Evidence map›Paper›PMID 34244997›Full record

ArticleEpilepsia2021

Clinical phenotypes within nonconvulsive status epilepticus.

Simona Lattanzi, Giada Giovannini, Francesco Brigo, Niccolò Orlandi, Eugen Trinka, Stefano Meletti

Abstract read
In one paragraph

Article in Epilepsia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
  5. Post-hypoxic status epilepticus - A distinct subtype of status epilepticus with poor prognosis.Epileptic disorders : international epilepsy journal with videotape · 2023
    Article
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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

6 authors.

Simona LattanziNeurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.ORCID 0000-0001-8748-0083
Giada GiovanniniNeurology Unit, Baggiovara Civil Hospital, AOU Modena, Modena, Italy.ORCID 0000-0002-3585-5872
Francesco BrigoDepartment of Neuroscience, Biomedicine, and Movement Science, University of Verona, Verona, Italy.ORCID 0000-0003-0928-1577
Niccolò OrlandiNeurology Unit, Baggiovara Civil Hospital, AOU Modena, Modena, Italy.ORCID 0000-0002-5717-7363
Eugen TrinkaDepartment of Neurology, Christian Doppler Clinic, Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-5950-2692
Stefano MelettiNeurology Unit, Baggiovara Civil Hospital, AOU Modena, Modena, Italy.ORCID 0000-0003-0334-539X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study aimed to identify distinct phenotypes within nonconvulsive status epilepticus (NCSE). Consecutive episodes of NCSE in patients at least 14 years old were included. The level of consciousness was assessed through the Glasgow Coma Scale (GCS). Etiology of NCSE was defined as symptomatic (acute, remote, progressive) or unknown. Electroencephalographic (EEG) recordings were searched for lateralized periodic discharges (LPDs), generalized sharply and/or triphasic periodic potentials (GPDs), and spontaneous burst suppression (BS). According to treatment response, NCSE was classified as responsive, refractory, or superrefractory. Average linkage hierarchical cluster analysis was performed with Pearson correlation as similarity measure. Two hundred twenty-nine episodes of NCSE were included. Three clusters were identified. The first cluster linked GCS score 3-8, presence of spontaneous BS on EEG, acute symptomatic etiology, and treatment superrefractoriness. The second cluster gathered GCS score 9-12, presence of LPDs or GPDs on EEG, unknown etiology, and treatment refractoriness. The third cluster associated GCS score 13-15, absence of LPDs, GPDs, and spontaneous BS on EEG, and progressive and remote symptomatic etiology with treatment responsiveness. Phenotyping the heterogeneity of NCSE into electroclinical clusters can contribute to understanding correlations between pathologic and clinical domains, assessing the intrinsic severity of NCSE episodes, and estimating the likelihood of treatment responsiveness.

Indexed as

Status EpilepticusAdolescentComaElectroencephalographyGlasgow Coma ScaleHumansPhenotypehierarchical cluster analysisphenotypesstatus epilepticus

Identifiers

PMID34244997
PMCPMC8456934

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.