Efficacy of intravenous immunoglobulin in children with drug-resistant epilepsy

Purpose: Inflammation may contribute to drug-resistant epilepsy (DRE) in children and immunomodulatory therapies, including intravenous immunoglobulin (IVIG), have been described to reduce seizure burden. This retrospective study assesses the effect of IVIG on seizures in a tertiary epilepsy center. Methods: We performed a retrospective chart review of children with DRE using our Pediatric Epilepsy Outcome-Informatics database, which contains standardized information on 3,650 pediatric epilepsy patients collected at the point of care. Inclusion criteria were refractory seizures, regular follow-up and treatment with IVIG for at least 1 year. Patients with autoimmune encephalitis were excluded from the analysis. Sex, etiology, epilepsy syndromes, seizure types, antiseizure medications (ASM), adverse effects, and seizure frequency scores prior, 3 months post-, and 1-year post-IVIG were collected and statistically compared. Results: = 0.019). These findings could not be explained by changes in other ASMs. Conclusion: Long-term use of IVIG in pediatric patients can be an effective treatment for refractory seizures, even if exact mechanisms remain unclear.

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Publication Details

Journal
Frontiers in Neurology
Published
2026-04-13
DOI
https://doi.org/10.3389/fneur.2026.1796553
Primary Topic
Epilepsy research and treatment
Type
article
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article

Efficacy of intravenous immunoglobulin in children with drug-resistant epilepsy

Morris H. Scantlebury, Aya Ebdalla, Julia Jacobs, Alice Ho et al.
Frontiers in Neurology
Epilepsy research and treatment
article

Efficacy of intravenous immunoglobulin in children with drug-resistant epilepsy

Morris H. Scantlebury, Aya Ebdalla, Julia Jacobs, Alice Ho, Juan P. Appendino
article en

Abstract

Purpose: Inflammation may contribute to drug-resistant epilepsy (DRE) in children and immunomodulatory therapies, including intravenous immunoglobulin (IVIG), have been described to reduce seizure burden. This retrospective study assesses the effect of IVIG on seizures in a tertiary epilepsy center. Methods: We performed a retrospective chart review of children with DRE using our Pediatric Epilepsy Outcome-Informatics database, which contains standardized information on 3,650 pediatric epilepsy patients collected at the point of care. Inclusion criteria were refractory seizures, regular follow-up and treatment with IVIG for at least 1 year. Patients with autoimmune encephalitis were excluded from the analysis. Sex, etiology, epilepsy syndromes, seizure types, antiseizure medications (ASM), adverse effects, and seizure frequency scores prior, 3 months post-, and 1-year post-IVIG were collected and statistically compared. Results: = 0.019). These findings could not be explained by changes in other ASMs. Conclusion: Long-term use of IVIG in pediatric patients can be an effective treatment for refractory seizures, even if exact mechanisms remain unclear.

Frontiers in NeurologyVol. 17
Allen Institute for Brain Science (US), University of Calgary (CA), Alberta Children's Hospital (CA), University of Saskatchewan (CA), Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute (CA)
Good health and well-being
Openalex Percentile: Top 20%
Epilepsy research and treatment
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