Tramadol Extended-Release for the Management of Pain due to Osteoarthritis.

ISRN Pain Pub Date : 2013-09-04 eCollection Date: 2013-01-01 DOI:10.1155/2013/245346
Chiara Angeletti, Cristiana Guetti, Antonella Paladini, Giustino Varrassi
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引用次数: 15

Abstract

Current knowledge on pathogenesis of osteoarticular pain, as well as the consequent several, especially on the gastrointestinal, renal, and cardiovascular systems, side effects of NSAIDs, makes it difficult to perform an optimal management of this mixed typology of pain. This is especially observable in elderly patients, the most frequently affected by osteoarthritis (OA). Tramadol is an analgesic drug, the action of which has a twofold action. It has a weak affinity to mu opioid receptors and, at the same time, can result in inhibition of the reuptake of noradrenaline and serotonin in nociceptorial descending inhibitory control system. These two mechanisms, "opioidergic" and "nonopioidergic," are the grounds for contrasting certain types of pain that are generally less responsive to opioids, such as neuropathic pain or mixed OA pain. The extended-release formulation of tramadol has good efficacy and tolerability and acts through a dosing schedule that allows a high level of patients compliance to therapies with a good recovery outcome for the patients' functional status.

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曲马多缓释治疗骨关节炎所致疼痛。
目前关于骨关节疼痛的发病机制,以及随之而来的一些非甾体抗炎药的副作用,特别是胃肠道、肾脏和心血管系统的副作用,使得很难对这种混合类型的疼痛进行最佳管理。这在最常受骨关节炎(OA)影响的老年患者中尤其明显。曲马多是一种镇痛药,其作用有双重作用。它对mu阿片受体有弱亲和力,同时在伤害感觉下降抑制控制系统中抑制去甲肾上腺素和血清素的再摄取。这两种机制,“阿片类能”和“非阿片类能”,是对比某些类型的疼痛的基础,这些疼痛通常对阿片类药物反应较弱,如神经性疼痛或混合性OA疼痛。曲马多缓释制剂具有良好的疗效和耐受性,其给药方案使患者对治疗的依从性较高,患者的功能状态恢复效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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