Kopman A F
Anesthesiology. 1986 Dec;65(6):572-8. doi: 10.1097/00000542-198612000-00002.
The ability of edrophonium and neostigmine to antagonize nondepolarizing neuromuscular blockade produced by steady-state infusions of atracurium, pancuronium, and vecuronium was studied in 71 adult patients anesthetized with nitrous oxide and halothane. Infusion rates of blocking drugs were adjusted so that single twitch depression as measured by the evoked integrated EMG of the hypothenar muscles was kept at 10% of control. Two minutes after the termination of the infusion either edrophonium (0.75 mg/kg) or neostigmine (0.05 mg/kg) was administered. Single twitch depression and train-of-four (T4/T1) fade was recorded during the recovery period. T4/T1 fade ratios observed at 20 min postreversal were 0.80 (atracurium-edrophonium); 0.76 (vecuronium-edrophonium); 0.44 (pancuronium-edrophonium); 0.95 (atracurium-neostigmine); 0.89 (vecuronium-neostigmine); and 0.68 (pancuronium-neostigmine). Under conditions of this study neostigmine produced more rapid and complete recovery than did edrophonium. Although edrophonium produced adequate antagonism of atracurium if 20-30 min were allowed to elapse, edrophonium reversal of pancuronium was rarely acceptable even at 30 min. Increasing the dose of edrophonium to 1.0 mg/kg produced single twitch values of 0.90 at 5 min postreversal but did not increase the rate of recovery of the train-of-four fade ratio. Neostigmine reversal of pancuronium, on the other hand, generally produced T4/T1 ratios of greater than 0.70 in 20-30 min. Although the pattern of recovery seen after reversal of vecuronium was in general quite similar to that seen after atracurium, two patients in the vecuronium-edrophonium group showed delayed recovery and also failed to respond significantly to subsequent doses of neostigmine.(ABSTRACT TRUNCATED AT 250 WORDS)
在71例接受氧化亚氮和氟烷麻醉的成年患者中,研究了依酚氯铵和新斯的明拮抗阿曲库铵、泮库溴铵和维库溴铵稳态输注所产生的非去极化神经肌肉阻滞的能力。调整阻滞药物的输注速率,以使由小鱼际肌诱发的积分肌电图测量的单颤搐抑制保持在对照值的10%。输注终止两分钟后,给予依酚氯铵(0.75mg/kg)或新斯的明(0.05mg/kg)。在恢复期记录单颤搐抑制和四个成串刺激(T4/T1)衰减情况。逆转后20分钟观察到的T4/T1衰减率分别为:阿曲库铵-依酚氯铵组0.80;维库溴铵-依酚氯铵组0.76;泮库溴铵-依酚氯铵组0.44;阿曲库铵-新斯的明组0.95;维库溴铵-新斯的明组0.89;泮库溴铵-新斯的明组0.68。在本研究条件下,新斯的明比依酚氯铵产生更快、更完全的恢复。尽管如果允许20 - 30分钟过去,依酚氯铵对阿曲库铵产生了足够的拮抗作用,但即使在30分钟时,依酚氯铵逆转泮库溴铵的效果也很少能令人满意。将依酚氯铵剂量增加到1.0mg/kg,逆转后5分钟单颤搐值为0.90,但未提高四个成串刺激衰减率的恢复速度。另一方面,新斯的明逆转泮库溴铵通常在20 - 30分钟内产生大于0.70的T4/T1比率。尽管维库溴铵逆转后观察到的恢复模式总体上与阿曲库铵逆转后相似,但维库溴铵-依酚氯铵组中有两名患者恢复延迟,并且对随后剂量的新斯的明也无明显反应。(摘要截断于250字)