Meheux Carlos J, McCulloch Patrick C, Lintner David M, Varner Kevin E, Harris Joshua D
Department of Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, Texas, U.S.A.
Department of Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, Texas, U.S.A..
Arthroscopy. 2016 Mar;32(3):495-505. doi: 10.1016/j.arthro.2015.08.005. Epub 2015 Oct 1.
To determine (1) whether platelet-rich plasma (PRP) injection significantly improves validated patient-reported outcomes in patients with symptomatic knee osteoarthritis (OA) at 6 and 12 months postinjection, (2) differences in outcomes between PRP and corticosteroid injections or viscosupplementation or placebo injections at 6 and 12 months postinjection, and (3) similarities and differences in outcomes based on the PRP formulations used in the analyzed studies.
PubMed, Cochrane Central Register of Controlled Trials, SCOPUS, and Sport Discus were searched for English-language, level I evidence, human in vivo studies on the treatment of symptomatic knee OA with intra-articular PRP compared with other options, with a minimum of 6 months of follow-up. A quality assessment of all articles was performed using the Modified Coleman Methodology Score (average, 83.3/100), and outcomes were analyzed using 2-proportion z-tests.
Six articles (739 patients, 817 knees, 39% males, mean age of 59.9 years, with 38 weeks average follow-up) were analyzed. All studies met minimal clinical important difference criteria and showed significant improvements in statistical and clinical outcomes, including pain, physical function, and stiffness, with PRP. All but one study showed significant differences in clinical outcomes between PRP and hyaluronic acid (HA) or PRP and placebo in pain and function. Average pretreatment Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scores were 52.36 and 52.05 for the PRP and HA groups, respectively (P = .420). Mean post-treatment WOMAC scores for PRP were significantly better than for HA at 3 to 6 months (28.5 and 43.4, respectively; P = .0008) and at 6 to 12 months (22.8 and 38.1, respectively; P = .0062). None of the included studies used corticosteroids.
In patients with symptomatic knee OA, PRP injection results in significant clinical improvements up to 12 months postinjection. Clinical outcomes and WOMAC scores are significantly better after PRP versus HA at 3 to 12 months postinjection. There is limited evidence for comparing leukocyte-rich versus leukocyte-poor PRP or PRP versus steroids in this study.
Level I, systematic review of Level I studies.
确定(1)富含血小板血浆(PRP)注射是否能在注射后6个月和12个月显著改善有症状的膝关节骨关节炎(OA)患者经验证的患者报告结局;(2)PRP与皮质类固醇注射、关节腔注射透明质酸钠或安慰剂注射在注射后6个月和12个月的结局差异;(3)基于分析研究中使用的PRP制剂的结局异同。
检索PubMed、Cochrane对照试验中心注册库、SCOPUS和Sport Discus,查找关于关节内注射PRP与其他方法相比治疗有症状膝关节OA的英文、I级证据的人体体内研究,随访时间至少6个月。使用改良科尔曼方法评分对所有文章进行质量评估(平均83.3/100),并使用双比例z检验分析结局。
分析了6篇文章(739例患者,817个膝关节,男性占39%,平均年龄59.9岁,平均随访38周)。所有研究均符合最小临床重要差异标准,且显示PRP能使疼痛、身体功能和僵硬等统计和临床结局显著改善。除一项研究外,所有研究均显示PRP与透明质酸(HA)或PRP与安慰剂在疼痛和功能的临床结局上存在显著差异。PRP组和HA组的平均治疗前西安大略和麦克马斯特大学骨关节炎指数(WOMAC)评分分别为52.36和52.05(P = 0.420)。PRP治疗后的平均WOMAC评分在3至6个月(分别为28.5和43.4;P = 0.0008)以及6至12个月(分别为22.8和38.1;P = 0.0062)时显著优于HA组。纳入的研究均未使用皮质类固醇。
在有症状的膝关节OA患者中,PRP注射在注射后12个月内可带来显著的临床改善。注射后3至12个月,PRP治疗后的临床结局和WOMAC评分显著优于HA组。本研究中比较富白细胞PRP与贫白细胞PRP或PRP与类固醇的证据有限。
I级,I级研究的系统评价。