Literature DB >> 25377998

Long-term outcome in children with infantile spasms treated with vigabatrin: a cohort of 180 patients.

Milena Djuric1, Ruzica Kravljanac, Biljana Tadic, Nataša Mrlješ-Popovic, Richard E Appleton.   

Abstract

OBJECTIVE: Evaluation of efficacy of vigabatrin as the first drug in infants with previously untreated infantile spasms (IS) and reporting the long-term outcome.
METHODS: We analyzed a cohort of 180 infants with infantile spasms treated with vigabatrin as the first drug. Following initial evaluation and a 48-h basal period for counting the spasms, vigabatrin was administered using the same protocol in all. After 14 days all infants were assessed for therapeutic response (primary outcome). Psychomotor development was evaluated by a psychologist and neurologist prior to the initiation of treatment and during the follow-up. Seizure outcomes were followed prospectively, by seizure types and epilepsy syndromes. Long-term (secondary) outcomes included neurologic status, occurrence of late epilepsy, and developmental/cognitive status.
RESULTS: Vigabatrin terminated the spasms in 101 patients (56.9%) at a mean period of 5 days. Patients with normal psychomotor development prior to the onset of spasms responded best. After follow-up of 2.4 to 18.9 years (mean 10.64; standard deviation [SD] 4.40), 38.1% of responders, treated with vigabatrin, had severe neurologic dysfunction, 42% had epilepsy, and 42.2% had unfavorable intellectual outcome. The group with symptomatic etiology and abnormal neurologic status at presentation demonstrated a significantly worse prognosis and a more unfavorable outcome than cryptogenic or idiopathic cases (85.1% and 81.6% versus 14.9% and 0%-p = 0.001). Idiopathic patients treated with vigabatrin were all intellectually normal, except the youngest patient who had borderline cognitive function. SIGNIFICANCE: The most important prognostic factors were the underlying etiology and preexisting developmental profile. Long-term outcome in the patients treated with vigabatrin was similar to the outcome in patients treated with adrenocorticotropic hormone (ACTH) or corticosteroids, as reported in earlier studies. The long-term prognosis of idiopathic cases treated with vigabatrin was favorable. Wiley Periodicals, Inc.
© 2014 International League Against Epilepsy.

Entities:  

Keywords:  Efficacy; Electroclinical outcome; Infantile spasms; Long-term outcome; Vigabatrin

Mesh:

Substances:

Year:  2014        PMID: 25377998     DOI: 10.1111/epi.12847

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  7 in total

1.  Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort.

Authors:  Kelly G Knupp; Erin Leister; Jason Coryell; Katherine C Nickels; Nicole Ryan; Elizabeth Juarez-Colunga; William D Gaillard; John R Mytinger; Anne T Berg; John Millichap; Douglas R Nordli; Sucheta Joshi; Renée A Shellhaas; Tobias Loddenkemper; Dennis Dlugos; Elaine Wirrell; Joseph Sullivan; Adam L Hartman; Eric H Kossoff; Zachary M Grinspan; Lorie Hamikawa
Journal:  Epilepsia       Date:  2016-09-12       Impact factor: 5.864

Review 2.  Improving Outcomes in Infantile Spasms: Role of Pharmacotherapy.

Authors:  Anand Iyer; Richard Appleton
Journal:  Paediatr Drugs       Date:  2016-10       Impact factor: 3.022

3.  Torin 1 partially corrects vigabatrin-induced mitochondrial increase in mouse.

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4.  Preclinical tissue distribution and metabolic correlations of vigabatrin, an antiepileptic drug associated with potential use-limiting visual field defects.

Authors:  Dana C Walters; Erwin E W Jansen; Garrett R Ainslie; Gajja S Salomons; Madalyn N Brown; Michelle A Schmidt; Jean-Baptiste Roullet; K M Gibson
Journal:  Pharmacol Res Perspect       Date:  2019-01-07

5.  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
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6.  Antiepileptogenic effects of rapamycin in a model of infantile spasms due to structural lesions.

Authors:  Ozlem Akman; Stephen W Briggs; Wenzhu B Mowrey; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia       Date:  2021-07-02       Impact factor: 6.740

7.  Epilepsy syndromes, etiologies, and the use of next-generation sequencing in epilepsy presenting in the first 2 years of life: A population-based study.

Authors:  Tommy Stödberg; Torbjörn Tomson; Michela Barbaro; Henrik Stranneheim; Britt-Marie Anderlid; Sofia Carlsson; Per Åmark; Anna Wedell
Journal:  Epilepsia       Date:  2020-09-23       Impact factor: 5.864

  7 in total

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