ACNS指南:经颅电刺激运动诱发电位监测。

A. Legatt, R. Emerson, C. Epstein, D. Macdonald, V. Deletis, R. Bravo, Jaime R. López
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引用次数: 101

摘要

运动诱发电位(MEPs)是神经组织或肌肉在中枢运动通路激活后记录的电信号。它们补充了其他临床神经生理学技术,如体感诱发电位(sep),用于评估神经系统,特别是在术中神经生理监测(IONM)期间。体感诱发电位仅直接评估脊髓的一部分,即背柱(Emerson, 1988),以及内侧小丘、丘脑皮质辐射和体感皮质。因为它们提供了对运动束的间接监测,使用它们已被证明可以改善脊柱手术期间的神经系统预后(Nuwer等,1995)。然而,当背柱不受损伤时,sep可能无法检测到脊髓运动通路的损伤(Ben-David等,1987;Ginsburg et al., 1985;Jones et al., 2003;Krieger et al., 1992;Legatt et al., 2014;Zornow et al., 1990);这导致了直接监测中枢运动通路技术的发展。大多数情况下,这是通过对大脑进行经颅电刺激(TES),并记录手术中危险区域的尾侧诱发神经或肌源性活动来完成的(Legatt, 2002)。在TES过程中,高强度的刺激必须传递到头皮,通过完整的头骨刺激大脑,刺激电压和电流水平远高于诱发sep的水平。如果开颅手术允许通过放置在大脑表面的电极直接刺激运动皮层,那么低强度的直接皮层刺激也可以用来引发IONM的mep (szelsamnyi et al., 2007;Taniguchi et al., 1993)。直接皮层刺激不在本指南的范围内,但此处关于记录经颅脑电刺激引起的mep的建议也适用于记录直接皮层刺激引起的mep。经颅磁刺激也被用于诱发mep,方法是在脑组织内诱导电流流动,而不通过头皮产生大量电流。这减少了对头皮、颅骨和脑膜疼痛纤维的刺激,使其成为清醒受试者MEP研究的实用技术(Chen et al., 2008)。然而,经颅磁刺激并不是IONM的最佳MEP技术,因为经颅磁刺激的麻醉抑制——MEP主要通过激发i波产生(见下文定义和生理学部分),并且线圈相对于患者头部的恒定位置难以维持(Legatt, 2004)。无论是单一刺激脉冲的TES还是经颅磁刺激,都不能始终产生适合IONM的强健的肌源性mep。商业上可用的刺激器可以传递高强度的电脉冲序列,这使得大多数患者使用TES进行可靠的MEP监测成为可能。目前,记录和解释tes - mep的技术已经足够成熟,可以保证制定这些指导方针。执行TES-MEP监测的人员必须认识到该技术的技术挑战和风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ACNS Guideline: Transcranial Electrical Stimulation Motor Evoked Potential Monitoring.
Motor evoked potentials (MEPs) are electrical signals recorded from neural tissue or muscle after activation of central motor pathways. They complement other clinical neurophysiology techniques, such as somatosensory evoked potentials (SEPs), in the assessment of the nervous system, especially during intraoperative neurophysiologic monitoring (IONM). Somatosensory evoked potentials directly assess only a part of the spinal cord, the dorsal columns (Emerson, 1988), and also the medial lemniscus, the thalamocortical radiations, and somatosensory cortex. Because they provide indirect surveillance of the motor tracts, their use has been shown to improve neurologic outcomes during spinal surgery (Nuwer et al., 1995). However, SEPs can fail to detect damage to the spinal cord motor pathways when the dorsal columns are spared (Ben-David et al., 1987; Ginsburg et al., 1985; Jones et al., 2003; Krieger et al., 1992; Legatt et al., 2014; Zornow et al., 1990); this led to the development of techniques for directly monitoring the central motor pathways. Most often, this is accomplished using transcranial electrical stimulation (TES) of the brain and recording of evoked neural or myogenic activity caudal to the area that is at risk during surgery (Legatt, 2002). During TES, high-intensity stimuli must be delivered to the scalp to stimulate the brain through the intact skull, with stimulus voltage and current levels far above those used to elicit SEPs. If a craniotomy permits direct stimulation of motor cortex by electrodes placed on the brain surface, low-intensity direct cortical stimulation can also be used to elicit MEPs for IONM (Szelényi et al., 2007b; Taniguchi et al., 1993). Direct cortical stimulation is outside the scope of this guideline, but the recommendations herein for the recording of the MEPs that are elicited by transcranial electrical brain stimulation would also apply to recording of MEPs elicited by direct cortical stimulation. Transcranial magnetic stimulation has also been used to elicit MEPs by inducing electrical current flows within the brain tissue without passing large amounts of current through the scalp. This reduces stimulation of pain fibers in the scalp, skull, and meninges and makes it a practical technique for MEP studies in awake subjects (Chen et al., 2008). However, transcranial magnetic stimulation is not the optimal MEP technique for IONM because of the anesthetic suppression of transcranial magnetic stimulation– MEPs which are generated mainly by eliciting I-waves (see section on Definitions and Physiology, below) and difficulties in maintaining a constant position of the coil relative to the patient’s head (Legatt, 2004). Neither TES with single stimulus pulses nor transcranial magnetic stimulation consistently produces robust myogenic MEPs suitable for IONM. The commercial availability of stimulators that can deliver trains of high-intensity electrical pulses has made reliable MEP monitoring using TES possible in most patients. At this time, the techniques for recording and interpreting TES-MEPs have become sufficiently well established to warrant the formulation of these guidelines. Personnel performing TES-MEP monitoring must be cognizant of the technical challenges and risks of the technique.
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