苍白球深部脑刺激治疗颅颈肌张力障碍的长期随访:苍白球内肌是最佳靶点吗?

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-06-01 DOI:10.3171/2024.3.FOCUS23890
Zhuoling Zhao, Zhiwei Ren, Yongsheng Hu, Kaijia Yu, Fangzhao Yin, Jianyu Li, Guojun Zhang
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引用次数: 0

摘要

目的:颅颈肌张力障碍(CCD)是节段性肌张力障碍的一种常见类型,是一种致残性疾病,经常被误诊。最初最常见的症状是眼睑痉挛或颈肌张力障碍。虽然对苍白球内肌(GPi)的脑深部刺激(DBS)已被广泛用于治疗CCD,但其临床效果主要是在小规模研究中进行评估。本研究探讨了 GPi DBS 对确诊为 CCD 患者的持续临床疗效:作者报告了 24 名难治性 CCD 患者(14 名女性,10 名男性)在 2016 年至 2023 年期间接受了 GPi DBS 治疗。使用伯克-法恩-马斯登肌张力障碍评分量表(Burke-Fahn-Marsden Dystonia Rating Scale,BFMDRS)评估了肌张力障碍的严重程度和残疾情况。BFMDRS评分在术前、术后6个月和最近一次随访时收集:患者发病时的平均年龄为(52.0 ± 11.0)岁(33-71 岁),平均病程为(63.3 ± 73.3)个月(7-360 个月)(连续变量的值以均值 ± SD 表示)。平均随访时间为 37.5 ± 23.5 个月(6-84 个月)。3 个不同时间点的 BFMDRS 运动总分平均值分别为:术前 13.3 ± 9.4,6 个月时 5.0 ± 4.7(改善 55.3%,p < 0.001),最后一次随访时 4.5 ± 3.6(改善 56.6%,p < 0.001)。有 6 人的治疗效果不佳:从研究结果中得出的推论表明,GPi DBS 在治疗难治性 CCD 方面具有持久的有效性和一定的局限性。临床结果并没有达到预期的稳定性。患有特定类型肌张力障碍的患者可考虑使用 GPi 以外的靶点进行更精确的治疗。
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Long-term follow-up of pallidal deep brain stimulation for craniocervical dystonia: is the globus pallidus internus the best target?

Objective: Craniocervical dystonia (CCD) is a common type of segmental dystonia, which is a disabling disease that has been frequently misdiagnosed. Blepharospasm or cervical dystonia is the most usual symptom initially. Although deep brain stimulation (DBS) of the globus pallidus internus (GPi) has been widely used for treating CCD, its clinical outcome has been primarily evaluated in small-scale studies. This research examines the sustained clinical effectiveness of DBS of the GPi in individuals diagnosed with CCD.

Methods: The authors report 24 patients (14 women, 10 men) with refractory CCD who underwent DBS of the GPi between 2016 and 2023. The severity and disability of the dystonia were evaluated using the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS). The BFMDRS scores were collected preoperatively, 6 months postoperatively, and at the most recent follow-up visit.

Results: The mean age at onset was 52.0 ± 11.0 years (range 33-71 years) and the mean disease duration was 63.3 ± 73.3 months (range 7-360 months) (values for continuous variables are expressed as the mean ± SD). The mean follow-up period was 37.5 ± 23.5 months (range 6-84 months). The mean total BFMDRS motor scores at the 3 different time points were 13.3 ± 9.4 preoperatively, 5.0 ± 4.7 (55.3% improvement, p < 0.001) at 6 months, and 4.5 ± 3.6 (56.6% improvement, p < 0.001) at last follow-up. The outcomes were deemed poor in 6 individuals.

Conclusions: Inferences drawn from the findings suggest that DBS of the GPi has long-lasting effectiveness and certain limitations in managing refractory CCD. The expected stability of the clinical outcome is not achieved. Patients with specific types of dystonia might consider targets other than GPi for a more precise therapy.

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