Literature DB >> 19638024

The quality of life of young people with Tourette syndrome.

D Cutler1, T Murphy, J Gilmour, I Heyman.   

Abstract

BACKGROUND: The study examined a UK sample of 57 young people with Tourette syndrome (TS). AIMS: The purpose of this study was to consider the impact of TS on young people's Quality of Life (QoL).
METHODS: The study used a mixed methods design, combining focus groups and questionnaire data. Child report questionnaires measured QoL and TS symptom severity.
RESULTS: The results showed that the QoL of children with TS was significantly worse than that of children in a UK normative sample. Analysis of transcripts from the groups identified four main themes; 'TS can be distressing and disabling', 'struggling to fit into society's expectations of normal behaviour', 'needing to control tics' and 'TS is one part of who I am'.
CONCLUSIONS: Poorer QoL was associated with increased symptom severity in terms of tics, Attention Deficit Hyperactivity Disorder diagnosis and obsessive compulsive behaviours.

Entities:  

Mesh:

Year:  2009        PMID: 19638024     DOI: 10.1111/j.1365-2214.2009.00983.x

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  32 in total

Review 1.  Stigma in youth with Tourette's syndrome: a systematic review and synthesis.

Authors:  Melina A Malli; Rachel Forrester-Jones; Glynis Murphy
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-08-28       Impact factor: 4.785

2.  Exploring the impact of chronic tic disorders on youth: results from the Tourette Syndrome Impact Survey.

Authors:  Christine A Conelea; Douglas W Woods; Samuel H Zinner; Cathy Budman; Tanya Murphy; Lawrence D Scahill; Scott N Compton; John Walkup
Journal:  Child Psychiatry Hum Dev       Date:  2011-04

3.  European clinical guidelines for Tourette syndrome and other tic disorders. Part III: behavioural and psychosocial interventions.

Authors:  Cara Verdellen; Jolande van de Griendt; Andreas Hartmann; Tara Murphy
Journal:  Eur Child Adolesc Psychiatry       Date:  2011-04       Impact factor: 4.785

4.  Quality of life and self-esteem in children with chronic tic disorder.

Authors:  Selma Tural Hesapçıoğlu; Mustafa Kemal Tural; Sema Kandil
Journal:  Turk Pediatri Ars       Date:  2014-12-01

5.  Quality of life in children with OCD before and after treatment.

Authors:  Bernhard Weidle; Tord Ivarsson; Per Hove Thomsen; Stian Lydersen; Thomas Jozefiak
Journal:  Eur Child Adolesc Psychiatry       Date:  2014-12-20       Impact factor: 4.785

6.  Cost of illness in patients with Gilles de la Tourette's syndrome.

Authors:  Ines Dodel; Jens Peter Reese; Norbert Müller; Alexander Münchau; Monika Balzer-Geldsetzer; Jürgen Wasem; Wolfgang H Oertel; Richard Dodel; Kirsten Müller-Vahl
Journal:  J Neurol       Date:  2010-02-24       Impact factor: 4.849

7.  Peer victimization in youth with Tourette syndrome and other chronic tic disorders.

Authors:  Samuel H Zinner; Christine A Conelea; Gwen M Glew; Douglas W Woods; Cathy L Budman
Journal:  Child Psychiatry Hum Dev       Date:  2012-02

8.  Quality of life in young people with Tourette syndrome: a controlled study.

Authors:  C M Eddy; R Rizzo; M Gulisano; A Agodi; M Barchitta; P Calì; M M Robertson; A E Cavanna
Journal:  J Neurol       Date:  2010-09-23       Impact factor: 4.849

9.  Living with tics: reduced impairment and improved quality of life for youth with chronic tic disorders.

Authors:  Joseph F McGuire; Elysse Arnold; Jennifer M Park; Joshua M Nadeau; Adam B Lewin; Tanya K Murphy; Eric A Storch
Journal:  Psychiatry Res       Date:  2014-12-04       Impact factor: 3.222

10.  The Impact of Tic Severity, Comorbidity and Peer Attachment on Quality of Life Outcomes and Functioning in Tourette's Syndrome: Parental Perspectives.

Authors:  Deirdre O'Hare; Edward Helmes; Valsamma Eapen; Rachel Grove; Kerry McBain; John Reece
Journal:  Child Psychiatry Hum Dev       Date:  2016-08
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