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Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review

OBJECTIVE: Deep brain stimulation (DBS) for treatment of advanced Parkinson’s disease (PD) has two anatomical targets: the subthalamic nucleus (STN) and the globus pallidus internus (GPI). The clinical effectiveness of these two stimulation targets was compared in the present study. METHODS: A syste...

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Autores principales: Xu, Hao, Zheng, Feng, Krischek, Boris, Ding, Wanhai, Xiong, Chi, Wang, Xin, Niu, Chaoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718722/
https://www.ncbi.nlm.nih.gov/pubmed/28701061
http://dx.doi.org/10.1177/0300060517708102
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author Xu, Hao
Zheng, Feng
Krischek, Boris
Ding, Wanhai
Xiong, Chi
Wang, Xin
Niu, Chaoshi
author_facet Xu, Hao
Zheng, Feng
Krischek, Boris
Ding, Wanhai
Xiong, Chi
Wang, Xin
Niu, Chaoshi
author_sort Xu, Hao
collection PubMed
description OBJECTIVE: Deep brain stimulation (DBS) for treatment of advanced Parkinson’s disease (PD) has two anatomical targets: the subthalamic nucleus (STN) and the globus pallidus internus (GPI). The clinical effectiveness of these two stimulation targets was compared in the present study. METHODS: A systematic review and meta-analysis was performed to evaluated the postoperative changes in the United Parkinson’s Disease Rating Scale (UPDRS) on- and off-phase, on-stimulation motor scores; activities of daily living score (ADLS); and levodopa equivalent dose (LED) after STN and GPI stimulation. Randomized and nonrandomized controlled trials of PD treated by STN and GPI stimulation were considered for inclusion. RESULTS: Eight published reports of eligible studies involving 599 patients met the inclusion criteria. No significant differences were observed between the STN and GPI groups in the on-medication, on-stimulation UPDRS motor score [mean difference, 2.15; 95% confidence interval (CI), −0.96–5.27] or ADLS (mean difference, 3.40; 95% CI, 0.95–7.76). Significant differences in favor of STN stimulation were noted in the off-medication, on-stimulation UPDRS motor score (mean difference, 1.67; 95% CI, 0.98–2.37) and LED (mean difference, 130.24; 95% CI, 28.82–231.65). CONCLUSION: The STN may be the preferred target for DBS in consideration of medication reduction, economic efficiency, and motor function improvement in the off phase. However, treatment decisions should be made according to the individual patient’s symptoms and expectations.
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spelling pubmed-57187222017-12-11 Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review Xu, Hao Zheng, Feng Krischek, Boris Ding, Wanhai Xiong, Chi Wang, Xin Niu, Chaoshi J Int Med Res Reviews OBJECTIVE: Deep brain stimulation (DBS) for treatment of advanced Parkinson’s disease (PD) has two anatomical targets: the subthalamic nucleus (STN) and the globus pallidus internus (GPI). The clinical effectiveness of these two stimulation targets was compared in the present study. METHODS: A systematic review and meta-analysis was performed to evaluated the postoperative changes in the United Parkinson’s Disease Rating Scale (UPDRS) on- and off-phase, on-stimulation motor scores; activities of daily living score (ADLS); and levodopa equivalent dose (LED) after STN and GPI stimulation. Randomized and nonrandomized controlled trials of PD treated by STN and GPI stimulation were considered for inclusion. RESULTS: Eight published reports of eligible studies involving 599 patients met the inclusion criteria. No significant differences were observed between the STN and GPI groups in the on-medication, on-stimulation UPDRS motor score [mean difference, 2.15; 95% confidence interval (CI), −0.96–5.27] or ADLS (mean difference, 3.40; 95% CI, 0.95–7.76). Significant differences in favor of STN stimulation were noted in the off-medication, on-stimulation UPDRS motor score (mean difference, 1.67; 95% CI, 0.98–2.37) and LED (mean difference, 130.24; 95% CI, 28.82–231.65). CONCLUSION: The STN may be the preferred target for DBS in consideration of medication reduction, economic efficiency, and motor function improvement in the off phase. However, treatment decisions should be made according to the individual patient’s symptoms and expectations. SAGE Publications 2017-07-12 2017-10 /pmc/articles/PMC5718722/ /pubmed/28701061 http://dx.doi.org/10.1177/0300060517708102 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Reviews
Xu, Hao
Zheng, Feng
Krischek, Boris
Ding, Wanhai
Xiong, Chi
Wang, Xin
Niu, Chaoshi
Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title_full Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title_fullStr Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title_full_unstemmed Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title_short Subthalamic nucleus and globus pallidus internus stimulation for the treatment of Parkinson’s disease: A systematic review
title_sort subthalamic nucleus and globus pallidus internus stimulation for the treatment of parkinson’s disease: a systematic review
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718722/
https://www.ncbi.nlm.nih.gov/pubmed/28701061
http://dx.doi.org/10.1177/0300060517708102
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