The impact of tourette syndrome in adults

Results from the tourette syndrome impact survey

Christine A. Conelea, Douglas W. Woods*, Samuel H. Zinner, Cathy L. Budman, Tanya K. Murphy, Lawrence D. Scahill, Scott N. Compton, John T. Walkup

*Corresponding author for this work

Research output: Contribution to journalArticle

40 Citations (Scopus)

Abstract

Chronic tic disorders (CTD) are characterized by motor and/or vocal tics. Existing data on the impact of tics in adulthood is limited by small, treatment-seeking samples or by data aggregated across adults and children. The current study explored the functional impact of tics in adults using a nationwide sample of 672 participants with a self-reported CTD. The impact of tics on physical, social, occupational/academic, and psychological functioning was assessed. Results suggested mild to moderate functional impairment and positive correlations between impairment and tic severity. Notable portions of the sample reported social or public avoidance and experiences of discrimination resulting from tics. Compared to previously reported population norms, participants had more psychological difficulties, greater disability, and lower quality of life. The current study suggests that CTDs can adversely impact functioning in adults and highlights the need for clinical interventions and systemic efforts to address tic-related impairments.

Original languageEnglish (US)
Pages (from-to)110-120
Number of pages11
JournalCommunity Mental Health Journal
Volume49
Issue number1
DOIs
StatePublished - Feb 1 2013

Fingerprint

Tics
Tourette Syndrome
adulthood
quality of life
discrimination
disability
Tic Disorders
Psychology
Surveys and Questionnaires
experience
Quality of Life

Keywords

  • Functional impact
  • Quality of life
  • Tic
  • Tourette

ASJC Scopus subject areas

  • Health(social science)
  • Public Health, Environmental and Occupational Health
  • Psychiatry and Mental health

Cite this

Conelea, Christine A. ; Woods, Douglas W. ; Zinner, Samuel H. ; Budman, Cathy L. ; Murphy, Tanya K. ; Scahill, Lawrence D. ; Compton, Scott N. ; Walkup, John T. / The impact of tourette syndrome in adults : Results from the tourette syndrome impact survey. In: Community Mental Health Journal. 2013 ; Vol. 49, No. 1. pp. 110-120.
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Conelea, CA, Woods, DW, Zinner, SH, Budman, CL, Murphy, TK, Scahill, LD, Compton, SN & Walkup, JT 2013, 'The impact of tourette syndrome in adults: Results from the tourette syndrome impact survey', Community Mental Health Journal, vol. 49, no. 1, pp. 110-120. https://doi.org/10.1007/s10597-011-9465-y

The impact of tourette syndrome in adults : Results from the tourette syndrome impact survey. / Conelea, Christine A.; Woods, Douglas W.; Zinner, Samuel H.; Budman, Cathy L.; Murphy, Tanya K.; Scahill, Lawrence D.; Compton, Scott N.; Walkup, John T.

In: Community Mental Health Journal, Vol. 49, No. 1, 01.02.2013, p. 110-120.

Research output: Contribution to journalArticle

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AU - Walkup, John T.

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