维库溴铵快速序列诱导和气管插管-有或没有启动剂量。

W J Cheng, Y L Wong, Y L Hui, Y W Wu, P P Tan
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引用次数: 0

摘要

本研究的目的是确定在快速序列诱导和气管插管中使用维库溴铵作为肌肉松弛剂时,事先给予小剂量、亚麻痹剂量的非去极化肌肉松弛剂维库溴铵是否比单次大剂量维库溴铵有更好的插管条件。本研究分为6组,每组15例患者(ASA I级或II级)。芬太尼2 ~ 3 mg/kg,硫喷妥4 ~ 5 mg/kg麻醉。1、2、3组均给予相同的起始剂量,均为0.1 mg/kg。4 min后,各组给予不同剂量的维库溴铵:0.09 mg/kg (Gp1)、0.14 mg/kg (Gp2)、0.19 mg/kg (Gp3)。4、5、6组不给维库溴铵起药,各组插管剂量分别为:0.1 mg/kg (Gp4)、0.15 mg/kg (Gp5)、0.2 mg/kg (Gp6)。60秒结束时,1组、2组、3组、4组、5组、6组插管情况优优者的比例分别为46.6%、66.6%、86.6%、20%、40%、80%。1、2、3、4、5、6组插管情况良好者分别为46.6%、33.4%、13.4%、46.6%、53.2%、20%。1组插管不良率6.8%,4组33.4%,5组6.8%,2、3、6组0%。所有接受启动剂量的患者都能维持头部抬起5秒,并且在启动剂量后3分钟没有出现任何呼吸不适。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid sequence induction and tracheal intubation with vecuronium--with or without a priming dose.

The purpose of this study was to determine whether prior administration of a small, sub-paralytic dose of nondepolarizing muscle relaxant, vecuronium, would have a better intubating condition than a single bolus dose when vecuronium was used as the muscle relaxant during rapid sequence induction and tracheal intubation. Six groups of 15 patients each (ASA class I or II) were involved in this study. Anesthesia was induced with fentanyl 2-3 micrograms/kg and thiopental 4-5 mg/kg. In group 1, 2 and 3, the patients were given the same priming dose of 0.1 mg/kg. Four min later, different doses of vecuronium were given to each group: 0.09 mg/kg (Gp1), 0.14 mg/kg (Gp2), and 0.19 mg/kg (Gp3). In group 4, 5 and 6, no priming vecuronium was given and the intubating doses given to each group were as follow: 0.1 mg/kg (Gp4), 0.15 mg/kg (Gp5) and 0.2 mg/kg (Gp6). At the end of a 60 sec, the percentage of patient with excellent intubating condition were 46.6%, 66.6%, 86.6%, 20%, 40% and 80% respectively for group 1, 2, 3, 4, 5 and 6 respectively. The percentage with good intubating condition were 46.6%, 33.4%, 13.4%, 46.6%, 53.2%, and 20% for group 1, 2, 3, 4, 5 and 6 respectively. The percentage of poor intubating condition were 6.8% in group 1, 33.4% in group 4, 6.8% in group 5 and 0% in group 2, 3, 6. All patients receiving a priming dose could sustain head lift for 5 sec and did not complain any respiratory discomfort 3 min after the priming dose.(ABSTRACT TRUNCATED AT 250 WORDS)

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