Abstract
Aims
The aim of this study was to report the outcomes of different treatment options for glenoid loosening following reverse shoulder arthroplasty (RSA) at a minimum follow-up of two years.
Patients and Methods
We retrospectively studied the records of 79 patients (19 men, 60 women; 84 shoulders) aged 70.4 years (21 to 87) treated for aseptic loosening of the glenosphere following RSA. Clinical evaluation included pre- and post-treatment active anterior elevation (AAE), external rotation, and Constant score.
Results
From the original cohort, 29 shoulders (35%) were treated conservatively, 27 shoulders (32%) were revised by revision of the glenosphere, and 28 shoulders (33%) were converted to hemiarthroplasty. At last follow-up, conservative treatment and glenoid revision significantly improved AAE, total Constant score, and pain, while hemiarthroplasty did not improve range of movement or clinical scores. Multivariable analysis confirmed that conservative treatment and glenoid revision achieved similar improvements in pain (glenoid revision vs conservative, beta 0.44; p = 0.834) but that outcomes were significantly worse following hemiarthroplasty (beta -5.00; p = 0.029).
Conclusion
When possible, glenoid loosening after RSA should first be treated conservatively, then by glenosphere revision if necessary, and last by salvage hemiarthroplasty
Cite this article: Bone Joint J 2019;101-B:461–469.
Take home message
Glenoid loosening may appear at the interface between the baseplate and the native scapula, the interface between the scapula and any bone graft used, or in the body of the scapula, medial to the baseplate screws.
Over one-third of glenoid loosening are treated conservatively, and another one-third by revision of the glenosphere, both of which granted better clinical improvements than hemiarthroplasty.
Given that secondary glenosphere stabilization is possible, passive or active movements during the first six weeks postoperatively, if immediate signs of loosening are observed, are not recommended.
Over recent years, the use of reverse shoulder arthroplasty (RSA) has increased as the indications for its use have expanded to include proximal humeral fractures, cases with humeral and glenoid bone loss, post-traumatic sequelae, and massive rotator cuff tears.1-5 As the use of RSA has increased and the indications have broadened, the frequency of observed complications has followed and the revision rate for both humeral and glenoid failure has increased. While the most common causes for revision of RSA are instability and infection, failure of the glenosphere has also been frequently reported,6 usually due to glenoid loosening.7
As glenoid loosening is an important complication of anatomical total shoulder arthroplasty (TSA), several revision options have already been investigated, including revision of the glenoid component, conversion to RSA, or conversion to hemiarthroplasty.8-11 Compared with TSA, failure of RSA due to aseptic glenoid loosening is rare, with a prevalence ranging from 1.7% to 3.5%,6,12-16 often attributed to excessive height or superior inclination of the glenosphere.6 There has been little investigation into the results of treatment options for glenoid loosening in RSA; current practice is to replace the glenosphere if there is sufficient bone stock, with salvage conversion to hemiarthroplasty being recommended when all other options are contraindicated.6,13,17
To the authors’ knowledge, there are no published investigations of failure characteristics and treatment options for glenoid loosening in RSA. The purpose of this study was to describe and analyze a consecutive series of failures following RSA due to glenoid loosening, and to report the outcomes of different treatment options at a minimum follow-up of two years.
Patients and Methods
Study design
The authors retrospectively studied the records of all patients treated for aseptic loosening of the glenosphere following RSA between 1998 and 2013 at seven centres. The inclusion criteria were adult patients with a minimum follow-up of two years. Cases of loosening due to infection were excluded as were those treated with excision arthroplasty. A total of 86 patients (91 shoulders) were screened for eligibility, of which five were excluded due to infection and two were treated using excision arthroplasty. This left a cohort of 79 patients (84 shoulders), 19 of whom were men (19 shoulders, 23%) and 60 of whom were women (65 shoulders, 77%), with a mean age of 70.4 years (21 to 87) at the time of index RSA (Table I). The dominant side was affected in 60 patients (60 shoulders, 71%). The study protocol received institutional review board approval (IRB #2018-01).
