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ABSTRACT: Objective
To explore the feasibility of home monitoring of epilepsy patients with a novel subcutaneous electroencephalography (EEG) device, including clinical implications, safety, and compliance via the first real-life test.Methods
We implanted a beta-version of the 24/7 EEG SubQ (UNEEG Medical A/S, Denmark) subcutaneously in nine participants with temporal lobe epilepsy. Data on seizures, adverse events, compliance in using the device, and use of antiepileptic drugs (AEDs) were collected. EEG was recorded for up to 3 months, and all EEG data were reviewed visually to identify electrographic seizures. These were descriptively compared to seizure counts and AED changes reported in diaries from the same period.Results
Four hundred ninety days of EEG and 338 electrogr
SUBMITTER: Weisdorf S
PROVIDER: S-EPMC6899579 | biostudies-literature | 2019 Nov
REPOSITORIES: biostudies-literature