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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Sevoflurane and isoflurane, but not propofol, decrease mivacurium requirements over time : (Le sevoflurane et l'isoflurane, mais pas le propofol, diminuent les besoins en mivacurium avec le temps).
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Sevoflurane and isoflurane, but not propofol, decrease mivacurium requirements over time : (Le sevoflurane et l'isoflurane, mais pas le propofol, diminuent les besoins en mivacurium avec le temps).

机译:七氟醚和异氟烷(但不是丙泊酚)会随着时间的推移降低米曲库铵的需求量:(七氟醚和异氟烷(但不是丙泊酚)会随着时间的推移降低米曲库铵的需求量)。

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PURPOSE: Volatile anesthetic agents potentiate neuromuscular blockade, but the magnitude of potentiation appears to be time dependent. The time course of this interaction was studied by measuring mivacurium infusion rates during sevoflurane, isoflurane and propofol anesthesia. METHODS: After informed consent, anesthesia was induced in 48 ASA physical status I-II adults with propofol, fentanyl and mivacurium 0.25 mg.kg(-1) and maintained with N(2)O (60%) and one of the three agents chosen at random: sevoflurane 1.9%; isoflurane 1.2%; or propofol 100-150 micro g.kg(-1).min(-1). Train-of-four stimulation was applied every 15 sec to the ulnar nerve. Neuromuscular blockade was monitored with accelerometry. At 5% recovery of the first twitch (T1), a mivacurium infusion was started and adjusted every five minutes to maintain 90-95% T1 depression. RESULTS: The time to 5% T1 recovery after the initial dose was similar in all groups (13-15 min). Fifteen minutes after the start of the infusion mivacurium requirements were greater (P < 0.05) in the propofol group (7.5 +/- 1.7 micro g.kg(-1).min(-1); mean +/- SD) than in either isoflurane (4.7 +/- 1.6 micro g.kg(-1).min(-1)) or sevoflurane (4.5 +/- 1.5 micro g.kg(-1).min(-1)) group. Then, the rate remained stable for propofol (6.2 +/- 1.4 micro g.kg(-1).min(-1) after 90 min of infusion) while it decreased with isoflurane to 2.9 +/- 1.6 micro g.kg(-1).min(-1) at 90 min (P < 0.05 vs propofol) and to 1.4 +/- 1.0 micro g.kg(-1).min(-1) in the sevoflurane group (P < 0.05 vs propofol and isoflurane). CONCLUSION: Sevoflurane and isoflurane do not prolong the effect of a bolus dose of mivacurium, but potentiation increases with time from 30-105 min of exposure. This interaction is greater with sevoflurane than isoflurane.
机译:用途:挥发性麻醉药可增强神经肌肉阻滞作用,但增强作用的程度似乎与时间有关。通过在七氟醚,异氟烷和丙泊酚麻醉期间测量米曲库铵输注速率来研究这种相互作用的时间过程。方法:在知情同意后,麻醉的48名ASA身体状态为I-II的成人使用丙泊酚,芬太尼和米伐库铵0.25 mg.kg(-1)进行麻醉,并用N(2)O(60%)和三种药物之一进行维持随机选择:七氟醚1.9%;异氟醚1.2%;或异丙酚100-150 micro g.kg(-1).min(-1)。每15秒对尺神经施加四次刺激。用加速计监测神经肌肉阻滞。第一次抽搐(T1)恢复5%时,开始输注米曲库铵,并每5分钟调整一次,以维持90%至95%的T1压抑。结果:所有组(13-15分钟)在初始剂量后达到5%T1恢复的时间相似。输注开始后十五分钟,丙泊酚组(7.5 +/- 1.7 micro g.kg(-1).min(-1);平均值+/- SD)比丙泊酚组更高(P <0.05)异氟烷(4.7 +/- 1.6 micro g.kg(-1).min(-1))或七氟醚(4.5 +/- 1.5 micro g.kg(-1).min(-1))组。然后,丙泊酚的速率保持稳定(输注90分钟后为6.2 +/- 1.4 micro g.kg(-1).min(-1)),但随着异氟烷的使用而降低至2.9 +/- 1.6 micro g.kg(-1)。在90分钟时-1).min(-1)(P <0.05 vs异丙酚)和七氟醚组中达到1.4 +/- 1.0 micro.g.kg(-1).min(-1)(P <0.05 vs异丙酚和异氟烷)。结论:七氟醚和异氟烷不能延长剂量的米曲库铵的作用,但是在暴露30-105分钟后,增强作用随时间的延长而增加。七氟醚的这种相互作用比异氟烷更大。

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