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Published in: European Child & Adolescent Psychiatry 3/2022

01-03-2022 | Tic Disorder | Review

European clinical guidelines for Tourette Syndrome and other tic disorders: patients’ perspectives on research and treatment

Authors: Seonaid Morag Anderson, on behalf of Tics and Tourette Around the Globe (TTAG) representing Tic and Tourette Syndrome (TS) patient associations around the world

Published in: European Child & Adolescent Psychiatry | Issue 3/2022

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Abstract

The formation of a new umbrella organisation called Tics and Tourette Across the Globe (TTAG) representing Tic and Tourette Syndrome (TS) patient associations around the world has led to a clearer voice for patients with Tourette Syndrome (TS). An opportunity has been created for this group to bridge research, clinical work and shared decision-making between researchers, clinicians and patients across Europe, with the result of improving the treatment and management of TS. A survey was sent out to capture the patients’ perspective on research and treatment, and 2269 participants responded. 71% of participants reported they would prefer research into how to treat TS and/or make symptoms better. The inclusion of patients’ perspectives on research and treatment in the updated European clinical guidelines for TS and other tic disorders highlights the new opportunities that have been created for the participation of patients in the discussion of TS research.
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Literature
1.
go back to reference Oliver S (2006) Patient involvement in setting research agendas. Eur J Gastroenterol Hepatol 18:935–938CrossRef Oliver S (2006) Patient involvement in setting research agendas. Eur J Gastroenterol Hepatol 18:935–938CrossRef
3.
go back to reference Abma TA, Nierse CJ, Widdershoven GA (2009) Patients as partners in responsive research: Methodological notions for collaborations in mixed research teams. Qual Health Res 19:401–415CrossRef Abma TA, Nierse CJ, Widdershoven GA (2009) Patients as partners in responsive research: Methodological notions for collaborations in mixed research teams. Qual Health Res 19:401–415CrossRef
5.
go back to reference Abma TA, Broerse JE (2010) Patient participation as dialogue: Setting research agendas. Health Expect 13:160–173CrossRef Abma TA, Broerse JE (2010) Patient participation as dialogue: Setting research agendas. Health Expect 13:160–173CrossRef
7.
go back to reference Biddle MSY et al (2021) (2021) Attitudes and approaches to patient and public involvement across Europe: a systematic review. Health Soc Care Community 29(1):18–27CrossRef Biddle MSY et al (2021) (2021) Attitudes and approaches to patient and public involvement across Europe: a systematic review. Health Soc Care Community 29(1):18–27CrossRef
10.
go back to reference Straus S, Richardson WS, Haynes RB (2019) Evidence-based Medicine: how to practice and teach EBM, Fifth ed., Elsevier publishers Straus S, Richardson WS, Haynes RB (2019) Evidence-based Medicine: how to practice and teach EBM, Fifth ed., Elsevier publishers
12.
go back to reference De Wit MP, Berlo SE, Aanerud GJ et al (2011) European League Against Rheumatism recommendations for the inclusion of patient representatives in scientific projects. Ann Rheum Dis 70:722–726CrossRef De Wit MP, Berlo SE, Aanerud GJ et al (2011) European League Against Rheumatism recommendations for the inclusion of patient representatives in scientific projects. Ann Rheum Dis 70:722–726CrossRef
13.
go back to reference Schipper K, Abma TA, van Zadelhoff E et al (2010) What does it mean to be a patient research partner? An ethnodrama. Qual Inq 16:501–510CrossRef Schipper K, Abma TA, van Zadelhoff E et al (2010) What does it mean to be a patient research partner? An ethnodrama. Qual Inq 16:501–510CrossRef
17.
go back to reference White MA, Verhoef MJ (2005) Toward a patient-centered approach: incorporating principles of participatory action research into clinical studies. Integr Cancer Ther 4(1):21–24CrossRef White MA, Verhoef MJ (2005) Toward a patient-centered approach: incorporating principles of participatory action research into clinical studies. Integr Cancer Ther 4(1):21–24CrossRef
Metadata
Title
European clinical guidelines for Tourette Syndrome and other tic disorders: patients’ perspectives on research and treatment
Authors
Seonaid Morag Anderson
on behalf of Tics and Tourette Around the Globe (TTAG) representing Tic and Tourette Syndrome (TS) patient associations around the world
Publication date
01-03-2022
Publisher
Springer Berlin Heidelberg
Published in
European Child & Adolescent Psychiatry / Issue 3/2022
Print ISSN: 1018-8827
Electronic ISSN: 1435-165X
DOI
https://doi.org/10.1007/s00787-021-01854-y

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