Evidence map›Paper›PMID 36208032›Full record

ArticleEpilepsia2022

Progressive slowing of clonic phase predicts postictal generalized EEG suppression.

Maria Vlachou, Philippe Ryvlin, Anca Adriana Arbune, Sidsel Armand Larsen, Annette Skraep Sidaros, Melita Cacic Hribljan, Martin Fabricius, Sándor Beniczky

Abstract read
In one paragraph

Article in Epilepsia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

8 authors.

Maria VlachouDepartment of Clinical Neurophysiology, Aarhus University Hospital and Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Philippe RyvlinDepartment of Clinical Neurosciences, Lausanne University Hospital, Lausanne, Switzerland.ORCID 0000-0001-7775-6576
Anca Adriana ArbuneDepartment of Clinical Neurophysiology, Danish Epilepsy Centre, Dianalund, Denmark.ORCID 0000-0002-9500-4498
Sidsel Armand LarsenDepartment of Clinical Neurophysiology, Danish Epilepsy Centre, Dianalund, Denmark.
Annette Skraep SidarosDepartment of Clinical Neurophysiology, Copenhagen University Hospital, Copenhagen, Denmark.
Melita Cacic HribljanDepartment of Clinical Neurophysiology, Copenhagen University Hospital, Copenhagen, Denmark.
Martin FabriciusDepartment of Clinical Neurophysiology, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0002-6959-6848
Sándor BeniczkyDepartment of Clinical Neurophysiology, Aarhus University Hospital and Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-6035-6581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePostictal generalized electroencephalography (EEG) suppression (PGES) is a surrogate marker of sudden unexpected death in epilepsy (SUDEP). It is still unclear which ictal phenomena lead to prolonged PGES and increased risk of SUDEP. Semiology features of generalized convulsive seizure (GCS type 1) have been reported as a predictor of prolonged PGES. Progressive slowing of clonic phase (PSCP) has been observed in GCSs, with gradually increasing inhibitory periods interrupting the tonic contractions. We hypothesized that PSCP is associated with prolonged PGES.

methodsWe analyzed 90 bilateral convulsive seizures in 50 consecutive patients (21 female; age: 11-62 years, median: 31 years) recruited to video-EEG monitoring. Five raters, blinded to all other data, independently assessed the presence of PSCP. PGES and seizure semiology were evaluated independently. We determined inter-rater agreement (IRA) for the presence of PSCP, and we evaluated its association, as well as that of other ictal features, with the occurrence of PGES, prolonged PGES (≥20 s) and very prolonged PGES (≥50 s) using multivariate logistic regression analysis.

resultsWe found substantial IRA for the presence of PSCP (percent agreement: 80%; beyond-chance agreement coefficient: .655). PSCP was an independent predictor of the occurrence of PGES and prolonged PGES (p < .001). All seizures with very prolonged PGES had PSCP. GCS type 1 was an independent predictor of occurrence of PGES (p = .02) and prolonged PGES (p = .03) but not of very prolonged PGES. Only half of the seizures with very prolonged PGES were GCS type 1. SIGNIFICANCE: PSCP predicts prolonged PGES, emphasizing the importance of gradually increasing inhibitory phenomena at the end of the seizures. Our findings shed more light on the ictal phenomena leading to increased risk of SUDEP. These phenomena may provide basis for algorithms implemented into wearable devices for identifying GCS with increased risk of SUDEP.

Indexed as

SeizuresAdolescentAdultChildFemaleHumansMiddle AgedYoung Adult

Identifiers

PMID36208032
PMCPMC10092045

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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.