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关节内多核苷酸治疗膝骨关节炎的疗效:一项随机、双盲临床试验。

Efficacy of intra-articular polynucleotides in the treatment of knee osteoarthritis: a randomized, double-blind clinical trial.

机构信息

IRCCS Foundation, Orthopaedic and Traumatology Department, S. Matteo Hospital Institute, University of Pavia, Pavia, Italy.

出版信息

Knee Surg Sports Traumatol Arthrosc. 2010 Jul;18(7):901-7. doi: 10.1007/s00167-009-1039-y. Epub 2010 Jan 29.

Abstract

This randomized, double-blind clinical trial was conducted over 16 weeks to assess the efficacy and safety profile of intra-articular polynucleotides gel injections in the treatment of knee osteoarthritis associated with persistent knee pain. 60 patients were enrolled and randomized to receive intra-articular polynucleotides (n = 30) or hyaluronan (n = 30); patients received five weekly intra-articular knee injections and the follow-up period was 3 months after the end of treatment. Primary endpoint was to determine polynucleotides (PN) efficacy in reducing knee pain at the end of the study, over baseline value and over standard hyaluronan viscosupplementation (HA). Pain levels were measured using a 0-10 cm Visual Analogue Scale (VAS). Secondary endpoints included Knee Osteoarthritis Outcome Score (KOOS), NSAIDs consumption, crackling during movement and articular mobility limitation. The mean global VAS pain decreased from 5.7 + or - 1.9 cm (T0) to 1.9 + or - 1.5 cm (T16) in polynucleotide group and from 4.9 + or - 2.0 cm (T0) to 2.1 + or - 1.4 cm (T16) in hyaluronan group. The reduction in pain was statistically significant for both groups. KOOS increases from baseline values were statistically significant in both groups. No significant adverse events were reported. These findings suggest that intra-articular polynucleotides can be a valid alternative to traditional hyaluronan supplementation for the treatment of knee osteoarthritis.

摘要

这项随机、双盲临床试验持续了 16 周,旨在评估关节内多核苷酸凝胶注射治疗持续性膝关节疼痛相关膝骨关节炎的疗效和安全性。共纳入 60 例患者并随机分为关节内多核苷酸(n = 30)或透明质酸(n = 30)组;患者接受每周 5 次膝关节腔内注射,治疗结束后随访 3 个月。主要终点是确定多核苷酸(PN)在研究结束时、与基线值和标准透明质酸粘弹性补充剂(HA)相比,降低膝关节疼痛的疗效。疼痛程度采用 0-10cm 视觉模拟量表(VAS)进行评估。次要终点包括膝关节骨关节炎结局评分(KOOS)、非甾体抗炎药(NSAIDs)消耗量、运动时的噼啪声和关节活动受限。多核苷酸组的平均总体 VAS 疼痛从 5.7±1.9cm(T0)降至 1.9±1.5cm(T16),透明质酸组从 4.9±2.0cm(T0)降至 2.1±1.4cm(T16)。两组疼痛减轻均具有统计学意义。两组的 KOOS 均较基线值显著增加。未报告明显的不良事件。这些发现表明,关节内多核苷酸可能是传统透明质酸补充剂治疗膝骨关节炎的有效替代方法。

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