Evidence map›Paper›PMID 38159134›Full record

ArticleEuropean child & adolescent psychiatry2025

Reframing stigma in Tourette syndrome: an updated scoping review.

Kelly Pring, Melina Malli, Brandy W Hardy, Stephen R Rapp, Eric A Storch, Jonathan W Mink, Jaclyn M Martindale

Open access · hybridAbstract readScoping Review
In one paragraph

Article in European child & adolescent psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  13. Tic-Talk: Voices on Tourette's Labelling.Movement disorders clinical practice · 2025
    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

7 authors at 4 institutions in 2 countries.

Kelly PringWake Forest University School of Medicine, Winston-Salem, NC, USA.
Melina MalliInstitute of Population Ageing, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-2744-4034
Brandy W HardyWake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID http://orcid.org/0000-0002-0358-3649
Stephen R RappDepartment of Psychology and Behavioral Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Eric A StorchMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-7631-3703
Jonathan W Mink, Pittsford, NY, USA.ORCID http://orcid.org/0000-0002-7867-3710
Jaclyn M MartindaleDepartment of Neurology, Wake Forest University School of Medicine, North Carolina, Winston-Salem, NC, USA. jmartind@wakehealth.edu.ORCID http://orcid.org/0000-0002-4919-8850
Wake Forest University · USBaylor College of Medicine · USScience Take-Out (United States) · USUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent tic disorders (PTD) such as Tourette's syndrome (TS) are common childhood-onset neurodevelopmental disorders. Stigmatization of individuals with these disorders remains an ongoing problem. The purpose of this scoping review is to serve as an updated review of the research regarding stigmatization in youth with PTD since the publication of the original systematic review about this topic in 2016. The electronic databases Embase, Web of Science, PubMed, PsycINFO, and CINAHL were searched. Of the 4751 initial articles screened after removing duplications, 47 studies met the inclusion criteria. The studies were examined under the social-ecological stigmatization model, which helps categorize stigmatization into individual, interpersonal, community, and structural levels and serves as a broader definition of stigmatization than the previous systematic review. On the individual level, youth with PTD had lower self-esteem than peers, often leading to fear of future stigmatization, avoidant behaviors, and self-stigmatization. They also experienced higher rates of bullying and other forms of abuse than peers at the interpersonal level. At the community level, youth with PTD faced discriminatory environments in school and work and limited availability of community services and healthcare access. At the structural level, knowledge about PTD was limited in the general population, often about the limited portrayals of PTD in the media. We hope that the broader scope of this review serves to help inform future efforts to decrease the stigmatization faced by this group.

Indexed as

Self ConceptSocial StigmaStereotypingTourette SyndromeAdolescentChildHumansDiscriminationScoping reviewSocial–ecologicalStigmaTicTourette syndrome

Identifiers

PMID38159134
PMCPMC11805784
OpenAlexW4390441338

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.