Volume 55, Issue 12 pp. 1918-1925
Full-Length Original Research

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

Milena Djuric

Corresponding Author

Milena Djuric

Institute of Mother and Child Healthcare of Serbia, Belgrade, Serbia

Faculty of Medicine, University of Belgrade, Belgrade, Serbia

Address correspondence to Milena Djuric, Svetozara Markovica 9, 11000 Belgrade, Serbia. E-mail: [email protected]Search for more papers by this author
Ruzica Kravljanac

Ruzica Kravljanac

Institute of Mother and Child Healthcare of Serbia, Belgrade, Serbia

Faculty of Medicine, University of Belgrade, Belgrade, Serbia

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Biljana Tadic

Biljana Tadic

Institute of Mother and Child Healthcare of Serbia, Belgrade, Serbia

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Nataša Mrlješ-Popovic

Nataša Mrlješ-Popovic

Institute of Mother and Child Healthcare of Serbia, Belgrade, Serbia

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Richard E. Appleton

Richard E. Appleton

Alder Hey Children's Hospital, Liverpool, United Kingdom

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First published: 06 November 2014
Citations: 44

Summary

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.

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