European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: pharmacological treatment

ESSTS · 2021 · Europe

Source and licence

Authors
Veit Roessner, Heike Eichele, Jeremy S. Stern et al.
Title
European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: pharmacological treatment
Journal
European Child & Adolescent Psychiatry, 2021
Licence
CC BY 4.0
Changes
Verbatim excerpts; formatting adapted

Full text retrieved 2026-10-27 from Europe PMC · PMC8940878

Licence statement of the original publication

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Abstract

In 2011, the European Society for the Study of Tourette Syndrome (ESSTS) published the first European guidelines for Tourette Syndrome (TS). We now present an update of the part on pharmacological treatment, based on a review of new literature with special attention to other evidence-based guidelines, meta-analyses, and randomized double-blinded studies. Moreover, our revision took into consideration results of a recent survey on treatment preferences conducted among ESSTS experts. The first preference should be given to psychoeducation and to behavioral approaches, as it strengthens the patients’ self-regulatory control and thus his/her autonomy. Because behavioral approaches are not effective, available, or feasible in all patients, in a substantial number of patients pharmacological treatment is indicated, alone or in combination with behavioral therapy. The largest amount of evidence supports the use of dopamine blocking agents, preferably aripiprazole because of a more favorable profile of adverse events than first- and second-generation antipsychotics. Other agents that can be considered include tiapride, risperidone, and especially in case of co-existing attention deficit hyperactivity disorder (ADHD), clonidine and guanfacine. This view is supported by the results of our survey on medication preference among members of ESSTS, in which aripiprazole was indicated as the drug of first choice both in children and adults. In treatment resistant cases, treatment with agents with either a limited evidence base or risk of extrapyramidal adverse effects might be considered, including pimozide, haloperidol, topiramate, cannabis-based agents, and botulinum toxin injections. Overall, treatment of TS should be individualized, and decisions based on the patient’s needs and preferences, presence of co-existing conditions, latest scientific findings as well as on the physician’s preferences, experience, and local regulatory requirements.

Contents of the original publication

The section headings of the original.

  • Introduction
  • Methodology of selection of agents and literature search strategy
  • Agents from recently published AAN guidelines
  • Agents mentioned in the ESSTS survey
  • Selection of agents to be discussed in detail
  • Dysfunction of transmitter systems as basis for psychopharmacological treatment
  • Dopamine-modulating agents
  • First-generation antipsychotics
  • Second- and third-generation antipsychotics
  • Benzamides
  • Noradrenergic agents
  • Other agents
  • Cannabis-based medicines
  • Botulinum toxin
  • Topiramate
  • Pharmacological treatment of tics in the context of co-existing psychiatric conditions
  • Attention-deficit/hyperactivity disorder (ADHD)
  • Obsessive–compulsive disorder (OCD)
  • Other co-existing psychiatric conditions
  • Clinical recommendations for the pharmacological treatment of TS
  • Current limitations and future directions

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