Evidence map›Paper›PMID 27208826›Full record

ReviewEpilepsy & behavior : E&B2016

Epilepsy misconceptions and stigma reduction: Current status in Western countries.

Lynn K Herrmann, Elisabeth Welter, Anne T Berg, Adam T Perzynski, Jamie R Van Doren, Martha Sajatovic

Open access · greenAbstract readReview
In one paragraph

Review in Epilepsy & behavior : E&B, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 3 pooled it
4.9field-weighted citation impact, top 5% of its field
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

32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 105 citations in OpenAlex.

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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

6 authors at 5 institutions in 1 country.

Lynn K HerrmannNorthern Illinois University, College of Health and Human Sciences, DeKalb, IL, United States.
Elisabeth WelterCase Western Reserve University School of Medicine, Neurological and Behavioral Outcomes Center, University Hospitals Case Medical Center, Cleveland, OH, United States.
Anne T BergAnn & Robert H. Lurie Children's Hospital of Chicago, Epilepsy Center, Northwestern Feinberg School of Medicine, Dept. of Pediatrics, Chicago, IL, United States.
Adam T PerzynskiCenter for Health Care Research and Policy, Case Western Reserve University, MetroHealth Medical Center, Cleveland, OH, United States.
Jamie R Van DorenCase Western Reserve University School of Medicine, Neurological and Behavioral Outcomes Center, University Hospitals Case Medical Center, Cleveland, OH, United States.
Martha SajatovicDepartment of Psychiatry and of Neurology, Case Western Reserve University School of Medicine, Neurological and Behavioral Outcomes Center, University Hospitals Case Medical Center, Cleveland, OH, United States. Electronic address: Martha.sajatovic@uhhospitals.org.
University Hospitals Cleveland Medical Center · USLurie Children's Hospital · USMetroHealth Medical Center · USNorthern Illinois University · USUniversity Hospitals of Cleveland · US

Funding

Prevention Research Center for Healthy NeighborhoodsU48DP005030 · DP · CASE WESTERN RESERVE UNIVERSITY · PI BORAWSKI, ELAINE A. · 2014 to 2018
$6.8M
ACL HHS U48DP005030NCCDPHP CDC HHS U48 DP005030
6 · The paper itself

Abstract

objectiveThis systematized literature review identified reports describing epilepsy misconceptions in the developed Western countries and research interventions focused on reducing these misconceptions. MATERIALS AND

methodsEnglish language publications from January 2004 to January 2015 that described original research conducted in Europe, North/Central/South America, or Australia on misconceptions about epilepsy among the general public were used for this review.

resultsEighty-one publications were selected. Most studies were conducted in the Americas (N=30) and Europe (N=31). Misconceptions and attitudes about epilepsy were assessed among clinical providers (N=9), family members of people with epilepsy (PWE) (N=5), teachers (N=11), students (N=22), and the general public (N=25). Most studies used structured questionnaires, sometimes adding open-ended questions. Misconceptions reflected socially exclusionary attitudes directed at PWE, ignorance about treatment, and overgeneralizations that are stigmatizing when applied to all PWE. Misconceptions were more prevalent in those with less education, lower socioeconomic status, and no exposure to PWE. There were only 12 intervention studies. While intervention studies were generally effective in improving attitudes, many were targeted to healthcare and education settings, were time-intensive, and impractical for broad general population implementation. None incorporated newer technology-based strategies regarding effective health communication approaches.

conclusionsTypes of epilepsy misconceptions were similar in reports published over the last decade, although most referred to misconceptions that have already been previously described. Existing questionnaires may fail to identify more subtle forms of current misconceptions and negative attitudes. Few interventional studies specifically target epilepsy stigma. Practical and broad scalable approaches to destigmatize epilepsy may help reduce misconceptions.

Indexed as

Social StigmaStereotypingAustraliaCentral AmericaEpilepsyEuropeFemaleHealth Knowledge, Attitudes, PracticeHumansMaleNorth AmericaPopulation GroupsPsychological DistanceSouth AmericaStudentsSurveys and QuestionnairesEpilepsyHealth communicationMisconceptionsSeizuresStigma

Identifiers

PMID27208826
PMCPMC6047062
OpenAlexW2399157057

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.