De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort.


Journal

Seizure
ISSN: 1532-2688
Titre abrégé: Seizure
Pays: England
ID NLM: 9306979

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 01 08 2019
revised: 12 10 2019
accepted: 31 10 2019
pubmed: 30 11 2019
medline: 6 5 2020
entrez: 29 11 2019
Statut: ppublish

Résumé

Absence Status epilepticus (AS) is a form of Non Convulsive Status Epilepticus defined as a prolonged, generalized and non-convulsive seizure, with an altered content of consciousness. We aim to describe a group of healthy children, who presented recurrent and unprovoked de novo AS as the only manifestation of their epilepsy, with an excellent response to antiepileptic drugs. We retrospectively reviewed the electroclinical and genetic features of 13 pediatric patients, referring to our epilepsy centers from 2005 to 2019, on the following criteria: (1) regular psychomotor development, (2) one or more unprovoked AS as the only epileptic manifestation, (3) normal blood testing, (4) normal neuroimaging, (5) EEG recording, (6) available follow-up (1-14 years). Patients are 7 females and 6 males, aged 7-22, with a mean age at AS onset of 9,3 years. All of them started an antiepileptic therapy, with an excellent response to Valproic Acid (VPA) or Ethosuximide (ETS). 5 patients did not start the therapy immediately after the first AS and they presented recurrent AS (from 2 to 4 episodes). 10 of them performed aCGH, karyotype, NGS panel or Whole Exome Sequencing. We suggest that de novo AS may be a well-defined age-related and self-limited epilepsy syndrome, with a good prognosis and excellent response to therapy, but it comes with a high risk of relapsing if not adequately treated with antiepileptic drugs.

Identifiants

pubmed: 31776058
pii: S1059-1311(19)30525-4
doi: 10.1016/j.seizure.2019.10.021
pii:
doi:

Substances chimiques

Anticonvulsants 0
Ethosuximide 5SEH9X1D1D
Valproic Acid 614OI1Z5WI

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-82

Informations de copyright

Copyright © 2019 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Auteurs

C Pepi (C)

Child Neurology Unit, Department of Neuroscience and Neurorehabilitation, Bambino Gesù Children's Hospital Research Institute, Rome, Italy; Child Neurology and Psychiatry Unit, System Medicine Unit, Tor Vergata University, Rome, Italy. Electronic address: chiara.pepi@opbg.net.

E Cesaroni (E)

Child Neuropsychiatric Unit, University of Ancona, Ancona, Italy.

P Striano (P)

Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, "G. Gaslini" Institute, University of Genoa, Genova, Italy.

D Maiorani (D)

Division of Pediatrics, Ospedale Belcolle, Viterbo, Rome, Italy.

D Pruna (D)

Pediatric Neurology and Epileptology Unit, Brotzu Hospital Trust, Cagliari, Italy.

S Cossu (S)

Pediatric Neurology and Epileptology Unit, Brotzu Hospital Trust, Cagliari, Italy.

M Di Capua (M)

Unit of Neurophysiology, Department of Neurosciences, Bambino Gesù Children's Hospital Research Institute, Rome, Italy.

F Vigevano (F)

Child Neurology Unit, Department of Neuroscience and Neurorehabilitation, Bambino Gesù Children's Hospital Research Institute, Rome, Italy.

N Specchio (N)

Child Neurology Unit, Department of Neuroscience and Neurorehabilitation, Bambino Gesù Children's Hospital Research Institute, Rome, Italy.

R Cusmai (R)

Unit of Neurophysiology, Department of Neurosciences, Bambino Gesù Children's Hospital Research Institute, Rome, Italy.

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Classifications MeSH