Clin Ther. 1992 Nov-Dec;14(6):924-38.
Midazolam, a short-acting benzodiazepine central nervous system (CNS) depressant widely used for the induction and maintenance of general anesthesia, is often supplemented with short-acting opioids for general anesthesia. Administered postoperatively, flumazenil, a specific benzodiazepine antagonist, reverses the CNS sedative effects of midazolam. In a double-blind clinical trial in hospitalized patients, flumazenil, administered postoperatively at an average intravenous dose of 0.89 mg (range: 0.4 mg to 1 mg), was more effective than placebo in reversing sedation and other residual effects of benzodiazepines in patients recovering from general anesthesia induced by midazolam (mean dose 29 mg) in conjunction with fentanyl (mean dose 0.4 mg) or sufentanil (mean dose 0.056 mg). Five minutes posttreatment, 87 (83%) of 124 flumazenil-treated patients and 6 (10%) of 60 placebo-treated patients had attained the criterion response for reversal of sedation. Of these patients, 60% in the flumazenil group, compared with 100% in the placebo group, retained their degree of alertness throughout the 3-hour observation period. Between-group differences were significant until 60 minutes posttreatment, when the effect of the benzodiazepines had spontaneously waned in the placebo group. The Physician's Global Efficacy Rating, providing an overall measure of efficacy 5 minutes after test drug administration, was good or excellent for 86% of the flumazenil-treated patients, as compared with 7% of the placebo-treated patients evaluated. Measurements of psychomotor function and memory also showed significant between-group differences. Flumazenil, compared with placebo, was not associated with a substantially greater frequency of operative-site pain. These results demonstrate that the efficacy and safety of flumazenil were not compromised by the addition of a short-acting opioid to the anesthetic regimen.
咪达唑仑是一种短效苯二氮䓬类中枢神经系统(CNS)抑制剂,广泛用于全身麻醉的诱导和维持,常与短效阿片类药物联合用于全身麻醉。术后给予特异性苯二氮䓬类拮抗剂氟马西尼可逆转咪达唑仑的CNS镇静作用。在一项针对住院患者的双盲临床试验中,术后平均静脉注射剂量为0.89 mg(范围:0.4 mg至1 mg)的氟马西尼,在逆转由咪达唑仑(平均剂量29 mg)联合芬太尼(平均剂量0.4 mg)或舒芬太尼(平均剂量0.056 mg)诱导的全身麻醉苏醒患者中苯二氮䓬类药物的镇静及其他残留效应方面,比安慰剂更有效。治疗后5分钟,124例接受氟马西尼治疗的患者中有87例(83%),60例接受安慰剂治疗的患者中有6例(10%)达到了镇静逆转的标准反应。在这些患者中,氟马西尼组60%的患者与安慰剂组100%的患者在整个3小时观察期内保持了警觉程度。治疗后60分钟前组间差异显著,此时安慰剂组中苯二氮䓬类药物的作用已自发减弱。给药后5分钟提供疗效总体评估的医生整体疗效评分显示,86%接受氟马西尼治疗的患者为良好或优秀,而接受安慰剂治疗的评估患者中这一比例为7%。心理运动功能和记忆力测量也显示组间存在显著差异。与安慰剂相比,氟马西尼与手术部位疼痛频率大幅增加无关。这些结果表明,麻醉方案中添加短效阿片类药物并未损害氟马西尼的疗效和安全性。