Evidence map›Paper›PMID 40669025›Full record

ArticleNeurology2025

Validation of the Seizure-Related Impact Assessment Scale: A Novel Patient-Reported Outcome Measure for Epilepsy.

Emma Foster, Alison Conquest, Chris Ewart, John-Paul Nicolo, Genevieve Rayner, Toby T Winton-Brown, Terence J O'Brien, Patrick Kwan, Charles Malpas, Jacqueline French

Abstract readValidation Study
In one paragraph

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

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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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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

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

10 authors.

Emma FosterDepartment of Neurosciences, Monash University, Melbourne, Australia.ORCID 0000-0001-8958-3844
Alison ConquestDepartment of Neurosciences, Monash University, Melbourne, Australia.ORCID 0009-0000-9388-1342
Chris EwartCommunity and Researcher Engagement (CaRE) Program, Monash University, Melbourne, Australia.
John-Paul NicoloMonash University, Melbourne, Australia.ORCID 0000-0002-0473-6475
Genevieve RaynerMelbourne School of Psychological Sciences, University of Melbourne, Australia.ORCID 0000-0002-0747-3877
Toby T Winton-BrownMonash University, Melbourne, Australia.
Terence J O'BrienDepartment of Neurosciences, Monash University, Melbourne, Australia.
Patrick KwanDepartment of Neurosciences, Monash University, Melbourne, Australia.ORCID 0000-0001-7310-276X
Charles MalpasDepartment of Neurosciences, Monash University, Melbourne, Australia.ORCID 0000-0003-0534-3718
Jacqueline FrenchNYU Comprehensive Epilepsy Center, New York.ORCID 0000-0003-2242-8027

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThere is a clear need in epilepsy clinical trials and practice for a measure that captures the trade-off between seizure and treatment-related adverse effects, which is reliable over time and across different treatment regimens. We aimed to create and validate the Seizure-Related Impact Assessment Scale (SERIAS) to fill this need.

methodsThis was a prospective longitudinal study of adults with epilepsy recruited from an Australian comprehensive epilepsy center. Participants completed SERIAS at baseline and 3 and 6 months later. SERIAS has 6 self-report items. Five items record the number of days per month that seizures or treatment-related adverse effects partially or fully affect work/home/school and family/social/nonwork activities. The final item is an epilepsy disability visual analog scale. SERIAS is scored by adding the days per month of disability, with scores ranging from 0 to 150 (higher scores indicate more disability). SERIAS was completed alongside 7 validated instruments measuring seizure-related and treatment-related adverse effects (Work and Social Adjustment Scale [WSAS], Liverpool Adverse Events Profile [LAEP]), mood disorders (Neurological Disorders Depression Inventory for Epilepsy [NDDI-E], Generalized Anxiety Disorder [GAD-7]), somatic symptoms (Somatic Symptom Scale [SSS-8]), and quality of life (Quality of Life in Epilepsy Inventory [QOLIE]-31, EuroQol 5 Dimensions [EQ-5D]). General linear mixed models were used to investigate the relationship between the SERIAS and other relevant clinical and psychometric data. Standardized model coefficients β are presented with 95% confidence intervals.

resultsA total of 90 patients (64.4% female, mean age 43.1 years) completed baseline SERIAS. Most patients reported at least 1 day of disability (62%, median SERIAS score = 3, interquartile range = 18.3). Greater disability was negatively correlated with QOLIE-31 total score (β = -0.17, 95% CI -0.27 to -0.07) and positively correlated with scores on 5-level EQ-5D (β = 0.15, 95% CI 0.04-0.25), NDDI-E (β = 0.22, 95% CI 0.13-0.31), GAD-7 (β = 0.21, 95% CI 0.09-0.32), SSS8 (β = 0.29, 95% CI 0.17-0.41), LAEP (β = 0.29, 95% CI 0.20-0.39), WSAS seizure-related adverse events (β = 0.23, 95% CI 0.14-0.33), and WSAS treatment-related adverse events (β = 0.36, 95% CI 0.26-0.46). Higher seizure frequency was associated with higher SERIAS score (β = 0.07, 95% CI 0.03-0.11). Psychometric reliability for the SERIAS was acceptable (all coefficients >0.70) as was test-retest reliability (n = 35 patients, intraclass correlation coefficient = 0.72, 95% CI 0.51-0.85). DISCUSSION: SERIAS shows good psychometric reliability and strong test-retest stability. These findings suggest that SERIAS is a valid scale to measure epilepsy-related disability.

Indexed as

EpilepsyPatient Reported Outcome MeasuresSeizuresAdultAgedAustraliaFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective StudiesQuality of LifeReproducibility of ResultsSelf ReportYoung Adult

Identifiers

PMID40669025
PMCPMC12264976

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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.