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Issue title: Researching Tourette syndrome in Europe
Article type: Research Article
Authors: Cavanna, Andrea Eugenio; | David, Kate | Bandera, Valentina | Termine, Cristiano | Balottin, Umberto | Schrag, Anette; | Selai, Caroline
Affiliations: Sobell Department of Movement Disorders, Institute of Neurology and University College London, London, UK | Department of Neuropsychiatry, BSMHFT and University of Birmingham, Birmingham, UK | Child Neuropsychiatry Unit, Department of Experimental Medicine, University of Insubria, Varese, Italy | Department of Child Neurology and Psychiatry, IRCCS 'C. Mondino' Foundation, University of Pavia, Pavia, Italy | Department of Neurology, Royal Free and University College Medical School, London, UK
Note: [] Corresponding author: Dr. Andrea Eugenio Cavanna, MD, PhD., Department of Neuropsychiatry, The Barberry National Centre for Mental Health, 25 Vincent Drive, Birmingham B15 2FG, UK. Tel.: +44 0121 3012317; Fax: +44 0121 3012291; E-mail: cavanna77@tin.it
Abstract: Gilles de la Tourette syndrome (GTS) is a neurodevelopmental condition characterised by multiple motor and phonic tics and associated behavioural problems, carrying a significant burden on patients' lives. Although the term health related-quality of life (HR-QOL) has only been used in recent years, several studies have long addressed the impact of GTS on physical, psychological and social aspects of wellbeing of both children and adults with GTS. We set out to answer the question "Is HR-QOL affected by GTS and, if so, in what domains?" by conducting a systematic literature review of published original studies addressing HR-QOL in both children and adult patients with GTS. This review focuses on the current evidence on the impact of GTS on patients' lives, mainly informed by studies using generic functional impairment and HR-QOL measures from the last decade, and expands on the new opportunities introduced by the recently developed GTS-specific HR-QOL scales (GTS-QOL and GTS-QOL-C&A). Analysis of the first decade of studies specifically addressing HR-QOL in GTS suggests that co-morbid conditions are key factors in determining HR-QOL in young patients, whilst the picture is more complex in adults with GTS. These findings offer some general directions for both current clinical practice and future research.
Keywords: Gilles de la Tourette syndrome, health-related quality of life, functional impairment, tics, behavioural problems
DOI: 10.3233/BEN-120296
Journal: Behavioural Neurology, vol. 27, no. 1, pp. 83-93, 2013
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