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通过体感和疼痛诱发诱发电位识别感觉阻滞。

Identification of sensory blockade by somatosensory and pain-induced evoked potentials.

作者信息

Schmidt Gunter N, Scharein Eckehard, Siegel Markus, Müller Jakob, Debener Stefan, Nitzschke Rainer, Engel Andreas, Bischoff Petra

机构信息

Department of Anesthesiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Anesthesiology. 2007 Apr;106(4):707-14. doi: 10.1097/01.anes.0000264774.09910.c6.

Abstract

BACKGROUND

To date, the anesthesia-induced blockade of nociceptive inputs is insufficiently reflected by commercially available electroencephalographic depth-of-anesthesia monitors. The aim of the current study was to evaluate the potential of somatosensory (SSEP) and intracutaneous pain evoked (iSEP) potentials during remifentanil and propofol anesthesia as electroencephalographic indicators of the nociceptive blockade.

METHODS

Ten healthy men were investigated in a double-blind crossover design during three sessions with remifentanil, propofol, and placebo administration. All dosages were increased in a step-by-step mode. SSEP and iSEP recordings were performed followed by subjective pain ratings and measurement of level of sedation (modified Observer's Assessment of Alertness and Sedation Scale). Changes from baseline in evoked potential components, pain ratings, and sedation scale were assessed by Bonferroni-Holms-corrected Wilcoxon tests.

RESULTS

Pain ratings were significantly reduced by remifentanil. Sedation scale was significantly reduced by propofol. Early SSEP components were not affected by medication. The amplitudes of the long latency SSEP components increased significantly with remifentanil, decreased with propofol, and did not change with placebo. The amplitudes of long latency components of the iSEP decreased significantly with both remifentanil and propofol and did not change with placebo.

CONCLUSION

Long latency components of the SSEP are differently affected by remifentanil and propofol administration. Further studies are needed to clarify whether they can serve as a specific indicator of the nociceptive blockade during anesthesia.

摘要

背景

迄今为止,市售的脑电图麻醉深度监测仪尚不能充分反映麻醉诱导的伤害性传入阻滞情况。本研究的目的是评估瑞芬太尼和丙泊酚麻醉期间体感诱发电位(SSEP)和皮内痛觉诱发电位(iSEP)作为伤害性阻滞脑电图指标的潜力。

方法

采用双盲交叉设计,对10名健康男性在三个阶段分别给予瑞芬太尼、丙泊酚和安慰剂进行研究。所有剂量均逐步增加。记录SSEP和iSEP,随后进行主观疼痛评分和镇静水平测量(改良的观察者警觉与镇静评分量表)。通过Bonferroni-Holms校正的Wilcoxon检验评估诱发电位成分、疼痛评分和镇静量表相对于基线的变化。

结果

瑞芬太尼显著降低疼痛评分。丙泊酚显著降低镇静量表评分。早期SSEP成分不受药物影响。瑞芬太尼使长潜伏期SSEP成分的波幅显著增加,丙泊酚使其降低,安慰剂则无变化。瑞芬太尼和丙泊酚均使iSEP长潜伏期成分的波幅显著降低,安慰剂则无变化。

结论

SSEP的长潜伏期成分受瑞芬太尼和丙泊酚给药的影响不同。需要进一步研究以明确它们是否可作为麻醉期间伤害性阻滞的特异性指标。

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