Short T G, Galletly D C
Department of Anaesthesia, Wellington School of Medicine, New Zealand.
Anaesth Intensive Care. 1989 Aug;17(3):290-7. doi: 10.1177/0310057X8901700309.
The ability of flumazenil to reverse the effects of midazolam sedation was examined in a randomised, crossover, placebo controlled study in six male volunteers. Subjects received intravenous injections of either (a) midazolam 10 mg followed 10 minutes later by flumazenil 1.0 mg or (b) midazolam 10 mg followed after 10 minutes by flumazenil 4 mg or (c) placebo followed after 10 minutes by placebo. Post reversal drug effects were examined using a psychomotor battery (critical flicker fusion, digit symbol substitution, tapping test, ball-bearing test, number recall, reflex time) and linear analogue mood scales. It was found that a residual psychomotor deficit was present following flumazenil and that this persisted for up to 125 minutes after the 1.0 mg dose and 65 minutes following 4 mg. A small deterioration in performance was apparent after initial reversal with 1.0 mg, the peak deterioration occurring at 35 minutes.
在一项针对6名男性志愿者的随机、交叉、安慰剂对照研究中,检测了氟马西尼逆转咪达唑仑镇静作用的能力。受试者静脉注射以下药物:(a) 咪达唑仑10毫克,10分钟后注射氟马西尼1.0毫克;(b) 咪达唑仑10毫克,10分钟后注射氟马西尼4毫克;(c) 安慰剂,10分钟后注射安慰剂。使用一组心理运动测试(临界闪烁融合、数字符号替换、敲击测试、滚珠测试、数字回忆、反射时间)和线性模拟情绪量表来检测药物逆转后的效果。结果发现,氟马西尼给药后存在残余的心理运动功能缺陷,1.0毫克剂量给药后这种缺陷持续长达125分钟,4毫克剂量给药后持续65分钟。1.0毫克剂量初始逆转后,表现出现轻微恶化,在35分钟时恶化达到峰值。