TY - JOUR
T1 - A multi-feature and multi-channel univariate selection process for seizure prediction
AU - D'Alessandro, Maryann
AU - Vachtsevanos, George
AU - Esteller, Rosana
AU - Echauz, Javier
AU - Cranstoun, Stephen
AU - Worrell, Greg
AU - Parish, Landi
AU - Litt, Brian
N1 - Funding Information:
This research has been funded by The Whitaker Foundation, The Esther and Joseph Klingenstein Foundation, The Dana Foundation, The American Epilepsy Society, The CURE Foundation, The Partnership for Pediatric Epilepsy and through a grant from the National Institutes of Health, Grant #R01NS041811-01.
PY - 2005/3
Y1 - 2005/3
N2 - Objective: To develop a prospective method for optimizing seizure prediction, given an array of implanted electrodes and a set of candidate quantitative features computed at each contact location. Methods: The method employs a genetic-based selection process, and then tunes a probabilistic neural network classifier to predict seizures within a 10 min prediction horizon. Initial seizure and interictal data were used for training, and the remaining IEEG data were used for testing. The method continues to train and learn over time. Results: Validation of these results over two workshop patients demonstrated a sensitivity of 100%, and 1.1 false positives per hour for Patient E, using a 2.4 s block predictor, and a failure of the method on Patient B. Conclusions: This study demonstrates a prospective, exploratory implementation of a seizure prediction method designed to adapt to individual patients with a wide variety of pre-ictal patterns, implanted electrodes and seizure types. Its current performance is limited likely by the small number of input channels and quantitative features employed in this study, and segmentation of the data set into training and testing sets rather than using all continuous data available. Significance: This technique theoretically has the potential to address the challenge presented by the heterogeneity of EEG patterns seen in medication-resistant epilepsy. A more comprehensive implementation utilizing all electrode sites, a broader feature library, and automated multi-feature fusion will be required to fully judge the method's potential for predicting seizures.
AB - Objective: To develop a prospective method for optimizing seizure prediction, given an array of implanted electrodes and a set of candidate quantitative features computed at each contact location. Methods: The method employs a genetic-based selection process, and then tunes a probabilistic neural network classifier to predict seizures within a 10 min prediction horizon. Initial seizure and interictal data were used for training, and the remaining IEEG data were used for testing. The method continues to train and learn over time. Results: Validation of these results over two workshop patients demonstrated a sensitivity of 100%, and 1.1 false positives per hour for Patient E, using a 2.4 s block predictor, and a failure of the method on Patient B. Conclusions: This study demonstrates a prospective, exploratory implementation of a seizure prediction method designed to adapt to individual patients with a wide variety of pre-ictal patterns, implanted electrodes and seizure types. Its current performance is limited likely by the small number of input channels and quantitative features employed in this study, and segmentation of the data set into training and testing sets rather than using all continuous data available. Significance: This technique theoretically has the potential to address the challenge presented by the heterogeneity of EEG patterns seen in medication-resistant epilepsy. A more comprehensive implementation utilizing all electrode sites, a broader feature library, and automated multi-feature fusion will be required to fully judge the method's potential for predicting seizures.
KW - Classification
KW - Feature extraction
KW - Multiple channels
KW - Multiple features
KW - Seizure prediction
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U2 - 10.1016/j.clinph.2004.11.014
DO - 10.1016/j.clinph.2004.11.014
M3 - Article
C2 - 15721064
AN - SCOPUS:13844298785
SN - 1388-2457
VL - 116
SP - 506
EP - 516
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
IS - 3
ER -