van den Broek L, Wierda J M, Smeulers N J, Proost J H
Research Group for Experimental Anesthesiology and Clinical Pharmacology, University Hospital, Groningen, The Netherlands.
Br J Anaesth. 1994 Sep;73(3):331-5. doi: 10.1093/bja/73.3.331.
We have evaluated in 10 anaesthetized patients the time course of action, infusion requirements, reversibility and pharmacokinetics of Org 9487. Org 9487 was administered as a bolus dose of 1.5 mg kg-1, followed by an infusion to maintain a block of 75-85% for 60 min. After recovery from the bolus dose, a mean dose of Org 9487 3.4 (SD 1.0) mg kg-1 h-1 was administered to maintain a mean neuromuscular block of 83 (3)%. During the final 15 min of infusion, the infusion requirements were 2.5 (1.1) mg kg-1 h-1. In the five patients who were allowed to recover spontaneously, a TOF ratio of 0.7 was reached 37.9 (12.4) min after stopping the infusion of Org 9487. In the five patients who received neostigmine, a TOF ratio of 0.7 was reached after 14.5 (6.1) min. Plasma clearance was 8.5 (30%) ml kg-1 min-1. Volume of distribution at steady state was 293 (55%) ml kg-1. Terminal half-life and mean residence time were 71.7 (34%) and 33.4 (31%) min, respectively. The concentration of the 3-OH metabolite remained relatively low. Urinary excretion of Org 9487 and its metabolites was 22% in 24 h. In conclusion, a 1-h infusion of the short-acting drug Org 9487 changed its time course characteristics gradually from that of a short-acting neuromuscular blocking agent to that of a neuromuscular blocker with an intermediate duration of action.
我们在10名接受麻醉的患者中评估了Org 9487的作用时程、输注需求量、可逆性及药代动力学。Org 9487以1.5 mg·kg⁻¹的推注剂量给药,随后进行输注以维持60分钟75% - 85%的阻滞。推注剂量作用恢复后,以平均剂量3.4(标准差1.0)mg·kg⁻¹·h⁻¹输注Org 9487以维持平均83(3)%的神经肌肉阻滞。在输注的最后15分钟,输注需求量为2.5(1.1)mg·kg⁻¹·h⁻¹。在5名允许自然恢复的患者中,停止输注Org 9487后37.9(12.4)分钟达到0.7的强直后计数(TOF)比值。在5名接受新斯的明的患者中,14.5(6.1)分钟后达到0.7的TOF比值。血浆清除率为8.5(30%)ml·kg⁻¹·min⁻¹。稳态分布容积为293(55%)ml·kg⁻¹。终末半衰期和平均驻留时间分别为71.7(34%)和33.4(31%)分钟。3 - OH代谢物的浓度相对较低。Org 9487及其代谢物的24小时尿排泄率为22%。总之,短效药物Org 9487输注1小时后,其时间进程特征逐渐从短效神经肌肉阻滞剂转变为中效神经肌肉阻滞剂。