Table I.
Characteristic | Value |
---|---|
Mean age, years (sd) | 70.4 (12.0) |
Mean body mass index, kg/m2 (sd) | 25.1 (4.1) |
Male gender, n (%) | 19 (23) |
Dominant arm, n (%) | 60 (71) |
Indication for index RSA, n (%) | |
Trauma sequelae | 10 (12) |
Cuff tear arthropathy (Hamada 3 to 5) | 34 (41) |
Rotator cuff tear (Hamada 1 to 2) | 16 (19) |
Failure of previous shoulder arthroplasty | 23 (27) |
Dislocation arthropathy | 1 (1) |
Comorbidities, n (%) | |
None | 50 (60) |
Weight-bearing arm (wheelchair) | 2 (2) |
Osteoporosis | 7 (8) |
Inflammatory arthritis | 14 (17) |
Diabetes | 2 (2) |
Tobacco use | 2 (2) |
Unknown | 7 (8) |
Implant model, n (%) | |
Aequalis (Tornier, Grenoble, France) | 25 (30) |
Delta (DePuy Synthes, Saint Priest, France) | 18 (21) |
Anatomical (Zimmer Biomet, Winterthur, Switzerland) | 31 (37) |
Other | 10 (12) |
Glenoid graft, n (%) | |
None | 51 (61) |
Autograft | 27 (32) |
Allograft | 2 (2) |
Unknown | 4 (5) |
Postoperative immobilization, n (%) | |
Abduction pillow | 12 (14) |
Sling | 63 (75) |
Unknown | 9 (11) |
Complications other than glenoid loosening, n (%) | |
Intraoperative | 13 (16) |
Postoperative | 11 (13) |
Unknown | 9 (11) |
Treatments
All shoulders had been treated either conservatively or surgically depending on the amount and quality of remaining glenoid bone. Conservative treatment comprised immobilization for six weeks, followed by progressive mobilization without physiotherapy or strengthening. Surgical treatment consisted of revision of the glenosphere or conversion to hemiarthroplasty. The treatment option was selected by each surgeon, based on their own experience and preferences, and informed by the mode of loosening of the glenoid and characteristics of the patient. Conservative treatment was preferred for patients with adequate secondary stabilization of their loosened glenoid components. Revision of the glenoid component was deemed necessary for patients with an unstable glenoid component, particularly those with broken screws but adequate glenoid bone stock. Conversion to hemiarthroplasty was performed as a salvage procedure for patients with an unstable glenoid component and severe glenoid bone loss, particularly in patients who had undergone two or more previous operations on the affected shoulder. The surgical approach was either deltopectoral or transdeltoid,18,19 depending on surgeon preference and clinical picture. There were no transfers of the latissimus dorsi.20 To compensate the glenoid bone loss, allografts were sometimes used in case of conversion to hemiarthroplasty and iliac crest autografts were systematically used to restore bone stock when the glenoid component was revised.21 The postoperative management was based on previously described protocols.22,23
Radiological evaluation
Radiographs were available for 56 of the 84 failed RSAs, including true anteroposterior, lateral scapular, and axillary views. Glenoid loosening was confirmed following the criteria of Mélis et al,24 the criteria being the presence of a radiolucent line > 2 mm thick. Radiographs were analyzed using Osirix (Pixmeo, Geneva, Switzerland) to describe loosening and/or migration of the glenosphere, screw breakage, or secondary stabilization. Secondary stabilization was defined by absence of additional movement of the implant over a six-month period, disappearance of radiolucent lines around the screws and the peg, and clinical improvement.
