Muscle Relaxants 2006: a clinical and basic science update and commentary

Chingmuh Lee MD , Ronald L. Katz MD
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Abstract

As muscle relaxants remain a mainstay of modern anesthesia practice, it behooves the anesthesiologists to keep themselves up-to-date on the theory and clinical practice of neuromuscular pharmacology. Progress continues to be made in the basic and clinical aspects of neuromuscular pharmacology, including mechanism of action, blocking drugs, and reversal agent. The new mechanism of action is based on the molecular shape of the relaxants. Although the so-called “ideal relaxant” is still not in sight, and may never be, the new relaxant AV430A and the new reversal agent Org 25969 hold potential to significantly improve patient care. AV430 has superior clinical profile, although it is still considerably slower and longer in action than succinylcholine. The fast onset of rocuronium combined with its complete and immediate reversibility with Org 25969 may match succinylcholine in onset and offset. Both drugs are undergoing clinical trials.

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肌肉松弛剂2006:临床和基础科学更新和评论
由于肌肉松弛剂仍然是现代麻醉实践的支柱,麻醉师有必要保持自己在神经肌肉药理学的理论和临床实践方面的最新进展。神经肌肉药理学的基础和临床研究不断取得进展,包括作用机制、阻断药物和逆转药物。新的作用机制是基于松弛剂的分子形状。虽然所谓的“理想松弛剂”还没有出现,而且可能永远不会出现,但新的松弛剂AV430A和新的逆转剂Org 25969具有显著改善患者护理的潜力。AV430具有优越的临床表现,尽管它仍然比琥珀酰胆碱慢得多,作用时间更长。罗库溴铵的快速起效及其与Org 25969的完全和立即可逆性可能在起效和偏移上与琥珀胆碱相匹配。这两种药物都在进行临床试验。
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