Evidence map›Paper›PMID 41250972›Full record

Trial reportEpilepsia2026

Dynamics of early electroencephalographic patterns and epileptic seizures in acute intracerebral hemorrhage: A prospective controlled study.

Ziad Al-Fatuhi-Al-Jundi, Salomé Avenas, Pierre Tankéré, Frédéric Philipeau, Pierre Garnier, Laure Mazzola, Nathalie Andre-Obadia, Sébastien Boulogne, Hélène Catenoix, Sylvain Rheims and 11 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Epilepsia, 2026. 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. Review
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

21 authors.

Ziad Al-Fatuhi-Al-JundiDepartment of Functional Neurology and Epileptology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0009-0002-5813-176X
Salomé AvenasDepartment of Biostatistics, Edouard Herriot Hospital, Lyon University Hospital, Lyon, France.
Pierre TankéréCenter for Sleep Medicine, Croix-Rousse Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-3793-7126
Frédéric PhilipeauStroke Unit, Department of Neurology, Fleyriat Hospital, Bourg en Bresse, France.
Pierre GarnierStroke Center, Department of Neurology, Saint-Etienne University Hospital, Saint-Etienne, France.
Laure MazzolaClinical Neurophysiology Unit, Department of Neurology, Saint-Etienne University Hospital, Saint-Etienne, France.ORCID https://orcid.org/0000-0001-7307-0809
Nathalie Andre-ObadiaDepartment of Functional Neurology and Epileptology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-0940-7224
Sébastien BoulogneDepartment of Functional Neurology and Epileptology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0001-8681-7369
Hélène CatenoixDepartment of Functional Neurology and Epileptology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-5574-8521
Sylvain RheimsDepartment of Functional Neurology and Epileptology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-4663-8515
Tae-Hee ChoStroke Center, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0001-8677-2447
Julia FontaineStroke Center, Neurological Hospital, University Hospital, Lyon, France.
Laura MechtouffStroke Center, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0001-9165-5763
Elodie OngStroke Center, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-3990-9241
Yves BerthezeneDepartment of Neuroradiology, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0001-6725-7861
Anne TermozPublic Health Unit, Clinical Research and Epidemiology Department, Lyon University Hospital, Lyon, France.ORCID https://orcid.org/0000-0003-4274-0114
Nathalie PerretonPublic Health Unit, Clinical Research and Epidemiology Department, Lyon University Hospital, Lyon, France.
Julie HaesebaertPublic Health Unit, Clinical Research and Epidemiology Department, Lyon University Hospital, Lyon, France.ORCID https://orcid.org/0000-0001-9109-5604
Muriel RabilloudDepartment of Biostatistics, Edouard Herriot Hospital, Lyon University Hospital, Lyon, France.ORCID https://orcid.org/0000-0003-1324-0356
Laurent DerexStroke Center, Neurological Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-0909-8900
Laure Peter-DerexCenter for Sleep Medicine, Croix-Rousse Hospital, University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-9938-9639

Funding

Ministère des Affaires Sociales et de la Santé PHRC-I grant 2013
6 · The paper itself

Abstract

objectiveAcute symptomatic seizures (ASyS) occur in up to 30% of patients with intracerebral hemorrhage (ICH) when continuous electroencephalography (cEEG) is used, potentially worsening outcomes. Identification of early EEG biomarkers of ASyS may help guide personalized antiseizure medication (ASM) prophylaxis. Here, we aimed to describe early interictal EEG patterns, their dynamics, and their association with seizure risk, considering the effect of prophylactic levetiracetam.

methodsThis prospective analysis used data from the PEACH phase 3 trial (2017-2020), which enrolled adults with acute spontaneous supratentorial ICH, randomized to receive levetiracetam or placebo. Patients underwent systematic 48-h cEEG within 48 h of symptom onset. Electrographic seizures and interictal EEG patterns were analyzed using standardized terminology of the American Clinical Neurophysiology Society. Associations between rhythmic and periodic patterns (RPPs) and seizures with clinical and radiological variables were assessed using univariate analyses. We also conducted exploratory testing of the CAV (cortical involvement, age < 65 years, volume > 10 mL) score for predicting ASyS, incorporating RPPs and ASM exposure.

resultsForty-two patients were included (median [Q1-Q3] age = 72 [60-79] years, 29% women), 19 in the levetiracetam group. Interictal EEG abnormalities were common and not influenced by ASM, including background asymmetry (73%), sporadic epileptiform discharges (62%), and RPPs (52%). RPPs were associated with ICH volume (p = .039) and cortical involvement (p = .003). Among patients with RPPs, 50% developed ASyS (20% in those treated with ASM vs. 75% in untreated patients, p = .030). Most patients (91.7%) with seizures had RPPs that preceded seizures, in >90% cases by 12 (Q1-Q3 = 4-25) h. Integrating RPPs into the CAV model led to an improvement of ASyS prediction (area under the curve = .949 vs. .918, p = .53) that was statistically nonsignificant. SIGNIFICANCE: RPPs are strong markers of ictogenesis in acute ICH and precede ASyS, thus offering a potential therapeutic window. These findings support the use of early cEEG for risk stratification and personalized ASM prophylaxis.

Indexed as

Cerebral HemorrhageElectroencephalographyEpilepsyLevetiracetamSeizuresAgedAnticonvulsantsFemaleHumansMaleMiddle AgedProspective StudiesAnticonvulsantsLevetiracetamacute symptomatic seizurescontinuous electroencephalographyinterictal epileptiform dischargesintracerebral hemorrhagerhythmic and periodic patterns

Identifiers

PMID41250972
PMCPMC13007832

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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.