Clinical evaluation
Baseline clinical parameters were collected at the index RSA operation, including patient age, gender, body mass index (BMI), comorbidities, and indications for surgery. Complications were reported according to the classification of Zumstein et al.16 Clinical evaluation included Constant score,25 active range of anterior elevation, and external rotation. Clinical evaluation was performed when the diagnosis of glenoid loosening was made and at a minimum of two years after initiation of conservative or surgical treatment. Patient satisfaction with the treatment of glenoid loosening was assessed as either ‘dissatisfied’, ‘satisfied’, or ‘very satisfied’.
Statistical analysis
Shapiro–Wilk tests were used to assess the normality of distributions. For non-Gaussian continuous data, differences between groups were evaluated using Mann–Whitney U test. For categorical data, differences between groups were evaluated using Fisher’s exact test. Multivariable linear regression was performed to determine associations between the pain component of the Constant score (the only outcome significantly associated with treatment option) and five independent variables (gender, age at index RSA, follow-up, indication for index RSA operation, and treatment option). Statistical analyses were performed using R version 3.3.3 (R Foundation for Statistical Computing, Vienna, Austria). A p-value < 0.05 was considered statistically significant.
Results
From the original cohort of 79 patients (84 shoulders), 28 patients (29 shoulders, 35%) were treated conservatively, 25 patients (27 shoulders, 32%) underwent revision of the glenosphere, and 27 patients (28 shoulders, 33%) were converted to hemiarthroplasty. At the index RSA operation, the three groups differed significantly in terms of BMI, indication for surgery, and implant type; in particular, conversion to hemiarthroplasty was more common when the index operation was a revision and when intraoperative complications occurred during index surgery (Table II).
Table II.
Characteristics | Conservative treatment (n = 29) | Glenosphere revision (n = 27) | Conversion to HA (n = 28) | p-value |
---|---|---|---|---|
Mean age, yrs (sd) | 68.7 (16.7) | 72.7 (7.9) | 69.8 (9.3) | 0.561* |
Mean body mass index, kg/m2 (sd) | 23.8 (3.1) | 26.6 (4.1) | 24.1 (4.5) | 0.036* |
Male gender, n (%) | 8 (27.6) | 7 (25.9) | 4 (14.3) | 0.440† |
Dominant arm, n (%) | 21 (72.4) | 18 (66.7) | 21 (75.0) | 0.792† |
Indication for index RSA, n (%) | 0.001† | |||
Trauma sequelae | 2 (6.9) | 5 (18.5) | 3 (10.7) | |
Cuff tear arthropathy (Hamada 3 to 5) | 15 (51.7) | 12 (44.4) | 7 (25.0) | |
Rotator cuff tear (Hamada 1 to 2) | 6 (20.7) | 8 (29.6) | 2 (7.1) | |
Failure of previous shoulder arthroplasty | 5 (17.2) | 2 (7.4) | 16 (57.1) | |
Dislocation arthropathy | 1 (3.4) | 0 (0) | 0 (0) | |
Comorbidities, n (%) | 0.334† | |||
None | 14 (48.3) | 17 (63.0) | 19 (67.9) | |
Weight-bearing arm (wheelchair) | 2 (6.9) | 0 (0) | 0 (0) | |
Osteoporosis | 3 (10.3) | 1 (3.7) | 3 (10.7) | |
Inflammatory arthritis | 7 (24.1) | 2 (7.4) | 5 (17.9) | |
Diabetes | 2 (6.9) | 0 (0) | 0 (0) | |
Tobacco use | 1 (3.4) | 1 (3.7) | 0 (0) | |
Unknown | 0 (0) | 6 (22.2) | 1 (3.6) | |
Implant model, n (%) | < 0.001† | |||
Aequalis (Tornier, Grenoble, France) | 7 (24.1) | 7 (25.9) | 11 (39.3) | |
Delta (DePuy Synthes, Saint Priest, France) | 1 (3.4) | 8 (29.6) | 9 (32.1) | |
Anatomical (Zimmer Biomet, Winterthur, Switzerland) | 19 (65.5) | 5 (18.5) | 7 (25.0) | |
Other | 2 (6.9) | 7 (25.9) | 1 (3.6) | |
Glenoid graft, n (%) | 0.828† | |||
None | 18 (62.1) | 16 (59.3) | 17 (60.7) | |
Autograft | 10 (34.5) | 7 (25.9) | 10 (35.7) | |
Allograft | 1 (3.4) | 0 (0) | 1 (3.6) | |
Unknown | 0 (0) | 4 (14.8) | 0 (0) | |
Postoperative immobilization, n (%) | 0.113† | |||
Abduction pillow | 8 (27.6) | 2 (7.4) | 2 (7.1) | |
Sling | 21 (72.4) | 18 (66.7) | 24 (85.7) | |
Unknown | 0 (0) | 7 (25.9) | 2 (7.1) | |
Complications other than glenoid loosening, n (%) | ||||
Intraoperative | 4 (13.8) | 0 (0) | 9 (32.1) | 0.008† |
Postoperative | 4 (13.8) | 1 (3.7) | 6 (21.4) | 0.205† |
Unknown | 0 (0) | 6 (22.2) | 3 (10.7) |
-
*
Kruskal–Wallis test
-
†
Fisher’s exact test
-
HA, hemiarthroplasty
The three groups did not differ in the inclination (Fig. 1) or degree of migration (Fig. 2) of the glenosphere, nor in the location of loosening (screws or central peg) (Fig. 3). The conservative treatment group, however, included fewer broken screws (5%) than the glenosphere revision (40%) and hemiarthroplasty (25%) groups (p = 0.023). As might be expected, more cases of secondary stabilization were seen in the conservative group (47%) than in the glenosphere revision (7%) and hemiarthroplasty (5%) groups (p = 0.001) (Table III).
Fig. 1
Fig. 2
Fig. 3
Table III.
Variable | Conservative (n = 21) | Revision (n = 15) | Hemiarthroplasty (n = 20) | p-value |
---|---|---|---|---|
Mean time from index RSA, mths (sd) | 4.1 (6.3) | 29.0 (44.4) | 22.4 (42.8) | 0.456* |
Glenosphere migration, n (%) | 11 (52) | 12 (80) | 17 (85) | 0.068† |
Glenosphere superior inclination, n (%) | 10 (48) | 6 (40) | 3 (15) | 0.095† |
Unknown | 1 (5) | 1 (7) | 2 (10) | |
Secondary stabilization, n (%) | 10 (48) | 1 (7) | 1 (5) | 0.001† |
Unknown | 1 (5) | 0 (0) | 0 (0) | |
Loosening signs, n (%) | ||||
Screws | 14 (67) | 10 (67) | 8 (40) | 0.275† |
Central peg | 14 (67) | 10 (67) | 9 (45) | 0.340† |
Unknown | 1 (5) | 1 (7) | 3 (15) | |
Broken screws, n (%) | 1 (5) | 6 (40) | 5 (25) | 0.023† |
Unknown | 0 (0) | 0 (0) | 1 (5) |
-
*
Kruskal–Wallis test
-
†
Fisher’s exact test
-
RSA, reverse shoulder arthroplasty
Post-treatment complications were noted in one shoulder that had been treated conservatively (periprosthetic fracture), in three shoulders that had revision of the glenosphere (one acromion fatigue fracture and two cases of scapular notching, of which one led to screw breakage), and in one shoulder that had undergone hemiarthroplasty (stress shielding of the proximal humerus). At last follow-up, external rotation did not improve in any of the three groups (Fig. 4). By contrast, conservative treatment and glenosphere revision significantly improved active anterior elevation (22.4° (sd 48.6°) and 38.6° (sd 53.0°)), the total Constant score (23.4 (sd 24.4) and 19.4 (sd 17.5)), and its pain component (5.7 (sd 6.7) and 4.3 (sd 4.3)). Hemiarthroplasty did not improve range of movement or clinical scores (Table IV, Fig. 5). Finally, revision of the glenosphere was associated with higher patient satisfaction (57%) than conservative treatment (20%) or hemiarthroplasty (6%) (p = 0.004).
