Seizure detection based on heart rate variability using a wearable electrocardiography device.


Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
10 2019
Historique:
received: 12 04 2019
revised: 29 08 2019
accepted: 29 08 2019
pubmed: 21 9 2019
medline: 15 4 2020
entrez: 21 9 2019
Statut: ppublish

Résumé

To assess the feasibility and accuracy of seizure detection based on heart rate variability (HRV) using a wearable electrocardiography (ECG) device. Noninvasive devices for detection of convulsive seizures (generalized tonic-clonic and focal to bilateral tonic-clonic seizures) have been validated in phase 2 and 3 studies. However, detection of nonconvulsive seizures still needs further research, since currently available methods have either low sensitivity or an extremely high false alarm rate (FAR). In this phase 2 study, we prospectively recruited patients admitted to long-term video-EEG monitoring (LTM). ECG was recorded using a dedicated wearable device. Seizures were automatically detected using HRV parameters computed off-line, blinded to all other data. We compared the performance of 26 automated algorithms with the seizure time-points marked by experts who reviewed the LTM recording. Patients were classified as responders if >66% of their seizures were detected. We recruited 100 consecutive patients and analyzed 126 seizures (108 nonconvulsive and 18 convulsive) from 43 patients who had seizures during monitoring. The best-performing HRV algorithm combined a measure of sympathetic activity with a measure of how quickly HR changes occurred. The algorithm identified 53.5% of the patients with seizures as responders. Among responders, detection sensitivity was 93.1% (95% CI: 86.6%-99.6%) for all seizures and 90.5% (95% CI: 77.4%-97.3%) for nonconvulsive seizures. FAR was 1.0/24 h (0.11/night). Median seizure detection latency was 30 s. Typically, patients with prominent autonomic nervous system changes were responders: An ictal change of >50 heartbeats per minute predicted who would be responder with a positive predictive value of 87% and a negative predictive value of 90%. The automated HRV algorithm, using ECG recorded with a wearable device, has high sensitivity for detecting seizures, including the nonconvulsive ones. FAR was low during the night. This approach is feasible in patients with prominent ictal autonomic changes.

Identifiants

pubmed: 31538347
doi: 10.1111/epi.16343
doi:

Types de publication

Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2105-2113

Subventions

Organisme : Lundbeck Foundation
Pays : International
Organisme : Health Research Fund of Central Denmark Region
Pays : International

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Wiley Periodicals, Inc. © 2019 International League Against Epilepsy.

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Auteurs

Jesper Jeppesen (J)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Anders Fuglsang-Frederiksen (A)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Peter Johansen (P)

Department of Engineering, Aarhus University, Aarhus, Denmark.

Jakob Christensen (J)

Department of Neurology, Aarhus University Hospital, Denmark.

Stephan Wüstenhagen (S)

Department of Clinical Neurophysiology, Danish Epilepsy Centre, Dianalund, Denmark.

Hatice Tankisi (H)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Erisela Qerama (E)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Alexander Hess (A)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Sándor Beniczky (S)

Department of Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Clinical Neurophysiology, Danish Epilepsy Centre, Dianalund, Denmark.

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