Evidence map›Paper›PMID 42595743›Full record

ArticleEpilepsia open2026

Impact of vigabatrin on risk of relapse of infantile spasms.

Yaretson I Carmenate, Hayoung E Ahn, Haley R Peters, Hiroki Nariai, Rajsekar R Rajaraman, Shaun A Hussain

Abstract read
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Article in Epilepsia open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yaretson I CarmenateDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0000-0003-0720-7621
Hayoung E AhnDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0009-0005-2278-1965
Haley R PetersDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0009-0000-8411-9129
Hiroki NariaiDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-8318-2924
Rajsekar R RajaramanDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-9685-7118
Shaun A HussainDivision of Pediatric Neurology, Department of Pediatrics, UCLA Mattel Children's Hospital and David Geffen School of Medicine, Los Angeles, California, USA.ORCID https://orcid.org/0000-0001-6947-8852

Funding

John C. Hench Foundation
6 · The paper itself

Abstract

objectiveVigabatrin is an effective treatment for infantile epileptic spasms syndrome (IESS), but relapse remains a clinical challenge. The ideal dose and duration of treatment after response are unknown. We set out to identify treatment-related predictors of IESS relapse after initial vigabatrin response.

methodsWe conducted a retrospective cohort study of infants with IESS who achieved electroclinical response within 30 days of vigabatrin initiation (alone or with hormonal therapy) and remained in remission for ≥ 30 days. Time to epileptic spasms relapse was analyzed using the Kaplan-Meier procedure and Cox proportional hazards regression. A linear regression-based propensity score (derived from etiology and latency to vigabatrin initiation) was included in Cox models to adjust for treatment duration confounding. Candidate predictors included age at IESS onset, presence of other seizure types at onset, developmental status, prior relapse, vigabatrin dose, and use of dual therapy (concomitant adrenocorticotropic hormone [ACTH] or prednisolone).

resultsOf 164 responders, 63 (38%) relapsed at a median of 7.5 months (IQR: 2.4-18.0) after response. Twenty-one (33.3%) relapses occurred following vigabatrin discontinuation. In propensity score-adjusted multivariable regression, increased relapse risk was associated with prior IESS relapse (HR 2.35; 95% CI 1.24-4.45; P = 0.009), other seizure types at IESS onset (HR 2.31; 95% CI 1.31-4.07; P = 0.004), and abnormal development at IESS diagnosis (HR 1.75; 95% CI 1.04-2.95; P = 0.035). Moderate dosing (100-149 mg/kg/day) was protective versus lower doses (HR 0.47; 95% CI 0.25-0.89; P = 0.020). In an underpowered analysis of vigabatrin exposure as a time-varying covariate, ongoing therapy was not significantly associated with latency to relapse (HR 0.77; 95% CI 0.39-1.49; P = 0.436). SIGNIFICANCE: Relapse after vigabatrin response is common and influenced by identifiable clinical factors. Continued vigabatrin treatment (> 100 mg/kg/day) may reduce relapse risk. Prospective validation is warranted to guide individualized relapse prevention strategies. PLAIN LANGUAGE SUMMARY: Infantile Epileptic Spasms Syndrome is a serious seizure disorder of infancy that can recur even after successful treatment with vigabatrin. In this study of 164 infants, we found that relapse was most common among children with prior relapses, other seizure types, or developmental delays. Infants treated with moderate vigabatrin doses (100-149 mg/kg/day) had the lowest relapse rates. These findings may help clinicians identify which infants face the highest risk and tailor treatment accordingly.

Indexed as

epileptic spasms syndromehypsarrhythmiaIESSrelapse preventiontuberous sclerosis complex

Identifiers

PMID42595743
PMCPMC13472970

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.