Fig. 4
Table IV.
Measurement | Conservative (n = 29) | p-value, pre vs post | Revision (n = 27) | p-value, pre vs post | Hemiarthroplasty (n = 28) | p-value, pre vs post | p-value |
---|---|---|---|---|---|---|---|
Mean last follow-up, mths (sd) | 46.2 (38.7); n = 29 | 35.5 (19.9); n = 27 | 30.0 (14.0); n = 28 | 0.078* | |||
Mean active anterior elevation, ° (sd) | 0.033† | 0.030† | 0.740* | ||||
At diagnosis | 61.3 (37.1); n = 27 | 72.0 (40.9); n = 15 | 61.7 (29.1); n = 24 | 0.759* | |||
At last follow-up | 85.2 (37.5); n = 26 | 107.8 (38.3); n = 25 | 68.7 (45.3); n = 19 | 0.014* | |||
Net improvement | 22.4 (48.6); n = 25 | 38.6 (53.0); n = 14 | 4.4 (47.5); n = 17 | 0.172* | |||
Mean external rotation, ° (sd) | 0.690† | 0.600† | 0.950* | ||||
At diagnosis | 14.1 (28.6); n = 27 | 11.3 (17.7); n = 15 | 14.4 (28.9); n = 24 | 0.949* | |||
At last follow-up | 14.0 (18.9); n = 25 | 10.4 (15.5); n = 24 | 9.2 (17.4); n = 19 | 0.736* | |||
Net improvement | 1.3 (21.3); n = 24 | -2.9 (18.2); n = 14 | -2.1 (33.8); n = 17 | 0.668* | |||
Mean Constant score, total (sd) | 0.001† | 0.002† | 0.078* | ||||
At diagnosis | 18.5 (15.1); n = 25 | 29.4 (11.5); n = 19 | 23.7 (10.9); n = 24 | 0.002* | |||
At last follow-up | 41.1 (19.8); n = 24 | 45.6 (17.0); n = 20 | 37.1 (19.3); n = 17 | 0.362* | |||
Net improvement | 23.4 (24.4); n = 22 | 19.4 (17.5); n = 15 | 13.8 (24.0); n = 16 | 0.384* | |||
Mean Constant score, pain component (sd) | 0.003† | 0.007† | 0.890* | ||||
At diagnosis | 4.6 (4.0); n = 22 | 7.1 (2.9); n = 17 | 7.8 (3.0); n = 18 | 0.012* | |||
At last follow-up | 9.3 (5.0); n = 26 | 11.9 (3.3); n = 22 | 8.6 (5.2); n = 18 | 0.052* | |||
Net improvement | 5.7 (6.7); n = 20 | 4.3 (4.3); n = 14 | 0.5 (5.8); n = 13 | 0.060* | |||
Post-treatment satisfaction, n (%) | 0.004‡ | ||||||
Very satisfied | 5 (17) | 13 (48) | 1 (4) | ||||
Satisfied | 13 (45) | 6 (22) | 8 (29) | ||||
Dissatisfied | 7 (24) | 4 (15) | 9 (32) | ||||
Unknown | 4 (14) | 4 (15) | 10 (36) |
-
*
Kruskal–Wallis test
-
†
Paired Mann–Whitney U test
-
‡
Fisher’s exact test pre, pre-treatment; post, post-treatment
Fig. 5
Univariable analysis revealed that improvements in pain were significantly smaller in younger patients (p = 0.028) and following hemiarthroplasty (p = 0.016). Multivariable analysis confirmed that revision of the glenosphere led to similar improvements in pain relief compared to conservative treatment (beta, 0.44; CI -3.76 to 4.63; p = 0.834), but that there were significantly worse results following hemiarthroplasty (beta, -5.00; CI -9.56 to -0.53; p = 0.029) (Table V).
Table V.
