Tissue and electrode capacitance reduce neural activation volumes during deep brain stimulation

被引:234
作者
Butson, CR [1 ]
McIntyre, CC [1 ]
机构
[1] Cleveland Clin Fdn, Dept Biomed Engn, Cleveland, OH 44195 USA
关键词
electrostatic; quasistatic; voltage-controlled stimulation; current-controlled stimulation; strength-duration relationship;
D O I
10.1016/j.clinph.2005.06.023
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The growing clinical acceptance of neurostimulation technology has highlighted the need to accurately predict neural activation as a function of stimulation parameters and electrode design. In this study we evaluate the effects of the tissue and electrode capacitance on the volume of tissue activated (VTA) during deep brain stimulation (DBS). Methods: We use a Fourier finite element method (Fourier FEM) to calculate the potential distribution in the tissue medium as a function of time and space simultaneously for a range of stimulus waveforms. The extracellular voltages are then applied to detailed multi-compartment cable models of myelinated axons to determine neural activation. Neural activation volumes are calculated as a function of the stimulation parameters and magnitude of the capacitive components. of the electrode-tissue interface. Results: Inclusion of either electrode or tissue capacitance reduces the VTA compared to electrostatic simulations in a manner dependent on the capacitance magnitude and the stimulation parameters (amplitude and pulse width). Electrostatic simulations with typical DBS parameter settings (-3V or -3mA, 90 mu s, 130Hz) overestimate the VTA by similar to 20% for voltage- or current-controlled stimulation. In addition, strength-duration time constants decrease and more closely match clinical measurements when explicitly accounting for the effects of voltage-controlled stimulation. Conclusions: Attempts to quantify the VTA from clinical neurostimulation devices should account for the effects of electrode and tissue capacitance. Significance: DBS has rapidly emerged as an effective treatment for movement disorders; however, little is known about the VTA during therapeutic stimulation. In addition, the influence of tissue and electrode capacitance has been largely ignored in previous models of neural stimulation. The results and methodology of this study provide the foundation for the quantitative analysis of the VTA during clinical neurostimulation. (c) 2005 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
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页码:2490 / 2500
页数:11
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