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静脉注射利多卡因对正中神经体感诱发电位的影响

[Effects of intravenous lidocaine administration on median nerve somatosensory evoked potentials].

作者信息

Kasaba T, Nonoue T, Yanagidani T, Maeda M, Kosaka Y

机构信息

Department of Anesthesia, Tottori Prefectural Central Hospital.

出版信息

Masui. 1991 May;40(5):713-6.

PMID:2072512
Abstract

The effect of lidocaine on the median nerve somatosensory evoked potential (SSEP) was investigated in 14 neurologically normal patients. Lidocaine 1.5 mg.kg-1.min-1 was injected intravenously over a 5 min period immediately followed by a continuous infusion of lidocaine 60 micrograms.kg-1.min-1. The peak latencies (N1, P2, N2) and amplitudes (N1-P2, P2-N2) of the SSEP response over the sensory cortex were recorded before and after lidocaine infusion. The peak latencies in the control group and in the experimental group after lidocaine infusion of N1, P1, N2 were 19.4 +/- 1.0 msec, 19.7 +/- 1.0 msec (N1), 24.6 +/- 1.4 msec, 25.0 +/- 1.5 msec (P2), 32.5 +/- 2.5 msec, and 33.3 +/- 2.8 msec (N2), respectively. The amplitudes in the control group and in the experimental group after lidocaine infusion of N1-P2, P2-N2 were 9.0 +/- 4.3 microV, 10.3 +/- 4.7 microV (N1-P2), 7.2 +/- 3.6 microV, 8.6 +/- 3.9 microV (P2-N2), respectively. Peak latencies of all components (N1, P2, N2) increased after lidocaine infusion compared with control values. Amplitude of N1-P2 and P2-N2 increased significantly following lidocaine infusion compared with control values. The data obtained in this study suggested that the changes in peak latencies and amplitude after epidural anesthesia with lidocaine were due to the systemic effect of lidocaine absorbed intravenously from the epidural space.

摘要

在14例神经系统正常的患者中研究了利多卡因对正中神经体感诱发电位(SSEP)的影响。在5分钟内静脉注射1.5毫克/千克·分钟的利多卡因,随后立即以60微克/千克·分钟的速度持续输注利多卡因。在利多卡因输注前后记录感觉皮层上SSEP反应的峰潜伏期(N1、P2、N2)和波幅(N1 - P2、P2 - N2)。利多卡因输注后,对照组和实验组中N1、P1、N2的峰潜伏期分别为19.4±1.0毫秒、19.7±1.0毫秒(N1),24.6±1.4毫秒、25.0±1.5毫秒(P2),32.5±2.5毫秒、33.3±2.8毫秒(N2)。利多卡因输注后,对照组和实验组中N1 - P2、P2 - N2的波幅分别为9.0±4.3微伏、10.3±4.7微伏(N1 - P2),7.2±3.6微伏、8.6±3.9微伏(P2 - N2)。与对照值相比,利多卡因输注后所有成分(N1、P2、N2)的峰潜伏期均增加。与对照值相比,利多卡因输注后N1 - P2和P2 - N2的波幅显著增加。本研究获得的数据表明,利多卡因硬膜外麻醉后峰潜伏期和波幅的变化是由于利多卡因从硬膜外间隙静脉吸收的全身效应所致。

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