University of Belgrade School of Medicine, Institute of Rheumatology, Belgrade, Serbia.
Institute of Rheumatology, Belgrade, Serbia.
J Int Med Res. 2023 Oct;51(10):3000605231203851. doi: 10.1177/03000605231203851.
This study was performed to assess the impact of autologous conditioned serum (ACS) when added to preceding intra-articular glucocorticoid therapy on pain, function, and quality of life outcomes over 24 weeks.
In this single-center, randomized controlled trial involving 40 patients with advanced knee osteoarthritis (Kellgren-Lawrence grades III and IV), ACS or saline placebo was injected after 40 mg triamcinolone acetonide (TA) intra-articular injection. Numerical rating scale (NRS) pain scores and Knee Injury and Osteoarthritis Outcome Score (KOOS) assessments were conducted at baseline and at weeks 3, 6, 12, and 24. The primary endpoint was the change in KOOS Pain at 24 weeks. Patient safety events were also monitored.
At week 24, TA + ACS significantly improved KOOS Pain, Symptoms, Activities of Daily Living, Quality of Life, and KOOS Sport scores. TA + ACS also outperformed TA + placebo in NRS pain scores (average and maximum intensity) at week 24 and NRS pain score (at rest) at weeks 12 and 24. The TA injection followed by ACS or placebo was well-tolerated.
ACS adds long-term pain relief and functional improvement to the short-term pain relief provided by glucocorticoids.
本研究旨在评估在先前关节内糖皮质激素治疗中加入自体条件血清(ACS)对 24 周内疼痛、功能和生活质量结果的影响。
在这项涉及 40 例晚期膝关节骨关节炎(Kellgren-Lawrence 分级 III 和 IV 级)患者的单中心随机对照试验中,在 40mg 曲安奈德(TA)关节内注射后,注射 ACS 或盐水安慰剂。在基线和第 3、6、12 和 24 周时进行数字评分量表(NRS)疼痛评分和膝关节损伤和骨关节炎结果评分(KOOS)评估。主要终点是 24 周时 KOOS 疼痛的变化。还监测了患者安全事件。
在第 24 周时,TA+ACS 显著改善了 KOOS 疼痛、症状、日常生活活动、生活质量和 KOOS 运动评分。与 TA+安慰剂相比,在第 24 周时,TA+ACS 还改善了 NRS 疼痛评分(平均和最大强度)和第 12 和 24 周时的 NRS 疼痛评分(休息时)。TA 注射后加 ACS 或安慰剂耐受性良好。
ACS 为糖皮质激素提供的短期疼痛缓解提供了长期的疼痛缓解和功能改善。