Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University of Greifswald, Greifswald, Germany.
ARCUS Sportklinik, Pforzheim, Germany.
Cartilage. 2023 Dec;14(4):393-399. doi: 10.1177/19476035231189840. Epub 2023 Aug 3.
The objective was to evaluate clinical outcome and safety of arthroscopic, autologous minced cartilage implantation for acetabular cartilage lesions observed during hip arthroscopy to treat femoroacetabular impingement syndrome (FAIS).
Eleven male patients, average age: 29.4 ± 5.4 years, average body mass index (BMI): 24.2 ± 2.2 kg/m, scheduled for hip arthroscopy due to FAIS accompanied by an acetabular cartilage lesion were included in the case series. Cartilage tissue was harvested and minced from the loose cartilage flap at the chondrolabral lesion by arthroscopic shaver, augmented with autologous conditioned plasma, implanted into the defect, and fixated by autologous thrombin. Concomitant interventions were performed as indicated. The patients were evaluated preoperatively and at 24-month follow-up, using the International Hip Outcome Tool-12 (iHOT-12) and Visual Analog Scale (VAS) pain score and by magnetic resonance imaging (MRI) using the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) grading scale at the 2-year follow-up.
The defect size was on average 3.5 cm (1.5-4.5 cm). From preoperatively to 2 years postoperatively, the iHOT-12 significantly improved from 50.2 ± 18 to 86.5 ± 19 ( < 0.0001), and pain score decreased from 5.6 ± 1.8 to 1.0 ± 1.5 ( < 0.0001) on the Visual Analog Scale pain score. Regarding functional outcome and pain, 10 of the 11 patients and all patients reached the minimal clinically important difference (MCID), respectively. The postoperative average MOCART score was 87.2 (± 9.2). No adverse events or reoperations were observed.
Arthroscopic, autologous minced cartilage implantation for treating full-thickness acetabular cartilage lesions in FAIS shows statistically and clinically significant improvement at short-term follow-up.
评估髋关节镜检查中治疗股骨髋臼撞击综合征(FAIS)时观察到的髋臼软骨病变的关节镜下自体软骨碎块植入的临床疗效和安全性。
本病例系列研究纳入了 11 名男性 FAIS 患者(平均年龄:29.4 ± 5.4 岁;平均体重指数(BMI):24.2 ± 2.2 kg/m),因 FAIS 合并髋臼软骨病变而行髋关节镜检查。通过关节镜刨削器从软骨-盂唇病变的松动软骨瓣上采集软骨组织并切碎,用自体条件血浆增强,植入缺损处,并用自体凝血酶固定。根据需要同时进行其他干预。在术前和 24 个月随访时,使用国际髋关节结局工具-12(iHOT-12)和视觉模拟评分(VAS)疼痛评分,以及在 2 年随访时使用磁共振观察软骨修复组织(MOCART)分级量表进行磁共振成像(MRI)评估。
缺损大小平均为 3.5 cm(1.5-4.5 cm)。从术前到术后 2 年,iHOT-12 从 50.2 ± 18 显著改善至 86.5 ± 19(<0.0001),VAS 疼痛评分从 5.6 ± 1.8 降低至 1.0 ± 1.5(<0.0001)。在功能结局和疼痛方面,11 名患者中有 10 名和所有患者均达到了最小临床重要差异(MCID)。术后平均 MOCART 评分为 87.2(±9.2)。未观察到不良事件或再次手术。
关节镜下自体软骨碎块植入术治疗 FAIS 中的全层髋臼软骨病变,在短期随访时具有统计学和临床意义上的显著改善。