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[非去极化肌松药神经肌肉阻滞起效的药效学分析——大剂量维库溴铵的药效学]

[A pharmacodynamic analysis of the onset of neuromuscular blockade by nondepolarizing muscle relaxants--the pharmacodynamics of a large dose of vecuronium].

作者信息

Yajima C, Sugai N, Hanaoka K, Numata K

机构信息

Department of Anesthesiology, Tokyo University.

出版信息

Masui. 1990 Jan;39(1):2-7.

PMID:1968108
Abstract

From Sheiner's equation on pharmacokinetics and pharmacodynamics, we derived a new equation which described the pharmacodynamics of nondepolarizing muscle relaxants during the onset phase. This equation showed that log (l0/l-1) had a linear relation to log (t) where "t" is the time after the administration of nondepolarizing muscle relaxant and "l" and "l0" are the twitch height at t = t and t = 0 respectively. It also implies that the administration dose (D) is inversely proportional to the onset time (OT), i.e., D.OT = const. We proved that these two relations held well for the actual 7 cases of vecuronium use in man. In conclusion, when vecuronium dose level was within 0.15-0.30 mg.kg-1 i.v., the dose was inversely proportional to the onset time which was defined as the time interval from the end of the administration of vecuronium until the single twitch was depressed under 5% of control value, i.e., Dose (mg.kg-1) x onset-time (sec) not equal to 24. During anesthesia with enflurane as well as during neuroleptanesthesia, a dose of vecuronium 0.3 mg.kg-1 (n = 7) was found to produce a duration of neuromuscular blocking action equal to the mean duration produced by pancuronium 0.1 mg.kg-1.

摘要

从谢纳的药代动力学和药效学方程出发,我们推导了一个新方程,该方程描述了非去极化肌松药起效阶段的药效学。此方程表明,log(l0/l - 1)与log(t)呈线性关系,其中“t”为非去极化肌松药给药后的时间,“l”和“l0”分别为t = t和t = 0时的单刺激颤搐高度。这也意味着给药剂量(D)与起效时间(OT)成反比,即D·OT =常数。我们证明这两个关系在人体实际使用维库溴铵的7个病例中表现良好。总之,当维库溴铵剂量水平在0.15 - 0.30 mg·kg-1静脉注射范围内时,剂量与起效时间成反比,起效时间定义为从维库溴铵给药结束至单刺激颤搐降至对照值的5%以下的时间间隔,即剂量(mg·kg-1)×起效时间(秒)≈24。在使用恩氟烷麻醉以及神经安定麻醉期间,发现0.3 mg·kg-1的维库溴铵剂量(n = 7)产生的神经肌肉阻滞作用持续时间与0.1 mg·kg-1的泮库溴铵产生的平均持续时间相等。

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