Seizure Detection in Continuous Inpatient EEG: A Comparison of Human vs Automated Review.


Journal

Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060

Informations de publication

Date de publication:
31 05 2022
Historique:
received: 11 04 2021
accepted: 08 02 2022
pubmed: 13 4 2022
medline: 3 6 2022
entrez: 12 4 2022
Statut: ppublish

Résumé

The aim of this work was to test the accuracy of Persyst commercially available automated seizure detection in critical care EEG by comparing automated seizure detections to human review in a manually reviewed cohort and on a large scale. Automated seizure detections (Persyst versions 12 and 13) were compared to human review in a pilot cohort of 229 seizures from 85 EEG records and then in an expanded cohort of 7,924 EEG records. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated for individual seizures (pilot cohort) and for entire records (pilot and expanded cohorts). We assessed EEG features associated with the accuracy of automated seizure detections. In the pilot cohort, accuracy of automated detection for individual seizures was modest (sensitivity 0.50, PPV 0.60). At the record level (did the recording contain seizures or not?), sensitivity was higher (pilot cohort 0.78, expanded cohort 0.91), PPV was low (pilot cohort 0.40, expanded cohort 0.08), and NPV was high (pilot cohort 0.88, expanded cohort 0.97). Different software versions (version 12 vs 13) performed similarly. Sensitivity was higher for records containing focal-onset seizures compared to generalized-onset seizures (0.93 vs 0.85, In critical care continuous EEG recordings, automated detection of individual seizures had rates of both false negatives and false positives that bring into question its utility as a seizure alarm in clinical practice. At the level of entire EEG records, the absence of automated detections accurately predicted EEG records without true seizures. The true value of Persyst automated seizure detection appears to lie in triaging of low-risk EEGs. This study provides Class II evidence that an automated seizure detection program cannot accurately identify EEG records that contain seizures.

Sections du résumé

BACKGROUND AND OBJECTIVES
The aim of this work was to test the accuracy of Persyst commercially available automated seizure detection in critical care EEG by comparing automated seizure detections to human review in a manually reviewed cohort and on a large scale.
METHODS
Automated seizure detections (Persyst versions 12 and 13) were compared to human review in a pilot cohort of 229 seizures from 85 EEG records and then in an expanded cohort of 7,924 EEG records. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated for individual seizures (pilot cohort) and for entire records (pilot and expanded cohorts). We assessed EEG features associated with the accuracy of automated seizure detections.
RESULTS
In the pilot cohort, accuracy of automated detection for individual seizures was modest (sensitivity 0.50, PPV 0.60). At the record level (did the recording contain seizures or not?), sensitivity was higher (pilot cohort 0.78, expanded cohort 0.91), PPV was low (pilot cohort 0.40, expanded cohort 0.08), and NPV was high (pilot cohort 0.88, expanded cohort 0.97). Different software versions (version 12 vs 13) performed similarly. Sensitivity was higher for records containing focal-onset seizures compared to generalized-onset seizures (0.93 vs 0.85,
DISCUSSION
In critical care continuous EEG recordings, automated detection of individual seizures had rates of both false negatives and false positives that bring into question its utility as a seizure alarm in clinical practice. At the level of entire EEG records, the absence of automated detections accurately predicted EEG records without true seizures. The true value of Persyst automated seizure detection appears to lie in triaging of low-risk EEGs.
CLASSIFICATION OF EVIDENCE
This study provides Class II evidence that an automated seizure detection program cannot accurately identify EEG records that contain seizures.

Identifiants

pubmed: 35410905
pii: WNL.0000000000200267
doi: 10.1212/WNL.0000000000200267
pmc: PMC9162163
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2224-e2232

Subventions

Organisme : NINDS NIH HHS
ID : DP1 NS122038
Pays : United States
Organisme : NINDS NIH HHS
ID : K23 NS121520
Pays : United States

Informations de copyright

© 2022 American Academy of Neurology.

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Auteurs

Taneeta Mindy Ganguly (TM)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Colin A Ellis (CA)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Danni Tu (D)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Russell T Shinohara (RT)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Kathryn A Davis (KA)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Brian Litt (B)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia.

Jay Pathmanathan (J)

From the Department of Neurology (T.M.G., C.A.E., K.A.D., B.L., J.P.), and Penn Statistics in Imaging and Visualization Endeavor (PennSIVE) Center of Excellence (D.T., R.T.S.), Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania; Department of Biostatistics, Epidemiology, & Informatics (D.T., R.T.S.) and Center for Biomedical Image Computing and Analytics (R.T.S.), University of Pennsylvania, Philadelphia. jay.pathmanathan@pennmedicine.upenn.edu.

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