Literature DB >> 34370120

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

Seonaid Morag Anderson1.   

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.
© 2021. Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  European Society for the Study of Tourette Syndrome (ESSTS); Guidelines; Patients; Patient and Public Involvement (PPI); Research; Tics; Tics and Tourette Around the Globe (TTAG); Tourette Syndrome

Mesh:

Year:  2021        PMID: 34370120     DOI: 10.1007/s00787-021-01854-y

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  6 in total

1.  Patients' participation in research projects as partners.

Authors:  D Mazzoni; Be van Leeuw; P Bednarova; F Marchiori; K Lerstrøm
Journal:  Lupus       Date:  2014-11-21       Impact factor: 2.911

2.  Evaluating patient and public involvement in research.

Authors:  Antoine Boivin; Tessa Richards; Laura Forsythe; Alexandre Grégoire; Audrey L'Espérance; Julia Abelson; Kristin L Carman
Journal:  BMJ       Date:  2018-12-06

3.  Editorial: Patient and public involvement in dementia research: Setting new standards.

Authors:  James Pickett; Matthew Murray
Journal:  Dementia (London)       Date:  2018-11

4.  Patients' roles and rights in research.

Authors:  Paul Wicks; Tessa Richards; Simon Denegri; Fiona Godlee
Journal:  BMJ       Date:  2018-07-25

5.  Patient involvement in research programming and implementation: A responsive evaluation of the Dialogue Model for research agenda setting.

Authors:  Tineke A Abma; Carina A C M Pittens; Merel Visse; Janneke E Elberse; Jacqueline E W Broerse
Journal:  Health Expect       Date:  2014-05-30       Impact factor: 3.377

6.  More than a method: trusting relationships, productive tensions, and two-way learning as mechanisms of authentic co-production.

Authors:  Sarah E Knowles; Dawn Allen; Ailsa Donnelly; Jackie Flynn; Kay Gallacher; Annmarie Lewis; Grace McCorkle; Manoj Mistry; Pat Walkington; Jess Drinkwater
Journal:  Res Involv Engagem       Date:  2021-05-31
  6 in total
  1 in total

Review 1.  Tourette syndrome research highlights from 2021.

Authors:  Andreas Hartmann; Per Andrén; Cyril Atkinson-Clement; Virginie Czernecki; Cécile Delorme; Nanette Marinette Debes; Natalia Szejko; Keisuke Ueda; Kevin Black
Journal:  F1000Res       Date:  2022-06-29
  1 in total

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