Pre-operative 3D glenoid planning improves component placement in terms of version, inclination, offset and orientation. Version and inclination measurements require the position of the inferior angle. As a consequence, current planning tools require a 3D model of the full scapula to accurately determine the glenoid parameters. Statistical shape models (SSMs) can be used to reconstruct the missing anatomy of bones. Therefore, the objective of this study is to develop and validate an SSM for the reconstruction of the inferior scapula, hereby reducing the irradiation exposure for patients. The training dataset for the statistical shape consisted of 110 CT images from patients without observable scapulae pathologies as judged by an experienced shoulder surgeon. 3D scapulae models were constructed from the segmented images. An open-source non-rigid B-spline-based registration algorithm was used to obtain point-to-point correspondences between the models. A statistical shape model was then constructed from the dataset using principal component analysis. Leave-one-out cross-validation was performed to evaluate the accuracy of the predicted glenoid parameters from virtual partial scans. Five types of virtual partial scans were created on each of the training set models, where an increasing amount of scapular body was removed to mimic a partial CT scan. The statistical shape model was reconstructed using the leave-one-out method, so the corresponding training set model is no longer incorporated in the shape model. Reconstruction was performed using a Monte Carlo Markov chain algorithm, random walk proposals included both shape and pose parameters, the closest fitting proposal was selected for the virtual reconstruction. Automatic 3D measurements were performed on both the training and reconstructed 3D models, including glenoid version, inclination, glenoid centre point position and glenoid offset. In terms of inclination and version we found a mean absolute difference between the complete model and the different virtual partial scan models of 0.5° (SD 0.4°). The maximum difference between models was 3° for inclination and 2° for version. For offset and centre point position the mean absolute difference was 0 mm with an absolute maximum of 1 mm. The magnitude of the mean and maximum differences for all anatomic measurements between the partial scan and complete models is smaller than the current surgical accuracy. Considering these findings, we believe a SSM based reconstruction technique can be used to accurately reconstruct the glenoid parameters from partial CT scans

Osteochondral glenoid loss is associated with recurrent shoulder instability. The critical threshold for surgical stabilization is multidimensional and conclusively unknown. The aim of this work was to provide a well- measurable surrogate parameter of an unstable shoulder joint for the frequent anterior-inferior dislocation direction. The shoulder stability ratio (SSR) of 10 paired human cadaveric glenoids was determined in anterior-inferior dislocation direction. Osteochondral defects were simulated by gradually removing osteochondral structures in 5%-stages up to 20% of the intact diameter. The glenoid morphological parameters glenoid depth, concavity gradient, and defect radius were measured at each stage by means of optical motion tracking. Based on these parameters, the osteochondral stability ratio (OSSR) was calculated. Correlation analyses between SSR and all morphological parameters, as well as OSSR were performed. The loss of SSR, concavity gradient, depth and OSSR with increasing defect size was significant (all p<0.001). The loss of SSR strongly correlated with the losses of concavity gradient (PCC = 0.918), of depth (PCC = 0.899), and of OSSR (PCC = 0.949). In contrast, the percentage loss based on intact diameter (defect size) correlated weaker with SSR (PCC=0.687). Small osteochondral defects (≤10%) led to significantly higher SSR decrease in small glenoids (diameter <25mm) compared to large (≥ 25mm) ones (p ≤ 0.009). From a biomechanical perspective, the losses of concavity gradient, glenoid depth and OSSR correlate strong with the loss of SSR. Therefore, especially the loss of glenoidal depth may be considered as a valid and reliable alternative parameter to describe shoulder instability. Furthermore, smaller glenoids are more vulnerable to become unstable in case of small osteochondral loosening. On the other hand, the standardly used percentage defect size based on intact diameter correlates weaker with the magnitude of instability and may therefore not be a valid parameter for judgement of shoulder instability

