Belmont M R, Lien C A, Quessy S, Abou-Donia M M, Abalos A, Eppich L, Savarese J J
New York Hospital-Cornell Medical Center, New York 10021, USA.
Anesthesiology. 1995 May;82(5):1139-45. doi: 10.1097/00000542-199505000-00008.
Atracurium is a mixture of ten stereoisomers. 51W89, one of these isomers, is a potent nondepolarizing intermediate-duration neuromuscular blocking agent. Preclinical studies have shown 51W89 to be significantly more potent than atracurium but with a similar neuromuscular blocking profile. This study was undertaken to establish the neuromuscular blocking potency and pharmacodynamics of 51W89 in patients undergoing elective surgical procedures.
Ninety-nine ASA physical status 1 or 2 patients undergoing elective surgical procedures under nitrous oxide/opioid/barbiturate anesthesia were studied. The neuromuscular blocking effect of 51W89 was assessed after administration of bolus doses from 0.015 to 0.4 mg/kg, as well as during and after continuous infusions from 11 to 249 min in length.
The calculated ED95 for inhibition of adductor pollicis twitch evoked at 0.15 Hz was 0.048 mg/kg. At 0.10 mg/kg, maximum block developed within 5.2 +/- 0.3 min, and recovery to 95% twitch height occurred 64.4 +/- 3.9 min after injection. At 0.4 mg/kg, onset was 1.9 +/- 0.1 min, and 95% recovery developed within 121.0 +/- 5.9 min. Comparative recovery indexes from 5% to 95% or from 25% to 75% twitch heights did not differ significantly among all dosage groups from 0.1 to 0.4 mg/kg (means ranged from 29.6 to 32.3 min and from 12.6 to 14.3 min, respectively). The average infusion rate necessary to maintain approximately 95% twitch suppression was 1.35 micrograms/kg/min. Recovery indexes from infusions were 5-95% 33.2 +/- 1.8 min and 25-75% 15.0 +/- 0.6 min, not differing significantly from recovery indexes from single bolus doses. Twenty-five patients received neostigmine (0.06 mg/kg) with atropine (0.03 mg/kg) at twitch height recovery of between 6% and 21%. Antagonism to 95% control twitch height developed within 6.8 +/- 0.3 min, and the neostigmine-accelerated 25-75% recovery index was 2.8 +/- 0.2 min.
51W89 is a potent nondepolarizing neuromuscular blocking agent that shows noncumulative intermediate-duration neuromuscular blocking pharmacodynamics.
阿曲库铵是十种立体异构体的混合物。其中一种异构体51W89是一种强效的非去极化中时效神经肌肉阻滞剂。临床前研究表明,51W89的效力明显高于阿曲库铵,但具有相似的神经肌肉阻滞特征。本研究旨在确定51W89在接受择期手术的患者中的神经肌肉阻滞效力和药效学。
对99例接受氧化亚氮/阿片类药物/巴比妥类麻醉的择期手术患者进行了研究,患者的美国麻醉医师协会(ASA)身体状况分级为1或2级。在给予0.015至0.4mg/kg的推注剂量后,以及在持续输注11至249分钟期间和之后,评估了51W89的神经肌肉阻滞效果。
抑制0.15Hz诱发的拇内收肌抽搐的计算ED95为0.048mg/kg。在0.10mg/kg时,最大阻滞在5.2±0.3分钟内出现,注射后64.4±3.9分钟恢复至抽搐高度的95%。在0.4mg/kg时,起效时间为1.9±0.1分钟,95%恢复在121.0±5.9分钟内出现。在0.1至0.4mg/kg的所有剂量组中,从5%至95%或从25%至75%抽搐高度的比较恢复指数无显著差异(平均值分别为29.6至32.3分钟和12.6至14.3分钟)。维持约95%抽搐抑制所需的平均输注速率为1.35μg/kg/min。输注后的恢复指数为5-95% 33.2±1.8分钟和25-75% 15.0±0.6分钟,与单次推注剂量后的恢复指数无显著差异。25例患者在抽搐高度恢复至6%至21%时接受了新斯的明(0.06mg/kg)加阿托品(0.03mg/kg)治疗。拮抗至95%对照抽搐高度在6.8±0.3分钟内出现,新斯的明加速的25-75%恢复指数为2.8±0.2分钟。
51W89是一种强效的非去极化神经肌肉阻滞剂,具有非累积性的中时效神经肌肉阻滞药效学。