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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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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. |
format | Online Article Text |
id | pubmed-4521224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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