Aims. The aim of this study was to determine whether there is a correlation between the grade of humeral osteoarthritis (OA) and the severity of glenoid morphology according to Walch. We hypothesized that there would be a correlation. Methods. Overal, 143 shoulders in 135 patients (73 females, 62 males) undergoing shoulder arthroplasty surgery for primary glenohumeral OA were included consecutively. Mean age was 69.3 years (47 to 85). Humeral head (HH), osteophyte length (OL), and morphology (transverse decentering of the apex, transverse, or coronal asphericity) on radiographs were correlated to the glenoid morphology according to Walch (A1, A2, B1, B2, B3), glenoid retroversion, and humeral subluxation on CT images. Results. Increased humeral OL correlated with a higher grade of glenoid morphology (A1-A2-B1-B2-B3) according to Walch (r = 0.672; p < 0.0001). It also correlated with glenoid retroversion (r = 0.707; p < 0.0001), and posterior humeral subluxation (r = 0.452; p < 0.0001). A higher humeral OL (odds ratio (OR) 1.17; 95% confidence interval (CI) 1.03 to 1.32; p = 0.013), posterior humeral subluxation (OR 1.11; 95% CI 1.01 to 1.22; p = 0.031), and glenoid retroversion (OR 1.48; 95% CI 1.30 to 1.68; p < 0.001) were independent factors for a higher glenoid morphology. More specifically, a humeral OL of ≥ 13 mm was indicative of eccentric glenoid types B2 and B3 (OR 14.20; 95% CI 5.96 to 33.85). Presence of an aspherical HH in the coronal plane was suggestive of glenoid types B2 and B3 (OR 3.34; 95% CI 1.67 to 6.68). Conclusion. The criteria of humeral OL and HH morphology are associated with increasing glenoid retroversion, posterior humeral subluxation, and eccentric glenoid wear. Therefore, humeral radiological parameters might hint at the morphology on the glenoid side. Cite this article: Bone Jt Open 2022;3(6):463–469

Introduction. Achieving prosthesis fixation in patients with glenoid defects can be challenging, particularly when the bony defects are large. To that end, this study quantifies the impact of 2 different sizes of large anterior glenoid defects on reverse shoulder glenoid fixation in a composite scapula model using the recently approved ASTM F 2028–14 reverse shoulder glenoid loosening test method. Methods. This rTSA glenoid loosening test was conducted according to ASTM F 2028–14; we quantified glenoid fixation of a 38mm reverse shoulder (Equinoxe, Exactech, Inc) in composite/dual density scapulae (Pacific Research, Inc) before and after cyclic testing of 750N for 10k cycles. Anterior defects of 8.5mm (31% of glenoid width and 21% of glenoid height; n=7) and 12.5mm (46% of glenoid width and 30% of glenoid height; n=7) were milled into the composite scapula along the S/I glenoid axis with the aid of a custom jig. The baseplate fixation in scapula with anterior glenoid defects was compared to that of scapula without an anterior glenoid defect (n = 7). For the non-defect scapula, initial fixation of the glenoid baseplates were achieved using 4, 4.5×30mm diameter poly-axial locking compression screws. To simulate a worst case condition in each anterior defect scapulae, no 4.5×30mm compression screw were used anteriorly, instead fixation was achieved with only 3 screws (one superior, one inferior, and one posterior). A one-tailed unpaired student's t-test (p < 0.05) compared prosthesis displacements relative to each scapula (anterior defect vs no-anterior defect). Results. All glenoid baseplates remained well-fixed after cyclic loading in composite scapula without a defect and those with an 8.5mm anterior glenoid defect. However, only 6 of the 7 glenoid baseplates remained well-fixed after cyclic loading in scapula with a 12.5mm anterior glenoid defect, where 1 device failed catastrophically at 5000 cycles by loosening from the substrate. As described in Table 1, the average pre- and post-cyclic glenoid baseplate displacement in scapula with 8.5mm and 12.5mm anterior glenoid defects was significantly greater than that of baseplates in scapula without an anterior glenoid defect in both the A/P and S/I directions. Similarly, the average pre- and post-cyclic glenoid baseplate displacement in scapula with 12.5mm anterior glenoid defects was significantly greater than that of baseplates in scapula with 8.5mm anterior glenoid defects in the both the A/P and S/I directions. Discussion and Conclusions. These results demonstrate that reverse shoulder glenoid baseplate fixation was achievable in scapula with an 8.5mm anterior glenoid defect. Given that one sample catastrophically loosened in the 12.5mm anterior defect model, supplemental bone grafting may be required to achieve fixation in 12.5mm anterior glenoid defects with reverse shoulder arthroplasty. Future work should evaluate whether adding additional screws mitigates the increased displacement observed in this anterior glenoid defect scenario. This study is limited by its use of polyurethane dual-density composite scapula

