摘要
背景 麻黄碱作为一种拟交感神经药,可通过增加心输出量加速非去极化肌松药到达神经肌肉接头的速度,进而缩短肌松药的起效时间. 目的 回顾麻黄碱在缩短非去极化肌松药起效时间方面的临床应用进展,为临床麻醉提供参考. 内容 主要对麻黄碱的作用机制、给药剂量、给药时机、副作用等方面予以阐述. 趋向 麻黄碱为临床麻醉中缩短非去极化肌松药的起效时间提供一种实用的方法.
Background Ephedrine,as a kind of sympathomimetic agent,can accelerate the delivery of non-depolarizing muscle relaxant to the neuromuscular junction by increasing cardiac output,thus shortening the onset time of muscle relaxant.Objective To review the advances of ephedrine use in shortening the onset time of non-depolarizing muscle relaxant and provide reference for clinical anesthesia.Content This article mainly elaborates the mechanism of ephedrine on shortening the onset time of non-depolarizing muscle relaxant,dosage,medication timing and adverse reactions.Trend Ephedrine has been proved to provide a practical way for shortening the onset time of non-depolarizing muscle relaxant in clinical anesthesia.
出处
《国际麻醉学与复苏杂志》
CAS
2014年第8期732-734,共3页
International Journal of Anesthesiology and Resuscitation
关键词
麻黄碱
非去极化肌松药
给药剂量
给药时机
起效时间
Ephedrine
Non-depolarizing muscular relaxant
Dosage
Medication occasion
Onset time