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Efficacy and tolerability of methylprednisolone pulse therapy in childhood epilepsies other than infantile spasms.
Bast, Thomas; Richter, Sarah; Ebinger, Friedrich; Rating, Dietz; Wiemer-Kruel, Adelheid; Schubert-Bast, Susanne.
Affiliation
  • Bast T; Kork Epilepsy Center, Kehl, Germany.
  • Richter S; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH, Campus Kiel), Kiel, Germany.
  • Ebinger F; Pediatric Clinic, St. Vincenz Hospital, Paderborn, Germany.
  • Rating D; Dr. Rating was previously associated with University Children's Hospital, Heidelberg, Germany. He has now retired.
  • Wiemer-Kruel A; Kork Epilepsy Center, Kehl, Germany.
  • Schubert-Bast S; University Children's Hospital, Heidelberg, Germany.
Neuropediatrics ; 45(6): 378-85, 2014 Dec.
Article in En | MEDLINE | ID: mdl-25184741
This retrospective study included 54 children with epilepsy. The treatment consisted of four pulses with single doses of 20 mg/kg/d methylprednisolone (MPR), administered every week on 3 consecutive days. After this initial phase, the intervals between the pulses were increased based on individual factors. MPR pulses were administered exclusively orally in 39 patients and 7.8% of all pulses were applied intravenously. After four pulses, 30 of 54 (56%) patients were responders, according to several clinical and electroencephalography criteria. A response was obtained in 12 of 20 (60%) cases with genetic, 7 of 17 (41%) with structural metabolic, and 11 of 17 (65%) with unknown etiology. Responder rates were 11 of 15 (73%) in patients with continuous spike-waves in slow sleep (CSWS) or Landau-Kleffner syndrome, 2 of 6 in patients with myoclonic astatic epilepsy or Lennox-Gastaut syndrome, and 17 of 31 (55%) in patients with unclassified epilepsies. A response was not correlated with any epilepsy-related clinical factor. The patients received a median of eight MPR pulses (range, 1-52), and the median duration of the therapy was 11 weeks. The response was maintained in 19 of 30 (63%) patients, and 3 of 24 (13%) without initial response became seizure-free (total responder rate at the end of the therapy 22/54 [41%]). The majority of patients experienced adverse effects that were typically mild and transient.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Methylprednisolone / Epilepsy Type of study: Observational_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Neuropediatrics Year: 2014 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Methylprednisolone / Epilepsy Type of study: Observational_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Neuropediatrics Year: 2014 Document type: Article Affiliation country: Country of publication: