Functional and Radiographic Outcomes of Bone Grafting for Severe Glenoid Defects in Reverse Shoulder Arthroplasty: A Minimum 5-Year Follow-up.

IF 4.3 1区 医学 Q1 ORTHOPEDICS
Adrik Da Silva, Michael A Moverman, Chance McCutcheon, Peter N Chalmers, Christopher D Joyce, Robert Z Tashjian
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引用次数: 0

Abstract

Background: 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.

Methods: 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.

Results: 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%.

Conclusions: 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.

Level of evidence: Therapeutic Level III . See Instructions for Authors for a complete description of levels of evidence.

反肩关节置换术中严重关节盂缺损植骨的功能和影像学结果:至少5年随访。
背景:严重肩关节缺损的逆行肩关节置换术(RSA)植骨治疗的结果难以预测。本研究的目的是描述利用带长中心柱的基板在RSA中对严重关节盂缺损进行关节盂骨移植的中期结果。方法:纳入2008 - 2018年RSA期间所有因严重盂骨缺损行盂骨移植术的患者,随访时间至少为5年。术前、术后即刻和术后至少5年的美国肩关节外科医生(American Shoulder and肘关节Surgeons, ASES)评分、视觉模拟评分(visual analogue scale, VAS)疼痛评分和x线片均被获取并回顾。由于植入物松动导致的基板切开或基板翻修被定义为基板失效。结果:56例接受植骨手术的肩胛骨中,14例因患者死亡而无法手术,1例因感染而被排除,其余41例肩胛骨可随访。有4个肩关节失访;因此,最终随访率为90%(41例中37例),平均随访6.8±2.4年。共进行了17次翻修手术和20次初级手术。自体肱骨头移植16例,同种异体股骨头移植21例。总的来说,8个基板失败(异体移植,7个[33.3%]失败);自体移植物,16例失败1例(6.3%);P = 0.104)。翻修手术(17例中有7例[41.2%])与初级手术(20例中有1例[5%])相比有更高的底板失败率(p = 0.014)。平均到底板失效时间为2.1±1.5年,其中2例术后4年失效。男性和较低的Charlson共病指数与底板失效相关(均p < 0.05)。5年总基底板生存率为78.4%。结论:在中期随访中,RSA关节盂骨移植术治疗严重关节盂缺损的总基底成活率为78.4%。自体自体植入术治疗严重缺损的原发性RSA存活率为95%,而同种异体移植重建的改良RSA存活率较低(58.8%)。虽然自体自体植骨重建的原发性RSA成功率很高,但使用中心桩基板的同种异体植骨重建的翻修RSA有较高的基板失败率,因此翻修RSA应考虑其他手术解决方案。证据等级:治疗性III级。有关证据水平的完整描述,请参见作者说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
7.50%
发文量
660
审稿时长
1 months
期刊介绍: The Journal of Bone & Joint Surgery (JBJS) has been the most valued source of information for orthopaedic surgeons and researchers for over 125 years and is the gold standard in peer-reviewed scientific information in the field. A core journal and essential reading for general as well as specialist orthopaedic surgeons worldwide, The Journal publishes evidence-based research to enhance the quality of care for orthopaedic patients. Standards of excellence and high quality are maintained in everything we do, from the science of the content published to the customer service we provide. JBJS is an independent, non-profit journal.
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