Abel M, Book W J, Eisenkraft J B
Department of Anesthesiology, Mount Sinai Medical Center, New York, New York.
Drug Saf. 1994 Jun;10(6):420-38. doi: 10.2165/00002018-199410060-00002.
Nondepolarising muscle relaxants block neuromuscular transmission, acting as antagonists of the nicotinic receptors at the neuromuscular junction. Their undesired effects are frequently caused by interaction with acetylcholine receptors outside this junction, and autonomic cardiovascular effects may result. Other adverse effects include anaphylactic or anaphylactoid reactions, and histamine release. Various disease states may present specific considerations in the use of nondepolarising muscle relaxants. Although many complications of these drugs (such as prolonged block or resistance) are easily treated, others may necessitate immediate intervention and vigorous therapy. Careful selection of an appropriate relaxant for a particular patient will usually prevent the occurrence of complications.
非去极化型肌松药可阻断神经肌肉传递,作为神经肌肉接头处烟碱样受体的拮抗剂发挥作用。其不良反应常由与该接头外的乙酰胆碱受体相互作用引起,可能导致自主心血管效应。其他不良反应包括过敏或类过敏反应以及组胺释放。在使用非去极化型肌松药时,各种疾病状态可能需要特殊考虑。尽管这些药物的许多并发症(如阻滞延长或耐药)易于治疗,但其他一些并发症可能需要立即干预和积极治疗。为特定患者精心选择合适的肌松药通常可预防并发症的发生。