Evidence map›Paper›PMID 39373091›Full record

ArticleEpilepsia2024

Health utilities of patients with epilepsy in a Canadian population.

Olayinka I Arimoro, Samuel Wiebe, Chantelle Q Y Lin, Colin B Josephson, Tolulope T Sajobi, Calgary Comprehensive Epilepsy Program

Abstract read
In one paragraph

Article in Epilepsia, 2024. 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

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

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

6 authors.

Olayinka I ArimoroDepartment of Community Health Sciences and O'Brien Institute of Public Health, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0009-0009-9464-589X
Samuel WiebeDepartment of Community Health Sciences and O'Brien Institute of Public Health, University of Calgary, Calgary, Alberta, Canada.
Chantelle Q Y LinDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Colin B JosephsonDepartment of Community Health Sciences and O'Brien Institute of Public Health, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0001-7052-1651
Tolulope T SajobiDepartment of Community Health Sciences and O'Brien Institute of Public Health, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0002-5696-5552
Calgary Comprehensive Epilepsy Program

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHealth state utilities are required to obtain quality adjusted life years, a common metric that informs clinical decision-making at individual, group, and health policy levels. Health state utilities are different from health-related quality of life, and their distribution across patients with epilepsy, as well as the factors that impact them, have not been studied in depth. We aimed to describe the distribution of health state utilities in people with epilepsy and the impact of different combinations of clinical and demographic factors on health state evaluation.

methodsWe performed a retrospective analysis of patients' data prospectively collected in the Calgary Comprehensive Epilepsy Program registry. Patient-reported health state utilities were measured using the 5-level EuroQol 5-Dimension scale (EQ-5D-5L) completed at their initial assessment. EQ-5D-5L index scores were derived via the time trade-off approach based on Canadian norms, and their distribution across different health states and patient characteristics was obtained. The Tobit regression model was used to evaluate the determinants of EQ-5D-5L index scores.

resultsOf 1446 patients included in this analysis, 724 (50.5%) were female. The median (interquartile range) Canada-normed EQ-5D-5L index score was .87 (.71-.91). Patients with significantly lower health utilities were more likely to be female (p = .008), to be older (p = .034), to be unmarried (p = .013), to have failed to achieve 1-year seizure freedom (p < .001), to have no postsecondary education (p = .028), to be depressed (p < .001), to have antiseizure medication side effects (p = .001), to be unemployed (p < .001), and to be unable to drive (p < .001). A look-up table of health utilities based on combinations of clinical-demographic characteristics was produced. SIGNIFICANCE: Health utility estimates for combinations of different health states in people with epilepsy attending specialty clinics are now available. These can help guide clinical decision-making in routine clinical practice, economic evaluations of treatment interventions, and health care policies.

Indexed as

EpilepsyHealth StatusQuality of LifeAdolescentAdultAgedCanadaFemaleHumansMaleMiddle AgedQuality-Adjusted Life YearsRetrospective StudiesYoung AdultepilepsyEQ‐5D‐5Lhealth‐related quality of lifehealth state utility

Identifiers

PMID39373091
PMCPMC11647436

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LicenceCC BY-NC-ND
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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.