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氟马西尼可加速无术前准备的健康患者七氟醚/瑞芬太尼麻醉的苏醒。

Flumazenil expedites recovery from sevoflurane/remifentanil anaesthesia when administered to healthy unpremedicated patients.

机构信息

Anaesthesiology Department, Thriassio General Hospital - NHS, Attica, Greece.

出版信息

Eur J Anaesthesiol. 2010 Nov;27(11):955-9. doi: 10.1097/EJA.0b013e3283398ef9.

Abstract

BACKGROUND AND OBJECTIVE

To investigate the hypothesis that 0.3 mg flumazenil administered to healthy unpremedicated patients at the end of deep surgical sevoflurane/remifentanil anaesthesia would expedite recovery. Flumazenil, an imidazobenzodiazepine derivative, antagonizes the hypnotic/sedative effects of benzodiazepines on γ-aminobutyric acid receptors. However, endogenous benzodiazepine ligands (endozepines) were isolated in mammalian tissues of individuals who had not received benzodiazepines.

METHODS

Twenty-four healthy unpremedicated patients, scheduled to undergo elective surgery requiring general anaesthesia, were randomly allocated to receive either a single dose of 0.3 mg flumazenil (n = 14) or placebo (n = 10) intravenously at the end of the surgical procedure just before the discontinuation of the volatile anaesthetic. After study drug administration, the authors compared various recovery parameters in the flumazenil and control groups.

RESULTS

Median time to spontaneous respiration, eye opening on verbal command, extubation and time to date of birth recollection was significantly shorter in the flumazenil group than in the control group [2.5 min (2.0-3.0) vs. 7.0 min (6.8-8.3), 3.4 min (3.0-4.0) vs. 8.1 min (6.9-10.2), 4.0 min (3.0-5.0) vs. 9.0 min (7.0-10.8) and 4.7 min (4.0-5.0) vs. 10.3 min (8.0-12.0), respectively].

CONCLUSION

Administration of a single dose of 0.3 mg flumazenil to healthy unpremedicated patients at the end of sevoflurane/remifentanil anaesthesia results in earlier emergence from anaesthesia and significantly expedites recovery. This could redefine the role of flumazenil in general anaesthesia, implicating endozepine-dependent mechanisms.

摘要

背景与目的

研究假设,在深度手术七氟醚/瑞芬太尼麻醉结束时,向健康未接受预用药的患者给予 0.3mg 氟马西尼,将加速恢复。氟马西尼是苯二氮䓬类衍生物,可拮抗苯二氮䓬类药物对γ-氨基丁酸受体的催眠/镇静作用。然而,在未接受苯二氮䓬类药物的个体的哺乳动物组织中分离出内源性苯二氮䓬配体(内源性苯二氮䓬)。

方法

选择 24 名计划接受全身麻醉的择期手术的健康未接受预用药患者,随机分为两组:在手术结束时即将停止挥发性麻醉时,静脉注射 0.3mg 氟马西尼(n=14)或安慰剂(n=10)。在给予研究药物后,比较氟马西尼组和对照组的各种恢复参数。

结果

氟马西尼组自主呼吸、按指令睁眼、拔管和回忆出生日期的时间中位数明显短于对照组[2.5 分钟(2.0-3.0)比 7.0 分钟(6.8-8.3),3.4 分钟(3.0-4.0)比 8.1 分钟(6.9-10.2),4.0 分钟(3.0-5.0)比 9.0 分钟(7.0-10.8)和 4.7 分钟(4.0-5.0)比 10.3 分钟(8.0-12.0)]。

结论

在七氟醚/瑞芬太尼麻醉结束时,向健康未接受预用药的患者给予 0.3mg 氟马西尼,可加速麻醉苏醒,显著加快恢复。这可能重新定义氟马西尼在全身麻醉中的作用,暗示了内源性苯二氮䓬依赖性机制的参与。

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