Brandom B W, Woelfel S K, Ference A, Dayal B, Cook D R, Kerls S
Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Pittsburgh, PA 15213, USA.
J Clin Anesth. 1998 May;10(3):195-9. doi: 10.1016/s0952-8180(98)00007-5.
To determine the neuromuscular blocking effect and recovery profile of cisatracurium besylate in children after administration of a bolus dose that was twice the estimated dose required to produce 95% of the maximum effect (2 x ED95; 0.08 mg/kg) followed by an infusion during halothane-nitrous oxide anesthesia.
Open-label study.
Teaching hospital.
30 male and female (ASA physical status I and II) patients, 2 to 10 years of age, scheduled for elective surgery of low to moderate risk.
After induction of general anesthesia, patients received cisatracurium 0.08 mg/kg administered over 5 to 10 seconds. For surgical procedures requiring neuromuscular block for at least 60 minutes, a second bolus dose of cisatracurium 0.02 mg/kg was administered after the first response to a train-of-four stimuli (T1) recovered to 25% of baseline. When T1 was 5% of baseline after the second dose, a 3 microg/kg/min infusion of cisatracurium was initiated and titrated to maintain 89% to 99% block for the duration of the surgery. For procedures requiring neuromuscular block of less than 60 minutes, one or more maintenance doses of 0.02 mg/kg cisatracurium were administered when T1 was 25% of baseline after the preceding dose. In 10 patients, recovery was facilitated with edrophonium 1.0 mg/kg administered when T1 was 26% to 48% of the final baseline.
Evoked muscular response at the adductor pollicis was measured by electromyography. With 0.08 mg/kg, onset time (mean +/- SEM) was 4.1 +/- 0.4 minutes, and clinically effective duration was 27.3 +/- 0.9 minutes. Mean 5% to 95% and 25% to 75% recovery indices were 28.4 +/- 2. 7 minutes and 11.2 +/- 0.8 minutes, respectively. The mean infusion rate necessary to maintain 89% to 99% T1 suppression for 17 to 145 minutes was 1.7 microg/kg/min. After termination of infusion, the mean 5% to 95% and 25% to 75% recovery indices were similar to those after a single bolus dose, and time to 95% recovery was 30.4 +/- 3.0 minutes. After administration of edrophonium, full recovery (T4:T1 > or = 70%) occurred in 1.5 +/- 0.4 minutes. No clinically significant changes in heart rate or blood pressure were noted during the first 5 minutes after administration of cisatracurium 0.08 mg/kg.
Cisatracurium provided maximal neuromuscular block, cardiovascular stability, and predictable recovery at the doses tested. In view of this finding, cisatracurium should be a useful intermediate-duration neuromuscular blocking drug for children during general anesthesia.
在氟烷 - 氧化亚氮麻醉期间,给予大剂量苯磺顺阿曲库铵(剂量为产生最大效应的95%所需估计剂量的两倍,即2×ED95;0.08mg/kg)后进行输注,以确定其对儿童的神经肌肉阻滞作用及恢复情况。
开放标签研究。
教学医院。
30例年龄在2至10岁、拟行低至中度风险择期手术的男女患者(美国麻醉医师协会身体状况分级为I级和II级)。
全身麻醉诱导后,患者在5至10秒内接受0.08mg/kg苯磺顺阿曲库铵静脉注射。对于需要神经肌肉阻滞至少60分钟的手术,在对四个成串刺激(T1)的首次反应恢复至基线的25%后,给予第二次苯磺顺阿曲库铵静脉注射,剂量为0.02mg/kg。当第二次给药后T1为基线的5%时,开始以3μg/kg/min的速度输注苯磺顺阿曲库铵,并进行滴定以在手术期间维持89%至99%的阻滞。对于需要神经肌肉阻滞少于60分钟的手术,当前一次给药后T1为基线的25%时,给予一次或多次0.02mg/kg苯磺顺阿曲库铵维持剂量。在10例患者中,当T1为最终基线的26%至48%时,给予1.0mg/kg依酚氯铵以促进恢复。
通过肌电图测量拇内收肌的诱发肌肉反应。给予0.08mg/kg时,起效时间(平均值±标准误)为4.1±0.4分钟,临床有效持续时间为27.3±0.9分钟。平均5%至95%和25%至75%恢复指数分别为28.4±2.7分钟和11.2±0.8分钟。维持17至145分钟89%至99%的T1抑制所需的平均输注速度为1.7μg/kg/min。输注结束后,平均5%至95%和25%至75%恢复指数与单次静脉注射后相似,95%恢复时间为30.4±3.0分钟。给予依酚氯铵后,1.5±0.4分钟内完全恢复(T4:T1≥70%)。给予0.08mg/kg苯磺顺阿曲库铵后的前5分钟内,心率或血压无临床显著变化。
在所测试的剂量下,苯磺顺阿曲库铵提供了最大程度的神经肌肉阻滞、心血管稳定性及可预测的恢复。鉴于此发现,苯磺顺阿曲库铵应是全身麻醉期间用于儿童的一种有用的中时效神经肌肉阻滞药物。