Caldwell J E, Robertson E N, Baird W L
Br J Anaesth. 1986 Nov;58(11):1285-9. doi: 10.1093/bja/58.11.1285.
The effectiveness of neostigmine 0.07 mg kg-1 and edrophonium 0.8 mg kg-1 as antagonists of profound neuromuscular blockade induced by vecuronium 0.1 mg kg-1 or atracurium 0.5 mg kg-1 was studied in 59 healthy patients. The antagonists were administered 5 min after total ablation of the twitch response and the end-point of recovery was a train-of-four ratio of 70%. In 30 patients given vecuronium the mean time to reach this point (duration TOF70) was 66.7 min in the control group (no antagonist), 43.5 min in the group given neostigmine and 59.8 min in the group given edrophonium. The duration TOF70 was shorter in the neostigmine group than in the control (P less than 0.01) and edrophonium (P less than 0.01) groups. The duration TOF70 did not differ from control in the edrophonium group. In 29 patients given atracurium, the durations TOF70 were 66.4, 44.1 and 54.9 min in the control, neostigmine and edrophonium groups, respectively. The durations TOF70 in the neostigmine (P less than 0.01) and edrophonium (P less than 0.01), groups were shorter than control. The duration TOF70 of the neostigmine group was shorter than in the edrophonium group (P less than 0.01). These results show that profound neuromuscular blockade cannot be rapidly antagonized by either of these two agents, but if reversal is required under these circumstances, neostigmine would be the more effective drug.
在59例健康患者中研究了0.07 mg/kg新斯的明和0.8 mg/kg依酚氯铵作为0.1 mg/kg维库溴铵或0.5 mg/kg阿曲库铵所致深度神经肌肉阻滞拮抗剂的有效性。在颤搐反应完全消失后5分钟给予拮抗剂,恢复终点为四个成串刺激比值达70%。在30例给予维库溴铵的患者中,对照组(未用拮抗剂)达到该点的平均时间(四个成串刺激比值达70%的持续时间,TOF70)为66.7分钟,新斯的明组为43.5分钟,依酚氯铵组为59.8分钟。新斯的明组的TOF70持续时间短于对照组(P<0.01)和依酚氯铵组(P<0.01)。依酚氯铵组的TOF70持续时间与对照组无差异。在29例给予阿曲库铵的患者中,对照组、新斯的明组和依酚氯铵组的TOF70持续时间分别为66.4、44.1和54.9分钟。新斯的明组(P<0.01)和依酚氯铵组(P<0.01)的TOF70持续时间短于对照组。新斯的明组的TOF70持续时间短于依酚氯铵组(P<0.01)。这些结果表明,这两种药物均不能迅速拮抗深度神经肌肉阻滞,但在这些情况下如需进行逆转,新斯的明将是更有效的药物。