A Systematic Clinical Framework for Postimplantation Monitoring in Thalamic Neuromodulation: Insights From Twiddler's Syndrome.

IF 4.4 2区 医学 Q1 CLINICAL NEUROLOGY
Shalin Shah, Ganne Chaitanya, Jeston Chin, Nicholas Delcimmuto, Jay R Gavvala
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Abstract

This case described a 25-year-old pregnant woman with refractory multifocal epilepsy, diagnosed in 2020 and treated with bilateral thalamic deep brain stimulation (DBS) targeting the centromedian and pulvinar nuclei. Prior to DBS, she experienced daily focal seizures, often progressing to generalized tonic-clonic seizures despite optimal medication. Presurgical evaluations revealed multifocal epilepsy with right hemispheric involvement and diffuse band heterotopia. Given the extensive neurophysiological and radiographic findings, DBS was chosen over resective surgery. Following implantation in December 2023, initial stimulation settings resulted in some seizure control but also development of new symptoms, including shock-like sensations down her neck. After 43 seizure-free days, she experienced a prolonged seizure in April 2024, prompting further investigation. Imaging revealed migration of the right pulvinar electrode, which was identified as the likely cause. This resultant displacement, called the "Twiddler's Syndrome," is a phenomenon where device manipulation causes malfunction or dislodgment. This resulted from the patient's habit of massaging her neck. After adjusting DBS settings and turning off right pulvinar stimulation, her symptoms resolved, and she remained seizure-free for two months. This case emphasizes the need for careful postimplantation monitoring, imaging, and awareness of hardware-related issues like Twiddler's Syndrome, highlighting the importance of well-planned surgical strategies to optimize outcomes in neuromodulation therapies.

丘脑神经调节植入后监测的系统临床框架:来自旋转者综合征的见解。
本病例描述了一名患有难治性多灶性癫痫的25岁孕妇,于2020年确诊,并接受双侧丘脑深部脑刺激(DBS)治疗,目标是正中核和枕核。在DBS之前,她经历了每天局灶性癫痫发作,经常进展到全身性强直阵挛发作,尽管最佳药物。术前评估显示多灶性癫痫伴右半球受累和弥漫性带异位。考虑到广泛的神经生理学和放射学发现,DBS被选择在切除手术。在2023年12月植入后,最初的刺激设置导致了一些癫痫控制,但也出现了新的症状,包括脖子上的电击样感觉。在43天无癫痫发作后,她于2024年4月经历了长时间的癫痫发作,促使进一步调查。影像学显示右侧枕侧电极迁移,这被确定为可能的原因。由此产生的移位,被称为“捻手综合征”,是一种操作设备导致故障或脱臼的现象。这是由于病人有按摩颈部的习惯。在调整DBS设置并关闭右侧丘脑刺激后,她的症状消失,两个月没有癫痫发作。本病例强调需要仔细的植入后监测,成像和硬件相关问题的意识,如旋转者综合征,强调精心规划的手术策略对优化神经调节治疗结果的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology Medicine-Neurology (clinical)
CiteScore
9.10
自引率
1.90%
发文量
218
审稿时长
8 weeks
期刊介绍: Annals of Clinical and Translational Neurology is a peer-reviewed journal for rapid dissemination of high-quality research related to all areas of neurology. The journal publishes original research and scholarly reviews focused on the mechanisms and treatments of diseases of the nervous system; high-impact topics in neurologic education; and other topics of interest to the clinical neuroscience community.
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