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口服羟吗啡酮治疗疼痛的综述。

Review of oral oxymorphone in the management of pain.

机构信息

University of Kentucky Medical Center, Department of Anesthesiology, Lexington, KY, USA.

出版信息

Ther Clin Risk Manag. 2008 Aug;4(4):777-87. doi: 10.2147/tcrm.s1784.

DOI:10.2147/tcrm.s1784
PMID:19209260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2621383/
Abstract

Chronic cancer and nonmalignant pain (CNMP) is a common and major health problem afflicting approximately 40 million persons in the US. Most cancer patients, and many patients with CNMP, require opioid analgesics to obtain adequate pain relief. Oral oxymorphone is a new formulation of an existing parenteral opioid that has become available for the treatment of significant pain: acute postoperative, chronic arthritis, chronic low back, and chronic cancer pain. Oxymorphone is a typical mu-opioid agonist that is effective in both immediate- and extended-release (IR and ER) formulations. Oxymorphone is more lipid soluble than morphine, resulting in a rapid onset of action when given in tablet formulation, with a duration of action of approximately 4-6 hours in IR and 12 hours in ER preparations. Oxymorphone provides excellent pain relief for significant pain, with typical opioid side effects that are usually mild or moderate in intensity. Multiple double-blind, prospective, placebo-controlled clinical trials have demonstrated the clinical efficacy and safety of this new oral opioid preparation. Oral oxymorphone is an effective opioid that provides a new therapeutic option for the physician.

摘要

慢性癌症和非恶性疼痛(CNMP)是一种常见且严重的健康问题,影响了美国约 4000 万人。大多数癌症患者和许多患有 CNMP 的患者需要阿片类镇痛药来获得足够的疼痛缓解。口服羟吗啡酮是一种新的现有注射用阿片类药物的配方,已可用于治疗严重疼痛:急性术后、慢性关节炎、慢性下腰痛和慢性癌症疼痛。羟吗啡酮是一种典型的μ-阿片类激动剂,在即时释放(IR)和延长释放(ER)制剂中均有效。羟吗啡酮比吗啡更具脂溶性,因此在片剂制剂中起效迅速,IR 制剂的作用持续时间约为 4-6 小时,ER 制剂为 12 小时。羟吗啡酮能为严重疼痛提供良好的疼痛缓解,通常具有典型的阿片类药物副作用,其强度通常为轻度或中度。多项双盲、前瞻性、安慰剂对照临床试验已经证明了这种新的口服阿片类药物制剂的临床疗效和安全性。口服羟吗啡酮是一种有效的阿片类药物,为医生提供了一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/37aba7b88fb6/tcrm-4-777f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/e963adf8b60d/tcrm-4-777f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/403c7aa5f351/tcrm-4-777f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/491acbc04efc/tcrm-4-777f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/d029bea514dd/tcrm-4-777f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/98d20b75ba86/tcrm-4-777f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/37aba7b88fb6/tcrm-4-777f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/e963adf8b60d/tcrm-4-777f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/403c7aa5f351/tcrm-4-777f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/491acbc04efc/tcrm-4-777f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/d029bea514dd/tcrm-4-777f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/98d20b75ba86/tcrm-4-777f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e836/2621383/37aba7b88fb6/tcrm-4-777f6.jpg

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