Suppr超能文献

关于较大剂量或重复给予非去极化肌松药后恢复时间延长的药代动力学解释。

A pharmacokinetic explanation for increasing recovery time following larger or repeated doses of nondepolarizing muscle relaxants.

作者信息

Fisher D M, Rosen J I

出版信息

Anesthesiology. 1986 Sep;65(3):286-91.

PMID:2875680
Abstract

The authors used pharmacokinetic and pharmacodynamic modeling to explain the time course of neuromuscular blockade following single or multiple doses of three nondepolarizing muscle relaxants. Published and unpublished pharmacokinetic and pharmacodynamic data for 13 normal subjects were used to simulate the duration of neuromuscular blockade (time from administration of the muscle relaxant to 25% recovery of control twitch tension) following six successive doses of atracurium (150-400 micrograms/kg initially, followed by 100 micrograms/kg), vecuronium, or pancuronium (30-80 micrograms/kg initially, followed by 20 micrograms/kg). With atracurium, duration of action was similar for the second and sixth doses, regardless of the initial dose. With vecuronium (initial doses of 30-80 micrograms/kg) and pancuronium (initial doses of 30-60 micrograms/kg), duration of action was longer after the sixth dose than after the second; with larger initial doses of pancuronium (70 and 80 micrograms/kg), duration of action was similar following the second and sixth doses. The authors also determined two recovery times (time for twitch tension to recover from 5-25% and from 25-75% of control value) for varying single doses of atracurium, vecuronium, or pancuronium. When the dose of atracurium was increased from 200 to 400 micrograms/kg, neither recovery time increased. When the dose of vecuronium was increased from 40 to 80 micrograms/kg, 5-25% recovery time increased from 6.0 +/- 2.5 min to 8.8 +/- 4.0 min (mean +/- SD) and 25-75% recovery time increased from 8.7 +/- 4.3 min to 12.6 +/- 4.4 min.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作者运用药代动力学和药效动力学模型来解释单次或多次给予三种非去极化肌松药后神经肌肉阻滞的时间过程。利用13名正常受试者已发表和未发表的药代动力学和药效动力学数据,模拟了连续六次给予阿曲库铵(初始剂量150 - 400微克/千克,随后为100微克/千克)、维库溴铵或泮库溴铵(初始剂量30 - 80微克/千克,随后为20微克/千克)后神经肌肉阻滞的持续时间(从给予肌松药至对照抽搐张力恢复25%的时间)。对于阿曲库铵,无论初始剂量如何,第二剂和第六剂的作用持续时间相似。对于维库溴铵(初始剂量30 - 80微克/千克)和泮库溴铵(初始剂量30 - 60微克/千克),第六剂后的作用持续时间长于第二剂;对于更大初始剂量的泮库溴铵(70和80微克/千克),第二剂和第六剂后的作用持续时间相似。作者还确定了不同单剂量阿曲库铵、维库溴铵或泮库溴铵的两个恢复时间(抽搐张力从对照值的5% - 25%和25% - 75%恢复所需的时间)。当阿曲库铵剂量从200微克/千克增加到400微克/千克时,两个恢复时间均未增加。当维库溴铵剂量从40微克/千克增加到80微克/千克时,5% - 25%恢复时间从6.0±2.5分钟增加到8.8±4.0分钟(均值±标准差),25% - 75%恢复时间从8.7±4.3分钟增加到12.6±4.4分钟。(摘要截选至250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验