Bedrin Michael D, Clark DesRaj M, Yow Bobby G, Dickens Jonathan F, Kilcoyne Kelly G
Department of Orthopaedic Surgery, Walter Reed National Military Medical Center, Bethesda, Maryland, U.S.A.
Uniformed Services University of Health Sciences, Bethesda, Maryland, U.S.A.
Arthrosc Sports Med Rehabil. 2023 Oct 15;5(6):100809. doi: 10.1016/j.asmr.2023.100809. eCollection 2023 Dec.
To determine clinical outcomes associated with micronized allogenic cartilage scaffold use for treatment of posterior glenoid cartilage defects at 2 years.
Case series.
A retrospective analysis of prospectively collected data was performed on a consecutive series of patients who underwent arthroscopic treatment of a symptomatic posterior glenoid cartilage defect with micronized allogenic cartilage scaffold between January 2019 and December 2020. The primary outcome was subjective shoulder value (SSV) at latest follow-up. Secondary outcomes included visual analog scale (VAS), recurrence of instability, and range of motion (ROM).
Seven patients, including 4 in the setting of primary posterior instability and 3 in the setting of recurrent symptoms after arthroscopic posterior glenohumeral stabilization, were included in the analysis with a mean follow up of 2.6 years (range, 2-3.7 years). Statistically significant improvements were seen in SSV (median = 40, interquartile range [IQR] = 40-50 before surgery; vs median = 85, IQR = 67.5-87.5 after surgery; = .018) and VAS (median = 4, IQR = 4-6.3 before surgery; vs median = 1, IQR = 0-1.5 after surgery; = .010). No significant differences were seen in ROM. There were no cases of recurrent instability or reoperation.
The use of micronized allogenic cartilage scaffold for glenoid cartilage defects is associated with clinical improvement at 2-year follow-up. This is the case when performed in conjunction with index posterior labral repair when there is a concomitant glenoid cartilage defect or when performed in the setting of persistent pain and mechanical symptoms after prior posterior labral repair.
Level IV, therapeutic case series.
确定使用微粉化同种异体软骨支架治疗肩胛盂后缘软骨缺损2年的临床疗效。
病例系列研究。
对2019年1月至2020年12月期间连续接受关节镜下使用微粉化同种异体软骨支架治疗有症状的肩胛盂后缘软骨缺损患者的前瞻性收集数据进行回顾性分析。主要结局是末次随访时的主观肩关节评分(SSV)。次要结局包括视觉模拟评分(VAS)、不稳定复发情况和活动范围(ROM)。
7例患者纳入分析,其中4例为原发性后向不稳定,3例为关节镜下肩胛盂肱关节后方稳定术后复发症状,平均随访2.6年(范围2 - 3.7年)。SSV有统计学意义的改善(术前中位数 = 40,四分位数间距[IQR] = 40 - 50;术后中位数 = 85,IQR = 67.5 - 87.5;P = 0.018),VAS也有改善(术前中位数 = 4,IQR = 4 - 6.3;术后中位数 = 1,IQR = 0 - 1.5;P = 0.010)。ROM无显著差异。无不稳定复发或再次手术病例。
使用微粉化同种异体软骨支架治疗肩胛盂软骨缺损在2年随访时与临床改善相关。当合并肩胛盂软骨缺损时与初次盂唇后修复联合进行,或在先前盂唇后修复后存在持续疼痛和机械症状时进行,均是如此。
IV级,治疗性病例系列。