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Stiripentol for the treatment of super-refractory status epilepticus with cross-sensitivity.
Uchida, Y; Terada, K; Madokoro, Y; Fujioka, T; Mizuno, M; Toyoda, T; Kato, D; Matsukawa, N.
Afiliação
  • Uchida Y; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Terada K; Department of Epileptology, National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan.
  • Madokoro Y; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Fujioka T; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Mizuno M; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Toyoda T; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Kato D; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Matsukawa N; Department of Neurology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Acta Neurol Scand ; 137(4): 432-437, 2018 Apr.
Article em En | MEDLINE | ID: mdl-29313881
ABSTRACT

BACKGROUND:

Cross-sensitivity of rash has been reported between various antiepileptic drugs (AEDs). However, few studies have determined the frequency and management of cross-sensitivity in patients with super-refractory status epilepticus (SRSE). AIMS OF THE STUDY To examine the optimal AED for treating SRSE with cross-sensitivity.

METHODS:

We performed a retrospective review of adult patients with SRSE treated at Nagoya City University Hospital, in which we investigated the frequency of cross-sensitivity among patients with SRSE and their clinical and medical profiles.

RESULTS:

We identified 10 adult patients with SRSE, 5 of whom had cross-sensitivity. Stiripentol (STP) was administered when previously used AEDs had demonstrated cross-sensitivity and failed to control seizures. After initiation of STP, the dose of general anaesthetics was reduced, and status epilepticus (SE) eventually ceased with co-administered AEDs without additional adverse effects. The mean time to SE cessation after initiation of STP was 30.8 days (range, 18-46 days), mean duration of general anaesthesia was 101.2 days (range, 74-128 days), and mean number of AEDs was 9.0 (range, 6-11).

CONCLUSIONS:

This study suggests that cross-sensitivity between AEDs is common in adults with SRSE and that STP may be useful for treating SRSE with cross-sensitivity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Toxidermias / Dioxolanos / Anticonvulsivantes Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Toxidermias / Dioxolanos / Anticonvulsivantes Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article