Multimodal nocturnal seizure detection in children with epilepsy: A prospective, multicenter, long‐term, in‐home trial

Author:

van Westrhenen Anouk12ORCID,Lazeron Richard H. C.34ORCID,van Dijk Johannes P.345ORCID,Leijten Frans S. S.6ORCID,Thijs Roland D.127ORCID,

Affiliation:

1. Stichting Epilepsie Instellingen Nederland (SEIN) Heemstede and Zwolle the Netherlands

2. Department of Neurology and Clinical Neurophysiology Leiden University Medical Center Leiden the Netherlands

3. Academic Center of Epileptology Kempenhaeghe Heeze the Netherlands

4. Faculty of Electrical Engineering Eindhoven University of Technology Eindhoven the Netherlands

5. Department of Orthodontics Ulm University Ulm Germany

6. Brain Center, Department of Neurology University Medical Center Utrecht Utrecht the Netherlands

7. UCL Queen Square Institute of Neurology London UK

Abstract

AbstractObjectiveThere is a pressing need for reliable automated seizure detection in epilepsy care. Performance evidence on ambulatory non‐electroencephalography‐based seizure detection devices is low, and evidence on their effect on caregiver's stress, sleep, and quality of life (QoL) is still lacking. We aimed to determine the performance of NightWatch, a wearable nocturnal seizure detection device, in children with epilepsy in the family home setting and to assess its impact on caregiver burden.MethodsWe conducted a phase 4, multicenter, prospective, video‐controlled, in‐home NightWatch implementation study (NCT03909984). We included children aged 4–16 years, with ≥1 weekly nocturnal major motor seizure, living at home. We compared a 2‐month baseline period with a 2‐month NightWatch intervention. The primary outcome was the detection performance of NightWatch for major motor seizures (focal to bilateral or generalized tonic–clonic [TC] seizures, focal to bilateral or generalized tonic seizures lasting >30 s, hyperkinetic seizures, and a remainder category of focal to bilateral or generalized clonic seizures and "TC‐like" seizures). Secondary outcomes included caregivers' stress (Caregiver Strain Index [CSI]), sleep (Pittsburgh Quality of Sleep Index), and QoL (EuroQol five‐dimension five‐level scale).ResultsWe included 53 children (55% male, mean age = 9.7 ± 3.6 years, 68% learning disability) and analyzed 2310 nights (28 173 h), including 552 major motor seizures. Nineteen participants did not experience any episode of interest during the trial. The median detection sensitivity per participant was 100% (range = 46%–100%), and the median individual false alarm rate was .04 per hour (range = 0–.53). Caregiver's stress decreased significantly (mean total CSI score = 8.0 vs. 7.1, p = .032), whereas caregiver's sleep and QoL did not change significantly during the trial.SignificanceThe NightWatch system demonstrated high sensitivity for detecting nocturnal major motor seizures in children in a family home setting and reduced caregiver stress.

Funder

ZonMw

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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