De Marziani Luca, Boffa Angelo, Franceschini Marco, Andriolo Luca, Di Martino Alessandro, Zaffagnini Stefano, Filardo Giuseppe
Clinica Ortopedica e Traumatologica 2, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Applied and Translational Research (ATR) Center, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Cartilage. 2025 Apr 15:19476035251322730. doi: 10.1177/19476035251322730.
ObjectiveThe aim of this study was to establish the minimal clinically important difference (MCID) thresholds for the International Knee Documentation Committee (IKDC) subjective and Visual Analogue Scale (VAS) pain scores in patients affected by knee chondral and osteochondral lesions treated with cell-free scaffold implantation.DesignFor the MCID definition, 186 patients who underwent an osteochondral scaffold implantation were included. Patients were evaluated through the IKDC subjective and VAS pain scores at baseline, 12 and 24 months. The MCID was calculated using a distribution-based method for both IKDC subjective and VAS pain scores at 12 and 24 months, as well as with an anchor-based method.ResultsThe MCID values were 10.1 and 1.5 for the IKDC subjective and VAS pain scores, respectively, both at 12 and 24 months of follow-up. The rate of patients who achieved the MCID was 83% at 12 months and 88% at 24 months. The anchor-based method led to higher MCID values. Factors identified to increase the probability to reach the MCID were younger age ( = 0.042), male sex ( = 0.042), and lateral femoral condyle lesions ( = 0.002), while patellar lesions were less likely to reach the MCID ( = 0.009).ConclusionsThis study defined the MCID values for the IKDC subjective and VAS pain scores after treatment with a cell-free biomimetic scaffold, with 88% of the patients achieving clinically relevant results at 2 years. Younger patients, males and lateral femoral condyle lesions were more likely to reach the MCID. However, the identified thresholds can be influenced by the method chosen, which warrants caution when interpreting study results.
目的
本研究的目的是确定接受无细胞支架植入治疗的膝关节软骨和骨软骨损伤患者国际膝关节文献委员会(IKDC)主观评分及视觉模拟量表(VAS)疼痛评分的最小临床重要差异(MCID)阈值。
设计
为定义MCID,纳入了186例行骨软骨支架植入的患者。在基线、12个月和24个月时通过IKDC主观评分及VAS疼痛评分对患者进行评估。使用基于分布的方法计算12个月和24个月时IKDC主观评分及VAS疼痛评分的MCID,同时也使用基于锚定的方法进行计算。
结果
在随访的12个月和24个月时,IKDC主观评分及VAS疼痛评分的MCID值分别为10.1和1.5。达到MCID的患者比例在12个月时为83%,在24个月时为88%。基于锚定的方法得出的MCID值更高。确定的增加达到MCID可能性的因素包括年龄较小(P = 0.042)、男性(P = 0.042)和股骨外侧髁损伤(P = 0.002),而髌骨损伤达到MCID的可能性较小(P = 0.009)。
结论
本研究确定了无细胞仿生支架治疗后IKDC主观评分及VAS疼痛评分的MCID值,88%的患者在2年时取得了临床相关结果。年轻患者、男性和股骨外侧髁损伤更有可能达到MCID。然而,所确定的阈值可能会受到所选方法的影响,这在解释研究结果时需谨慎。