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Perampanel: A therapeutic alternative in refractory status epilepticus associated with MELAS syndrome.
Santamarina, Estevo; Alpuente, Alicia; Maisterra, Olga; Sueiras, María; Sarria, Silvana; Guzman, Lorena; Abraira, Laura; Salas-Puig, Javier; Toledo, Manuel.
Afiliação
  • Santamarina E; Epilepsy Unit, Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Alpuente A; Epilepsy Unit, Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Maisterra O; Neurovascular Unit, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Sueiras M; EEG Unit, Department of Neurophysiology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Sarria S; MRI Unit, Department of Neuroradiology, Spain.
  • Guzman L; EEG Unit, Department of Neurophysiology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Abraira L; Epilepsy Unit, Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Salas-Puig J; Epilepsy Unit, Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Toledo M; Epilepsy Unit, Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain.
Epilepsy Behav Case Rep ; 11: 92-95, 2019.
Article em En | MEDLINE | ID: mdl-30834194
ABSTRACT
To our knowledge, there are no reports of status epilepticus (SE) associated with mitochondrial diseases and treated with perampanel (PER). We present three cases of patients with refractory SE associated with MELAS syndrome who responded favorably to PER. All cases were diagnosed as non-convulsive SE (focal without impairment of level of consciousness). After an initial treatment with other anti-seizure drugs, PER was added in all cases (8, 16 and 12 mg) and cessation of SE was observed within the next 4-8 hours. All the cases involved a stroke-like lesion present on brain MRI. In our patients, PER was an effective option in SE associated with MELAS syndrome.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article