摘要
右美托咪啶为新型高选择性α2肾上腺素能受体激动剂,它具有剂量依赖性的镇静催眠作用,还具有镇痛、抑制交感活性、无呼吸抑制等药理性质。1999年美国FDA批准将其用于重症监护病房的镇静。在围术期"规定范围之外"的应用表明,右美托咪啶还具有稳定血流动力学、抑制应激反应、减少麻醉剂及阿片类药物的用量和抗寒颤等作用。本文对右美托咪啶的药理学性质以及围术期临床应用进展进行介绍。
Dexmedetomidine is a novel and highly selective a2-adrenoceptor agonist. Dexmedetomidine offers beneficial pharmacological properties, providing dose-dependent sedation, analgesia, sympatholysis and without relevant respiratory depression. Dexmedetomidine was approved for sedation in the intensive care unit in the USA in 1999. The ‘off-label’ use of dexmedetomidine during the perioperative period has proved that it can attenuate hemodynamic responses to anesthesia and surgery, decrease sympathetic tone, reduce anesthetic and opioid requirements and prevent postanesthetic shivering. This review aims to present and discuss the pharmacological properties and perioperative use of dexmedetomidine.
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2007年第6期466-470,共5页
The Chinese Journal of Clinical Pharmacology