Evidence map›Paper›PMID 40760363›Full record

ArticleActa neurologica Belgica2025

Navigating pediatric post-stroke epilepsy: comparative assessment of treatment strategies.

Çağatay Günay, Semra Hız Kurul, Uluç Yiş, Adem Aydın, Ayşe İpek Polat

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Acta neurologica Belgica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Çağatay GünayDepartment of Pediatric Neurology, Siirt Training and Research Hospital, Siirt, Turkey. cagataygunaymd@gmail.com.ORCID http://orcid.org/0000-0001-7860-6297
Semra Hız KurulDepartment of Pediatric Neurology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-8020-4884
Uluç YişDepartment of Pediatric Neurology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0001-8355-1411
Adem AydınDepartment of Pediatric Neurology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-8480-2857
Ayşe İpek PolatDepartment of Pediatric Neurology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-8270-3249

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough post-stroke epilepsy (PSE) is a prevalent complication in children, optimal management remains challenging. This study evaluated the impact of different treatment modalities and antiseizure medications (ASM) on the development and management of pediatric PSE following arterial ischemic stroke.

methodsWe conducted a retrospective cohort analysis over 20 years, examining pediatric patients who experienced seizures during the course of arterial ischemic stroke. Exclusions included neonatal stroke, hemorrhagic stroke, and sinovenous thrombosis. Cut-off point of seven days were accepted as early seizures and PSE. Treatments included acute stroke therapies such as intravenous tissue plasminogen activator, mechanical thrombectomy, anti-edema therapies, and antithrombotic treatments. Medications for seizure control were categorized as acute seizure management agents (benzodiazepines and phenytoin), which are not used for long-term post-stroke epilepsy control, and long-term antiseizure medications (levetiracetam and carbamazepine) for PSE management.

resultsAmong 153 patients, 99 were male, with a median age of 23 months. PSE was diagnosed in 59.5% of the cohort. Cardiac disorders were the primary etiology (32.7%). Hyperacute treatments and anti-edema therapies showed no significant impact on PSE development. Benzodiazepines and phenytoin also did not affect PSE rates. Levetiracetam was associated with a higher PSE rate (66.7%) compared to carbamazepine (45.1%) (p = 0.010). Carbamazepine demonstrated superior seizure freedom at 6 and 24 months (p = 0.024 and p = 0.014, respectively). Seizure control was achieved in 19.8% of PSE patients through dose titration, with carbamazepine showing higher efficacy (p = 0.037). ASM discontinuation rates were higher with carbamazepine (95.7%) compared to levetiracetam (79.4%).

conclusionAcute stroke therapies, anti-edema, and antithrombotic treatments did not lower the PSE development. Benzodiazepines and phenytoin were not effective in preventing PSE. Carbamazepine may be more effective than levetiracetam in managing pediatric PSE, providing better seizure control and higher ASM discontinuation rates. Further research is needed to confirm these findings.

Indexed as

AnticonvulsantsEpilepsyIschemic StrokeStrokeAdolescentChildChild, PreschoolCohort StudiesFemaleHumansInfantMaleRetrospective StudiesTreatment OutcomeAnticonvulsantsAntiseizure medicationsCarbamazepineLevetiracetamPediatric strokePost-stroke epilepsy

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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.