Yuan H B, Yang M W, Chan K H, Lee T Y
Department of Anesthesiology, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1994 Oct;54(4):259-64.
Diazepam, known to possess myorelaxation property, has been widely used clinically to control muscular rigidity and spasticity. The interactions of diazepam with neuromuscular blocking agents have been extensively studied, yet the results reported are somewhat controversial and inconclusive.
The interaction of diazepam with one of the neuromuscular blocking agents, vecuronium, was studied in 20 ASA I-II patients undergoing elective surgery. They were randomly assigned to two groups with ten in each group. Anesthesia was induced with fentanyl, thiopental and vecuronium and maintained with 1% halothane and 70% N2O in O2. The experimental group received diazepam (0.2 mg/kg) 3 minutes prior to vecuronium (0.1 mg/kg) during induction while the control group received vecuronium (0.1 mg/kg) straight without diazepam. Control records of the integrated electromyography showed the response to train-of-four supramaximal stimulation by a Datex Relaxograph during induction. In no time when the first twitch (T1) recovered to 25% of the control, it was topped up again with another intraoperative dose of vecuronium (0.025 mg/kg). From the derived data, the following parameters were calculated and analysed: (1) onset time T10 (the time from the end of injection of vecuronium during induction to depression of T1 to 10% of control twitch height); (2) duration time T25 (the time from administering vecuronium during induction to the time when T1 recovered to 25% of the original twitch height); (3) topup time T25-25 (the time from administering the top dose of vecuronium to the time when T1 returned to 25% of control twitch height again) and (4) recovery time T25-50 (the time of recovery of T1 from 25% to 50% of the control twitch height at the end of the operation).
Significant differences between both groups were found in T10 (221.8 +/- 62.2 vs 135.4 +/- 23.3 sec, p < 0.01) and T25 (41.9 +/- 10.2 vs 50.6 +/- 9.4 min, p < 0.05). The results of T25-25 and T25-50 did not differ much (26.6 +/- 6.9 vs 29.3 +/- 4.4 min, p > 0.05 and 15.0 +/- 8.9 vs 16.9 +/- 8.7 min, p > 0.05 respectively).
The administration of diazepam (0.2 mg/kg) three minutes prior to vecuronium (0.1 mg/kg) during induction may hasten the onset of vecuronium and prolong its duration of action.
地西泮具有肌松特性,临床上已被广泛用于控制肌肉强直和痉挛。地西泮与神经肌肉阻滞剂之间的相互作用已得到广泛研究,但所报道的结果在一定程度上存在争议且尚无定论。
在20例接受择期手术的美国麻醉医师协会(ASA)I-II级患者中研究了地西泮与一种神经肌肉阻滞剂维库溴铵之间的相互作用。他们被随机分为两组,每组10例。诱导麻醉采用芬太尼、硫喷妥钠和维库溴铵,维持麻醉采用1%氟烷和70%氧化亚氮与氧气混合气体。实验组在诱导期于维库溴铵(0.1mg/kg)给药前3分钟给予地西泮(0.2mg/kg),而对照组直接给予维库溴铵(0.1mg/kg),不给予地西泮。通过Datex Relaxograph记录诱导期对四个成串超强刺激的复合肌电图反应作为对照。当第一个肌颤搐(T1)恢复到对照值的25%时,立即给予另一术中剂量的维库溴铵(0.025mg/kg)进行补充。根据所得数据,计算并分析以下参数:(1)起效时间T10(从诱导期维库溴铵注射结束至T1降至对照肌颤搐高度的10%的时间);(2)持续时间T25(从诱导期给予维库溴铵至T1恢复到原始肌颤搐高度的25%的时间);(3)补充时间T25-25(从给予维库溴铵补充剂量至T1再次恢复到对照肌颤搐高度的25%的时间)和(4)恢复时间T25-50(手术结束时T1从对照肌颤搐高度的25%恢复到50%的时间)。
两组在T10(221.8±62.2秒对135.4±23.3秒,p<0.01)和T25(41.9±10.2分钟对50.6±9.4分钟,p<0.05)方面存在显著差异。T25-25和T25-50的结果差异不大(分别为26.6±6.9分钟对29.3±4.4分钟,p>0.05和15.0±8.9分钟对16.9±8.7分钟,p>0.05)。
诱导期在维库溴铵(0.1mg/kg)给药前3分钟给予地西泮(0.2mg/kg)可能会加速维库溴铵的起效并延长其作用持续时间。