Polyacrylamide Hydrogel Injection for Knee Osteoarthritis: A 6 Months Prospective Study

H. Bliddal, A. Overgaard, A. Hartkopp, J. Beier, P. Conaghan, M. Henriksen
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引用次数: 5

Abstract

Objective: Intra-Articular (IA) injection of polyacrylamide hydrogel (PAAG) is a possible treatment for symptomatic Osteoarthritis (OA) of the knee. This study evaluated the efficacy and safety of a single injection of 6 ml intra-articular PAAG over 26 weeks. Methods: Open-label study in patients with symptomatic and radiographically confirmed knee OA . Primary outcome was change in WOMAC pain after 13 weeks. Secondary outcomes were WOMAC stiffness and function subscales, Patient Global Assessment of disease impact (PGA) and proportion of OMERACT-OARSI responders. Follow-up time points were 4, 13 and 26 weeks. Results: 49 patients (31 females) received PAAG, with 48 patients completing the 13 and 46 the 26 weeks assessments. Mean change in WOMAC pain after 13 weeks was -18.3 points [95% CI-23.4 to -13.3]; P<.0001 and at 26 weeks -20.8 points [95% CI -26.3 to -15.3]; P<0.0001 with similar benefits for WOMAC stiffness, physical function, and PGA. After 13 weeks 64.6% were OMERACT-OARSI responders and this was maintained at 26 weeks.. During the 13 weeks, 18 patients reported 23 adverse events, 13 of which were related to PAAG, none severe. Two serious adverse events, atrial fibrillation and gastrointestinal pain, were assessed as ‘not related’ to PAAG. Conclusions: PAAG can be delivered in a single 6 ml injection and this non-randomized trial in patients with knee OA demon-strated beneficial clinical effects at 13 and 26 weeks. No serious adverse events were seen with PAAG. These encouraging results need to be confirmed in controlled studies.
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聚丙烯酰胺水凝胶注射治疗膝骨关节炎:6个月的前瞻性研究
目的:聚丙烯酰胺水凝胶(PAAG)关节内注射是治疗膝关节症状性骨关节炎(OA)的一种可能方法。本研究评估了单次注射6ml关节内PAAG 26周的疗效和安全性。方法:对有症状和影像学证实的膝关节OA患者进行开放标签研究。主要结局是13周后WOMAC疼痛的改变。次要结局是WOMAC僵硬和功能亚量表、患者疾病影响总体评估(PGA)和OMERACT-OARSI应答者的比例。随访时间分别为4周、13周和26周。结果:49例患者(31名女性)接受了PAAG治疗,其中48例完成了13周评估,46例完成了26周评估。13周后WOMAC疼痛的平均变化为-18.3点[95% CI-23.4至-13.3];P <。0001和26周时-20.8点[95% CI -26.3至-15.3];P<0.0001,在WOMAC刚度、物理功能和PGA方面具有相似的益处。13周后,64.6%的患者对OMERACT-OARSI有反应,这一数据在26周时保持不变。在13周内,18例患者报告了23例不良事件,其中13例与PAAG相关,无严重事件。心房颤动和胃肠道疼痛这两个严重不良事件被评估为与PAAG“无关”。结论:PAAG可以通过单次6ml注射给药,这项针对膝关节OA患者的非随机试验在13周和26周时显示出有益的临床效果。PAAG未见严重不良事件。这些令人鼓舞的结果需要在对照研究中得到证实。
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