Variable | Univariable (n = 84) | p-value* | Multivariable (n = 47) | p-value† |
---|---|---|---|---|
Continuous | ||||
Age, yrs (95% CI) | 0.21 (0.02 to 0.40) | 0.028 | 0.14 (-0.08 to 0.36) | 0.207 |
Last follow-up, mths (95% CI) | 0.08 (-0.03 to 0.20) | 0.150 | 0.05 (-0.06 to 0.16) | 0.384 |
Categorical Indication for index RSA (95% CI) | ||||
Rotator cuff tears | Referent | Referent | ||
Cuff tear arthropathy | 2.13 (-2.74 to 6.99) | 0.384 | 0.98 (-3.73 to 5.69) | 0.677 |
Trauma sequelae | -3.73 (-9.87 to 2.41) | 0.227 | -4.07 (-9.78 to 1.64) | 0.158 |
Failure of previous shoulder arthroplasty | 2.35 (-3.42 to 8.11) | 0.416 | 3.74 (-2.16 to 9.64) | 0.207 |
Male gender | -1.97 (-5.96 to 2.02) | 0.326 | -0.46 (-4.76 to 3.83) | 0.828 |
Glenoid loosening treatment (95% CI) | ||||
Conservative treatment | Referent | Referent | ||
Glenosphere revision | -1.36 (-5.44 to 2.71) | 0.503 | 0.44 (-3.76 to 4.63) | 0.834 |
Conversion to hemiarthroplasty | -5.19 (-9.35 to -1.02) | 0.016 | -5.00 (-9.46 to -0.53) | 0.029 |
-
*
Univariable linear regression with analysis of variance
-
†
Multivariable linear regression with analysis of variance
-
RSA, reverse shoulder arthroplasty
Discussion
The purpose of this study was to evaluate a consecutive series of RSA failures due to glenoid loosening and to report functional improvements following different treatments. Over one-third of these shoulders were treated conservatively, and another one-third were treated by revision of the glenosphere, both of which granted better clinical improvements than hemiarthroplasty.
Glenoid loosening after RSA is a rare but burdensome complication (1.7% to 3.5%),6,12-16 which may be related to infection,24 poor bone stock,13,26,27 design of the glenoid component,28,29 technique of fixation,13 or excessive shear forces (Table VI). In this series, we excluded cases of glenoid loosening due to infection, in order to focus on mechanical failures. Following RSA, the lever arm of the deltoid muscle is increased, thereby improving abduction range.30,31 In abduction, the glenosphere provides the stable fulcrum, to allow shoulder elevation and prosthetic stability.30 The increase in compressive forces has a stabilizing effect on the glenosphere,32 while shear forces could contribute to destabilizing this semi-constrained component,33 potentially leading to glenoid loosening.
Table VI.
Possible causes |
---|
Preoperative |
Pathological insufficiency of bone (osteoporosis, tumour) |
Poor bone stock |
Intraoperative |
Fracture of the scapular neck or glenoid |
Baseplate specificities |
Baseplate implanted too high on the glenoid |
Superior tilt of the glenosphere |
Bone graft with a central peg that was too short and did not reach the native bone |
A central glenoid hole that was too large, excessively reamed glenoid, medial vault penetration, poor screw placement |
Non-assemblage of the glenosphere on the baseplate |
Postoperative |
Excessive shear forces in case of superior tilt, large or lateralized glenosphere, excessive deltoid retensioning, associated latissimus dorsal transfer |
Grade 4 scapular notching or osteolysis due to wear particles from the polyethylene acetabular component |
Infection |
Different locations and modes of failure have been observed. Loosening may appear at the interface between the baseplate and the native scapula, the interface between the scapula and any bone graft used, or in the body of the scapula, medial to the baseplate screws. This is important as it dictates the type of revision surgery possible.
