Evidence map›Paper›PMID 42064976›Full record

ArticleFrontiers in neurology

Efficacy of intravenous immunoglobulin in children with drug-resistant epilepsy.

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

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Aya EbdallaDepartment of Pediatrics and Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Morris H ScantleburyDepartment of Pediatrics and Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Juan P AppendinoDivision of Pediatric Neurology, Department of Pediatrics, University of Saskatchewan, Saskatoon, SK, Canada.
Alice HoDepartment of Pediatrics and Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Julia JacobsDepartment of Pediatrics and Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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: Sixty patients aged 2-18 years (mean ± SD, 11.8 ± 4.13) were included. Patients exhibited focal (38.3%, Conclusion: Long-term use of IVIG in pediatric patients can be an effective treatment for refractory seizures, even if exact mechanisms remain unclear.

Indexed as

drug-resistant epilepsyepilepsyIVIgpediatric epilepsyseizure

Identifiers

PMID42064976
PMCPMC13127252

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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.