Fleming N W, Macres S, Antognini J F, Vengco J
Department of Anesthesiology, University of California, Davis 95616-8634, USA.
Br J Anaesth. 1996 Oct;77(4):492-5. doi: 10.1093/bja/77.4.492.
The reported effects of edrophonium on a subsequent dose of suxamethonium are variable and the effects of pyridostigmine have not been evaluated extensively. We have studied this interaction in patients anaesthetized with propofol and sufentanil. After recovery from an initial bolus (1 mg kg-1) of suxamethonium, vecuronium was infused to produce 75% block. After 30 min, the infusion was discontinued and saline 5 ml, edrophonium 0.75 mg kg-1, pyridostigmine 0.24 mg kg-1 or neostigmine 0.05 mg kg-1 was given. Fifteen minutes later the mean durations of a second bolus of suxamethonium were: 10.5 (SD 3.9) min (saline), 10.9 (3.7) min (edrophonium), 18.7 (5.4) min (pyridostigmine) and 23.8 (7.4) min (neostigmine). Corresponding plasma cholinesterase activities (percentage of baseline) were: 91 (18), 87 (9), 21 (10) and 52 (26). When both treatment groups and individual patients were compared, the changes in duration of action did not correlate with changes in cholinesterase activity. These data suggest that other mechanisms in addition to cholinesterase inhibition may contribute to this drug interaction.
据报道,依酚氯铵对随后一剂琥珀酰胆碱的影响各不相同,而吡啶斯的明的影响尚未得到广泛评估。我们在使用丙泊酚和舒芬太尼麻醉的患者中研究了这种相互作用。在初始推注(1mg/kg)琥珀酰胆碱恢复后,输注维库溴铵以产生75%的阻滞。30分钟后,停止输注,并给予5ml生理盐水、0.75mg/kg依酚氯铵、0.24mg/kg吡啶斯的明或0.05mg/kg新斯的明。15分钟后,第二次推注琥珀酰胆碱的平均持续时间为:10.5(标准差3.9)分钟(生理盐水)、10.9(3.7)分钟(依酚氯铵)、18.7(5.4)分钟(吡啶斯的明)和23.8(7.4)分钟(新斯的明)。相应的血浆胆碱酯酶活性(基线百分比)分别为:91(18)、87(9)、21(10)和52(26)。当比较治疗组和个体患者时,作用持续时间的变化与胆碱酯酶活性的变化不相关。这些数据表明,除了胆碱酯酶抑制作用外,其他机制可能也参与了这种药物相互作用。