Literature DB >> 23010167

Surgical versus conservative treatment in patients with cerebral cavernomas and non refractory epilepsy.

Santiago Fernández1, Júlia Miró, Mercé Falip, Alejandro Coello, Gerard Plans, Sara Castañer, Juan José Acebes.   

Abstract

PURPOSE: The optimal therapy of patients with cerebral cavernoma (CCs) and new onset epilepsy, sporadic seizures, or non well established refractory epilepsy is still not clear. The aim of this study was to compare the incidence of seizures in patients with CCs both operated and non operated, in order to obtain more information on the correct management of these patients.
MATERIALS AND METHODS: We studied retrospectively 43 patients with non refractory epilepsy secondary to CCs. Twenty-six of them (60.5%) underwent surgery and made up the surgical group, and 17 patients were treated medically and constituted the medical group. Seizure frequency and other clinical variables were compared between both groups.
RESULTS: At two years, out of the 26 operated patients, 19 (73%) remained seizure free, 4 (15%) had less than a seizure per month, and one patient (4%) had more than one seizure per month. At five years, 15 patients of the surgical group remained for analysis. Of them, 11 (73.3%) were seizure free, and 4 (26.7%) had less than one seizure a month. In the medical group, 12 out of 17 patients were seizure free (70.6%). There were no significant differences between the two groups (p=0.2 and p=0.3, respectively). Seven patients had postoperative neurological sequelae.
CONCLUSION: Surgical treatment of patients with non refractory epilepsy due to CCs did not significantly reduce the likelihood of seizures when compared to medical treatment. It must also be considered that surgery carries serious risks. A prospective and randomized study must be carried out to further clarify our findings.
Copyright © 2012 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23010167     DOI: 10.1016/j.seizure.2012.09.004

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


  4 in total

Review 1.  Familial Cerebral Cavernous Malformations.

Authors:  Atif Zafar; Syed A Quadri; Mudassir Farooqui; Asad Ikram; Myranda Robinson; Blaine L Hart; Marc C Mabray; Catherine Vigil; Alan T Tang; Mark L Kahn; Howard Yonas; Michael T Lawton; Helen Kim; Leslie Morrison
Journal:  Stroke       Date:  2019-05       Impact factor: 7.914

Review 2.  Management of cerebral cavernous malformations: from diagnosis to treatment.

Authors:  Nikolaos Mouchtouris; Nohra Chalouhi; Ameet Chitale; Robert M Starke; Stavropoula I Tjoumakaris; Robert H Rosenwasser; Pascal M Jabbour
Journal:  ScientificWorldJournal       Date:  2015-01-05

3.  Outcome after surgical or conservative management of cerebral cavernous malformations.

Authors:  Fiona Moultrie; Margaret A Horne; Colin B Josephson; Julie M Hall; Carl E Counsell; Jo J Bhattacharya; Vakis Papanastassiou; Robin J Sellar; Charles P Warlow; Gordon D Murray; Rustam Al-Shahi Salman
Journal:  Neurology       Date:  2014-07-03       Impact factor: 9.910

4.  Surgical management of epilepsy due to cerebral cavernomas using neuronavigation and intraoperative MR imaging.

Authors:  Bjoern Sommer; Burkhard Sebastian Kasper; Roland Coras; Ingmar Blumcke; Hajo Martinus Hamer; Michael Buchfelder; Karl Roessler
Journal:  Neurol Res       Date:  2013-09-30       Impact factor: 2.448

  4 in total

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