Evidence map›Paper›PMID 40230985›Full record

ReviewEpilepsy & behavior reports2025

Frequently asked questions and answers on Visually-Provoked (Photosensitive) epilepsy.

Dorothée Kasteleijn-Nolst Trenité, Jayant Acharya, Fiona Mitchell Baumer, Roy Beran, Dana Craiu, Jaqueline French, Pasquale Parisi, Jessica Solodar, Jerzy P Szaflarski, Yukitoshi Takahashi and 4 more

Abstract readReview
In one paragraph

Review in Epilepsy & behavior reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

14 authors.

Dorothée Kasteleijn-Nolst TrenitéNesmos Department Sapienza University Rome Italy.
Jayant AcharyaDepartment of Neurology Southern Illinois University School of Medicine Springfield IL USA.
Fiona Mitchell BaumerDepartment of Neurology Stanford University School of Medicine Stanford CA USA.
Roy BeranSouth Western Clinic School, University of NSW Sydney Australia.
Dana CraiuDepartment of Pediatric Neurology University of Medicine Bucharest Romania.
Jaqueline FrenchNYU Comprehensive Epilepsy Center New York NY USA.
Pasquale ParisiNesmos Department Sapienza University Rome Italy.
Jessica SolodarWriter on Health LLC Boston MA USA.
Jerzy P SzaflarskiDepartment of Neurology, University of Alabama at Birmingham, USA.
Yukitoshi TakahashiNHO Shizuoka Institute of Epilepsy and Neurological Disorders Shizuoka Japan.
Liu Lin ThioDepartments of Neurology, Pediatrics and Neuroscience , Washington University School of Medicine St. Louis MO USA.
Ben TolchinDepartment of Neurology, Yale School of Medicine New Haven CT USA.
Arnold WilkinsDepartment of Psychology, University of Essex Essex UK.
Robert S FisherDepartment of Neurology Stanford University School of Medicine Stanford CA USA.

Funding

Speaking of Spikes: Connectivity and Language in Benign Epilepsy with Centrotemporal SpikesK23NS116110 · NINDS · STANFORD UNIVERSITY · PI BAUMER, FIONA MITCHELL · 2020 to 2024
$1.1M
NINDS NIH HHS K23 NS116110
6 · The paper itself

Abstract

Clinical experts associated with national epilepsy-related societies, led by the Epilepsy Foundation, collected, collated and answered "Frequently asked questions (FAQ)" of broad interest pertaining to visually-provoked seizures. Questions emerged from people with epilepsy, caretakers and healthcare professionals from different countries around the world. Focus is on practical implications of visually-provoked seizures. The top 5 most frequently asked questions were.1.How does a doctor make a diagnosis of visually-provoked seizures?2.What can I do in general to prevent visually-provoked seizures?3.Will I need antiseizure medications for my visually-provoked seizures?"4.Will I outgrow visually-provoked seizures? How will I know if I've outgrown them?5.How do I enable safety features to block content that could trigger seizures on social media, websites, phones, laptops and tablets?Answers were based on scientific evidence, where such information was available [1] and expert opinion when formal evidence was insufficient. Key answers included distinction of photoparoxysmal EEG findings versus light-provoked seizures. Typical provocation is by flashes at 10-25 per second or certain moving patterns. There is a genetic risk, which is outgrown in about half. Covering one or both eyes can prevent a light-provoked seizure. TV, videogames, virtual reality and 3D images are not in themselves provocative, but their content can be. Topics covered included: 1. Photosensitive epilepsy diagnosis; 2. Preventing visually-provoked seizures; 3. Do treatments help; 4. Life and behavioral decisions; 5. School; 6. Multi-media; 7. Children and youth.

Indexed as

EpilepsyPattern-sensitive seizuresPhotosensitive seizuresReflex EpilepsyVideo game seizures

Identifiers

PMID40230985
PMCPMC11995705

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.