Evidence map›Paper›PMID 29655171›Full record

ArticleEpilepsy research2018

Alterations of network synchrony after epileptic seizures: An analysis of post-ictal intracranial recordings in pediatric epilepsy patients.

Samuel B Tomlinson, Ankit N Khambhati, Camilo Bermudez, Rebecca M Kamens, Gregory G Heuer, Brenda E Porter, Eric D Marsh

Open access · greenAbstract read
In one paragraph

Article in Epilepsy research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Samuel B TomlinsonDepartment of Pediatrics, Division of Child Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, United States; School of Medicine and Dentistry, University of Rochester Medical Center, Rochester, NY, 14642, United States. Electronic address: samuel_tomlinson@urmc.rochester.edu.
Ankit N KhambhatiDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, United States; Penn Center for Neuroengineering and Therapeutics, University of Pennsylvania, Philadelphia, PA, 19104, United States.
Camilo BermudezDepartment of Pediatrics, Division of Child Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, United States.
Rebecca M KamensDepartment of Pediatrics, Division of Child Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, United States.
Gregory G HeuerDepartment of Pediatrics, Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, United States.
Brenda E PorterDepartment of Neurology and Neurological Science, Stanford School of Medicine, Palo Alto, CA, 94304, United States.
Eric D MarshDepartment of Pediatrics, Division of Child Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, United States; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, United States.
Children's Hospital of Philadelphia · USStanford Medicine · USUniversity of Pennsylvania · US

Funding

The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI ROBINSON, MICHAEL BYRNE · 2016 to 2020
$6.3M
Virtual Resection to Treat EpilepsyR01NS099348 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI BASSETT, DANIELLE SMITH, LITT, BRIAN · 2016 to 2019
$2.3M
NICHD NIH HHS U54 HD086984NINDS NIH HHS R01 NS099348
6 · The paper itself

Abstract

objectivePost-ictal EEG alterations have been identified in studies of intracranial recordings, but the clinical significance of post-ictal EEG activity is undetermined. The purpose of this study was to examine the relationship between peri-ictal EEG activity, surgical outcome, and extent of seizure propagation in a sample of pediatric epilepsy patients.

methodsIntracranial EEG recordings were obtained from 19 patients (mean age = 11.4 years, range = 3-20 years) with 57 seizures used for analysis (mean = 3.0 seizures per patient). For each seizure, 3-min segments were extracted from adjacent pre-ictal and post-ictal epochs. To compare physiology of the epileptic network between epochs, we calculated the relative delta power (Δ) using discrete Fourier transformation and constructed functional networks based on broadband connectivity (conn). We investigated differences between the pre-ictal (Δ

resultsDistributed-network (DN) seizures exhibited increased post-ictal delta power and global EEG connectivity compared to focal-network (FN) seizures. Following DN seizures, patients with seizure-free outcomes exhibited a 14.7% mean increase in delta power and an 8.3% mean increase in global connectivity compared to pre-ictal baseline, which was dramatically less than values observed among seizure-persistent patients (29.6% and 47.1%, respectively). SIGNIFICANCE: Post-ictal differences between DN and FN seizures correlate with post-operative seizure persistence. We hypothesize that post-ictal deactivation of subcortical nuclei recruited during seizure propagation may account for this result while lending insights into mechanisms of post-operative seizure recurrence.

Indexed as

ElectrocorticographyAdolescentBrainChildChild, PreschoolDelta RhythmEpilepsyFemaleHumansMalePrognosisRetrospective StudiesSeizuresTime FactorsTreatment OutcomeYoung AdultEpilepsy surgeryIntracranial electroencephalographyNetwork connectivityPediatric epilepsyPost-ictal

Identifiers

PMID29655171
PMCPMC7003130
OpenAlexW2803865420

What OpenQuestion holds

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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.