首页> 外文期刊>The journal of pain: official journal of the American Pain Society >A single-blind, placebo run-in study of duloxetine for activity-limiting osteoarthritis pain.
【24h】

A single-blind, placebo run-in study of duloxetine for activity-limiting osteoarthritis pain.

机译:度洛西汀治疗活动受限的骨关节炎疼痛的单盲,安慰剂试验研究。

获取原文
获取原文并翻译 | 示例
       

摘要

Osteoarthritis pain is a significant problem for our aging population. Antidepressants that are serotonin-norepinephrine reuptake inhibitors are effective for other forms of chronic pain and may provide a new treatment option for osteoarthritis pain. We performed a single-blind, placebo run-in trial of 60 to 90 mg of duloxetine in 25 subjects with activity-limiting osteoarthritis pain. Each subject received 2 weeks of placebo followed by 10 weeks of duloxetine. The primary outcome was reduction in average pain intensity between 2 and 12 weeks for subjects completing the trial. Average pain on the Brief Pain Inventory (BPI) was 5.7 at baseline, 4.8 after the 2-week placebo run-in, and 3.5 at 12 weeks for the 17 patients completing the trial (28% decrease between 2 and 12 weeks, P = .122). Eight of 15 study completers who had nonmissing BPI results (53%) reported at least 30% pain reduction between weeks 2 and 12. The Western Ontario McMaster Osteoarthritis Index (WOMAC) pain score at baseline was 2.3, 1.8 after 2 weeks, and 1.3 after 12 weeks (30% decrease between 2 and 12 weeks, P = .018). Ten of 17 patients (59%) reported at least 30% pain relief between weeks 2 and 12 on the WOMAC. Significant improvements in self-reported physical and role function were reported but observed physical function did not improve. PERSPECTIVE: Duloxetine did not significantly reduce pain intensity on the BPI but did improve pain intensity and self-reported function on the WOMAC. Duloxetine warrants further investigation as a novel treatment for osteoarthritis pain.
机译:骨关节炎疼痛是我们人口老龄化的重要问题。抗抑郁药是5-羟色胺-去甲肾上腺素再摄取抑制剂,对其他形式的慢性疼痛有效,并且可能为骨关节炎疼痛提供新的治疗选择。我们在25名活动受限的骨关节炎疼痛受试者中进行了60至90 mg度洛西汀的单盲安慰剂试验。每个受试者接受2周安慰剂治疗,然后接受10周度洛西汀治疗。主要结果是完成试验的受试者在2至12周之间平均疼痛强度降低。在完成试验的17位患者中,简短疼痛清单(BPI)的平均疼痛在基线时为5.7,在2周安慰剂磨合后为4.8,在12周时为3.5(在2周和12周之间降低了28%,P = .122)。 BPI成绩未丢失的15个研究完成者中有8个(53%)报告说在第2周到第12周之间疼痛减轻至少30%。基线时,西安大略麦克马斯特骨关节炎指数(WOMAC)疼痛评分为2.3、2周后为1.8,而1.3 12周后(在2周和12周之间下降30%,P = .018)。在WOMAC上,第2周到第12周之间,有17位患者中的10位(59%)报告了至少30%的疼痛缓解。据报告自我报告的身体和角色功能有显着改善,但观察到的身体功能并未改善。观点:度洛西汀并未显着降低BPI上的疼痛强度,但确实改善了WOMAC上的疼痛强度和自我报告的功能。度洛西汀值得进一步研究,作为骨关节炎疼痛的新疗法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号