Evidence map›Paper›PMID 41042536›Full record

ArticleEpilepsia2026

Digital Response Test in Epilepsy assesses interictal epileptiform discharge effects in real time.

Andreas von Allmen, Diyuan Lu, Caroline Jagella, Yasmina Abukhadra, Rune Markhus, Jochen Triesch, Margaret Gopaul, Lawrence J Hirsch, Felix Rosenow, Hal Blumenfeld and 1 more

Abstract read
In one paragraph

Article 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

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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

2 citing papers in PubMed.

  1. 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

11 authors.

Andreas von AllmenDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.
Diyuan LuFrankfurt Institute for Advanced Studies, Frankfurt am Main, Germany.
Caroline JagellaDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.
Yasmina AbukhadraDepartment of Neuroscience, Yale School of Medicine, New Haven, Connecticut, USA.
Rune MarkhusNational Centre for Epilepsy, full member of European Reference Network on Rare and Complex Epilepsies EpiCARE, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway.
Jochen TrieschFrankfurt Institute for Advanced Studies, Frankfurt am Main, Germany.
Margaret GopaulDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.
Lawrence J HirschDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0002-6333-832X
Felix RosenowDepartment of Neurology, Epilepsy Center Frankfurt Rhine-Main, University Medical Center Frankfurt and Center for Personalized Translational Epilepsy Research (CePTR), Goethe University, Frankfurt am Main, Germany.
Hal BlumenfeldDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0003-0812-8132
Heinz KrestelDepartment of Neurology, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0001-8742-0232

Funding

Horizon 2020 99791
6 · The paper itself

Abstract

objectiveInterictal epileptiform discharges (IEDs) in people with epilepsy (PWE) can impair cognitive functions and increase reaction time (RT) and the likelihood of missed reactions. These effects are not routinely assessed, because reliable methods for detecting IEDs of variable appearance in real time and suitable tests to measure IED effects do not yet exist. The objective was to assess different IED effects using new artificial intelligence and medical electronics.

methodsThe Digital Response Test in Epilepsy (DigRTEpi) consisted of a laptop and electronic circuits in a closed loop. Our model with Markov Transition Fields and a deep neural network (ResNet34) visualized the electroencephalogram (EEG) and classified the resulting images. IED detection triggered stimuli in a driving game or in a new cognitive assessment, the interictal Automated Responsiveness Test (iART). DigRTEpi was validated in a prospective case series with 20 people with focal and generalized epilepsies. During offline analysis, sensitivity, specificity, false-positive IED detection rate, latency of EEG classification, IED-induced RT prolongation, virtual crashes, and impaired responses to neuropsychological tasks were determined.

resultsThe model detected IEDs with 84% sensitivity and 96% specificity in our training dataset. In the prospective study with 20 PWE, median sensitivity was 90% (95% confidence interval [CI] = .81-.95), and false-positive IED detection rate was 2.8 (95% CI 2.1-5.9). The ongoing EEG was classified window-by-window in a median 98.7 ms (95% CI = 98.0-99.4). Median RT prolongation and crash probability due to IEDs were 43.8 ms (95% CI = 20.3-64.7) and .9% (95% CI = 0-6.0) per person, respectively. Two patients (10%) had delays of >100 ms, found to be clinically relevant in our prior publication. IEDs caused four patients (20%) each to respond incorrectly or miss answers to neuropsychological tasks. The median false-positive IED detection rates were 2.8/min (95% CI = 2.1-5.9; driving game) and 2.1/min (95% CI = 1.5-3.2; iART). SIGNIFICANCE: By effectively detecting IEDs of variable morphology in real time, DigRTEpi assessed the severity of IED-associated transitory impairment of virtual driving and cognition to improve personalized care.

Indexed as

ElectroencephalographyEpilepsyAdolescentAdultFemaleHumansMaleMiddle AgedNeural Networks, ComputerNeuropsychological TestsProspective StudiesReaction TimeSensitivity and SpecificityYoung Adultdriving safetyEEGinterictal epileptiform discharge effectmachine learningtransitory cognitive impairment

Identifiers

PMID41042536
PMCPMC12893249

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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.