Suppr超能文献

丙泊酚与芬太尼麻醉短期和长期给药后有无血-效应室平衡时的苏醒丙泊酚浓度

Awakening propofol concentration with and without blood-effect site equilibration after short-term and long-term administration of propofol and fentanyl anesthesia.

作者信息

Kazama T, Ikeda K, Morita K, Sanjo Y

机构信息

Department of Anesthesiology and Intensive Care, Hamamatsu University, School of Medicine, Japan.

出版信息

Anesthesiology. 1998 Apr;88(4):928-34. doi: 10.1097/00000542-199804000-00012.

Abstract

BACKGROUND

The propofol awakening concentration can vary. However, the effect site awakening propofol concentration will be a fixed value. The purpose of this study was to determine the awakening propofol concentrations obtained from infusion Schede using abrupt discontinuation of propofol (half-maximal effective concentration [EC50]) or a descending decrease in concentration to allow blood-effect site equilibration (EC50eq).

METHODS

Patients undergoing short-term (group 1) and long-term (group 2) elective surgery were anesthetized with computer-assisted continuous infusion of propofol and fentanyl, with both groups receiving the same propofol (3 microg/ml) and fentanyl (1 ng/ml) concentrations 20-30 min before the end of surgery until the end. Then both groups were further divided into two subgroups: subgroup A abrupt discontinuation, and subgroup B descending concentrations of propofol (15-min duration per concentration). In the A subgroups, the response to verbal command was evaluated every 30 s. In the B subgroups, the blood propofol concentrations just permitting and just preventing response to command were averaged individually. The EC50 and EC50eq values were determined by probit analysis.

RESULTS

The EC50 of group 1A was 1 microg/ml, which was significantly less than the 1.6 microg/ml of group 2A (P < 0.05). The awakening time of group 1A was 5.2 +/- 1.8 min, which was significantly shorter than the 9.3 +/- 3.5 min of group 2A (means +/- SD). The EC50eq of both groups 1B and 2B was 2.2 microg/ml.

CONCLUSIONS

The EC50eq was independent of propofol infusion length, compared with the EC50. Thus the potential for hysteresis during emergence from propofol anesthesia was confirmed.

摘要

背景

丙泊酚的苏醒浓度会有所不同。然而,效应室苏醒丙泊酚浓度将是一个固定值。本研究的目的是确定通过丙泊酚突然停药(半数有效浓度[EC50])或浓度逐渐下降以使血药-效应室达到平衡(EC50eq)的输注方案所获得的丙泊酚苏醒浓度。

方法

接受短期(1组)和长期(2组)择期手术的患者采用计算机辅助持续输注丙泊酚和芬太尼进行麻醉,两组在手术结束前20 - 30分钟直至结束均接受相同浓度的丙泊酚(3微克/毫升)和芬太尼(1纳克/毫升)。然后两组再进一步分为两个亚组:A亚组为突然停药,B亚组为丙泊酚浓度逐渐下降(每个浓度持续15分钟)。在A亚组中,每30秒评估一次对语言指令的反应。在B亚组中,分别计算刚好允许和刚好阻止对指令反应的血丙泊酚浓度平均值。通过概率分析确定EC50和EC50eq值。

结果

1A组的EC50为1微克/毫升,显著低于2A组的1.6微克/毫升(P < 0.05)。1A组的苏醒时间为5.2 +/- 1.8分钟,显著短于2A组的9.3 +/- 3.5分钟(均值 +/- 标准差)。1B组和2B组的EC50eq均为2.2微克/毫升。

结论

与EC50相比,EC50eq与丙泊酚输注时长无关。因此证实了丙泊酚麻醉苏醒过程中存在滞后现象的可能性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验