Buprenorphine: Considerations for pain management

被引:197
作者
Johnson, RE
Fudala, PJ
Payne, R
机构
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Behav Pharmacol Res Unit, Baltimore, MD 21205 USA
[2] Univ Penn, Sch Med, VA Med Ctr, Dept Psychiat, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, VA Med Ctr, Behav Hlth Serv, Philadelphia, PA 19104 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Neurol, New York, NY 10021 USA
关键词
buprenorphine; pharmacology; pharmacodynamics; pharmacokinetics; pain management; partial agonists; formulations; opioids;
D O I
10.1016/j.jpainsymman.2004.07.005
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
New effective analgesics are needed for the treatment of pain. Buprenorphine, a partial muopioid agonist which has been in clinical use for over 25 years, has been found to be amenable to new formulation technology based on its physiochemical and pharmacological profile. Buprenorphine is marketed as parenteral, sublingual, and transdermal formulations. Unlike full mu-opioid agonists, at higher doses, buprenorphine's physiological and subjective effects, including euphoria, reach a plateau. This ceiling may limit the abuse potential and may result in a wider safety margin. Buprenorphine has been used for the treatment of acute and chronic pain, as a supplement to anesthesia, and for behavioral and psychiatric disorders including treatment for opioid addiction. Prolonged use of buprenorphine can result in physical dependence. However, withdrawal symptoms appear to be mild to moderate in intensity compared with those of full mu agonists. Overdoses have primarily involved buprenorphine taken in combination with other central nervous system depressants. (c) 2005 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:297 / 326
页数:30
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