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七氟醚和静脉麻醉期间米库氯铵阻滞的时间过程和四个成串刺激衰减

Time course and train-of-four fade of mivacurium block during sevoflurane and intravenous anaesthesia.

作者信息

Barrio J, SanMiguel G, Asensio I, Molina I, López F, García V

机构信息

Hospital Arnau de Vilanova, Department of Anaesthesiology, Valencia, Spain.

出版信息

Eur J Anaesthesiol. 2005 Apr;22(4):303-6. doi: 10.1017/s0265021505000517.

Abstract

BACKGROUND AND OBJECTIVE

Volatile anaesthetics inhibit nicotinic acetylcholine receptors at clinically relevant concentrations with higher affinity for the neuronal nicotinic receptor. The inhibitory effects of propofol on nicotinic receptors have only been documented at supraclinical concentrations. The aim of this study was to determine recovery properties and train-of-four (TOF) fade of mivacurium during sevoflurane and propofol anaesthesia, in order to examine any differences both in the enhancement of the neuromuscular block (postjunctional effects) and in TOF fade (prejunctional effects).

METHODS

Twenty ASA I-II adult patients were randomly allocated to maintenance of anaesthesia with sevoflurane (end-tidal concentration 2%) or propofol. Neuromuscular block was assessed by acceleromyography and a single dose of mivacurium (0.15 mg kg(-1)) was administered (in the sevoflurane group after 30 min of exposure to sevoflurane). We measured time for recovery of the first twitch of the TOF (T1) from 25-75%, time from 25% recovery of T1 to achieving a TOF ratio (TOFR) of 0.8, TOFR at 50%, 75% and 90% recovery of T1, and height of T1 at TOFR of 0.7 and 0.9. Data were tested using t-test for independent samples.

RESULTS

Recovery times (mean (95% confidence interval, CI)) of mivacurium in the sevoflurane group (T1 25-75%, 11.3 (8.1-14.5) min; T1 25%-TOFR0.8, 19.1 (15.7-22.5) min) were significantly longer (P < 0.05) than in the propofol group (T1 25-75%, 6.5 (5.2-7.7) min; T1 25%-TOFR0.8, 11.3 (7.8-10.3) min). No differences were found in the relations between TOFR and T1 or vice versa, between the groups.

CONCLUSIONS

Recovery times after a single dose of mivacurium were prolonged by sevoflurane compared with propofol but no differences in TOF fade were observed between the two anaesthetics.

摘要

背景与目的

挥发性麻醉剂在临床相关浓度下可抑制烟碱型乙酰胆碱受体,且对神经元烟碱型受体具有更高的亲和力。丙泊酚对烟碱型受体的抑制作用仅在超临床浓度下有文献记载。本研究旨在确定七氟醚和丙泊酚麻醉期间米库氯铵的恢复特性及四个成串刺激(TOF)衰减情况,以检查在神经肌肉阻滞增强(接头后效应)和TOF衰减(接头前效应)方面是否存在差异。

方法

20例美国麻醉医师协会(ASA)分级为I-II级的成年患者被随机分配接受七氟醚(呼气末浓度2%)或丙泊酚维持麻醉。通过加速度肌电图评估神经肌肉阻滞,并给予单剂量米库氯铵(0.15mg/kg)(七氟醚组在吸入七氟醚30分钟后给药)。我们测量了TOF第一个颤搐(T1)从25%-75%恢复的时间、T1从25%恢复到TOF比值(TOFR)达到0.8的时间、T1恢复50%、75%和90%时的TOFR,以及TOFR为0.7和0.9时T1的高度。数据采用独立样本t检验进行分析。

结果

七氟醚组米库氯铵的恢复时间(平均值(95%置信区间,CI))(T1 25%-75%,11.3(8.1-14.5)分钟;T1 25%-TOFR0.8,19.1(15.7-22.5)分钟)显著长于丙泊酚组(T1 25%-75%,6.5(5.2-7.7)分钟;T1 25%-TOFR0.8,11.3(7.8-10.3)分钟)(P<0.05)。两组之间在TOFR与T1的关系方面未发现差异,反之亦然。

结论

与丙泊酚相比,七氟醚使单剂量米库氯铵后的恢复时间延长,但两种麻醉剂之间在TOF衰减方面未观察到差异。

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