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中度至重度慢性疼痛患者使用羟考酮缓释片与纳洛酮联合制剂的长期评估:两项III期试验延长期的汇总分析

Long-term evaluation of combined prolonged-release oxycodone and naloxone in patients with moderate-to-severe chronic pain: pooled analysis of extension phases of two Phase III trials.

作者信息

Blagden M, Hafer J, Duerr H, Hopp M, Bosse B

机构信息

Avondale Surgery, Chesterfield, UK.

出版信息

Neurogastroenterol Motil. 2014 Dec;26(12):1792-801. doi: 10.1111/nmo.12463. Epub 2014 Oct 23.

DOI:10.1111/nmo.12463
PMID:25346155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4265251/
Abstract

BACKGROUND

While opioids provide effective analgesia, opioid-induced constipation (OIC) can severely impact quality of life and treatment compliance. This pooled analysis evaluated the maintenance of efficacy and safety during long-term treatment with combined oxycodone/naloxone prolonged-release tablets (OXN PR) in adults with moderate-to-severe chronic pain.

METHODS

Patients (N = 474) received open-label OXN PR during 52-week extension phases of two studies, having completed 12-week, double-blind, randomized treatment with oxycodone prolonged-release tablets (Oxy PR) or OXN PR. Analgesia and bowel function were assessed at each study visit using 'Average pain over last 24 h scale and Bowel Function Index (BFI), respectively. Treatment Satisfaction Questionnaire for Medication was assessed at study end only.

KEY RESULTS

Improvement in bowel function was particularly marked in patients who switched from Oxy PR in the double-blind phase to OXN PR during the extension phase, resulting in a clinically meaningful reduction (≥12 points) in BFI score: at the start of the extension phases, mean (SD) BFI score was 44.3 (28.13), and was 29.8 (26.36) for patients who had received OXN PR in the double-blind phase. One week later, BFI scores were similar for the two groups (26.5 [24.40] and 27.5 [25.60], respectively), as was observed throughout the following months. Fewer than 10% of patients received laxatives regularly. Mean 24-h pain scores were low and stable throughout the extension phases. No unexpected adverse events were observed.

CONCLUSIONS & INFERENCES: Pooled data demonstrate OXN PR is an effective long-term therapy for patients with chronic non-cancer pain, and can address symptoms of OIC. No new safety issues were observed which were attributable to the long-term administration of OXN PR.

摘要

背景

虽然阿片类药物能提供有效的镇痛效果,但阿片类药物引起的便秘(OIC)会严重影响生活质量和治疗依从性。这项汇总分析评估了中度至重度慢性疼痛成人患者长期使用羟考酮/纳洛酮缓释片(OXN PR)联合治疗期间疗效和安全性的维持情况。

方法

在两项研究的52周延长期中,患者(N = 474)接受了开放标签的OXN PR治疗,他们之前已完成了为期12周的羟考酮缓释片(Oxy PR)或OXN PR双盲随机治疗。每次研究访视时分别使用“过去24小时平均疼痛量表”和“肠功能指数(BFI)”评估镇痛效果和肠道功能。仅在研究结束时评估药物治疗满意度问卷。

主要结果

在延长期从双盲期的Oxy PR转换为OXN PR的患者中,肠道功能改善尤为明显,导致BFI评分出现具有临床意义的降低(≥12分):在延长期开始时,平均(标准差)BFI评分为44.3(28.13),而在双盲期接受OXN PR的患者为29.8(26.36)。一周后,两组的BFI评分相似(分别为26.5 [24.40]和27.5 [25.60]),在接下来的几个月中均如此。定期接受泻药治疗的患者不到10%。在整个延长期,平均24小时疼痛评分较低且稳定。未观察到意外不良事件。

结论与推论

汇总数据表明,OXN PR是慢性非癌性疼痛患者的一种有效的长期治疗方法,并且可以解决OIC的症状。未观察到因长期服用OXN PR而导致的新的安全问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/4918cb33f0f4/nmo0026-1792-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/3c2af3a3c233/nmo0026-1792-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/9871aa5570fd/nmo0026-1792-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/4918cb33f0f4/nmo0026-1792-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/3c2af3a3c233/nmo0026-1792-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/9871aa5570fd/nmo0026-1792-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bb/4265251/4918cb33f0f4/nmo0026-1792-f3.jpg

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Validated in vitro/in vivo correlation of prolonged-release oxycodone/naloxone with differing dissolution rates in relation to gastrointestinal transit times.验证了延长释放羟考酮/纳洛酮与不同溶解速率与胃肠道转运时间的体外/体内相关性。
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Opioid-induced bowel dysfunction: pathophysiology and management.
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