Evidence map›Paper›PMID 40387211›Full record

ArticleEpilepsia2025

Risk of unprovoked seizures after discontinuation of antiseizure medication at discharge following acute symptomatic seizures.

Vineet Punia, MarieElena Byrnes, Nicolas R Thompson, Neishay Ayub, Clio Rubinos, Sahar Zafar, Adithya Sivaraju, PASSION (Post‐Acute Symptomatic Seizure Investigation and Outcomes Network) investigators

Abstract read
In one paragraph

Article in Epilepsia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

8 authors.

Vineet PuniaEpilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID https://orcid.org/0000-0002-0552-6736
MarieElena ByrnesEpilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID https://orcid.org/0000-0002-2646-2735
Nicolas R ThompsonDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Neishay AyubRhode Island Hospital, Brown University, Providence, Rhode Island, USA.
Clio RubinosUniversity of North Carolina, Chapel Hill, North Carolina, USA.ORCID https://orcid.org/0000-0002-1680-2302
Sahar ZafarMassachusetts General Hospital, Harvard University, Cambridge, Massachusetts, USA.
Adithya SivarajuYale New Haven Hospital, Yale University, New Haven, Connecticut, USA.ORCID https://orcid.org/0000-0002-6027-9205
PASSION (Post‐Acute Symptomatic Seizure Investigation and Outcomes Network) investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe aimed to investigate whether the risk of unprovoked seizures differs between patients receiving a brief antiseizure medication (ASM) course during hospitalization and those treated beyond hospital discharge following acute symptomatic seizures (ASyS).

methodsWe performed a single-center, retrospective cohort study of all consecutive adults without epilepsy who received maintenance ASM (≥48 h) after ASyS. All patients underwent continuous electroencephalographic (EEG) monitoring and were divided into those receiving ASMs only during hospitalization and those discharged on ASMs. We used propensity score matching to balance covariates between groups. Cause-specific Cox proportional hazards models analyzed the time to the first unprovoked seizure; death was treated as a competing risk.

resultsA total of 144 adults (mean age = 57.4 ± 18.6 years, 48% females) included 118 (82%) patients discharged on ASMs and 26 (18%) who received ASM during hospitalization. During a median follow-up of 24.6 months, 15% experienced an unprovoked seizure. The cumulative incidence of unprovoked seizures at 3, 12, and 36 months was 7.2%, 11.5%, and 17.9%, respectively. ASM status at discharge was significantly associated with electrographic seizures on EEG, etiology, mental status at the time of ASyS, and functional outcome at discharge. After a well-balanced propensity score matching, there was no significant difference in time to unprovoked seizure between patients discharged on ASMs and those who received ASMs only during hospitalization. SIGNIFICANCE: We found that unprovoked seizure risk may not differ significantly between ASyS patients receiving a brief ASM course during hospitalization and those treated for a longer duration after discharge. Although our findings need confirmation in larger studies, they underscore the need for investigating optimal ASM duration in this patient population.

Indexed as

AnticonvulsantsPatient DischargeSeizuresAdultAgedCohort StudiesElectroencephalographyFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesAnticonvulsantscontinuous EEGepileptogenesislate onset seizurepropensity matchingsymptomatic epilepsy

Identifiers

PMID40387211
PMCPMC12455424

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LicenceCC BY-NC-ND
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Registered trials

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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.