Literature DB >> 29687739

Vigabatrin for Epileptic Spasms and Tonic Seizures in Tuberous Sclerosis Complex.

Emma A van der Poest Clement1, Mustafa Sahin2, Jurriaan M Peters1.   

Abstract

Vigabatrin is recommended as first-line treatment for infantile spasms in tuberous sclerosis complex (TSC), but other indications in children with tuberous sclerosis complex are less known. We retrospectively reviewed 201 children with tuberous sclerosis complex, and identified 21 children older than 1 year started on vigabatrin for any indication and with sufficient follow-up data. The indication for vigabatrin was epileptic spasms (n = 13), tonic seizures (n = 5), both (n = 2), and status epilepticus (n = 1). Mean age of treatment onset was 4.0 years (range 1.1-18.3). All but 1 patient had a reduction in seizures. Ten patients became seizure free and 4 had an improvement of >90%. In 9 patients, vigabatrin was tapered successfully after 8 to 33 months. Side effects reported included rash (n = 1) and behavioral decline (n = 1). No retinal toxicity was detected in 14 of 21 patients with adequate ophthalmologic surveillance data. In conclusion, vigabatrin may be an effective treatment for epileptic spasms and tonic seizures beyond the infantile age.

Entities:  

Keywords:  antiepileptic drugs; children; epilepsy; infantile spasms; tuberous sclerosis complex

Mesh:

Substances:

Year:  2018        PMID: 29687739     DOI: 10.1177/0883073818768309

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  7 in total

Review 1.  Update on Drug Management of Refractory Epilepsy in Tuberous Sclerosis Complex.

Authors:  Emma van der Poest Clement; Floor E Jansen; Kees P J Braun; Jurriaan M Peters
Journal:  Paediatr Drugs       Date:  2020-02       Impact factor: 3.022

2.  Metabolomic analyses of vigabatrin (VGB)-treated mice: GABA-transaminase inhibition significantly alters amino acid profiles in murine neural and non-neural tissues.

Authors:  Dana C Walters; Erland Arning; Teodoro Bottiglieri; Erwin E W Jansen; Gajja S Salomons; Madalyn N Brown; Michelle A Schmidt; Garrett R Ainslie; Jean-Baptiste Roullet; K Michael Gibson
Journal:  Neurochem Int       Date:  2019-02-26       Impact factor: 3.921

Review 3.  Modeling epileptic spasms during infancy: Are we heading for the treatment yet?

Authors:  Libor Velíšek; Jana Velíšková
Journal:  Pharmacol Ther       Date:  2020-05-15       Impact factor: 12.310

4.  Clinical profile of children with West syndrome: A retrospective chart review.

Authors:  Virender K Gehlawat; Vandana Arya; Harish Bhardwaj; Narain D Vaswani; Jaya S Kaushik
Journal:  J Family Med Prim Care       Date:  2021-01-30

Review 5.  Psychobehavioural and Cognitive Adverse Events of Anti-Seizure Medications for the Treatment of Developmental and Epileptic Encephalopathies.

Authors:  Adam Strzelczyk; Susanne Schubert-Bast
Journal:  CNS Drugs       Date:  2022-10-04       Impact factor: 6.497

Review 6.  Review of the treatment options for epilepsy in tuberous sclerosis complex: towards precision medicine.

Authors:  Susanne Schubert-Bast; Adam Strzelczyk
Journal:  Ther Adv Neurol Disord       Date:  2021-07-17       Impact factor: 6.570

7.  A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies.

Authors:  Tobias Baumgartner; Mar Carreño; Rodrigo Rocamora; Francesca Bisulli; Antonella Boni; Milan Brázdil; Ondrej Horak; Dana Craiu; Cristina Pereira; Renzo Guerrini; Victoria San Antonio-Arce; Andreas Schulze-Bonhage; Sameer M Zuberi; Tove Hallböök; Reetta Kalviainen; Lieven Lagae; Sylvie Nguyen; Sofia Quintas; Ana Franco; J Helen Cross; Matthew Walker; Alexis Arzimanoglou; Sylvain Rheims; Tiziana Granata; Laura Canafoglia; Cecilie Johannessen Landmark; Arjune Sen; Rohini Rattihalli; Rima Nabbout; Elena Tartara; Manuela Santos; Rui Rangel; Pavel Krsek; Petr Marusic; Nicola Specchio; Kees P J Braun; Patricia Smeyers; Vicente Villanueva; Katarzyna Kotulska; Rainer Surges
Journal:  Epilepsia Open       Date:  2021-01-13
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.