Introduction. Due to the predictability of outcomes achieved with reverse shoulder arthroplasty (rTSA), rTSA is increasingly being used in patients where glenoid fixation is compromised due to presence of glenoid wear. There are various methods to achieve glenoid fixation in patients with glenoid wear, including the use of bone grafting behind the glenoid baseplate or the use of augmented glenoid baseplates. This clinical study quantifies clinical outcomes achieved using both techniques in patients with severe glenoid wear at 2 years minimum follow-up. Methods. 80 patients (mean age: 71.6yrs) with 2 years minimum follow-up were treated by 7 fellowship trained orthopaedic surgeons using rTSA with bone graft behind the baseplate or rTSA with an augmented glenoid baseplate in patients with severe posterior glenoid wear. 39 rTSA patients (14 female, avg: 73.1 yrs; 25 male, avg: 71.5 yrs) received an augmented glenoid (cohort composed of 24 patients with an 8° posterior augment baseplate and 15 patients with a 10° superior augment baseplate) for treatment of CTA, RCT, and OA with a medially eroded scapula. 41 rTSA patients (27 female, avg: 73.0 yrs; 14 male, avg: 66.9 yrs) received glenoid bone graft (cohort composed of 5 patients with allograft and 36 patients with autograft) for treatment of CTA, RCT, and OA with a medially eroded scapula. Outcomes were scored using SST, UCLA, ASES, Constant, and SPADI metrics; active abduction, forward flexion, and internal/external rotation were also measured to quantify function. Average follow-up was 31.2 months (augment 28.3; graft 34.1). A two-tailed, unpaired t-test identified differences (p<0.05) in pre-operative, post-operative, and pre-to-post improvements. Results. A comparison of pre-operative, post-operative, and pre-to-post improvement in outcomes are presented in Tables 1–3, respectively. No difference was noted in pre-operative, post-operative, and pre-to-post improvement in outcomes between cohorts. The augmented glenoid baseplate rTSA cohort had 0 complications for a complication rate of 0%; whereas, the rTSA glenoid bone graft cohort had 6 complications (including 2 glenoid loosenings/graft failures) for a complication rate of 14.6%. Additionally, radiographic follow-up information was available for 30 of 39 augmented baseplate patients (76.9%) and 27 of 41 bone graft patients (65.9%); where the augmented baseplate rTSA cohort had a scapular notching rate of 10.0% with an average scapular notching grade of 0.1; whereas, the rTSA glenoid bone graft cohort had a scapular notching rate of 18.5% with an average scapular notching grade of 0.19. Conclusions. These results demonstrate positive outcomes can be achieved at 2 years minimum follow-up in patients with severe glenoid wear using either augmented glenoid baseplates or bone graft behind the glenoid baseplate with rTSA. While no statistical difference was noted between pre-operative, post-operative, and pre-to-post improvement in outcomes between rTSA cohorts, a substantial difference in the complication rate was noted between cohorts which may factor into the surgeon's decision of the choice of treatment technique for these patients. Additional and longer-term follow-up is needed to confirm these outcomes and trends

