Stockham R J, Stanley T H, Pace N L, Gillmor S, Groen F, Hilkens P
Department of Anesthesiology, University of Utah School of Medicine, Salt Lake City 84132.
Anaesth Intensive Care. 1988 May;16(2):171-6. doi: 10.1177/0310057X8801600207.
Haemodynamic changes and side-effects of induction of anaesthesia with etomidate were evaluated in 60 ASA Class I or II patients. The objective was to find an optimal pre-induction dose of fentanyl which eliminated haemodynamic changes and side-effects during induction and intubation without introducing other problems. Patients were randomly assigned to four groups according to the pretreatment dose of fentanyl (Group I = 2 ml normal saline; Group II = 100 micrograms of fentanyl; Group III = 250 micrograms of fentanyl; Group IV = 500 micrograms of fentanyl) administered intravenously five minutes prior to induction of anaesthesia with etomidate, 0.3 mg/kg. There was an increasing incidence of apnoea (53, 87, 87 and 100% in Groups I-IV respectively) and a decreasing incidence of myoclonus (60, 33, 13 and 0% in Groups I-IV respectively) and injection pain (53, 13, 7 and 0% in Groups I-IV respectively), P less than 0.002 chi-square test for linear trends, with increasing fentanyl dosage. The incidences of postoperative nausea and vomiting were similar in the four groups. There were also significant linear regression relationships (P less than 0.01 ANOVA for linear regression) between increasing doses of fentanyl administered before etomidate and the prevention of increases in systolic blood pressure and heart rate during the induction-intubation sequence. The data demonstrate that increasing pre-induction doses of fentanyl are more effective at minimising side-effects and preventing increases in systolic arterial blood pressure and heart rate but also increase the incidence of apnoea during induction. The results suggest that 500 micrograms of fentanyl is an ideal pretreatment dose in fit patients prior to anaesthetic induction with etomidate.
在60例美国麻醉医师协会(ASA)I级或II级患者中评估了依托咪酯诱导麻醉时的血流动力学变化和副作用。目的是找到一种最佳的诱导前芬太尼剂量,该剂量能消除诱导和插管过程中的血流动力学变化和副作用,同时不引发其他问题。患者在接受0.3mg/kg依托咪酯诱导麻醉前五分钟,根据静脉注射的芬太尼预处理剂量随机分为四组(I组 = 2ml生理盐水;II组 = 100微克芬太尼;III组 = 250微克芬太尼;IV组 = 500微克芬太尼)。随着芬太尼剂量增加,呼吸暂停的发生率逐渐升高(I - IV组分别为53%、87%、87%和100%),肌阵挛(I - IV组分别为60%、33%、13%和0%)和注射痛(I - IV组分别为53%、13%、7%和0%)的发生率逐渐降低,线性趋势卡方检验P < 0.002。四组术后恶心和呕吐的发生率相似。依托咪酯给药前增加芬太尼剂量与诱导 - 插管过程中收缩压和心率升高的预防之间也存在显著的线性回归关系(线性回归方差分析P < 0.01)。数据表明,增加诱导前芬太尼剂量在最小化副作用以及预防收缩动脉血压和心率升高方面更有效,但也会增加诱导期间呼吸暂停的发生率。结果表明,对于身体状况良好的患者,在依托咪酯麻醉诱导前,500微克芬太尼是理想的预处理剂量。