Literature DB >> 31465970

Multi-feature localization of epileptic foci from interictal, intracranial EEG.

Jan Cimbalnik1, Petr Klimes2, Vladimir Sladky3, Petr Nejedly2, Pavel Jurak4, Martin Pail5, Robert Roman6, Pavel Daniel5, Hari Guragain7, Benjamin Brinkmann8, Milan Brazdil9, Greg Worrell8.   

Abstract

OBJECTIVE: When considering all patients with focal drug-resistant epilepsy, as high as 40-50% of patients suffer seizure recurrence after surgery. To achieve seizure freedom without side effects, accurate localization of the epileptogenic tissue is crucial before its resection. We investigate an automated, fast, objective mapping process that uses only interictal data.
METHODS: We propose a novel approach based on multiple iEEG features, which are used to train a support vector machine (SVM) model for classification of iEEG electrodes as normal or pathologic using 30 min of inter-ictal recording.
RESULTS: The tissue under the iEEG electrodes, classified as epileptogenic, was removed in 17/18 excellent outcome patients and was not entirely resected in 8/10 poor outcome patients. The overall best result was achieved in a subset of 9 excellent outcome patients with the area under the receiver operating curve = 0.95.
CONCLUSION: SVM models combining multiple iEEG features show better performance than algorithms using a single iEEG marker. Multiple iEEG and connectivity features in presurgical evaluation could improve epileptogenic tissue localization, which may improve surgical outcome and minimize risk of side effects. SIGNIFICANCE: In this study, promising results were achieved in localization of epileptogenic regions by SVM models that combine multiple features from 30 min of inter-ictal iEEG recordings.
Copyright © 2019 International Federation of Clinical Neurophysiology. All rights reserved.

Entities:  

Keywords:  Connectivity; Drug resistant epilepsy; Epileptogenic zone localization; High frequency oscillations; Machine learning; Multi-feature approach

Mesh:

Year:  2019        PMID: 31465970      PMCID: PMC6759804          DOI: 10.1016/j.clinph.2019.07.024

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  50 in total

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