Clinica Ortopedica e Traumatologica 2, IRCCS Istituto Ortopedico Rizzoli, Via Di Barbiano, 1/10, 40136, Bologna, Italy.
Clinica Mediterranea, Via Orazio 2, 80122, Napoli, Italy.
Knee Surg Sports Traumatol Arthrosc. 2022 Dec;30(12):3958-3967. doi: 10.1007/s00167-021-06793-4. Epub 2021 Nov 12.
The purpose of this double-blind randomized controlled trial (RCT) was to compare clinical improvement and radiographic findings up to 2 years of follow-up of a single intra-articular injection of bone marrow aspirate concentrate (BMAC) versus hyaluronic acid (HA) for the treatment of knee osteoarthritis (OA). The hypothesis was that BMAC injection could lead to better clinical and radiographic results compared to viscosupplementation.
Patients with bilateral knee OA were randomized to one intra-articular injection of tibial-derived BMAC in one knee and one HA injection in the contralateral knee. Sixty patients were enrolled, and 56 were studied up to the final follow-up (35 men, 21 women, mean age 57.8 ± 8.9 years), for a total of 112 knees. Patients were evaluated before the injection and at 1, 3, 6, 12, and 24 months with the IKDC subjective score, VAS for pain, and the KOOS score. Minimal clinically important difference (MCID), patient treatment judgement, and adverse events were documented, as well as bilateral X-Rays (Rosenberg view) before and after treatment.
No severe adverse events nor differences were reported in terms of mild adverse events (7.1% vs 5.4%, p = ns) and treatment failures (10.7% vs 12.5%, p = ns) in BMAC and HA groups, respectively. The IKDC subjective score improved from baseline to all follow-ups for BMAC (p < 0.0005), while it improved up to 12 months (p < 0.0005) and then decreased at 24 months (p = 0.030) for HA. Compared to HA, BMAC showed a higher improvement for VAS pain at 12 (2.2 ± 2.6 vs 1.7 ± 2.5, p = 0.041) and 24 months (2.2 ± 2.6 vs 1.4 ± 2.8, p = 0.002). The analysis based on OA severity confirmed this difference only in Kellgren-Lawrence 1-2 knees, while comparable results were observed in moderate/severe OA. Radiographic evaluation did not show knee OA deterioration for both treatment groups, without intergroup differences.
BMAC did not demonstrate a clinically significant superiority at short-term compared to viscosupplementation, reporting overall comparable results in terms of clinical scores, failures, adverse events, radiographic evaluation, MCID achievement, and patient treatment judgment. However, while HA results decreased over time, BMAC presented more durable results in mild OA knees.
Level I.
本双盲随机对照试验(RCT)的目的是比较单次关节内注射骨髓抽吸浓缩物(BMAC)与透明质酸(HA)治疗膝关节骨关节炎(OA)的临床改善和影像学结果,随访时间长达 2 年。假设 BMAC 注射可能比滑液补充剂带来更好的临床和影像学结果。
将双侧膝 OA 患者随机分为膝关节内注射胫骨源性 BMAC 与对侧膝关节内注射 HA。共纳入 60 例患者,56 例患者完成了最终随访(35 例男性,21 例女性,平均年龄 57.8±8.9 岁),共 112 膝。患者在注射前和 1、3、6、12 和 24 个月时接受 IKDC 主观评分、疼痛 VAS 和 KOOS 评分评估。记录了最小临床重要差异(MCID)、患者治疗判断和不良事件,以及治疗前后的双侧 X 射线(Rosenberg 视图)。
在 BMAC 和 HA 组中,均未报告严重不良事件,且轻度不良事件(7.1%比 5.4%,p=0.12)和治疗失败(10.7%比 12.5%,p=0.43)也无差异。与 HA 相比,BMAC 的 IKDC 主观评分从基线到所有随访时间均有改善(p<0.0005),而在 12 个月时(p<0.0005)改善,然后在 24 个月时(p=0.030)下降。与 HA 相比,BMAC 在 12 个月(2.2±2.6 比 1.7±2.5,p=0.041)和 24 个月(2.2±2.6 比 1.4±2.8,p=0.002)时的 VAS 疼痛改善更显著。基于 OA 严重程度的分析仅在 Kellgren-Lawrence 1-2 级膝关节中证实了这一差异,而在中重度 OA 中观察到了类似的结果。影像学评估显示两组均未出现膝 OA 恶化,且无组间差异。
与滑液补充剂相比,BMAC 在短期并未表现出明显的临床优势,在临床评分、失败、不良事件、影像学评估、MCID 获得和患者治疗判断方面报告了总体相当的结果。然而,尽管 HA 的结果随时间下降,BMAC 在轻度 OA 膝关节中表现出更持久的结果。
I 级。