Abstract
Objective. High frequency oscillations (HFOs) are a promising biomarker of tissue that instigates seizures. However, ambiguous data and random background fluctuations can cause any HFO detector (human or automated) to falsely label non-HFO data as an HFO (a false positive detection). The objective of this paper was to identify quantitative features of HFOs that distinguish between true and false positive detections. Approach. Feature selection was performed using background data in multi-day, interictal intracranial recordings from ten patients. We selected the feature most similar between randomly selected segments of background data and HFOs detected in surrogate background data (false positive detections by construction). We then compared these results with fuzzy clustering of detected HFOs in clinical data to verify the feature’s applicability. We validated the feature is sensitive to false versus true positive HFO detections by using an independent data set (six subjects) scored for HFOs by three human reviewers. Lastly, we compared the effect of redacting putative false positive HFO detections on the distribution of HFOs across channels and their association with seizure onset zone (SOZ) and resected volume (RV). Main results. Of the 15 analyzed features, the analysis selected only skewness of the curvature (skewCurve). The feature was validated in human scored data to be associated with distinguishing true and false positive HFO detections. Automated HFO detections with higher skewCurve were more focal based on entropy measures and had increased localization to both the SOZ and RV. Significance. We identified a quantitative feature of HFOs which helps distinguish between true and false positive detections. Redacting putative false positive HFO detections improves the specificity of HFOs as a biomarker of epileptic tissue.
Highlights
Over 50 million people worldwide have epilepsy, with about one third of them being unable to obtain seizure control from medications (Kwan and Brodie 2000)
We quantified whether the putative true positive High frequency oscillations (HFOs) were less diffusely distributed over channels; see figures 6(C) and (D)
The goal of this paper was to identify and validate quantitative HFO features to identify and redact false positive detections in order to improve the association of HFOs with epileptic tissue
Summary
Over 50 million people worldwide have epilepsy, with about one third of them being unable to obtain seizure control from medications (Kwan and Brodie 2000). For these patients with refractory epilepsy, resective surgery is a primary treatment option. This surgery seeks to remove the region of the brain instigating seizures, the hypothesized epileptogenic zone. One of the main modalities for identifying SOZ is intracranial EEG, which involves placement of electrodes on the cortical surface or deep within the brain followed by days of hospitalization to observe spontaneous seizures. Less than 60% of patients have a seizure-free outcome after resective surgery informed by intracranial EEG (Edelvik et al 2013, Noe et al 2013, Yu et al 2014)
Published Version
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