In our series, one-third of RSA failures due to glenoid loosening were treated conservatively, with comparable clinical improvements to revision of the glenosphere. A study of 16 consecutive glenosphere revisions after failed RSA34 reported pain relief and improved function but higher complication rates than primary RSA. We, therefore, suggest treating RSA failures due to glenoid loosening conservatively whenever possible. If conservative treatment fails, revision of the glenosphere could be considered as a subsequent option,35 and conversion to hemiarthroplasty should remain a last salvage option.
Our practice has been informed by the results of this study. Given that secondary stabilization is possible, we do not recommend passive or active movements during the first six weeks postoperatively if immediate signs of loosening are observed. For the same reason, we recommend that shoulders with acute superior glenosphere migration and inferior inclination should first be treated conservatively rather than revised immediately, as they may go on to stabilize with a good functional outcome. Finally, in primary surgery where glenoid fixation is found to be suboptimal intraoperatively, we recommend conversion to a two-stage revision procedure.
Established risk factors for glenoid loosening include female gender, younger age (less than 70 years), superior tilt of the glenoid component, use of bone grafts and non-locking screws, and the superolateral approach.7,14,36-38 Over three-quarters of our cases (77%) of glenoid loosening were in women, which would appear to corroborate the existence of female gender as a risk factor, but we do not know the gender distribution of the cohort as a whole once successful RSA is included. In our series, 17% of patients had inflammatory osteoarthritis, which is above the 11% prevalence in a recent nationwide database study, suggesting that this may represent a risk factor for loosening.39
This study has limitations typical of retrospective designs, including missing preoperative, radiological, and clinical data. As a result, only improvements in external rotation, anterior elevation and Constant scores could be analyzed. Moreover, the choice of treatment was not randomized but based on subjective assessment of remaining glenoid bone volume and quality, which rendered direct comparisons among the treatment groups difficult. The hemiarthroplasty group comprised patients who had worse clinical scores prior to revision and the poor results in this group are at least partly a result of this difference at baseline. Because of missing data, some confounding factors could not be controlled for in the multivariable analysis. The strengths of this study include the fact that it is large (given that this is a rare complication) and, by conducting the study over a number of centres, we can reflect the experience of a large group of experienced shoulder surgeons. Future prospective trials are needed to confirm our findings.
This study has demonstrated that better clinical improvements are achieved by conservative treatment and glenoid revision compared to salvage hemiarthroplasty in cases of glenoid loosening in RSA. We recommend that, when possible, glenoid loosening after RSA should ideally be treated conservatively, then by revision of the glenosphere, and last by salvage hemiarthroplasty. Further prospective studies with larger cohorts are needed to identify risks factors for each treatment to help surgeons choose the most suitable treatment based on patient characteristics.
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Author contributions
A. Lädermann: Designed the study, Collected the data, Wrote the manuscript.
A. J. Schwitzguebel: Analyzed the data, Performed the statistical analysis.
T. B. Edwards: Wrote the manuscript.
A. Godeneche: Designed the study, Collected the data.
L. Favard: Collected the data.
G. Walch: Designed the study, Edited the manuscript.
F. Sirveaux: Collected the data.
P. Boileau: Collected the data.
C. Gerber: Collected the data, Edited the manuscript.
Funding statement
The author or one or more of the authors have received or will receive benefits for personal or professional use from a commercial party related directly or indirectly to the subject of this article.
ICMJE COI statement
A.Godeneche reports consulting fees from Wright, Arthrex, and Conmed related to this study. G. Walch reports consulting fees from Wright related to this study. C. Gerber reports consulting fees from Zimmer Biomet related to this study, as the designer of the anatomical shoulder arthroplasty system.
Acknowledgements
The authors are grateful to Hugo Bothorel and Mo Saffarini for their assistance with data management, statistical analysis, and manuscript redaction.
Ethical review statement
This study received institutional review board approval (IRB #2018-01).
Open access statement
This is an open-access article distributed under the terms of the Creative Commons Attributions license (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
This article was primary edited by A. D. Liddle and first proof edited by G. Scott.
Follow A. Lädermann @Laedermann