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表皮内伤害性电刺激 A-δ 纤维对伤害性感觉诱发电位的麻醉效应。

Effects of anesthetics on nociceptive sensory evoked potentials by intraepidermal noxious electrical stimulation of A-δ fibers.

机构信息

Department of Anesthesiology and Resuscitology, Shinshu University School of Medicine, 3-1-1, Asahi, Matsumoto, Nagano, 390-8621, Japan.

出版信息

J Anesth. 2023 Dec;37(6):841-852. doi: 10.1007/s00540-023-03243-y. Epub 2023 Aug 19.

Abstract

PURPOSE

Generation of nociceptive sensory evoked potentials (NEPs) by selective stimulation of nociceptive intraepidermal nerve fibers is a simple technique which could be used as intraoperative nociception monitor. We evaluated the effects of remifentanil, propofol and sevoflurane on NEPs by this technique.

METHODS

Patients undergoing general anesthesia were assigned to groups in two studies. A-δ fiber selective NEPs were recorded. Study 1: NEPs were recorded at control, under anesthetics administration: remifentanil at an effect-site concentration (Ce) of 1.0 ng/mL (n = 10), propofol at Ce of 0.5 µg/mL (n = 10), or sevoflurane at 0.2 minimum alveolar concentration (MAC) (n = 10), and recovery from the anesthetics. Study 2: NEPs were recorded at control and under administration of higher dose anesthetics: propofol at Ce of 0.5 and 1.0 µg/mL (n = 10) or sevoflurane at 0.2 and 0.5 MAC (n = 10). A P-value < 0.016 was considered statistically significant in multiple analyses.

RESULTS

Study 1: Remifentanil at Ce of 1.0 ng/mL significantly suppressed the amplitude of NEPs (mean amplitude (standard deviation) of control vs. remifentanil administration: 16.8 µV (3.8) vs. 10.1 µV (2.5), P < 0.001). Propofol and sevoflurane did not suppress the amplitude significantly. Study 2: Propofol at Ce of 0.5 and 1.0 µg/mL and sevoflurane at 0.2 and 0.5 MAC did not suppress the amplitude significantly.

CONCLUSION

The amplitude of A-δ fiber selective NEPs was suppressed by remifentanil but not propofol or sevoflurane. NEPs with intraepidermal electrical stimulation can assess the analgesic effect of anesthetics.

CLINICAL TRIAL NUMBER

UMIN000038214 REGISTRY URL: https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043328.

摘要

目的

通过选择性刺激伤害性表皮内神经纤维来产生伤害性感觉诱发电位(NEP)是一种简单的技术,可以用作术中伤害性监测。我们通过这种技术评估了瑞芬太尼、丙泊酚和七氟醚对 NEP 的影响。

方法

接受全身麻醉的患者在两项研究中被分为几组。记录 A-δ 纤维选择性 NEP。研究 1:在对照、麻醉药物给药下(瑞芬太尼效应部位浓度(Ce)为 1.0ng/mL(n=10)、丙泊酚 Ce 为 0.5μg/mL(n=10)或七氟醚 0.2 最低肺泡浓度(MAC)(n=10)和麻醉恢复时)记录 NEP。研究 2:在对照和更高剂量麻醉药物给药下(丙泊酚 Ce 为 0.5 和 1.0μg/mL(n=10)或七氟醚 0.2 和 0.5 MAC(n=10))记录 NEP。在多次分析中,P 值<0.016 被认为具有统计学意义。

结果

研究 1:瑞芬太尼 Ce 为 1.0ng/mL 显著抑制 NEP 的幅度(对照与瑞芬太尼给药时的平均幅度(标准差):16.8µV(3.8)与 10.1µV(2.5),P<0.001)。丙泊酚和七氟醚对幅度没有显著抑制作用。研究 2:丙泊酚 Ce 为 0.5 和 1.0μg/mL 和七氟醚 0.2 和 0.5 MAC 对幅度没有显著抑制作用。

结论

A-δ 纤维选择性 NEP 的幅度被瑞芬太尼抑制,但丙泊酚或七氟醚不抑制。表皮内电刺激的 NEP 可以评估麻醉药物的镇痛效果。

临床试验编号

UMIN000038214 注册网址:https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043328。

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