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Lacosamide monotherapy for the treatment of childhood epilepsy with centrotemporal spikes.
Okanishi, Tohru; Fujii, Yuji; Sakuma, Satoru; Shiraishi, Hideaki; Motoi, Hirotaka; Yazaki, Kotaro; Enoki, Hideo; Fujimoto, Ayataka.
Afiliação
  • Okanishi T; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan; Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital Hamamatsu, Japan. Electronic address: t.okanishi@tottori-u.ac.jp.
  • Fujii Y; Department of Pediatrics, Hiroshima City Funairi Citizens Hospital, Hiroshima, Japan.
  • Sakuma S; Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Shiraishi H; Department of Pediatrics, Hokkaido University Hospital, Sapporo, Japan.
  • Motoi H; Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan.
  • Yazaki K; Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Enoki H; Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital Hamamatsu, Japan.
  • Fujimoto A; Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital Hamamatsu, Japan.
Brain Dev ; 44(6): 380-385, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35241306
ABSTRACT

OBJECTIVE:

Childhood epilepsy with centrotemporal spikes (CECTS) is known as age-limited focal epilepsy syndrome in childhood. Lacosamide is a third-generation antiepileptic drug. This study aimed to evaluate the efficacy of lacosamide monotherapy for the treatment of CECTS.

METHODS:

We enrolled 18 patients (6 girls and 12 boys) who met the following criteria 1) the age of onset of the seizures was between 3 and 13 years of age; 2) showing at least hemifacial and/or oropharyngeal seizures; 3) interictal discharges in central and/or middle temporal electrodes; 4) no intellectual disability; 5) treatment duration of lacosamide monotherapy over 6 months. We retrospectively collected and analyzed clinical data and treatment information. We evaluated the seizure occurrences during 0-3, 4-6, and 7-12 months from the treatment initiation and the last 6 months of the follow-up. We also evaluated the outcomes as seizure-free if the patients developed no seizures both over 6 months and 3 times of pretreatment mean seizure interval at the last follow-up.

RESULTS:

Of the patients, 39%, 67% and 72% were seizure-free during 0-3, 4-6, and 7-12 months from treatment initiation, respectively. Finally, 83% of the patients achieved seizure freedom. Seizure freedom was achieved in 72% during the first 4 months of treatment. All patients continued lacosamide monotherapy during the study, although four patients showed transient fatigue or somnolence.

CONCLUSIONS:

Lacosamide showed good efficacy for controlling seizures with fewer adverse effects, and therefore may be a good candidate as a first-line medication for the treatment of new-onset CECTS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Anticonvulsivantes Tipo de estudo: Observational_studies Limite: Female / Humans / Infant / Male Idioma: En Revista: Brain Dev Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Anticonvulsivantes Tipo de estudo: Observational_studies Limite: Female / Humans / Infant / Male Idioma: En Revista: Brain Dev Ano de publicação: 2022 Tipo de documento: Article