Robertson E N, Booij L H, Fragen R J, Crul J F
Br J Anaesth. 1983 Feb;55(2):125-9. doi: 10.1093/bja/55.2.125.
The potency, histamine releasing ability, cardiovascular effects, and pharmacodynamics of vecuronium and atracurium were investigated in 64 healthy patients following administration i.v. Cumulative dose-response curves showed vecuronium to be 4.4 times as potent as atracurium. Using the calculated ED90 of each drug (43 micrograms kg-1 for vecuronium and 188 micrograms kg-1 for atracurium), vecuronium had a significantly more rapid onset time and shorter duration of action than atracurium. When three times the ED90 doses were used (129 micrograms kg-1 for vecuronium and 564 micrograms kg-1 for atracurium), no statistically significant differences in the pharmacodynamics were seen between the two drugs, although vecuronium tended to be shorter-acting. There was no clinical evidence of histamine release during the study. No clinically significant changes in arterial pressure or heart rate were seen after the injection of either drug, although vecuronium caused a statistically significant decrease in heart rate (approximately 5%) at 5 and 10 min after administration. Both drugs would appear to have certain advantages over existing non-depolarizing neuromuscular blocking drugs.
在64例健康患者静脉注射后,研究了维库溴铵和阿曲库铵的效价、组胺释放能力、心血管效应及药效学。累积剂量-反应曲线显示,维库溴铵的效价是阿曲库铵的4.4倍。使用每种药物计算出的ED90(维库溴铵为43微克/千克,阿曲库铵为188微克/千克),维库溴铵的起效时间明显更快,作用持续时间比阿曲库铵更短。当使用3倍ED90剂量时(维库溴铵为129微克/千克,阿曲库铵为564微克/千克),两种药物在药效学上无统计学显著差异,尽管维库溴铵的作用时间有缩短趋势。研究期间无组胺释放的临床证据。注射任何一种药物后,动脉压或心率均无临床显著变化,尽管维库溴铵在给药后5分钟和10分钟导致心率有统计学显著下降(约5%)。与现有的非去极化神经肌肉阻滞药物相比,这两种药物似乎都有一定优势。