Tzschentke Thomas M, Jahnel Ulrich, Kogel Babette, Christoph Thomas, Englberger Werner, De Vry Jean, Schiene Klaus, Okamoto Akiko, Upmalis David, Weber Horst, Lange Claudia, Stegmann Jens-Ulrich, Kleinert Regina
Grunenthal GmbH, Aachen, Germany.
Drugs Today (Barc). 2009 Jul;45(7):483-96. doi: 10.1358/dot.2009.45.7.1395291.
Tapentadol exerts its analgesic effects through micro opioid receptor agonism and noradrenaline reuptake inhibition in the central nervous system. Preclinical studies demonstrated that tapentadol is effective in a broad range of pain models, including nociceptive, inflammatory, visceral, mono- and polyneuropathic models. Moreover, clinical studies showed that tapentadol effectively relieves moderate to severe pain in various pain care settings. In addition, it was reported to be associated with significantly fewer treatment discontinuations due to a significantly lower incidence of gastrointestinal-related adverse events compared with equivalent doses of oxycodone. The combination of these reduced treatment discontinuation rates and tapentadol efficacy for the relief of moderate to severe nociceptive and neuropathic pain may offer an improvement in pain therapy by increasing patient compliance with their treatment regimen.
曲马多通过中枢神经系统中的微阿片受体激动作用和去甲肾上腺素再摄取抑制发挥其镇痛作用。临床前研究表明,曲马多在广泛的疼痛模型中有效,包括伤害性、炎症性、内脏性、单神经和多神经病变模型。此外,临床研究表明,曲马多在各种疼痛护理环境中均能有效缓解中度至重度疼痛。此外,据报道,与等效剂量的羟考酮相比,由于胃肠道相关不良事件的发生率显著降低,曲马多导致的治疗中断明显减少。这些降低的治疗中断率与曲马多缓解中度至重度伤害性和神经性疼痛的疗效相结合,可能通过提高患者对治疗方案的依从性来改善疼痛治疗。