Effect of Lacosamide on Interictal Epileptiform Discharges in Pediatric Patients With Newly Diagnosed Focal Epilepsy.

Electroencephalogram (EEG) Exacerbation Focal epilepsy Interictal epileptiform discharge (IED) Lacosamide (LCM) Seizure

Journal

Pediatric neurology
ISSN: 1873-5150
Titre abrégé: Pediatr Neurol
Pays: United States
ID NLM: 8508183

Informations de publication

Date de publication:
10 2023
Historique:
received: 10 08 2022
revised: 24 04 2023
accepted: 27 06 2023
medline: 5 9 2023
pubmed: 28 7 2023
entrez: 27 7 2023
Statut: ppublish

Résumé

The purpose of this study was to determine the efficacy of lacosamide (LCM) on interictal epileptiform discharges (IEDs) and evaluate the relationships between IEDs and seizure outcome in pediatric patients with focal epilepsy. Patient inclusion criteria included (1) newly diagnosed focal epilepsy with unknown etiology; and (2) electroencephalogram recorded twice (before and after starting LCM) under the same conditions. The difference between the highest number of IEDs over five successive minutes (IEDs/5 min) and the location of IEDs was determined. Seizure outcome was evaluated one year after achieving the maintenance dose of LCM. Responders were identified as showing a ≥50% reduction in the pre-LCM seizure frequency. Of 22 patients, 10 showed an increase in IEDs/5 min after starting LCM. The median IEDs/5 min before and after starting LCM was not significantly different, at 1.5 (interquartile range: 0, 31.75) and 10.5 (0, 80.5), respectively. No relationship was identified between the difference in IEDs/5 min and seizure outcome. Patients with multiple regional or diffuse IEDs had significantly poorer seizure outcome compared with patients without those IEDs (P = 0.036 and P = 0.039, respectively). Of 10 patients with single regional IEDs, a tendency of IEDs to disappear was observed between patients with frontal and non-frontal IEDs. The effects of LCM on the number of IEDs may be unrelated to seizure outcome. LCM may be ineffective at improving seizure outcomes in patients with multiple regional or diffuse IEDs.

Sections du résumé

BACKGROUND
The purpose of this study was to determine the efficacy of lacosamide (LCM) on interictal epileptiform discharges (IEDs) and evaluate the relationships between IEDs and seizure outcome in pediatric patients with focal epilepsy.
METHODS
Patient inclusion criteria included (1) newly diagnosed focal epilepsy with unknown etiology; and (2) electroencephalogram recorded twice (before and after starting LCM) under the same conditions. The difference between the highest number of IEDs over five successive minutes (IEDs/5 min) and the location of IEDs was determined. Seizure outcome was evaluated one year after achieving the maintenance dose of LCM. Responders were identified as showing a ≥50% reduction in the pre-LCM seizure frequency.
RESULTS
Of 22 patients, 10 showed an increase in IEDs/5 min after starting LCM. The median IEDs/5 min before and after starting LCM was not significantly different, at 1.5 (interquartile range: 0, 31.75) and 10.5 (0, 80.5), respectively. No relationship was identified between the difference in IEDs/5 min and seizure outcome. Patients with multiple regional or diffuse IEDs had significantly poorer seizure outcome compared with patients without those IEDs (P = 0.036 and P = 0.039, respectively). Of 10 patients with single regional IEDs, a tendency of IEDs to disappear was observed between patients with frontal and non-frontal IEDs.
CONCLUSION
The effects of LCM on the number of IEDs may be unrelated to seizure outcome. LCM may be ineffective at improving seizure outcomes in patients with multiple regional or diffuse IEDs.

Identifiants

pubmed: 37499552
pii: S0887-8994(23)00206-0
doi: 10.1016/j.pediatrneurol.2023.06.022
pii:
doi:

Substances chimiques

Lacosamide 563KS2PQY5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-8

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Hiroki Hoshino (H)

Department of Pediatrics, Toho University Medical Center Sakura Hospital, Sakura, Chiba, Japan. Electronic address: hiroki.hoshino@med.toho-u.ac.jp.

Yoshihiro Miyasato (Y)

Department of Pediatrics, Toho University Medical Center Sakura Hospital, Sakura, Chiba, Japan.

Takayuki Handa (T)

Department of Pediatrics, Toho University Medical Center Sakura Hospital, Sakura, Chiba, Japan; Department of Pediatrics, Toho University Medical Center Omori Hospital, Ota, Tokyo, Japan.

Yutaro Tomi (Y)

Department of Pediatrics, Toho University Medical Center Sakura Hospital, Sakura, Chiba, Japan; Department of Pediatrics, Toho University Medical Center Omori Hospital, Ota, Tokyo, Japan.

Hideaki Kanemura (H)

Department of Pediatrics, Toho University Medical Center Sakura Hospital, Sakura, Chiba, Japan.

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