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非去极化肌松药的四个成串刺激衰减:对预箭毒化机制的深入了解

Train-of-four fade of non depolarizing muscle relaxants: an insight into the mechanism of precurarization.

作者信息

Erkola O

机构信息

Department of Anaesthesia, Töölö Hospital, Helsinki University Central Hospital, Finland.

出版信息

Ann Fr Anesth Reanim. 1988;7(4):299-304. doi: 10.1016/S0750-7658(88)80032-7.

Abstract

This study was carried out to assess the prejunctional effect of non depolarizing muscle relaxants during the onset of neuromuscular blockade using the train-of-four ratio (TR). The prejunctional effect was compared with previous results concerning the ability of the relaxants to prevent suxamethonium-induced fasciculations. Fifty-three adult patients were relaxed with small incremental doses of either alcuronium (0.03 mg.kg-1), atracurium (0.04 mg.kg-1), pancuronium (0.01 mg.kg-1), d-tubocurarine (0.05 mg.kg-1) or vecuronium (0.01 mg.kg-1) during anaesthesia with thiopentone, fentanyl and nitrous oxide in oxygen. The muscle relaxant was given after recovery from an initial suxamethonium blockade needed for tracheal intubation. The evoked integrated EMG response to supramaximal train-of-four (2 Hz) stimulation was recorded every 20 s. TR % was calculated at different first twitch (T1) levels during the onset of neuromuscular blockade. Significant changes occurred at the 100% and 90% T1 levels, alcuronium having the lowest mean TR values. Atracurium, pancuronium and vecuronium gave similar TR values. Results with d-tubocurarine placed it between alcuronium and the others. These train-of-four ratio results were compared with the ability of non depolarizing muscle relaxants to prevent fasciculations. In conclusion, the stronger the train-of-four fade, the greater was the ability of the relaxant to prevent suxamethonium-induced fasciculations. This supports the theory that the blockade of prejunctional cholinergic receptors is the mechanism of action of precurarization.

摘要

本研究旨在使用四个成串刺激比率(TR)评估非去极化肌松药在神经肌肉阻滞起效期间的接头前效应。将该接头前效应与先前关于这些肌松药预防琥珀胆碱诱发肌束颤动能力的结果进行比较。53例成年患者在硫喷妥钠、芬太尼和氧化亚氮-氧气麻醉期间,用小剂量递增的阿库氯铵(0.03mg·kg-1)、阿曲库铵(0.04mg·kg-1)、泮库溴铵(0.01mg·kg-1)、d-筒箭毒碱(0.05mg·kg-1)或维库溴铵(0.01mg·kg-1)使其肌肉松弛。在气管插管所需的初始琥珀胆碱阻滞恢复后给予肌松药。每20秒记录一次对超强四个成串(2Hz)刺激诱发的复合肌电图反应。在神经肌肉阻滞起效期间,于不同的第一个肌颤搐(T1)水平计算TR%。在T1为100%和90%水平时出现显著变化,阿库氯铵的平均TR值最低。阿曲库铵、泮库溴铵和维库溴铵的TR值相似。d-筒箭毒碱的结果介于阿库氯铵和其他药物之间。将这些四个成串刺激比率结果与非去极化肌松药预防肌束颤动的能力进行比较。总之,四个成串刺激衰减越强,肌松药预防琥珀胆碱诱发肌束颤动的能力就越强。这支持了接头前胆碱能受体阻滞是预箭毒化作用机制的理论。

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