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帕金森病中的运动皮层刺激

Motor cortex stimulation in Parkinson's disease.

作者信息

De Rose Marisa, Guzzi Giusy, Bosco Domenico, Romano Mary, Lavano Serena Marianna, Plastino Massimiliano, Volpentesta Giorgio, Marotta Rosa, Lavano Angelo

机构信息

Department of Neurosurgery, University Hospital of Germaneto, Campus "Salvatore Venuta", Viale Europa, 88100 Catanzaro, Italy.

出版信息

Neurol Res Int. 2012;2012:502096. doi: 10.1155/2012/502096. Epub 2012 Nov 8.

Abstract

Motor Cortex Stimulation (MCS) is less efficacious than Deep Brain Stimulation (DBS) in Parkinson's disease. However, it might be proposed to patients excluded from DBS or unresponsive to DBS. Ten patients with advanced PD underwent unilateral MCS contralaterally to the worst clinical side. A plate electrode was positioned over the motor cortex in the epidural space through single burr hole after identification of the area with neuronavigation and neurophysiological tests. Clinical assessment was performed by total UPDRS, UPDRS III total, UPDRS III-items 27-31, UPDRS IV, and UPDRS II before implantation in off-medication and on-medication states and after surgery at 1, 3, 6, 12, 18, 24, and 36 months in on-medication/on-stimulation and off-medication/on-stimulation states. We assessed changes of quality of life, throughout the Parkinson's disease quality of life scale (PDQoL-39), and the dose of anti-Parkinson's disease medications, throughout the Ldopa equivalent daily dose (LEDD). During off-medication state, we observed moderate and transitory reduction of total UPDRS and UPDRS total scores and significant and long-lasting improvement in UPDRS III items 27-31 score for axial symptoms. There was marked reduction of UPDRS IV score and LEDD. PDQL-39 improvement was also significant. No important complications and adverse events occurred.

摘要

在帕金森病中,运动皮层刺激(MCS)的疗效不如深部脑刺激(DBS)。然而,对于被排除在DBS之外或对DBS无反应的患者,可能会建议采用MCS。10例晚期帕金森病患者在临床症状最严重的对侧进行了单侧MCS。在通过神经导航和神经生理学测试确定区域后,通过单个骨孔将板状电极放置在硬膜外间隙的运动皮层上方。在植入前的非服药和服药状态下,以及术后1、3、6、12、18、24和36个月的服药/刺激状态和非服药/刺激状态下,通过总统一帕金森病评定量表(UPDRS)、UPDRS III总分、UPDRS III项目27 - 31、UPDRS IV和UPDRS II进行临床评估。我们通过帕金森病生活质量量表(PDQoL - 39)评估生活质量的变化,并通过左旋多巴等效日剂量(LEDD)评估抗帕金森病药物的剂量。在非服药状态下,我们观察到总UPDRS和UPDRS总分有中度和短暂的降低,以及UPDRS III项目27 - 31中轴性症状评分有显著且持久的改善。UPDRS IV评分和LEDD有明显降低。PDQL - 39的改善也很显著。未发生重要并发症和不良事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d2c/3504447/6b420a278e66/NRI2012-502096.001.jpg

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