • Tinuper P; Department of Biomedical and Neuromotor Sciences, University of Bologna, Milan, Italy.
  • D'Orsi G; Epilepsy Centre, Clinic of Nervous System Diseases, Ospedali Riuniti, University of Foggia, Foggia, Italy.
  • Cassina M; Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Manara R; Neuroradiology, Department of Neuroscience, University of Padova, Padova, Italy.
Pediatr Neurol ; 141: 58-64, 2023 04.
Article em En | MEDLINE | ID: mdl-36773408
ABSTRACT

BACKGROUND:

Subcortical band heterotopia (SBH) is a rare malformation of the cortical development characterized by a heterotopic band of gray matter between cortex and ventricles. The clinical presentation typically includes intellectual disability and epilepsy.

PURPOSE:

To evaluate if the Extended Glasgow Outcome Scale-pediatric version (EGOS-ped) is a feasible tool for evaluating the functional disability of patients with (SBH).

METHOD:

Cross-sectional multicenter study of a cohort of 49 patients with SBH (female n = 30, 61%), recruited from 23 Italian centers.

RESULTS:

Thirty-nine of 49 (80%) cases showed high functional disability at EGOS-ped assessment. In the poor result subgroup (EGOS-ped >3) motor deficit, language impairment, and lower intelligence quotient were more frequent (P < 0.001, P = 0.02, and P = 0.01, respectively); the age at epilepsy onset was remarkably lower (P < 0.001); and the prevalence of epileptic encephalopathy (West syndrome or Lennox-Gastaut-like encephalopathy) was higher (P = 0.04). The thickness and the extension of the heterotopic band were associated with EGOS-ped score (P < 0.01 and P = 0.02). Pachygyria was found exclusively among patients with poor outcome (P < 0.01).

CONCLUSIONS:

The EGOS-ped proved to be a reliable tool for stratifying the functional disability of patients with SBH. According to this score, patients could be dichotomized group 1 (80%) is characterized by a poor overall functionality with early epilepsy onset, thick heterotopic band, and pachygyria, whereas group 2 (20%) is characterized by a good overall functionality with later epilepsy onset and thinner heterotopic band.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia / Lissencefalias Clássicas e Heterotopias Subcorticais em Banda Tipo de estudo: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Pediatr Neurol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia / Lissencefalias Clássicas e Heterotopias Subcorticais em Banda Tipo de estudo: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Pediatr Neurol Ano de publicação: 2023 Tipo de documento: Article