Directional Deep Brain Stimulation of the Thalamic Ventral Intermediate Area for Essential Tremor Increases Therapeutic Window

被引:28
|
作者
Bruno, Sabine [1 ,2 ]
Nikolov, Petyo [1 ,2 ]
Hartmann, Christian J. [1 ,2 ]
Trenado, Carlos [2 ]
Slotty, Philipp J. [3 ]
Vesper, Jan [3 ]
Schnitzler, Alfons [1 ,2 ]
Groiss, Stefan J. [1 ,2 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Med Fac, Dept Neurol, Dusseldorf, Germany
[2] Heinrich Heine Univ Dusseldorf, Med Fac, Inst Clin Neurosci & Med Psychol, Dusseldorf, Germany
[3] Heinrich Heine Univ Dusseldorf, Med Fac, Dept Funct Neurosurg & Stereotaxy, Dusseldorf, Germany
来源
NEUROMODULATION | 2021年 / 24卷 / 02期
关键词
Deep brain stimulation; directional stimulation; essential tremor; segmented leads; side effects; therapeutic window; RATING-SCALE; GAIT ATAXIA; RELIABILITY; FORM;
D O I
10.1111/ner.13234
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives Deep brain stimulation (DBS) of the posterior subthalamic area (PSA) and the ventral intermediate thalamic nucleus (VIM) is a well-established therapy for essential tremor (ET), but it is frequently associated with side effects like dysarthria or gait ataxia. Directional DBS (dDBS) may be a way to activate fiber tracts more selectively. Is dDBS for ET superior to omnidirectional DBS (oDBS) regarding therapeutic window and clinically as effective as oDBS? Materials and Methods Ten patients with ET treated with PSA/VIM-DBS were recruited. Therapeutic window served as primary outcome parameter; clinical efficacy, volume of neuronal activation, and total electrical energy delivered (TEED) served as secondary outcome parameters. Therapeutic window was calculated for all three dDBS directions and for oDBS by determining therapeutic thresholds and side effect thresholds. Clinical efficacy was assessed by comparing the effect of best dDBS and oDBS on tremor and ataxia rating scales, and accelerometry. Volume of neural activation and TEED were also calculated for both paradigms. Results For best dDBS, therapeutic window was wider and therapeutic threshold was lower compared to oDBS. While side effect threshold did not differ, volume of neural activation was larger for dDBS. In terms of clinical efficacy, dDBS was as effective as oDBS. Conclusions dDBS for ET widens therapeutic window due to reduction of therapeutic threshold. Larger volume of neural activation for dDBS at side effect threshold supports the notion of persistent directionality even at higher intensities. dDBS may compensate for slightly misplaced leads and should be considered first line for PSA/VIM-DBS.
引用
收藏
页码:343 / 352
页数:10
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