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Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years

OBJECTIVE: Observational study to evaluate the long-term motor and non-motor effects of deep brain stimulation (DBS) of the globus pallidus internus (GPi) on medically refractory dystonia. BACKGROUND: Dystonia is a chronic disease affecting mainly young patients with a regular life expectancy and li...

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Autores principales: Krause, P., Völzmann, S., Ewert, S., Kupsch, A., Schneider, G. H., Kühn, Andrea A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592956/
https://www.ncbi.nlm.nih.gov/pubmed/32055996
http://dx.doi.org/10.1007/s00415-020-09745-z
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author Krause, P.
Völzmann, S.
Ewert, S.
Kupsch, A.
Schneider, G. H.
Kühn, Andrea A.
author_facet Krause, P.
Völzmann, S.
Ewert, S.
Kupsch, A.
Schneider, G. H.
Kühn, Andrea A.
author_sort Krause, P.
collection PubMed
description OBJECTIVE: Observational study to evaluate the long-term motor and non-motor effects of deep brain stimulation (DBS) of the globus pallidus internus (GPi) on medically refractory dystonia. BACKGROUND: Dystonia is a chronic disease affecting mainly young patients with a regular life expectancy and lifelong need for therapy. Pallidal DBS is an established treatment for severe isolated dystonia but long-term data are sparse. METHODS: We considered 36 consecutive patients with isolated generalized (n = 14) and cervical/segmental (n = 22) dystonia operated at Charité-University Hospital between 2000 and 2007 in a retrospective analysis for long-term outcome of pallidal DBS. In 19 of these patients, we could analyze dystonic symptoms and disability rated by the Burke–Fahn–Marsden Dystonia Rating scale (BFMDRS) at baseline, short-term (ST-FU, range 3–36 months) and long-term follow-up (LT-FU, range 93–197 months). Quality of life and mood were evaluated using the SF36 and Beck Depression Index (BDI) questionnaires. RESULTS: Patients reached an improvement in motor symptoms of 63.8 ± 5.7% (mean ± SE) at ST-FU and 67.9 ± 6.1% at LT-FU. Moreover, a significant and stable reduction in disability was shown following DBS (54.2 ± 9.4% at ST-FU and 53.8 ± 9.2% at LT-FU). BDI and SF36 had improved by 40% and 23%, respectively, at LT-FU (n = 14). Stimulation-induced adverse events included swallowing difficulties, dysarthria, and bradykinesia. Pulse generator (n = 3) and electrodes (n = 5) were revised in seven patients due to infection. CONCLUSIONS: Pallidal DBS is a safe and efficacious long-term treatment for dystonia with sustained effects on motor impairment and disability, accompanied by a robust improvement in mood and quality of life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-09745-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-85929562021-11-24 Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years Krause, P. Völzmann, S. Ewert, S. Kupsch, A. Schneider, G. H. Kühn, Andrea A. J Neurol Original Communication OBJECTIVE: Observational study to evaluate the long-term motor and non-motor effects of deep brain stimulation (DBS) of the globus pallidus internus (GPi) on medically refractory dystonia. BACKGROUND: Dystonia is a chronic disease affecting mainly young patients with a regular life expectancy and lifelong need for therapy. Pallidal DBS is an established treatment for severe isolated dystonia but long-term data are sparse. METHODS: We considered 36 consecutive patients with isolated generalized (n = 14) and cervical/segmental (n = 22) dystonia operated at Charité-University Hospital between 2000 and 2007 in a retrospective analysis for long-term outcome of pallidal DBS. In 19 of these patients, we could analyze dystonic symptoms and disability rated by the Burke–Fahn–Marsden Dystonia Rating scale (BFMDRS) at baseline, short-term (ST-FU, range 3–36 months) and long-term follow-up (LT-FU, range 93–197 months). Quality of life and mood were evaluated using the SF36 and Beck Depression Index (BDI) questionnaires. RESULTS: Patients reached an improvement in motor symptoms of 63.8 ± 5.7% (mean ± SE) at ST-FU and 67.9 ± 6.1% at LT-FU. Moreover, a significant and stable reduction in disability was shown following DBS (54.2 ± 9.4% at ST-FU and 53.8 ± 9.2% at LT-FU). BDI and SF36 had improved by 40% and 23%, respectively, at LT-FU (n = 14). Stimulation-induced adverse events included swallowing difficulties, dysarthria, and bradykinesia. Pulse generator (n = 3) and electrodes (n = 5) were revised in seven patients due to infection. CONCLUSIONS: Pallidal DBS is a safe and efficacious long-term treatment for dystonia with sustained effects on motor impairment and disability, accompanied by a robust improvement in mood and quality of life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-09745-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-02-13 2020 /pmc/articles/PMC8592956/ /pubmed/32055996 http://dx.doi.org/10.1007/s00415-020-09745-z Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/ 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Krause, P.
Völzmann, S.
Ewert, S.
Kupsch, A.
Schneider, G. H.
Kühn, Andrea A.
Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title_full Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title_fullStr Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title_full_unstemmed Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title_short Long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
title_sort long-term effects of bilateral pallidal deep brain stimulation in dystonia: a follow-up between 8 and 16 years
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592956/
https://www.ncbi.nlm.nih.gov/pubmed/32055996
http://dx.doi.org/10.1007/s00415-020-09745-z
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