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经颅电刺激后,在氧化亚氮麻醉期间记录的胫前肌运动诱发电位的变异性。

Variability of motor-evoked potentials recorded during nitrous oxide anesthesia from the tibialis anterior muscle after transcranial electrical stimulation.

作者信息

Woodforth I J, Hicks R G, Crawford M R, Stephen J P, Burke D J

机构信息

Department of Anesthesia and Intensive Care, Price of Wales Hospital, Sydney, Australia.

出版信息

Anesth Analg. 1996 Apr;82(4):744-9. doi: 10.1097/00000539-199604000-00012.

Abstract

When recorded as a compound muscle action potential (CMAP), the motor-evoked potential (MEP) is affected by volatile anesthetics and nitrous oxide. However, MEPs recorded using epidural electrodes in the presence of nitrous oxide are highly reproducible from trial to trial. We wished to establish the reproducibility over time of the CMAP produced by supramaximal transcranial electrical stimulation of the human motor cortex. Cascades of 100 successive CMAPs were recorded from the tibialis anterior muscles of six anesthetized patients undergoing scoliosis surgery, in response to transcranial electrical stimuli of > 500 V. Satisfactory CMAPs could be recorded in the presence of nitrous oxide, but not isoflurane. Latencies and amplitudes were reproducible in repeated sequences of 100 responses. However, amplitude and, to a lesser extent, latency, were highly variable within a sequence. In addition, occasional individual stimuli, although rarely successive ones, failed to evoke a CMAP. CMAPs have a much higher trial-to-trial variability than corticospinal volleys recorded from the epidural space. Using the present methodology it would be difficult to rely on CMAP recordings as an indicator of corticospinal function in the clinical monitoring situation.

摘要

当作为复合肌肉动作电位(CMAP)记录时,运动诱发电位(MEP)会受到挥发性麻醉剂和氧化亚氮的影响。然而,在氧化亚氮存在的情况下,使用硬膜外电极记录的MEP在不同试验之间具有高度的可重复性。我们希望确定由人类运动皮层的超强经颅电刺激产生的CMAP随时间的可重复性。从6名接受脊柱侧弯手术的麻醉患者的胫前肌记录了100个连续CMAP的序列,以响应大于500V的经颅电刺激。在氧化亚氮存在的情况下可以记录到满意的CMAP,但异氟烷存在时则不行。在100次反应的重复序列中,潜伏期和波幅是可重复的。然而,在一个序列中,波幅以及在较小程度上潜伏期具有高度变异性。此外,偶尔有个别刺激,虽然很少是连续的刺激,未能诱发CMAP。与从硬膜外间隙记录的皮质脊髓冲动相比,CMAP在不同试验之间的变异性要高得多。使用目前的方法,在临床监测情况下很难依靠CMAP记录作为皮质脊髓功能的指标。

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