Da Silva Adrik, Moverman Michael A, McCutcheon Chance, Chalmers Peter N, Joyce Christopher D, Tashjian Robert Z
Department of Orthopaedic Surgery, University of Utah, Salt Lake City, Utah.
J Bone Joint Surg Am. 2025 May 28;107(13):1450-1460. doi: 10.2106/JBJS.24.01052.
The outcomes of bone grafting for severe glenoid defects in reverse shoulder arthroplasty (RSA) are unpredictable. The purpose of this study was to describe the intermediate-term outcomes of glenoid bone grafting in RSA for severe glenoid defects utilizing a baseplate with a long central post.
All patients who underwent glenoid bone grafting for severe glenoid defects during RSA from 2008 to 2018, with a minimum of 5-year follow-up, were included. Preoperative, immediate postoperative, and minimum 5-year postoperative American Shoulder and Elbow Surgeons (ASES) scores and visual analog scale (VAS) pain scores and radiographs were obtained and reviewed. Baseplate failure was defined as gross radiographic baseplate cutout or baseplate revision due to implant loosening.
Of the 56 shoulders that underwent bone grafting, 14 were not available because the patients had died and 1 was excluded because of infection, leaving 41 shoulders available for follow-up. There were 4 shoulders in which the patients were lost to follow-up; therefore, the final follow-up rate was 90% (37 of 41) at a mean of 6.8 ± 2.4 years. There were 17 revision procedures and 20 primary procedures performed. Autograft humeral head was utilized in 16 shoulders, and femoral head allograft was utilized in 21 shoulders. Overall, 8 baseplates failed (allograft, 7 [33.3% failure] of 21; autograft, 1 [6.3% failure] of 16; p = 0.104). Revision surgery (7 [41.2%] of 17) was associated with a higher rate of baseplate failure (p = 0.014) than primary procedures (1 [5%] of 20). The mean time to baseplate failure was 2.1 ± 1.5 years, with 2 cases having failure after 4 years postoperatively. Male sex and a lower Charlson Comorbidity Index were associated with baseplate failure (all p < 0.05). The 5-year overall baseplate survivorship was 78.4%.
Glenoid bone grafting with RSA for severe glenoid defects had an overall baseplate survivorship rate of 78.4% at the intermediate-term follow-up. Primary RSA with autografting for severe defects yielded survivorship of 95%, whereas revision RSA with allograft reconstruction had poorer survivorship (58.8%). Although primary RSA with autograft reconstruction resulted in a high success rate, revision RSA with allograft reconstruction using a central-post baseplate had an elevated baseplate failure rate and alternative surgical solutions for revision RSA should be considered.
Therapeutic Level III . See Instructions for Authors for a complete description of levels of evidence.
在反肩关节置换术(RSA)中,用于严重肩胛盂缺损的骨移植结果不可预测。本研究的目的是描述使用带有长中央柱的基板对严重肩胛盂缺损进行RSA时肩胛盂骨移植的中期结果。
纳入2008年至2018年期间在RSA中因严重肩胛盂缺损接受肩胛盂骨移植且至少随访5年的所有患者。获取并回顾术前、术后即刻以及术后至少5年的美国肩肘外科医师(ASES)评分、视觉模拟量表(VAS)疼痛评分和X线片。基板失败定义为X线片上明显的基板穿出或因植入物松动而进行的基板翻修。
在接受骨移植的56例肩部中,14例因患者死亡而无法获取资料,1例因感染被排除,剩余41例肩部可供随访。有4例患者失访;因此,最终随访率为90%(41例中的37例),平均随访时间为6.8±2.4年。共进行了17例翻修手术和20例初次手术。16例肩部使用自体肱骨头移植,21例肩部使用同种异体股骨头移植。总体而言,8块基板失败(同种异体移植,21例中的7例[失败率33.3%];自体移植,16例中的1例[失败率6.3%];p = 0.104)。翻修手术(17例中的7例[41.2%])的基板失败率(p = 0.014)高于初次手术(20例中的1例[5%])。基板失败的平均时间为2.1±1.5年,2例在术后4年出现失败。男性和较低的Charlson合并症指数与基板失败相关(所有p < 0.05)。5年总体基板生存率为78.4%。
对于严重肩胛盂缺损进行RSA时肩胛盂骨移植,在中期随访时总体基板生存率为78.4%。严重缺损的初次RSA自体移植生存率为95%,而同种异体移植重建的翻修RSA生存率较差(58.8%)。尽管初次RSA自体移植重建成功率较高,但使用中央柱基板进行同种异体移植重建的翻修RSA基板失败率升高,应考虑翻修RSA的替代手术方案。
治疗性III级。有关证据水平的完整描述,请参阅作者指南。