Literature DB >> 25976064

Effectiveness of a hybrid corticosteroid treatment regimen on refractory childhood seizures and a review of other corticosteroid treatments.

Dewi P Bakker1, Coriene E Catsman-Berrevoets1, Rinze F Neuteboom2.   

Abstract

BACKGROUND: Many different corticosteroid treatment schedules have been used in order to treat refractory epileptic seizures with encouraging effects on seizure reduction in many epileptic syndromes.
OBJECTIVE: The objective is to report our experience with a hybrid treatment regimen for refractory seizures in children with epilepsies other than West and Landau-Kleffner syndrome. We hypothesized that a pulse of corticosteroids effectively reduces seizures while low-dosage maintenance treatment reduces side effects. The results are compared with results from a review of reported corticosteroid and ACTH treatments.
METHODS: In this retrospective observational study, 26 children diagnosed with epilepsy with refractory seizures other than West syndrome and Landau-Kleffner syndrome were eligible for a treatment regimen consisting of three days intravenous methylprednisolone (20 mg per kilogram per day) followed by twelve weeks oral prednisolone (0.5 mg per kilogram on alternate days), concluded with a taper phase. Data on effectiveness and side effects were obtained. End-points were the percentages of patients who became seizure free or responded well.
RESULTS: Twenty-one patients received the study treatment. Nine (43%) responded well and 6 (29%) became seizure free. All but one patient had a relapse of seizures. Four patients had reversible adverse effects. Data extracted from the literature were consistent with a good response in 48% of 192 children treated with different corticosteroids and in 69% of 103 patients treated with ACTH.
CONCLUSION: This new hybrid therapy of a pulse of intravenous methylprednisolone and alternate day oral prednisolone is effective with a favourable side effect profile. Results on efficacy and safety justify a randomized controlled trial.
Copyright © 2015 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Corticosteroid; Epilepsy; Lennox–Gastaut syndrome; Myoclonic astatic epilepsy; Refractory seizure

Mesh:

Substances:

Year:  2015        PMID: 25976064     DOI: 10.1016/j.ejpn.2015.04.006

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  5 in total

1.  Intravenous Corticosteroids as an Adjunctive Treatment for Refractory and Super-Refractory Status Epilepticus: An Observational Cohort Study.

Authors:  Vasiliki Pantazou; Jan Novy; Andrea O Rossetti
Journal:  CNS Drugs       Date:  2019-02       Impact factor: 5.749

2.  Does Autoimmunity have a Role in Myoclonic Astatic Epilepsy? A Case Report of Voltage Gated Potassium Channel Mediated Seizures.

Authors:  Deepa Sirsi; Alison Dolce; Benjamin M Greenberg; Drew Thodeson
Journal:  Ann Clin Case Rep       Date:  2016-11-03

Review 3.  Expanding the Treatment Landscape for Lennox-Gastaut Syndrome: Current and Future Strategies.

Authors:  Adam Strzelczyk; Susanne Schubert-Bast
Journal:  CNS Drugs       Date:  2021-01-21       Impact factor: 5.749

4.  Pharmacological treatment for continuous spike-wave during slow wave sleep syndrome and Landau-Kleffner Syndrome.

Authors:  Luca Moresco; Matteo Bruschettini; Maria Grazia Calevo; Laura Siri
Journal:  Cochrane Database Syst Rev       Date:  2020-11-06

5.  Pediatric autoimmune encephalitis: Recognition and diagnosis.

Authors:  Marienke A A M de Bruijn; Arlette L Bruijstens; Anna E M Bastiaansen; Agnes van Sonderen; Marco W J Schreurs; Peter A E Sillevis Smitt; Rogier Q Hintzen; Rinze F Neuteboom; Maarten J Titulaer
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2020-02-11
  5 in total

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