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苍白球深部脑刺激术治疗双侧苍白球切开术和选择性周围神经切断术治疗的肌张力障碍患者。

Pallidal Deep Brain Stimulation in Patients with Prior Bilateral Pallidotomy and Selective Peripheral Denervation for Treatment of Dystonia.

机构信息

Department of Neurosurgery, Hannover Medical School, Hannover, Germany,

Department of Neurosurgery, Hannover Medical School, Hannover, Germany.

出版信息

Stereotact Funct Neurosurg. 2021;99(1):1-5. doi: 10.1159/000509822. Epub 2020 Oct 20.

Abstract

INTRODUCTION

Deep brain stimulation (DBS) of the globus pallidus internus has become an accepted treatment for severe isolated idiopathic and inherited dystonia. Patients who had other forms of surgery earlier, such as radiofrequency lesioning or selective peripheral denervation, however, usually are not considered candidates for DBS.

OBJECTIVE

The aim of this study was to evaluate the long-term outcome of pallidal DBS in a rare subgroup of patients who had undergone both pallidotomy and selective peripheral denervation previously with a waning effect over the years.

METHODS

Pallidal DBS was performed according to a prospective study protocol in 2 patients with isolated idiopathic dystonia, and patients were followed for a period of at least 6 years.

RESULTS

Both patients benefitted from long-lasting amelioration of dystonia after pallidal DBS, which was comparable to that of patients who did not have previous surgeries. In a 62-year-old female with cervical dystonia both the Burke-Fahn-Marsden (BFM) and the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) motor scores were improved at follow-up 8 years after surgery (50 and 39%). In a 32-year-old male with generalized dystonia, the BFM motor and disability scores showed marked improvement at 6.5 years of follow-up (82 and 66%).

CONCLUSIONS

Pallidal DBS can yield marked and long-lasting improvement in patients who underwent both pallidotomy and selective peripheral denervation earlier. Therefore, such patients, in general, should not be excluded from DBS.

摘要

简介

深部脑刺激(DBS)已成为治疗严重孤立性特发性和遗传性肌张力障碍的一种公认方法。然而,以前接受过其他手术形式(如射频消融或选择性外周神经切断术)的患者通常不被认为是 DBS 的候选者。

目的

本研究的目的是评估在一组罕见的患者中,行苍白球切开术和选择性外周神经切断术联合治疗后,多年来疗效逐渐减退的情况下,行苍白球 DBS 的长期疗效。

方法

根据前瞻性研究方案,对 2 例孤立性特发性肌张力障碍患者行苍白球 DBS,并对患者进行至少 6 年的随访。

结果

2 例患者在接受苍白球 DBS 后均获得了持久的肌张力障碍缓解,与未行手术的患者相当。在一名 62 岁的女性患者中,颈肌张力障碍的 Burke-Fahn-Marsden (BFM)和多伦多西部痉挛性斜颈评定量表(TWSTRS)运动评分在术后 8 年的随访时改善(分别为 50 和 39%)。在一名 32 岁的男性患者中,广泛性肌张力障碍的 BFM 运动和残疾评分在 6.5 年的随访时明显改善(分别为 82 和 66%)。

结论

对于先前接受过苍白球切开术和选择性外周神经切断术的患者,苍白球 DBS 可以产生显著和持久的改善。因此,一般来说,不应将此类患者排除在 DBS 之外。

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