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羟考酮/纳洛酮缓释片:在缓解阿片类药物引起的便秘的同时用于治疗慢性疼痛的用途介绍。

Oxycodone/Naloxone prolonged-release: a review of its use in the management of chronic pain while counteracting opioid-induced constipation.

机构信息

Adis, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, North Shore 0754, Auckland, New Zealand,

出版信息

Drugs. 2014 Mar;74(3):353-75. doi: 10.1007/s40265-014-0177-9.

Abstract

A combination of prolonged-release (PR) oxycodone with PR naloxone (Targin(®), Targiniq(®), Targinact(®)) in one tablet with a fixed 2:1 ratio is available for the treatment of patients with severe pain, which can only be adequately managed with opioid analgesics. The aim of this formulation is to counteract opioid-induced constipation through the local antagonist effect of naloxone in the gut wall, while maintaining analgesia due to the low bioavailability of oral naloxone. Three large, 12-week, randomized, double-blind, phase III trials in patients with moderate to severe, chronic, non-malignant pain, plus a prospectively planned pooled analysis of two of these studies, demonstrated that oxycodone/naloxone PR improved bowel function, as measured by the bowel function index, compared with oxycodone PR. Additionally, oxycodone/naloxone PR relieved pain more effectively than placebo and no less effectively than oxycodone PR after 12 weeks. Phase II efficacy data in cancer patients are consistent with those observed in patients with non-malignant pain. Oxycodone/naloxone PR was generally well tolerated; the most frequently reported adverse events were of gastrointestinal origin, consistent with those known to occur with opioid therapy. Of note, numerically lower rates of constipation were observed in the oxycodone/naloxone PR group compared with the oxycodone PR group. A cost-utility analysis predicted that oxycodone/naloxone PR would be a cost-effective option compared with oxycodone PR in patients with non-malignant pain. Although more comparative data are needed, oxycodone/naloxone PR is an effective option for use in patients with severe chronic pain, particularly among those with opioid-induced constipation.

摘要

一种将延长释放(PR)羟考酮与 PR 纳洛酮(Targin(®)、Targiniq(®)、Targinact(®))组合在一片固定 2:1 比例的片剂中,可用于治疗需要阿片类镇痛药才能充分控制的严重疼痛患者。这种配方的目的是通过纳洛酮在肠壁上的局部拮抗剂作用来对抗阿片类药物引起的便秘,同时由于口服纳洛酮的生物利用度低而保持镇痛作用。三项为期 12 周、随机、双盲、III 期临床试验,评估了中度至重度、慢性、非恶性疼痛患者,加上两项研究中的两项前瞻性计划的汇总分析,表明与 PR 羟考酮相比,PR 羟考酮/纳洛酮改善了肠道功能,以肠道功能指数衡量。此外,与安慰剂相比,PR 羟考酮/纳洛酮 PR 在 12 周后更有效地缓解疼痛,与 PR 羟考酮一样有效。在癌症患者中的 II 期疗效数据与非恶性疼痛患者观察到的数据一致。PR 羟考酮/纳洛酮通常具有良好的耐受性;最常报告的不良事件是胃肠道来源的,与阿片类药物治疗已知的不良事件一致。值得注意的是,与 PR 羟考酮组相比,PR 羟考酮/纳洛酮组观察到便秘的发生率较低。成本效益分析预测,与 PR 羟考酮相比,PR 羟考酮/纳洛酮在非恶性疼痛患者中是一种具有成本效益的选择。尽管需要更多的比较数据,但 PR 羟考酮/纳洛酮是严重慢性疼痛患者的有效选择,特别是在那些有阿片类药物引起的便秘的患者中。

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