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氟马西尼对未行预用药患者七氟醚/芬太尼全身麻醉后麻醉恢复和脑电双频指数的影响。

Effect of flumazenil on recovery from anesthesia and the bispectral index after sevoflurane/fentanyl general anesthesia in unpremedicated patients.

机构信息

Department of Anesthesiology and Pain Medicine, School of Medicine, Ewha Womans University, Seoul, Korea.

出版信息

Korean J Anesthesiol. 2012 Jan;62(1):19-23. doi: 10.4097/kjae.2012.62.1.19. Epub 2012 Jan 25.

Abstract

BACKGROUND

Benzodiazepines have a hypnotic/sedative effect through the inhibitory action of γ-aminobutyric acid type A receptor. Flumazenil antagonizes these effects via competitive inhibition, so it has been used to reverse the effect of benzodiazepines. Recently, flumazenil has been reported to expedite recovery from propofol/remifentanil and sevoflurane/remifentanil anesthesia without benzodiazepines. Endogenous benzodiazepine ligands (endozepines) were isolated in several tissues of individuals who had not received benzodiazepines.

METHODS

Forty-five healthy unpremedicated patients were randomly allocated to either flumazenil or a control groups. Each patient received either a single dose of 0.3 mg of flumazenil (n = 24) or placebo (n = 21). After drug administration, various recovery parameters and bispectral index (BIS) values in the flumazenil and control groups were compared.

RESULTS

Mean time to spontaneous respiration, eye opening on verbal command, hand squeezing on verbal command, extubation and time to date of birth recollection were significantly shorter in the flumazenil group than in the control group (P = 0.004, 0.007, 0.005, 0.042, and 0.016, respectively). The BIS value was significantly higher in flumazenil group than in the control group beginning 6 min after flumazenil administration.

CONCLUSIONS

Administration of a single dose of 0.3 mg of flumazenil to healthy, unpremedicated patients at the end of sevoflurane/fentanyl anesthesia without benzodiazepines resulted in earlier emergence from anesthesia and an increase in the BIS value. This may indicate that flumazenil could have an antagonistic effect on sevoflurane or an analeptic effect through endozepine-dependent mechanisms.

摘要

背景

苯二氮䓬类药物通过 GABA 受体的抑制作用产生催眠/镇静作用。氟马西尼通过竞争性抑制拮抗这些作用,因此被用于逆转苯二氮䓬类药物的作用。最近,有报道称氟马西尼可在没有苯二氮䓬类药物的情况下加速丙泊酚/瑞芬太尼和七氟醚/瑞芬太尼麻醉的恢复。内源性苯二氮䓬类配体(内源性苯二氮䓬类)在未接受苯二氮䓬类药物的个体的几种组织中被分离出来。

方法

45 名健康未用药的患者被随机分配到氟马西尼组或对照组。每位患者接受单剂量 0.3 mg 氟马西尼(n = 24)或安慰剂(n = 21)。给药后,比较氟马西尼组和对照组的各项恢复参数和脑电双频指数(BIS)值。

结果

与对照组相比,氟马西尼组自主呼吸时间、口头命令睁眼时间、口头命令手捏时间、拔管时间和出生日期回忆时间均明显缩短(P = 0.004、0.007、0.005、0.042 和 0.016)。氟马西尼给药后 6 分钟,氟马西尼组的 BIS 值明显高于对照组。

结论

在没有苯二氮䓬类药物的七氟醚/芬太尼麻醉结束时,健康未用药患者单次给予 0.3 mg 氟马西尼可使麻醉更快苏醒,并增加 BIS 值。这可能表明氟马西尼可能通过内源性苯二氮䓬类依赖机制对七氟醚产生拮抗作用或苏醒作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13a8/3272523/83697273906d/kjae-62-19-g001.jpg

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