Foldes F F, Nagashima H, Nguyen H D, Duncalf D, Goldiner P L
Department of Anesthesiology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10467.
Can J Anaesth. 1990 Jul;37(5):549-55. doi: 10.1007/BF03006324.
Pipecuronium bromide (Arduan) is a bisquaternary, steroid-type neuromuscular blocking agent in clinical use in Eastern Europe. Before its introduction into clinical practice in the USA, in the first phase of this study the neuromuscular potency of pipecuronium was determined under "balanced" and enflurance anaesthesia by the cumulative log dose-response method in 30 patients each. In the second phase the intubation and onset times, clinical duration of the first and repeated doses, spontaneous recovery index, reversibility of its residual neuromuscular effect by an anticholinesterase and its effect on heart rate and blood pressure was compared with the same variables observed in patients, anaesthetized with identical techniques but who had received vecuronium or pancuronium. The neuromuscular potency of pipecuronium was greater under enflurane (ED95 = 23.6 +/- 1.1 micrograms.kg-1 (mean +/- SEM)] than under balanced (ED95 = 35.1 +/- 17 micrograms.kg-1) anaesthesia. Pipecuronium was more potent than vecuronium under both balanced (ED95 = 45.8 micrograms.kg-1) and enflurane anaesthesia (ED95 = 27.4 micrograms.kg-1). Following the administration of 2 x ED95 doses there were no clinically significant differences in the intubation or onset times of pipecuronium, vecuronium and pancuronium. Under balanced anaesthesia the clinical duration of 2 x ED95 dose of pipecuronium (110.5 +/- 0.3 min) or pancuronium (115.8 +/- 8.1 min) were similar and about three times longer than that of vecuronium (36.3 +/- 2.1 min). The recovery indices of pipecuronium (44.5 +/- 8.2 min) and pancuronium (41.3 +/- 4.2 min) were also similar and about three times longer than that of vecuronium (14.3 +/- 1.4 min).(ABSTRACT TRUNCATED AT 250 WORDS)
哌库溴铵(阿端)是一种双季铵类固醇类神经肌肉阻滞剂,在东欧临床使用。在美国将其引入临床实践之前,在本研究的第一阶段,通过累积对数剂量反应法,在30例患者中分别在“平衡”麻醉和安氟醚麻醉下测定了哌库溴铵的神经肌肉效能。在第二阶段,将哌库溴铵、维库溴铵和泮库溴铵分别给予采用相同技术麻醉但接受不同药物的患者,比较了它们的插管和起效时间、首次及重复给药的临床持续时间、自主恢复指数、抗胆碱酯酶对其残余神经肌肉效应的逆转作用以及对心率和血压的影响。在安氟醚麻醉下哌库溴铵的神经肌肉效能(ED95 = 23.6±1.1微克·千克-1(均值±标准误))高于平衡麻醉(ED95 = 35.1±1.7微克·千克-1)。在平衡麻醉(ED95 = 45.8微克·千克-1)和安氟醚麻醉(ED95 = 2..4微克·千克-1)下,哌库溴铵均比维库溴铵效能更强。给予2倍ED95剂量后,哌库溴铵、维库溴铵和泮库溴铵的插管或起效时间无临床显著差异。在平衡麻醉下,2倍ED95剂量的哌库溴铵(110.5±0.3分钟)或泮库溴铵(115.8±8.1分钟)的临床持续时间相似,约为维库溴铵(36.3±2.1分钟)的3倍。哌库溴铵(44.5±8.2分钟)和泮库溴铵(41.3±4.2分钟)的恢复指数也相似,约为维库溴铵(14.3±1.4分钟)的3倍。(摘要截短于250字)