Unidad Cirugía Artroscópica (USP Clínica la Esperanza), Vitoria, Spain.
Arthroscopy. 2012 Aug;28(8):1070-8. doi: 10.1016/j.arthro.2012.05.011.
This multicenter, double-blind clinical trial evaluated and compared the efficacy and safety of PRGF-Endoret (BTI Biotechnology Institute, Vitoria-Gasteiz, Spain), an autologous biological therapy for regenerative purposes, versus hyaluronic acid (HA) as a short-term treatment for knee pain from osteoarthritis.
We randomly assigned 176 patients with symptomatic knee osteoarthritis to receive infiltrations with PRGF-Endoret or with HA (3 injections on a weekly basis). The primary outcome measure was a 50% decrease in knee pain from baseline to week 24. As secondary outcomes, we also assessed pain, stiffness, and physical function using the Western Ontario and McMaster Universities Osteoarthritis Index; the rate of response using the criteria of the Outcome Measures for Rheumatology Committee and Osteoarthritis Research Society International Standing Committee for Clinical Trials Response Criteria Initiative (OMERACT-OARSI); and safety.
The mean age of the patients was 59.8 years, and 52% were women. Compared with the rate of response to HA, the rate of response to PRGF-Endoret was 14.1 percentage points higher (95% confidence interval, 0.5 to 27.6; P = .044). Regarding the secondary outcome measures, the rate of response to PRGF-Endoret was higher in all cases, although no significant differences were reached. Adverse events were mild and evenly distributed between the groups.
Plasma rich in growth factors showed superior short-term results when compared with HA in a randomized controlled trial, with a comparable safety profile, in alleviating symptoms of mild to moderate osteoarthritis of the knee.
Level I, randomized controlled multicenter trial.
本多中心、双盲临床试验评估并比较了富血小板纤维蛋白(PRGF-Endoret)(西班牙维多利亚-加斯泰兹的 BTI 生物技术研究所)与透明质酸(HA)作为膝骨关节炎短期治疗方法的疗效和安全性。
我们将 176 例有症状的膝骨关节炎患者随机分为两组,分别接受 PRGF-Endoret 或 HA 浸润治疗(每周 3 次注射)。主要终点是自基线至第 24 周时膝关节疼痛缓解 50%。次要终点包括使用 Western Ontario and McMaster Universities Osteoarthritis Index 评估疼痛、僵硬和身体功能;使用 OMERACT-OARSI 标准评估反应率;以及安全性。
患者的平均年龄为 59.8 岁,52%为女性。与 HA 的反应率相比,PRGF-Endoret 的反应率高 14.1 个百分点(95%置信区间,0.5 至 27.6;P =.044)。在次要结局方面,PRGF-Endoret 的反应率在所有情况下均更高,但未达到显著差异。不良反应轻微且两组分布均匀。
在随机对照试验中,富含生长因子的血浆在缓解轻至中度膝骨关节炎症状方面的短期疗效优于 HA,且安全性相当。
I 级,随机对照多中心试验。