脑深部电刺激治疗小儿肌张力障碍的长期疗效

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY
Camille Malatt, M. Tagliati
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引用次数: 5

摘要

背景:脑深部电刺激(DBS)用于治疗儿童药物难治性肌张力障碍已有20多年的历史。对遗传性、孤立性和特发性病例有短期疗效,对遗传性退行性和获得性肌张力障碍疗效较差。长期结果的持续发表保证了对现有信息的关键评估,因为儿科患者预计将在这些植入物中度过大部分生命。摘要:我们对21岁以下接受DBS手术治疗肌张力障碍的患者,在植入DBS 5年或更长时间后,除并发症外,运动和神经精神预后的文献资料进行了回顾。我们找到了20篇文章,包括78名患者DBS后长期运动结果的个人数据。此外,我们发现5篇文章报道了9例肌张力障碍患者DBS后的长期结果。大多数患者植入内苍白球,只有少数病例针对丘脑下核和丘脑腹外侧后核。平均随访时间为8.5年,最长可达22年。长期结果显示持续的运动益处,在不同的肌张力障碍亚型中,伯克-法恩-马斯登肌张力障碍评分改善的中位数从2.5%到93.2%不等。遗传性、孤立性和特发性肌张力障碍患者比遗传性退行性和获得性肌张力障碍患者有更大的改善。生活质量的持续改善也有报道,没有发生显著的认知或精神合并症。后期不良事件往往与硬件相关,刺激诱导的影响最小。关键信息:虽然关于长期结果的数据有些有限,特别是关于神经精神结果和不良事件,但运动结果的改善似乎在DBS放置后保持了5年以上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-Term Outcomes of Deep Brain Stimulation for Pediatric Dystonia
Background: Deep brain stimulation (DBS) has been utilized for over two decades to treat medication-refractory dystonia in children. Short-term benefit has been demonstrated for inherited, isolated, and idiopathic cases, with less efficacy in heredodegenerative and acquired dystonia. The ongoing publication of long-term outcomes warrants a critical assessment of available information as pediatric patients are expected to live most of their lives with these implants. Summary: We performed a review of the literature for data describing motor and neuropsychiatric outcomes, in addition to complications, 5 or more years after DBS placement in patients undergoing DBS surgery for dystonia at an age younger than 21. We identified 20 articles including individual data on long-term motor outcomes after DBS for a total of 78 patients. In addition, we found five articles reporting long-term outcomes after DBS in 9 patients with status dystonicus. Most patients were implanted within the globus pallidus internus, with only a few cases targeting the subthalamic nucleus and ventrolateral posterior nucleus of the thalamus. The average follow-up was 8.5 years, with a range of up to 22 years. Long-term outcomes showed a sustained motor benefit, with median Burke-Fahn-Marsden dystonia rating score improvement ranging from 2.5% to 93.2% in different dystonia subtypes. Patients with inherited, isolated, and idiopathic dystonias had greater improvement than those with heredodegenerative and acquired dystonias. Sustained improvements in quality of life were also reported, without the development of significant cognitive or psychiatric comorbidities. Late adverse events tended to be hardware-related, with minimal stimulation-induced effects. Key Messages: While data regarding long-term outcomes is somewhat limited, particularly with regards to neuropsychiatric outcomes and adverse events, improvement in motor outcomes appears to be preserved more than 5 years after DBS placement.
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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