Knowledge of the premorbid glenoid shape and the morphological changes the bone undergoes in patients with glenohumeral arthritis can improve surgical outcomes in total and reverse shoulder arthroplasty. Several studies have previously used scapular statistical shape models (SSMs) to predict premorbid glenoid shape and evaluate glenoid erosion properties. However, current literature suggests no studies have used scapular SSMs to examine the changes in glenoid surface area in patients with glenohumeral arthritis. Therefore, the purpose of this study was to compare the glenoid articular surface area between pathologic glenoid cavities from patients with glenohumeral arthritis and their predicted premorbid shape using a scapular SSM. Furthermore, this study compared pathologic glenoid surface area with that from virtually eroded glenoid models created without influence from internal bone remodelling activity and osteophyte formation. It was hypothesized that the pathologic glenoid cavities would exhibit the greatest glenoid surface area despite the eroded nature of the glenoid and the medialization, which in a vault shape, should logically result in less surface area. Computer tomography (CT) scans from 20 patients exhibiting type A2 glenoid erosion according to the Walch classification [Walch et al., 1999] were obtained. A scapular SSM was used to predict the premorbid glenoid shape for each scapula. The scapula and humerus from each patient were automatically segmented and exported as 3D object files along with the scapular SSM from a pre-operative planning software. Each scapula and a copy of its corresponding SSM were aligned using the coracoid, lateral edge of the acromion, inferior glenoid tubercule, scapular notch, and the trigonum spinae. Points were then digitized on both the pathologic humeral and glenoid surfaces and were used in an iterative closest point (ICP) algorithm in MATLAB (MathWorks, Natick, MA, USA) to align the humerus with the glenoid surface. A Boolean subtraction was then performed between the scapular SSM and the humerus to create a virtual erosion in the scapular SSM that matched the erosion orientation of the pathologic glenoid. This led to the development of three distinct glenoid models for each patient: premorbid, pathologic, and virtually eroded (Fig. 1). The glenoid surface area from each model was then determined using 3-Matic (Materialise, Leuven, Belgium). Figure 1. (A) Premorbid glenoid model, (B) pathologic glenoid model, and (C) virtually eroded glenoid model. The average glenoid surface area for the pathologic scapular models was 70% greater compared to the premorbid glenoid models (P < 0 .001). Furthermore, the surface area of the virtual glenoid erosions was 6.4% lower on average compared to the premorbid glenoid surface area (P=0.361). The larger surface area values observed in the pathologic glenoid cavities suggests that sufficient bone remodelling exists at the periphery of the glenoid bone in patients exhibiting A2 type glenohumeral arthritis. This is further supported by the large difference in glenoid surface area between the pathologic and virtually eroded glenoid cavities as the virtually eroded models only considered humeral anatomy when creating the erosion. For any figures or tables, please contact the authors directly

Purpose: The causes of glenoid loosening are multifactorial (implant design, surgical technique, bone properties, soft tissue properties). This biomechanical study was conducted to evaluate the consequences of two clinical problems often encountered in shoulder arthroplasty: subscapular tension and glenoid retroversion. Material and methods: We developed a 3D model of the shoulder including the rotator cuff. A total prosthesis was implanted by digital modellisation. The humeral prosthesis imitated the adaptable third-generation implants, with a stem and a portion of a metal sphere, were used to achieve anatomic reconstruction of the proximal humerus. The polyethylene glenoid, cemented to bone, had a central stem and a flat base. Two subscapular tension (normal and twice normal) and two glenoid positions (0° and 20° retroversion) were tested. External rotation (0–40°) and internal rotation (0–60°) were simulated. We calculated displacement of the glenohumeral contact point, joint forces and contact pressures, interosseous glenoid stress, and micromovement of the bone-cement-implant interfaces. Results: Subscapular tension produced increased forces and joint pressures, associated with moderate posterior translation of the glenohumeral contact point. Retroversion induced more marked posterior displacement of the contact point, leading to significantly higher intraosseous glenoid stress and micromovements at the interfaces. The association of subscapular tension and glenoid retroversion produced important concentration of stress forces in the posterior part of the glenoid and increased all the micromovements. Discussion: Subscapular tension and retroversion of the glenoid implant have significant biomechanical effects which can favour glenoid loosening. Correction of these two parameters must be carefully controlled during shoulder arthroplasty

Purpose of the study: Posterior glenoid erosio is a common finging in patients with degenerative joint disease of the shoulder. Anterior release is usually recommended, almost always with correction of the glenoid retroversion. There is no real consensus on the gravity of these posterior lesions nor on the appropriate attitude. The purpose of this study was to define the limitations of asymmetrical reaming during correction of excessive glenoid retroversion during total shoulder arthroplasty. Material and methods: Five fresh cadaver shoulders were used. The size of the glenoid cavity and the humeral head were measured to select the optimal size for the glenoid implant. The scapula was embedded in resin. Posterior glenoid erosion was created by reaming to simulate wear producing retroversion greater than 15°. A control computed tomography (CT) was obtained to verify the lesion. The glenoid cavity was then prepared in the same manner as for prosthesis implantation, restoring neutral version to enable implantation of the prosthetic component of the size initially determined. A second CT was obtained to confirm the correction of the retroversion. Results: The retroversion was corrected in all cases. At least one point of the implant penetrated the glenoid wall in all cases. In three cases, four points were outside the wall. In one case, reaming caused a fracture of the anterior glenoid rim. Finally, in one case, the size of the implant had to be reduced to avoid an oversized implant. Discussion: The limitations for asymmetrical reaming to correct for posterior wear yet leave enough bone stock for implantation of a glenoid prosthesis are not defined. This study shows that asymmetrical reaming of the anterior rim of the glenoid cavity cannot satisfactorily correct for glenoid retroverson greater than 15° because of the frailness of the anterior wall and the risk the points will penetrate the rim. These complications compromise the primary stablity of the prosthesis and probably secondary short-term and mid-term stability. Conclusion: If the glenoid retroversion is excessive (> 15°), it would be advisable to graft the posterior defect

Abstract. Aim. Excessive glenoid retroversion and posterior wear leads to technical challenges when performing anatomic shoulder replacement. Various techniques have been described to correct glenoid version, including eccentric reaming, bone graft, posterior augmentation and custom prosthesis. Clinical outcomes and survivorship of a Stemless humeral component with cemented pegged polyethylene glenoid with eccentric reaming to partially correct retroversion are presented. Patients and Methods. Between 2010– 2019, 115 Mathys Affinis Stemless Shoulder Replacements were performed. 50 patients with significant posterior wear and retroversion (Walch type B1, B2, B3 and C) were identified. Measurement of Pre-operative glenoid retroversion and Glenoid component version on a post op axillary view was performed by method as described by Matsen FA. Relative correction was correlated with clinical and radiological outcome. Results. 4 were lost to follow up. 46 patients were therefore reviewed. The mean follow up was 4 years (2–8.9 years). Walch B1, Pre op Retroversion: 12 (8–20), post op retroversion :11.8 (−4 to 19), correction= 0.2. Walch B2, Pre op Retroversion :18.4 (10–32), post op retroversion: 13.2 (1 −22), correction= 5.2. Walch B3, Pre op Retroversion: 19.1 (13–32)post op retroversion : 16.1 (9–25), correction= 3.0. Walch C, Pre op Retroversion: 33.3 (28–42) post op retroversion: 16.0 (6–27), correction= 17.3. 3 patients required revision surgery for rotator cuff failure. Conclusion. Partial correction of glenoid retroversion with eccentric reaming and implantation of cemented pegged polyethylene component leads to satisfactory clinical outcomes at midterm follow up. No revisions for aseptic loosening of the glenoid were required

