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小脑深部脑刺激治疗脑瘫运动障碍。

Cerebellar deep brain stimulation for the treatment of movement disorders in cerebral palsy.

机构信息

Departments of1Neurological Surgery.

2Radiology & Biomedical Imaging, and.

出版信息

J Neurosurg. 2023 Feb 10;139(3):605-614. doi: 10.3171/2023.1.JNS222289. Print 2023 Sep 1.

Abstract

OBJECTIVE

Cerebral palsy (CP) represents the most common childhood physical disability that encompasses disorders of movement and posture attributed to nonprogressive disturbances that occurred in the developmental fetal or infant brain. Dyskinetic CP (DCP), the second most common type of CP after spastic forms, refers to a subset of patients in whom dystonia and choreoathetosis are the predominant motor manifestations. Most children with CP have abnormal brain MRI studies indicative of cortical and deep gray matter damage consistent with hypoxic ischemic encephalopathy, which may preclude or suggest decreased efficacy of standard deep brain stimulation (DBS) targets. The cerebellum has been posited as an attractive target for treatment of DCP because it is frequently spared from hypoxic ischemic damage and has shown promise in alleviating patient symptoms both in early work in the 1970s and in more recent case series with DBS.

METHODS

The authors performed bilateral cerebellar DBS implantation, targeting the dentate nucleus (DN) and cerebellar outflow pathway, in 3 patients with DCP. Leads were connected to a pulse generator that senses local field potentials during chronic continuous DBS. The authors report their surgical methods, examples of chronic cerebellar local field potential recordings, and preliminary clinical outcomes. Motor outcomes were assessed using the Burke-Fahn-Marsden Dystonia Rating Scale.

RESULTS

Three patients 14-22 years old with DCP and MRI evidence of structural damage to the basal ganglia were offered cerebellar stimulation targeting the DN. All patients tolerated the procedure well and demonstrated improvement in subjective motor function as well as objective improvement in the Burke-Fahn-Marsden Dystonia Rating Scale movement subscale, although the range of responses was variable (19%-40%). Patients experienced subjective improvement in motor function including ease of hand movements and coordination, gait, head control, speech, decreased overflow, and diminished muscle tightness.

CONCLUSIONS

DBS of the dentate nuclei in patients with DCP appears to be safe and shows preliminary evidence of clinical benefit. New chronic sensing technology may allow for determination of in vivo mechanisms of network disruption in DCP and allow for further understanding of the effects of neuromodulation on brain physiology. Larger studies with long-term follow up will be required to further elucidate the clinical benefits of this therapy. This report addresses a gap in the literature regarding the technical approach to image-based stereotactic targeting and chronic neural recording in the DN.

摘要

目的

脑瘫(CP)是最常见的儿童身体残疾,包括运动和姿势障碍,这些障碍归因于在发育中的胎儿或婴儿大脑中发生的非进行性紊乱。运动障碍型脑瘫(DCP)是继痉挛型脑瘫之后的第二大常见类型,是指一组以肌张力障碍和舞蹈手足徐动症为主要运动表现的患者。大多数脑瘫患儿的大脑 MRI 研究显示存在皮质和深部灰质损伤,提示存在缺氧缺血性脑病,这可能会降低或提示标准深部脑刺激(DBS)靶点的疗效。小脑已被认为是治疗 DCP 的一个有吸引力的目标,因为它通常免受缺氧缺血性损伤的影响,并且在 20 世纪 70 年代的早期工作以及最近的 DBS 病例系列中都显示出了缓解患者症状的潜力。

方法

作者对 3 例 DCP 患者进行了双侧小脑 DBS 植入,以齿状核(DN)和小脑传出通路为靶点。导线连接到一个脉冲发生器,该发生器在慢性连续 DBS 期间感知局部场电位。作者报告了他们的手术方法、慢性小脑局部场电位记录的示例以及初步的临床结果。运动结果采用 Burke-Fahn-Marsden 肌张力障碍评定量表进行评估。

结果

3 例 14-22 岁的 DCP 患者,MRI 显示基底节结构损伤,接受了靶向 DN 的小脑刺激治疗。所有患者均能很好地耐受该手术,并在主观运动功能和 Burke-Fahn-Marsden 肌张力障碍评定量表运动分量表上均有客观改善,尽管反应范围各不相同(19%-40%)。患者主观上改善了运动功能,包括手部运动和协调、步态、头部控制、言语、减少溢出、减轻肌肉紧张等。

结论

DCP 患者的齿状核 DBS 似乎是安全的,并初步显示出临床获益的证据。新的慢性感应技术可能有助于确定 DCP 中网络紊乱的体内机制,并进一步了解神经调节对大脑生理学的影响。需要进行更大规模的长期随访研究,以进一步阐明这种治疗方法的临床益处。本报告填补了文献中关于基于图像的立体定向靶向和 DN 慢性神经记录的技术方法的空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1078/10726727/59a88c963eaf/nihms-1947496-f0001.jpg

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