Evidence map›Paper›PMID 37349955›Full record

ArticleEpilepsia2023

Focal to bilateral tonic-clonic seizures predict pharmacoresistance in focal cortical dysplasia-related epilepsy.

Phat Chang, Hua Xie, Venkata Sita Priyanka Illapani, Xiaozhen You, Tayyba Anwar, Archana Pasupuleti, Thuy-Anh Vu, L Gilbert Vezina, Taha Gholipour, Chima O Oluigbo and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Epilepsia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. ILAE neuroimaging task force highlight: MRI detection of early life epilepsy caused by focal cortical dysplasia.Epileptic disorders : international epilepsy journal with videotape · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. 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

13 authors at 2 institutions in 1 country.

Phat ChangCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Hua XieCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Venkata Sita Priyanka IllapaniCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Xiaozhen YouCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Tayyba AnwarCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Archana PasupuletiCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Thuy-Anh VuCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
L Gilbert VezinaCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Taha GholipourCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Chima O OluigboCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.
Anqing ZhangDivision of Biostatistics and Study Methodology, Children's National Research Institute, Washington, District of Columbia, USA.
William Davis GaillardCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.ORCID 0000-0001-5709-0033
Nathan T CohenCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, District of Columbia, USA.ORCID 0000-0002-1410-3487
George Washington University Hospital · USChildren's National · US

Funding

Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
Neurobehavioral Evaluation CoreP50HD105328 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI WILLIAM Davis GAILLARD · 2021 to 2026
$9.3M
NCATS NIH HHS UL1 TR001876NICHD NIH HHS P50 HD105328
6 · The paper itself

Abstract

objectiveFocal cortical dysplasia (FCD) is the most common etiology of surgically-remediable epilepsy in children. Eighty-seven percent of patients with FCD develop epilepsy (75% is pharmacoresistant epilepsy [PRE]). Focal to bilateral tonic-clonic (FTBTC) seizures are associated with worse surgical outcomes. We hypothesized that children with FCD-related epilepsy with FTBTC seizures are more likely to develop PRE due to lesion interaction with restricted cortical neural networks.

methodsPatients were selected retrospectively from radiology and surgical databases from Children's National Hospital. INCLUSION CRITERIA: 3T magnetic resonance imaging (MRI)-confirmed FCD from January 2011 to January 2020; ages 0 days to 22 years at MRI; and 18 months of documented follow-up. FCD dominant network (Yeo 7-network parcellation) was determined. Association of FTBTC seizures with epilepsy severity, surgical outcome, and dominant network was tested. Binomial regression was used to evaluate predictors (FTBTC seizures, age at seizure onset, pathology, hemisphere, lobe) of pharmacoresistance and Engel outcome. Regression was used to evaluate predictors (age at seizure onset, pathology, lobe, percentage default mode network [DMN] overlap) of FTBTC seizures.

resultsOne hundred seventeen patients had a median age at seizure onset of 3.00 years (interquartile range [IQR] .42-5.59 years). Eighty-three patients had PRE (71%); 34 had pharmacosensitive epilepsy (PSE) (29%). Twenty patients (17%) had FTBTC seizures. Seventy-three patients underwent epilepsy surgery. Multivariate regression showed that FTBTC seizures are associated with an increased risk of PRE (odds ratio [OR] 6.41, 95% confidence interval [CI] 1.21-33.98, p = .02). FCD hemisphere/lobe was not associated with PRE. Percentage DMN overlap predicts FTBTC seizures. Seventy-two percent (n = 52) overall and 53% (n = 9) of patients with FTBTC seizures achieved Engel class I outcome. SIGNIFICANCE: In a heterogeneous population of surgical and non-operated patients with FCD-related epilepsy, the presence of FTBTC seizures is associated with a tremendous risk of PRE. This finding is a recognizable marker to help neurologists identify those children with FCD-related epilepsy at high risk of PRE and can flag patients for earlier consideration of potentially curative surgery. The FCD-dominant network also contributes to FTBTC seizure clinical expression.

Indexed as

EpilepsyFocal Cortical DysplasiaMalformations of Cortical DevelopmentChildHumansMagnetic Resonance ImagingRetrospective StudiesSeizuresTreatment Outcomedefault mode networkdrug-resistant epilepsyFCDpharmacoresistant epilepsy

Identifiers

PMID37349955
PMCPMC10529443
OpenAlexW4381716773

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.