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      Role of electrode design on the volume of tissue activated during deep brain stimulation.

      1 ,
      Journal of neural engineering
      IOP Publishing

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          Abstract

          Deep brain stimulation (DBS) is an established clinical treatment for a range of neurological disorders. Depending on the disease state of the patient, different anatomical structures such as the ventral intermediate nucleus of the thalamus (VIM), the subthalamic nucleus or the globus pallidus are targeted for stimulation. However, the same electrode design is currently used in nearly all DBS applications, even though substantial morphological and anatomical differences exist between the various target nuclei. The fundamental goal of this study was to develop a theoretical understanding of the impact of changes in the DBS electrode contact geometry on the volume of tissue activated (VTA) during stimulation. Finite element models of the electrodes and surrounding medium were coupled to cable models of myelinated axons to predict the VTA as a function of stimulation parameter settings and electrode design. Clinical DBS electrodes have cylindrical contacts 1.27 mm in diameter (d) and 1.5 mm in height (h). Our results show that changes in contact height and diameter can substantially modulate the size and shape of the VTA, even when contact surface area is preserved. Electrode designs with a low aspect ratio (d/h) maximize the VTA by providing greater spread of the stimulation parallel to the electrode shaft without sacrificing lateral spread. The results of this study provide the foundation necessary to customize electrode design and VTA shape for specific anatomical targets, and an example is presented for the VIM. A range of opportunities exist to engineer DBS systems to maximize stimulation of the target area while minimizing stimulation of non-target areas. Therefore, it may be possible to improve therapeutic benefit and minimize side effects from DBS with the design of target-specific electrodes.

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          Author and article information

          Journal
          J Neural Eng
          Journal of neural engineering
          IOP Publishing
          1741-2560
          1741-2552
          Mar 2006
          : 3
          : 1
          Affiliations
          [1 ] Department of Biomedical Engineering, Cleveland Clinic Foundation, Cleveland, OH, USA.
          Article
          S1741-2560(06)05977-5 NIHMS76079
          10.1088/1741-2560/3/1/001
          2583360
          16510937
          aeef98cd-d2bf-486a-a608-d968c9bc9cce
          History

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