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[阿曲库铵:重复给药时的神经肌肉阻滞]

[Atracurium: neuromuscular blockade in repeated administration].

作者信息

Kube D, Schuh F T

出版信息

Anaesthesist. 1985 Dec;34(12):639-44.

PMID:2869712
Abstract

The neuromuscular blocking action of repeated injections of atracurium and vecuronium was studied in 74 surgical patients during balanced anaesthesia (methohexitone or etomidate, intubation after suxamethonium, fentanyl, droperidol, N2O). The initial bolus dose (ID) of atracurium was 0.25 mg/kg and of vecuronium 0.05 mg/kg followed by repeated increments (RD) of atracurium 0.1 mg/kg and vecuronium 0.0125 mg/kg when neuromuscular function (EMG) had recovered to about 30% of pre-relaxant control. Dose-response relationships revealed atracurium to be about 1/5 as potent as vecuronium; the ED50 of atracurium was 0.13 +/- 0.03 mg/kg and of vecuronium 0.023 +/- 0.007 mg/kg. The ID of both relaxants produced a neuromuscular blockade of about 90% within 4 min. The duration from the time of injection to 30% recovery was slightly longer in atracurium 26 +/- 9 min. In all patients the RD produced within 3.5 min satisfactory muscle relaxation with a neuromuscular block of about 85%. The mean duration of atracurium (18 min) was 5-10 min longer than of vecuronium (12 min). To maintain good surgical relaxation (more than 70% blockade) atracurium 0.32 mg/kg X h and vecuronium 0.056 mg/kg X h were required. No cumulation could be measured after repeated injections. The recovery time of atracurium and vecuronium at the end of anaesthesia was 10-12 min. Neither cardiovascular side-effects nor signs of histamine release were observed after both relaxants in our particular dose range. It is concluded, that atracurium is a favourable blocker for anaesthetic practice: The time of onset is approximately the same compared with vecuronium. The duration of action, however, is slightly longer but still truly intermediate long.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在74例接受平衡麻醉(甲己炔巴比妥或依托咪酯、琥珀胆碱插管、芬太尼、氟哌利多、氧化亚氮)的外科手术患者中,研究了重复注射阿曲库铵和维库溴铵的神经肌肉阻滞作用。阿曲库铵的初始推注剂量(ID)为0.25mg/kg,维库溴铵为0.05mg/kg,当神经肌肉功能(肌电图)恢复到松弛前对照的约30%时,随后重复递增注射阿曲库铵0.1mg/kg和维库溴铵0.0125mg/kg。剂量-反应关系显示阿曲库铵的效力约为维库溴铵的1/5;阿曲库铵的ED50为0.13±0.03mg/kg,维库溴铵为0.023±0.007mg/kg。两种肌松药的ID在4分钟内均可产生约90%的神经肌肉阻滞。阿曲库铵从注射到恢复30%的时间稍长,为26±9分钟。在所有患者中,重复递增注射在3.5分钟内产生了满意的肌肉松弛,神经肌肉阻滞约为85%。阿曲库铵的平均作用时间(18分钟)比维库溴铵(12分钟)长5 - 10分钟。为维持良好的手术松弛状态(阻滞超过70%),需要阿曲库铵0.32mg/kg·小时和维库溴铵0.056mg/kg·小时。重复注射后未检测到蓄积现象。麻醉结束时阿曲库铵和维库溴铵的恢复时间为10 - 12分钟。在我们特定的剂量范围内,两种肌松药均未观察到心血管副作用或组胺释放迹象。得出结论,阿曲库铵是麻醉实践中一种有利的阻滞剂:起效时间与维库溴铵大致相同。然而,作用时间稍长,但仍属真正的中长效。(摘要截短于250字)

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