European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: pharmacological treatment
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 guideline...
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Published in | European child & adolescent psychiatry Vol. 31; no. 3; pp. 425 - 441 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.03.2022
Springer Nature B.V Springer Verlag (Germany) |
Subjects | |
Online Access | Get full text |
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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. |
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AbstractList | 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. 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.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. |
Author | Cath, Danielle Cavanna, Andrea E. Termine, Cristiano Szejko, Natalia Münchau, Alexander Verdellen, Cara Debes, Nanette Mol Hartmann, Andreas Ganos, Christos Roessner, Veit Stern, Jeremy S. Müller-Vahl, Kirsten R. Rizzo, Renata Nagy, Péter Plessen, Kerstin J. Hoekstra, Pieter J. Rothenberger, Aribert Eichele, Heike Skov, Liselotte |
Author_xml | – sequence: 1 givenname: Veit surname: Roessner fullname: Roessner, Veit email: veit.roessner@uniklinikum-dresden.de organization: Department of Child and Adolescent Psychiatry, TU Dresden – sequence: 2 givenname: Heike surname: Eichele fullname: Eichele, Heike organization: Department of Biological and Medical Psychology, Faculty of Psychology, University of Bergen, Regional Resource Center for Autism, ADHD, Tourette Syndrome and Narcolepsy Western Norway, Division of Psychiatry, Haukeland University Hospital – sequence: 3 givenname: Jeremy S. surname: Stern fullname: Stern, Jeremy S. organization: Department of Neurology, St George’s Hospital, St George’s University of London – sequence: 4 givenname: Liselotte surname: Skov fullname: Skov, Liselotte organization: Paediatric Department, Herlev University Hospital – sequence: 5 givenname: Renata surname: Rizzo fullname: Rizzo, Renata organization: Child and Adolescent Neurology and Psychiatry, Department of Clinical and Experimental Medicine, University of Catania – sequence: 6 givenname: Nanette Mol surname: Debes fullname: Debes, Nanette Mol organization: Paediatric Department, Herlev University Hospital – sequence: 7 givenname: Péter surname: Nagy fullname: Nagy, Péter organization: Vadaskert Child Psychiatric Hospital and Outpatient Clinic – sequence: 8 givenname: Andrea E. surname: Cavanna fullname: Cavanna, Andrea E. organization: Institute of Clinical Sciences, University of Birmingham – sequence: 9 givenname: Cristiano surname: Termine fullname: Termine, Cristiano organization: Child Neuropsychiatry Unit, Department of Medicine and Surgery, University of Insubria – sequence: 10 givenname: Christos surname: Ganos fullname: Ganos, Christos organization: Department of Neurology, Charité Universitätsmedizin Berlin – sequence: 11 givenname: Alexander surname: Münchau fullname: Münchau, Alexander organization: Institute of Systems Motor Science, University of Lübeck – sequence: 12 givenname: Natalia surname: Szejko fullname: Szejko, Natalia organization: Department of Neurology, Medical University of Warsaw, Department of Bioethics, Medical University of Warsaw, Division of Neurocritical Care and Emergency Neurology, Department of Neurology, Yale School of Medicine – sequence: 13 givenname: Danielle surname: Cath fullname: Cath, Danielle organization: Department of Psychiatry, University Medical Center Groningen, Rijks Universiteit Groningen, GGZ Drenthe Mental Health Institution – sequence: 14 givenname: Kirsten R. surname: Müller-Vahl fullname: Müller-Vahl, Kirsten R. organization: Clinic of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School – sequence: 15 givenname: Cara surname: Verdellen fullname: Verdellen, Cara organization: PsyQ Nijmegen, Parnassia Group, TicXperts – sequence: 16 givenname: Andreas surname: Hartmann fullname: Hartmann, Andreas organization: Department of Neurology, Sorbonne Université, Pitié-Salpetriere Hospital, National Reference Center for Tourette Disorder, Pitié Salpetiere Hospital – sequence: 17 givenname: Aribert surname: Rothenberger fullname: Rothenberger, Aribert organization: Clinic for Child and Adolescent Psychiatry and Psychotherapy, University Medical Center Gottingen – sequence: 18 givenname: Pieter J. surname: Hoekstra fullname: Hoekstra, Pieter J. organization: Department of Child and Adolescent Psychiatry, University of Groningen, University Medical Center Groningen – sequence: 19 givenname: Kerstin J. surname: Plessen fullname: Plessen, Kerstin J. organization: Division of Child and Adolescent Psychiatry, Department of Psychiatry, Lausanne University Hospital, University of Lausanne, Child and Adolescent Mental Health Centre, Mental Health Services, Capital Region of Denmark |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34757514$$D View this record in MEDLINE/PubMed https://hal.sorbonne-universite.fr/hal-03454248$$DView record in HAL |
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Keywords | Pharmacotherapy Medication Tics Treatment Tourette syndrome |
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Snippet | 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... |
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SubjectTerms | Adult Agents Antipsychotics Aripiprazole Attention Deficit Disorder with Hyperactivity - drug therapy Attention deficit hyperactivity disorder Autonomy Behavior Behavior modification Blocking Botulinum toxin Cannabis Child Child & adolescent psychiatry Child and Adolescent Psychiatry Clinical practice guidelines Clonidine Combination therapy Critical incidents Dopamine Drug therapy Drugs Extrapyramidal system Female Gilles de la Tourette syndrome Guanfacine - therapeutic use Haloperidol Human health and pathology Humans Life Sciences Literature reviews Male Marijuana Medicine Medicine & Public Health Neurons and Cognition Patients Pediatrics Pimozide Polls & surveys Preferences Psychiatry Psychoeducational treatment Review Risperidone Risperidone - therapeutic use Side effects Tic Disorders - complications Tic Disorders - drug therapy Topiramate Tourette syndrome Tourette Syndrome - complications Tourette Syndrome - drug therapy Treatment methods |
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Title | European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: pharmacological treatment |
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