Morphine-6-glucuronide (M6G) for postoperative pain relief

被引:36
作者
Dahan, Albert [1 ]
van Dorp, Eveline [1 ]
Smith, Terry [2 ]
Yassen, Ashraf [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Anesthesiol, NL-2300 RC Leiden, Netherlands
[2] CeNeS Ltd, Cambridge CB24 9ZR, England
关键词
pain; opioid; morphine; endogenous morphine-6-glucuronide; PCA; respiratory depression; metabolism; PK/PD modeling; blood-brain barrier;
D O I
10.1016/j.ejpain.2007.07.009
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Morphine-6-glucuronide (M6G) is morphine's active metabolite acting at the mu-opioid receptor. Recent experimental human studies and 5 of 6 randomized clinical trials indicate that M6G causes adequate and long lasting pain relief comparable to morphine. There are various observations that M6G is associated with a reduction in the severity of side effects normally associated with opioid use, such as reduced postoperative nausea and vomiting (PONV) and reduced respiratory depression. The present drug profile provides a review of the pharmacological properties of M6G, the clinical evidence relating to its efficacy and safety, and discusses its future role in the treatment of postoperative pain. (C) 2007 European Federation of Chapters of the International Association for the Study of Pain. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:403 / 411
页数:9
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