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小儿患者吸入氟烷麻醉时罗库溴铵的药效动力学。

The pharmacodynamics of rocuronium in pediatric patients anesthetized with halothane.

机构信息

Department of Anesthesiology, University of Miami School of Medicine, P.O. Box 016370, 33101, Miami, FL, USA.

出版信息

J Anesth. 1994 Sep;8(3):256-60. doi: 10.1007/BF02514645.

Abstract

The aim of this study was to determine the neuromuscular blocking potency of rocuronium (ORG 9426) in 4-to 14-year old children anesthetized with halothane. After induction of anesthesia, the ulnar nerve was stimulated with electrical impulses of 0.2 ms duration every 12 s and the force of contraction of the thumb (P) was continuously recorded. Doses of 0.12, 0.16, 0.20, and 0.24 mg·kg(-1) rocuronium were administered, in a randomized fashion, to 4 groups of 12 patients each. The ED50, ED90, and ED95 of rocuronium determined from the log dose-probit regression lines were 0.18, 0.34, and 0.40 mg·kg(-1), respectively. To facilitate tracheal intubation, after the development of the maximal effect of the first dose, a variable second dose of rocuronium was administered to increase the total dose to 0.3 mg·kg(-1). If after the second dose P was greater than 10% of control, additional 0.025-0.1 mg·kg(-1) increments of rocuronium were administered until P became less than 10% of control. At this time the trachea was intubated. Muscular relaxation was maintained with 0.075, 0.1, or 0.125 mg·kg(-1) rocuronium, administered whenever P recovered to 25% of control. The clinical duration of these doses was 6.9±2.8, 6.1±0.4, and 8.1±0.6 min, respectively. On repeated administration of three 0.1 or 0.125 mg·kg(-1) doses, rocuronium showed little cumulative tendency. Time for spontaneous recovery of P from 25% to 75%, 8.4±0.39 min and from 10% to 90%, 16.19±0.15 min, of control, were relatively short. When at termination of anesthesia T4/T1 ratios were lower than 0.75, the residual neuromuscular block could be antagonized with 0.5 mg·kg(-1) edrophonium in 2 min. Rocuronium, 0.3 mg·kg(-1) caused a 13.5% increase of heart rate but had no effect on blood pressure. In conclusion, in 4 to 14-year-old children, rocuronium appears to have a more rapid onset and shorter duration of action than other steroid-type muscle relaxants.

摘要

本研究旨在确定氟烷麻醉下 4 至 14 岁儿童罗库溴铵(ORG 9426)的神经肌肉阻滞作用。在麻醉诱导后,用持续 0.2 毫秒、间隔 12 秒的电脉冲刺激尺神经,持续记录拇指(P)的收缩力。将 0.12、0.16、0.20 和 0.24mg·kg(-1)的罗库溴铵以随机方式分配给每组 12 名患者。从对数剂量概率回归线中得出罗库溴铵的 ED50、ED90 和 ED95 分别为 0.18、0.34 和 0.40mg·kg(-1)。为了便于气管插管,在第一剂量产生最大作用后,给予可变的第二剂量罗库溴铵,将总剂量增加至 0.3mg·kg(-1)。如果第二剂量后 P 大于对照的 10%,则给予 0.025-0.1mg·kg(-1)的罗库溴铵递增剂量,直到 P 小于对照的 10%。此时进行气管插管。当 P 恢复至对照的 25%时,给予 0.075、0.1 或 0.125mg·kg(-1)的罗库溴铵以维持肌肉松弛。这些剂量的临床持续时间分别为 6.9±2.8、6.1±0.4 和 8.1±0.6 分钟。重复给予三个 0.1 或 0.125mg·kg(-1)剂量时,罗库溴铵显示出很少的累积趋势。从 25%到 75%、8.4±0.39 分钟和从 10%到 90%、16.19±0.15 分钟,P 从对照的恢复时间相对较短。当麻醉结束时 T4/T1 比值低于 0.75 时,用 0.5mg·kg(-1)的依酚氯铵可在 2 分钟内拮抗残余的神经肌肉阻滞。罗库溴铵 0.3mg·kg(-1)使心率增加 13.5%,但对血压无影响。总之,在 4 至 14 岁儿童中,罗库溴铵的起效更快,作用持续时间更短,优于其他甾体类肌肉松弛剂。

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