Abstract

There are different techniques to address severe glenoid erosion during reverse shoulder arthroplasty (RSA). This study assessed the clinical and radiological outcomes of RSA with combined bony and metallic augment (BMA) glenoid reconstruction compared to bony augmentation (BA) alone. A review of patients who underwent RSA with severe glenoid bone loss requiring reconstruction from January 2017 to January 2019 was performed. Patients were divided into two groups: BMA versus BA alone. Clinical outcome measurements included two years postoperative ROM, Constant score, subjective shoulder value (SSV), and the American Shoulder and Elbow Surgeons Shoulder (ASES) score. Radiological outcomes included radiographic evidence of scapular complications and graft incorporation. The BMA group had significantly different glenoid morphology (p < 0.001) and greater bone loss thickness than the BA group (16.3 ± 3.8 mm vs. 12.0 ± 0.0 mm, p = 0.020). Both groups had significantly improved ROM (anterior forward flexion and external rotation) and clinical scores (Constant, SSV and ASES scores) at 2 years. Greater improvement was observed in the BMA group in terms of anterior forward flexion (86.3° ± 27.9° vs. 43.8° ± 25.6°, p = 0.013) and Constant score (56.6 ± 10.1 vs. 38.3 ± 16.7, p = 0.021). The BA group demonstrated greater functional and clinical improvements with higher postoperative active external rotation and ASES results (active external rotation, 49.4° ± 17.0° vs. 29.4° ± 14.7°, p = 0.017; ASES, 89.1 ± 11.3 vs. 76.8 ± 11.0, p = 0.045). The combination use of bone graft and metallic augments in severe glenoid bone loss during RSA is safe and effective and can be considered in cases of severe glenoid bone loss where bone graft alone may be insufficient.

Highlights

  • Addressing severe glenoid deficiency during shoulder arthroplasty is technically challenging

  • Between January 2017 and January 2019, all patients who had an reverse shoulder arthroplasty (RSA) by either a combination of bony and metallic augments or bony augments alone were considered potentially eligible for inclusion in this retrospective analysis of data prospectively collected during the SHOUT (Shoulder OUTcome) multi-center study

  • Patient characteristics showed no significant differences in terms of patient age, gender, BMI, tobacco usage, or affected side

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Summary

Introduction

Addressing severe glenoid deficiency during shoulder arthroplasty is technically challenging. Glenoid deficiencies have been reported in up to 39% of patients undergoing reverse shoulder arthroplasty (RSA). Such glenoid bone loss may occur in any part of the 4.0/). The excessive medialization results in increased scapular notching with inferomedial glenoid bone erosion and polyethylene wear [6]. In superior glenoid bone loss, there is a risk of placing the glenoid baseplate in superior inclination. This has been shown to be an important risk factor for aseptic loosening as it increases shear forces and decreases compressive forces that otherwise stabilize RSA [7,8]

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