Gupta A, Lind S, Eklund A, Lennmarken C
Department of Anaesthesia and Intensive Care, University Hospital, Linkoping, Sweden.
J Clin Anesth. 1997 Feb;9(1):21-5. doi: 10.1016/S0952-8180(96)00214-0.
To determine the effects of midazolam and its antagonism with flumazenil on psychomotor function as assessed by the perceptive accuracy test (PAT) and choice reaction time (CRT).
Double-blind, cross-over, randomized, placebo-controlled study.
Department of Anaesthesiology, University Hospital, Linköping, Sweden.
11 healthy volunteers (6 females, 5 males, mean age 32 years).
Midazolam 0.1 mg/kg (Group MH), midazolam 0.035 mg/kg (Group ML), or placebo (Group PL) were injected intravenously (IV) in a cross-over design. Flumazenil 0.5 mg was injected after 60 minutes. Plasma concentrations of midazolam were measured at 3, 30, 60 and 75 minutes.
Baseline values were first obtained on psychomotor tests including the PAT and CRT. These tests were then repeated 30 and 60 minutes after the IV injection of midazolam or placebo, and repeated 15 and 30 minutes following the injection of flumazenil. A dose-dependent effect of midazolam was seen on the PAT and CRT. Flumazenil completely reversed the psychomotor effects of midazolam in Group ML at 60 minutes but not in Group MH, and this action was clearly detected by the PAT. Psychomotor tests had returned to baseline values when the plasma concentration of midazolam was below 33 ng/ml. A marked inter-individual variation was seen on the PAT, CRT, and in the correlation between the plasma concentration and the results on the PAT.
There was a dose-dependent deterioration in psychomotor performance in subjects given midazolam. The PAT was sensitive in the detection of these residual effects, but a large inter-individual variation in the psychomotor effects of midazolam was evident that could be due to pharmacodynamic and pharmacokinetic variability between individuals. Flumazenil in a dose of 0.5 mg IV completely reversed the effects of low-dose, but not high-dose, midazolam.
通过感知准确性测试(PAT)和选择反应时间(CRT)来确定咪达唑仑及其与氟马西尼的拮抗作用对精神运动功能的影响。
双盲、交叉、随机、安慰剂对照研究。
瑞典林雪平大学医院麻醉科。
11名健康志愿者(6名女性,5名男性,平均年龄32岁)。
采用交叉设计静脉注射(IV)咪达唑仑0.1mg/kg(MH组)、咪达唑仑0.035mg/kg(ML组)或安慰剂(PL组)。60分钟后注射氟马西尼0.5mg。在3、30、60和75分钟时测量咪达唑仑的血浆浓度。
首先在包括PAT和CRT的精神运动测试中获得基线值。然后在静脉注射咪达唑仑或安慰剂后30和60分钟重复这些测试,并在注射氟马西尼后15和30分钟重复。在PAT和CRT上观察到咪达唑仑的剂量依赖性效应。氟马西尼在60分钟时完全逆转了ML组中咪达唑仑的精神运动效应,但在MH组中未逆转,并且这种作用通过PAT可明显检测到。当咪达唑仑的血浆浓度低于33ng/ml时,精神运动测试已恢复到基线值。在PAT、CRT以及血浆浓度与PAT结果之间的相关性方面存在明显的个体间差异。
给予咪达唑仑的受试者精神运动表现出现剂量依赖性恶化。PAT对这些残留效应的检测很敏感,但咪达唑仑的精神运动效应存在明显的个体间差异,这可能是由于个体之间的药效学和药代动力学变异性所致。静脉注射0.5mg的氟马西尼完全逆转了低剂量但非高剂量咪达唑仑的效应。