Shoulder Service, Florida Orthopaedic Institute (FOI), Tampa, FL, USA.
Department of Translational Research, Foundation for Orthopaedic Research and Education (FORE), Tampa, FL, USA.
J Shoulder Elbow Surg. 2023 Jun;32(6S):S32-S38. doi: 10.1016/j.jse.2022.12.022. Epub 2023 Jan 18.
Revision shoulder arthroplasty often requires management of glenoid bone defects. Options include using allograft, harvesting iliac crest autograft, or using augmented metal components. The purpose of this study is to report outcomes of revision shoulder arthroplasty requiring management of glenoid bone defects with femoral head allograft in a large cohort of patients using a single reverse shoulder implant system and compare them to a matched cohort based on the indication for surgery. Outcomes of patients who had successful glenoid reconstruction were compared to those that required a re-revision, and to a control group that was revised without the need for bone graft.
This was a retrospective review of data collected from 2009 to 2018. There were 36 patients in the bone graft group and 52 in the control group. All patients underwent revision to a reverse shoulder arthroplasty to manage a failed total shoulder arthroplasty (n = 29 and 11), hemiarthroplasty (n = 1 and 24), or reverse shoulder arthroplasty (n = 6 and 17). All patients had a minimum of 2 yr of clinical follow-up. The primary endpoint was survival of baseplate fixation. Secondary outcomes included range of motion and functional outcome scores. Patients that had recurrent baseplate failure and were re-revised were compared to patients with bone graft that did not require additional surgery, and to patients who were revised without the need for bone graft. Patients who required revisions for reasons other than recurrent baseplate failure were also recorded.
Five of 36 (14%) patients had recurrent baseplate failure. Mean time to failure was 12 mo. Three of 5 had successful re-implantation of another baseplate. Two of 5 were revised to a hemi arthroplasty after failure of their revisions. Preoperative American Shoulder and Elbow Surgeons scores were 31 in the grafted patients that did not require re-revision, 39 in the grafted patients that required re-revision, and 33 in the control group. Final American Shoulder and Elbow Surgeons scores were 64, 36, and 56, respectively. One patient required revision surgery not related to baseplate failure. There were no baseplate failures in the control group.
The use of femoral head allograft to manage glenoid bone defects in the revision setting produces predictable improvement in functional outcomes that is not inferior to those in patients revised without bone graft. However, there is a 14% rate of baseplate failure.
肩部翻修手术常常需要处理肩胛盂骨缺损。处理方案包括使用同种异体移植物、取自体髂嵴骨移植物,或使用增强型金属组件。本研究的目的是报告在大量使用单一反式肩植入物系统的患者中,使用股骨头同种异体移植物处理肩胛盂骨缺损的翻修肩部关节成形术的结果,并将其与基于手术指征的匹配队列进行比较。比较了成功进行肩胛盂重建的患者与需要再次翻修的患者,以及无需植骨的对照组的结果。
这是一项回顾性研究,对 2009 年至 2018 年期间收集的数据进行了分析。骨移植组有 36 例患者,对照组有 52 例患者。所有患者均接受了反式肩关节成形术翻修,以治疗失败的全肩关节成形术(n=29 例和 11 例)、半肩关节成形术(n=1 例和 24 例)或反式肩关节成形术(n=6 例和 17 例)。所有患者的临床随访时间均至少为 2 年。主要终点是基板固定的存活率。次要结果包括活动范围和功能结果评分。与需要再次手术的骨移植患者相比,发生基板再次失效的患者(n=5)与接受植骨但无需进一步手术的患者(n=36)和无需植骨的患者(n=52)相比,活动范围和功能结果评分较差。记录了因基板再次失效以外的其他原因而需要进行翻修的患者。
36 例患者中有 5 例(14%)出现基板再次失效。平均失效时间为 12 个月。5 例中有 3 例成功重新植入另一块基板。5 例中有 2 例在翻修失败后改为半关节成形术。未再次手术的植骨患者的术前美国肩肘外科医生评分(American Shoulder and Elbow Surgeons,ASES)为 31 分,再次手术的植骨患者为 39 分,对照组为 33 分。最终的美国肩肘外科医生评分分别为 64、36 和 56。1 例患者需要进行与基板失败无关的翻修手术。对照组无基板失败。
在翻修手术中使用股骨头同种异体移植物来处理肩胛盂骨缺损可产生可预测的功能改善,其结果与未接受植骨的患者相似。然而,仍有 14%的基板失败率。