College of Pharmacy, University of Georgia, Athens, Georgia 30602, USA.
Clin Ther. 2009 Dec;31(12):2804-18. doi: 10.1016/j.clinthera.2009.12.003.
Tapentadol hydrochloride is a centrally acting oral analgesic approved by the US Food and Drug Administration in November 2008 for the treatment of moderate to severe acute pain. It is available as immediate-release 50-, 75-, and 100-mg tablets.
The purpose of this article is to review animal studies, pharmacokinetic studies, drug-drug interaction studies, and Phase II/III trials of tapentadol in various conditions producing moderate to severe pain. Efficacy and tolerability data from these studies are summarized.
A search of MEDLINE and International Pharmaceutical Abstracts was conducted from January 2005 through June 30, 2009. Search terms included tapentadol, tapentadol hydrochloride, and (-)-(1R,2R)-3-(3-Dimethylamino-1-ethyl-2-methyl-propyl)-phenol hydrochloride. Relevant information was extracted from the identified articles, and the reference lists of these articles were reviewed for additional pertinent publications. The manufacturer was contacted for clinical trials, abstracts, and poster presentations that were not identified by the literature search. ClinicalTrials.gov was searched to identify recently completed studies.
Tapentadol produces analgesia through a dual mechanism of action: mu-opioid-receptor activation and norepinephrine reuptake inhibition. Its efficacy has been reported in a number of animal studies, as well as in Phase II/III clinical trials. Primary pain disorders in which efficacy has been reported include dental extraction pain, pain after bunionectomy surgery, osteoarthritis pain of the knee and hip, and low back pain. Major adverse effects reported in Phase II/III trials primarily involved the gastrointestinal system (2%-66% of subjects) and the central nervous system (4%-65% of subjects). The occurrence of gastrointestinal adverse effects appeared to be less frequent in tapentadol recipients than in those receiving oxycodone.
Tapentadol appears to be a well-tolerated and effective analgesic for the treatment of moderate to severe acute pain. Although not currently approved for the management of chronic pain, tapentadol has been reported to be effective in managing pain associated with osteoarthritis and low back pain.
盐酸他喷他多是一种中枢作用的口服镇痛药,于 2008 年 11 月获得美国食品和药物管理局批准,用于治疗中重度急性疼痛。它有速释 50mg、75mg 和 100mg 片剂。
本文旨在回顾盐酸他喷他多在各种产生中重度疼痛的情况下的动物研究、药代动力学研究、药物相互作用研究和 II/III 期临床试验。总结了这些研究的疗效和耐受性数据。
从 2005 年 1 月到 2009 年 6 月 30 日,对 MEDLINE 和国际药学文摘进行了检索。检索词包括他喷他多、盐酸他喷他多和(-)-(1R,2R)-3-(3-二甲基氨基-1-乙基-2-甲基-丙基)-苯酚盐酸盐。从确定的文章中提取相关信息,并审查这些文章的参考文献以获取其他相关出版物。联系制造商以获取未通过文献检索识别的临床试验、摘要和海报展示。在 ClinicalTrials.gov 上搜索了最近完成的研究。
盐酸他喷他多通过双重作用机制产生镇痛作用:μ-阿片受体激活和去甲肾上腺素再摄取抑制。它的疗效已在许多动物研究以及 II/III 期临床试验中得到报道。报告疗效的主要原发性疼痛疾病包括拔牙疼痛、拇囊炎手术后疼痛、膝关节炎和髋关节疼痛以及腰痛。II/III 期试验中报告的主要不良反应主要涉及胃肠道系统(2%-66%的受试者)和中枢神经系统(4%-65%的受试者)。与接受羟考酮的受试者相比,接受他喷他多的受试者胃肠道不良反应的发生频率似乎较低。
盐酸他喷他多似乎是一种耐受良好且有效的镇痛药,可用于治疗中重度急性疼痛。尽管目前尚未批准用于治疗慢性疼痛,但报告称他喷他多在治疗骨关节炎和腰痛相关疼痛方面有效。