Cheeva-Akrapan Vorasilp, Turajane Thana
Biotechnological Research and Development Center, Police General Hospital, Bangkok, THA.
Cureus. 2023 Mar 1;15(3):e35632. doi: 10.7759/cureus.35632. eCollection 2023 Mar.
Knee osteoarthritis (KOA) is a musculoskeletal disease that leads to pain, stiffness, and deformity of the load-bearing knee joints. Biologic products including platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) are now in the spotlight for the treatment of KOA owing to their role of disease-modifying potential effect. There are still limited studies on the survival rate of KOA treated with biological intervention. We conducted this study to evaluate the primary outcome as the survival rate of KOA treated with PRP enhanced with injectable PRF that helps avoid unnecessary surgical intervention.
There were 368 participants who met the inclusion and exclusion criteria. Participants were informed about this prospective cohort study protocol and signed written consent forms. Each participant received one injection of 4 ml of PRP and 4 ml of injectable PRF (iPRF), the so-called "PRP enhanced with iPRF". Clinical assessment was evaluated with the visual analog scale (VAS) at the second, fourth, sixth, 12th, 18th, 24th, 30th, and 36th-month post-treatment. If the VAS pain score improved by more than 80% compared to the previous treatment, there was no need for a repeated dose. If the pain scores improved by 50% to 80% compared to the previous treatment, the participants were advised a repeated dose. However, if the pain scores improved by less than 50% compared to the previous treatment, the participants were advised to undergo surgical intervention instead of a repeated dose. The primary outcome was recorded as any surgical treatment (either arthroscopic knee surgery, unicondylar arthroplasty, or total knee arthroplasty) at any time point post-treatment. The secondary outcome was recorded as the interval (months) between first-to-second, second-to-third, and third-to-fourth injections.
The overall survival rate of knees that did not require surgical intervention during the 36-month follow-up was 80.18%. The mean number of injections was 2.52±0.07 times for overall participants. The mean interval time was 5.42±0.36, 8.92±0.47, and 9.58±0.55 months for the first-to-second, second-to-third, and third-to-fourth injections.
This study supports the usage of PRP enhanced with iPRF as a biologic modality for the treatment of KOA. This treatment modality provides a satisfactory survival rate at the 36-month follow-up. The longer interval between each injection supports the disease-modifying effect of PRP enhanced with iPRF.
膝关节骨关节炎(KOA)是一种肌肉骨骼疾病,会导致负重膝关节疼痛、僵硬和畸形。包括富血小板血浆(PRP)和富血小板纤维蛋白(PRF)在内的生物制品,因其具有疾病修饰潜在作用,目前在KOA治疗中备受关注。关于生物干预治疗KOA的生存率研究仍然有限。我们开展本研究以评估主要结局,即使用可注射PRF增强的PRP治疗KOA的生存率,这有助于避免不必要的手术干预。
368名参与者符合纳入和排除标准。向参与者告知了这项前瞻性队列研究方案,并签署了书面知情同意书。每位参与者接受一次4毫升PRP和4毫升可注射PRF(iPRF)的注射,即所谓的“iPRF增强的PRP”。在治疗后的第2、4、6、12、18、24、30和36个月,使用视觉模拟量表(VAS)进行临床评估。如果VAS疼痛评分较前一次治疗改善超过80%,则无需重复给药。如果疼痛评分较前一次治疗改善50%至80%,则建议参与者重复给药。然而,如果疼痛评分较前一次治疗改善不足50%,则建议参与者接受手术干预而非重复给药。主要结局记录为治疗后任何时间点的任何手术治疗(关节镜下膝关节手术、单髁置换术或全膝关节置换术)。次要结局记录为首次注射至第二次注射、第二次注射至第三次注射以及第三次注射至第四次注射之间的间隔时间(月)。
在36个月的随访期间,无需手术干预的膝关节总体生存率为80.18%。所有参与者的平均注射次数为2.52±0.07次。首次注射至第二次注射、第二次注射至第三次注射以及第三次注射至第四次注射的平均间隔时间分别为5.42±0.36、8.92±0.47和9.58±0.55个月。
本研究支持使用iPRF增强的PRP作为治疗KOA的生物治疗方式。这种治疗方式在36个月的随访中提供了令人满意的生存率。每次注射之间较长的间隔时间支持了iPRF增强的PRP的疾病修饰作用。