Literature DB >> 28873364

Refractory spasms of focal onset-A potentially curable disease that should lead to rapid surgical evaluation.

Mathilde Chipaux1, Georg Dorfmüller2, Martine Fohlen3, Nathalie Dorison3, Marie-Astrid Metten4, Olivier Delalande3, Sarah Ferrand-Sorbets3, Delphine Taussig3.   

Abstract

PURPOSE: Infantile spasms (IS) can occur as the only seizure type in children with surgically amenable epilepsies. Although early surgery has shown positive effects, little is known regarding outcomes.
METHODS: We retrospectively reviewed all children with IS referred to our tertiary center between 2002 and 2014 and try to define factors of outcome.
RESULTS: Sixty-eight children with focal onset seizures were referred: twenty children with a hemispheric implication and 48 with one or more lobes involved. The age of onset was significantly earlier in the hemispheric population (8.0 versus 16.7 months in the focal population). There was no difference in the age of onset between anterior and posterior onset zones, as we could expect regarding the maturation gradient. The epilepsy began earlier in life in tuberous sclerosis than in DNET. Only three children of the 48 non-hemispheric patients had a normal MRI at the time of the surgery. Temporal lobe was involved only in a third of the population. More than 86% of the patients were operated on. Patients with hemispheric lesions were operated on younger (2.6 years+/- 2.1 years) compared to 4.6+/- 3.5 years in the whole population. The most frequent etiologies were in descending order: dysplasia, ganglioglioma or dysembryoplastic tumours and tuberous sclerosis. The global seizure outcome was favorable (Engel 1a) in 74.6% of the patients, and 87.9% if the delay between the first seizure and the surgery was less than 36 months. It fell to 64.7% if the delay exceeded 50 months.
CONCLUSION: Spasms of focal onset have a similar postsurgical outcome as other seizure types so surgery may be an excellent option for treating selected patients with focal infantile spasms. Volume and type but not topography of the lesion influence the age of onset. MRI is very helpful to locate the pathology in the pediatric population, since only a small portion had a normal MRI.
Copyright © 2017 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Epilepsy surgery; Focal epilepsy; Infantile spasms; Invasive EEG monitoring; Surgical outcome

Mesh:

Year:  2017        PMID: 28873364     DOI: 10.1016/j.seizure.2017.08.010

Source DB:  PubMed          Journal:  Seizure        ISSN: 1059-1311            Impact factor:   3.184


  5 in total

Review 1.  Stereoelectroencephalography Versus Subdural Electrodes for Localization of the Epileptogenic Zone: What Is the Evidence?

Authors:  Joel S Katz; Taylor J Abel
Journal:  Neurotherapeutics       Date:  2019-01       Impact factor: 7.620

Review 2.  Impact of predictive, preventive and precision medicine strategies in epilepsy.

Authors:  Rima Nabbout; Mathieu Kuchenbuch
Journal:  Nat Rev Neurol       Date:  2020-10-19       Impact factor: 42.937

3.  Infantile Spasms in Tuberous Sclerosis Complex: Lesion or Network?

Authors:  Charuta Joshi; Joshua J Bear
Journal:  Epilepsy Curr       Date:  2021-07-28       Impact factor: 7.500

4.  Lesional Intractable Epileptic Spasms in Children: Electroclinical Localization and Postoperative Outcomes.

Authors:  Shuang Wang; Chang Liu; Hongwei Zhang; Qingzhu Liu; Taoyun Ji; Ying Zhu; Yan Fan; Hao Yu; Guojing Yu; Wen Wang; Dongming Wang; Lixin Cai; Xiaoyan Liu
Journal:  Front Neurol       Date:  2022-07-22       Impact factor: 4.086

Review 5.  Corpus Callosotomy for Controlling Epileptic Spasms: A Proposal for Surgical Selection.

Authors:  Tohru Okanishi; Ayataka Fujimoto
Journal:  Brain Sci       Date:  2021-12-01
  5 in total

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