Fragen R J, Avram M J, Henthorn T K, Caldwell N J
Anesth Analg. 1983 Jul;62(7):654-60.
An etomidate infusion regimen for hypnosis as part of balanced, totally intravenous anesthesia was designed to maintain plasma etomidate concentrations above the awakening concentration of 300 ng/ml while avoiding dose-related side effects. The etomidate infusion regimen of 0.1 mg/kg/min for 3 min, 0.02 mg/kg/min for 27 min, and 0.01 mg/kg/min for the remainder of the anesthesia was used together with intravenous bolus doses of fentanyl, droperidol, and pancuronium. This was evaluated in 11 patients and the kinetics of etomidate were reexamined. The anesthetic technique seemed clinically satisfactory for the infusion periods of 30-109 min. The average time and plasma concentration at the end of the infusion was 59.5 min and 583 ng/ml, at awakening was 9.3 min and 307 ng/ml, and at alertness was 19.5 min and 227 ng/ml. The main difference between the kinetics observed in the present study and those of previous studies is in the elimination clearance. The average plasma elimination clearance of the present study was 1210 ml/min and the whole-blood clearance was estimated to be 1357 ml/min, giving an apparent hepatic extraction ratio of approximately 0.90. The negative correlation of patient mass and elimination clearance normalized for body mass suggests that the terminal infusion should not be adjusted to body mass.
作为平衡全静脉麻醉一部分的依托咪酯催眠输注方案,旨在维持血浆依托咪酯浓度高于300 ng/ml的清醒浓度,同时避免剂量相关的副作用。依托咪酯输注方案为:先以0.1 mg/kg/min输注3分钟,再以0.02 mg/kg/min输注27分钟,麻醉剩余时间以0.01 mg/kg/min输注,并与芬太尼、氟哌利多和泮库溴铵静脉推注剂量联合使用。对11例患者进行了评估,并重新检查了依托咪酯的动力学。在30 - 109分钟的输注期间,该麻醉技术在临床上似乎令人满意。输注结束时的平均时间和血浆浓度分别为59.5分钟和583 ng/ml,苏醒时为9.3分钟和307 ng/ml,警觉时为19.5分钟和227 ng/ml。本研究观察到的动力学与先前研究的主要差异在于消除清除率。本研究的平均血浆消除清除率为1210 ml/min,全血清除率估计为1357 ml/min,表观肝脏提取率约为0.90。患者体重与体重标准化后的消除清除率呈负相关,这表明终末输注不应根据体重进行调整。