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双侧苍白球深部脑刺激治疗肌张力障碍的长期疗效:8 至 16 年随访结果。

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

机构信息

Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité, University Medicine Berlin, Campus Mitte, Charitéplatz 1, 10117, Berlin, Germany.

Department of Neurology and Stereotactic Neurosurgery, University Medicine of Magdeburg, Magdeburg, Germany.

出版信息

J Neurol. 2020 Jun;267(6):1622-1631. doi: 10.1007/s00415-020-09745-z. Epub 2020 Feb 13.

Abstract

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.

摘要

目的

观察研究评估深部脑刺激(DBS)对内侧苍白球(GPi)治疗药物难治性肌张力障碍的长期运动和非运动效应。

背景

肌张力障碍是一种影响主要为年轻患者的慢性疾病,他们具有正常的预期寿命和终生的治疗需求。苍白球 DBS 是一种治疗严重孤立性肌张力障碍的既定方法,但长期数据稀缺。

方法

我们回顾性分析了 2000 年至 2007 年期间在 Charité-University 医院接受手术的 36 例连续孤立性全身性(n=14)和颈/节段性(n=22)肌张力障碍患者的长期 GPi-DBS 结果。在其中 19 例患者中,我们可以分析基线、短期(ST-FU,范围 3-36 个月)和长期随访(LT-FU,范围 93-197 个月)时用 Burke-Fahn-Marsden 肌张力障碍评定量表(BFMDRS)评定的肌张力障碍症状和残疾。使用 SF36 和贝克抑郁指数(BDI)问卷评估生活质量和情绪。

结果

患者在 ST-FU 时达到运动症状改善 63.8±5.7%(平均值±SE),在 LT-FU 时达到 67.9±6.1%。此外,DBS 后显示出显著且稳定的残疾程度降低(ST-FU 时为 54.2±9.4%,LT-FU 时为 53.8±9.2%)。LT-FU 时 BDI 和 SF36 分别改善了 40%和 23%(n=14)。刺激诱导的不良反应包括吞咽困难、构音障碍和运动迟缓。由于感染,7 例患者更换了脉冲发生器(n=3)和电极(n=5)。

结论

苍白球 DBS 是一种安全有效的肌张力障碍长期治疗方法,对运动障碍和残疾有持续的疗效,同时情绪和生活质量有显著改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bca3/8592956/7777109d8e64/415_2020_9745_Fig1_HTML.jpg

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