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双侧苍白球深部脑刺激术后难治性迟发性肌张力障碍患者的长期获益得以维持。

Long-term benefit sustained after bilateral pallidal deep brain stimulation in patients with refractory tardive dystonia.

作者信息

Chang Edward F, Schrock Lauren E, Starr Philip A, Ostrem Jill L

机构信息

Department of Neurological Surgery, University of California, San Francisco, CA 94143, USA.

出版信息

Stereotact Funct Neurosurg. 2010;88(5):304-10. doi: 10.1159/000316763. Epub 2010 Jun 24.

Abstract

BACKGROUND/AIMS: Tardive dystonia (TD) can be a highly disabling, permanent condition related to the use of dopamine-receptor-blocking medications. Our aim was to evaluate the long-term effect of bilateral pallidal deep brain stimulation (DBS) for TD.

METHODS

Five consecutive patients with disabling TD who underwent stereotactic placement of bilateral globus pallidus internus DBS leads were included. All patients had a history of mood disorder or schizophrenia previously treated with neuroleptic medication, with a mean duration of motor symptoms of 10.2 years. Dystonia severity was measured using the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) movement score by a blinded neurologist reviewing pre- and postoperative videotaped examinations.

RESULTS

The mean baseline movement BFMDRS score was 49.7 (range 20-88). Overall, we observed a mean reduction of 62% in the BFMDRS movement score within the first year after surgery. Persistent improvement in dystonia (71%) was seen at the last follow-up ranging from 2 to 8 years after surgery.

CONCLUSION

Our experience suggests that pallidal DBS can be an effective therapy with long-term benefits for patients with TD.

摘要

背景/目的:迟发性肌张力障碍(TD)可能是一种与使用多巴胺受体阻断药物相关的高度致残的永久性疾病。我们的目的是评估双侧苍白球深部脑刺激(DBS)治疗TD的长期效果。

方法

纳入5例连续接受双侧内侧苍白球DBS电极立体定向植入的致残性TD患者。所有患者既往均有情绪障碍或精神分裂症病史,曾接受抗精神病药物治疗,运动症状平均持续时间为10.2年。由一名不知情的神经科医生通过回顾术前和术后的录像检查,使用伯克-法恩-马斯登肌张力障碍评定量表(BFMDRS)运动评分来评估肌张力障碍的严重程度。

结果

平均基线运动BFMDRS评分为49.7(范围20 - 88)。总体而言,我们观察到术后第一年BFMDRS运动评分平均降低了62%。在术后2至8年的最后一次随访中,肌张力障碍持续改善(71%)。

结论

我们的经验表明,苍白球DBS对TD患者可能是一种有效的治疗方法,具有长期益处。

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