Electroencephalographic biomarkers of epilepsy development in patients with acute brain injury: a matched, parallel cohort study.
Journal
Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
28
08
2019
revised:
18
09
2019
accepted:
18
09
2019
pubmed:
28
10
2019
medline:
22
9
2020
entrez:
29
10
2019
Statut:
ppublish
Résumé
This study was designed to investigate if highly epileptic electroencephalogram (EEG) findings in patients with acute brain injury increase the long-term risk of epilepsy development. Adults patients, lacking epilepsy history, with electrographic seizures or lateralized periodic discharges (LPDs) (cases) were identified and matched based on age, mental status, and etiology with the ones lacking any epileptiform activity (controls) on continuous EEG (cEEG) during hospitalization. The primary outcome of clinical seizures after hospital discharge and their antiepileptic drug (AED) status was determined using a telephonic interview. Logistic regression models using generalized estimating equations to account for the matched nature of the data were performed. A total of 70 cases [16 (22.9%) "LPDs only," 34 (48.6%) "electrographic seizure only," and 20 (28.6%) "both"] and controls were enrolled. A total of 22 (31.4%) cases developed epilepsy after a mean follow-up duration of 20.6 ± 5.0 months compared to three (4.3%) controls. After adjusting for cEEG indication and follow-up duration, the odds of cases developing epilepsy were almost 15 times higher compared to the controls (OR = 14.8, 95% CI = 2.4-92.3, P = 0.004). This elevated risk was despite a 10 times higher likelihood of cases to be taking AEDs at the last follow-up (OR = 10.34, 95% CI = 3.7-29, P < 0.001). Highly epileptic EEG findings in patients with acute brain injury may serve as prognostic biomarkers of epilepsy development. Although prospective studies are required to confirm our findings, it seems that with epilepsy developing in almost one-third cases in less than 2-year follow-up period, such patients may potentially be ideal candidates for epilepsy prevention clinical trials.
Identifiants
pubmed: 31657134
doi: 10.1002/acn3.50925
pmc: PMC6856614
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2230-2239Informations de copyright
© 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association.
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