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Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?

BACKGROUND: Gilles de la Tourette Syndrome (GTS) is a complex neuropsychiatric disorder, characterized by chronic motor and vocal tics, associated in 50–90% of cases with psychiatric comorbidities. Patients with moderate and severe clinical picture are treated with psychotherapy and pharmacological...

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Autores principales: Zekaj, Edvin, Saleh, Christian, Porta, Mauro, Servello, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521224/
https://www.ncbi.nlm.nih.gov/pubmed/26290773
http://dx.doi.org/10.4103/2152-7806.161242
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author Zekaj, Edvin
Saleh, Christian
Porta, Mauro
Servello, Domenico
author_facet Zekaj, Edvin
Saleh, Christian
Porta, Mauro
Servello, Domenico
author_sort Zekaj, Edvin
collection PubMed
description BACKGROUND: Gilles de la Tourette Syndrome (GTS) is a complex neuropsychiatric disorder, characterized by chronic motor and vocal tics, associated in 50–90% of cases with psychiatric comorbidities. Patients with moderate and severe clinical picture are treated with psychotherapy and pharmacological therapy. Deep brain stimulation (DBS) is reserved for pharmacological refractory GTS patients. As GTS tends to improve with time and potentially resolves in the second decade of life, the major concern of DBS in GTS is the age at which the patient undergoes surgical procedure. Some authors suggest performing DBS after 18 years, others after 25 years of age. CASE DESCRIPTION: We present a 25-year-old patient with GTS, who was aged 17 years and was treated with thalamic DBS. DBS resulted in progressive and sustained improvement of tics and co-morbidities. After 6 years of DBS treatment, it was noted that the clinical improvement was maintained also in OFF stimulation setting, so it was decided to keep it off. After 2 years in off-setting and stable clinical picture the entire DBS device was removed. Six months after DBS device removal the patient remained symptom-free. CONCLUSIONS: DBS is a therapeutic option reserved for severe and refractory GTS cases. In our opinion DBS might be considered as a temporary application in GTS.
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spelling pubmed-45212242015-08-19 Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach? Zekaj, Edvin Saleh, Christian Porta, Mauro Servello, Domenico Surg Neurol Int Case Report BACKGROUND: Gilles de la Tourette Syndrome (GTS) is a complex neuropsychiatric disorder, characterized by chronic motor and vocal tics, associated in 50–90% of cases with psychiatric comorbidities. Patients with moderate and severe clinical picture are treated with psychotherapy and pharmacological therapy. Deep brain stimulation (DBS) is reserved for pharmacological refractory GTS patients. As GTS tends to improve with time and potentially resolves in the second decade of life, the major concern of DBS in GTS is the age at which the patient undergoes surgical procedure. Some authors suggest performing DBS after 18 years, others after 25 years of age. CASE DESCRIPTION: We present a 25-year-old patient with GTS, who was aged 17 years and was treated with thalamic DBS. DBS resulted in progressive and sustained improvement of tics and co-morbidities. After 6 years of DBS treatment, it was noted that the clinical improvement was maintained also in OFF stimulation setting, so it was decided to keep it off. After 2 years in off-setting and stable clinical picture the entire DBS device was removed. Six months after DBS device removal the patient remained symptom-free. CONCLUSIONS: DBS is a therapeutic option reserved for severe and refractory GTS cases. In our opinion DBS might be considered as a temporary application in GTS. Medknow Publications & Media Pvt Ltd 2015-07-21 /pmc/articles/PMC4521224/ /pubmed/26290773 http://dx.doi.org/10.4103/2152-7806.161242 Text en Copyright: © 2015 Zekaj E. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Zekaj, Edvin
Saleh, Christian
Porta, Mauro
Servello, Domenico
Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title_full Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title_fullStr Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title_full_unstemmed Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title_short Temporary deep brain stimulation in Gilles de la Tourette syndrome: A feasible approach?
title_sort temporary deep brain stimulation in gilles de la tourette syndrome: a feasible approach?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521224/
https://www.ncbi.nlm.nih.gov/pubmed/26290773
http://dx.doi.org/10.4103/2152-7806.161242
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