This paper presents an ongoing review of the use of a wedge-shaped porous metal augments in the shoulder to address glenoid retroversion as part of anatomical total shoulder arthroplasty (aTSA). Seventy-five shoulders in 66 patients (23 women and 43 men, aged 42 to 85 years) with Walch grade B2 or C glenoids underwent porous metal glenoid augment (PMGA) insertion as part of aTSA. Patients received either a 15º or 30º PMGA wedge (secured by screws to the native glenoid) to correct excessive glenoid retroversion before a standard glenoid component was implanted using bone cement. Neither patient-specific guides nor navigation were used. Patients were prospectively assessed using shoulder functional assessments (Oxford Shoulder Score [OSS], American Shoulder and Elbow Standardized Shoulder Assessment Form [ASES], visual analogue scale [VAS] pain scores and forward elevation [FE]) preoperatively, at three, six, and 12 months, and yearly thereafter, with similar radiological surveillance. Forty-nine consecutive series shoulders had a follow-up of greater than 24 months, with a median follow-up of 48 months (range: 24–87 months). Median outcome scores improved for OSS (21 to 44), ASES (24 to 92), VAS (7 to 0), and FE (90º to 140º). Four patients died, but no others were lost to follow-up. Apart from one infection at 18 months postoperatively and one minor peg perforation, there were no complications, hardware failures, implant displacements, significant lucency or posterior re-subluxations. Radiographs showed good incorporation of the wedge augment with correction of glenoid retroversion from median 22º (13º to 46º) to 4º. All but four glenoids were corrected to within the target range (less than 10º retroversion). The porous metal wedge-shaped augments effectively addressed posterior glenoid deficiency as part of aTSA for rotator cuff intact osteoarthritis, producing satisfactory clinical outcomes with no signs of impending future failure

Ideberg-Goss type VI/AO F2(4) glenoid fossa fractures are a rare and complex injury. Although some advocate non-operative management, grossly displaced glenoid fossa fractures in the young patient may warrant fixation. Current approaches still describe difficulty with access of the entirety of the glenoid, particularly the postero-superior quadrant. We present 2 cases of Ideberg-Goss type VI/AO F2(4) glenoid fossa fractures treated with fixation through a novel “Deltoid Takedown” approach, which allows safe access to the whole glenoid with satisfactory clinical results at 5 and 7 years respectively

Aims. To report early (two-year) postoperative findings from a randomized controlled trial (RCT) investigating disease-specific quality of life (QOL), clinical, patient-reported, and radiological outcomes in patients undergoing a total shoulder arthroplasty (TSA) with a second-generation uncemented trabecular metal (TM) glenoid versus a cemented polyethylene glenoid (POLY) component. Methods. Five fellowship-trained surgeons from three centres participated. Patients aged between 18 and 79 years with a primary diagnosis of glenohumeral osteoarthritis were screened for eligibility. Patients were randomized intraoperatively to either a TM or POLY glenoid component. Study intervals were: baseline, six weeks, six-, 12-, and 24 months postoperatively. The primary outcome was the Western Ontario Osteoarthritis Shoulder QOL score. Radiological images were reviewed for metal debris. Mixed effects repeated measures analysis of variance for within and between group comparisons were performed. Results. A total of 93 patients were randomized (46 TM; 47 POLY). No significant or clinically important differences were found with patient-reported outcomes at 24-month follow-up. Regarding the glenoid components, there were no complications or revision surgeries in either group. Grade 1 metal debris was observed in three (6.5%) patients with TM glenoids at 24 months but outcomes were not negatively impacted. Conclusion. Early results from this RCT showed no differences in disease-specific QOL, radiographs, complication rates, or shoulder function between uncemented second-generation TM and cemented POLY glenoids at 24 months postoperatively. Revision surgeries and reoperations were reported in both groups, but none attributed to glenoid implant failure. At 24 months postoperatively, Grade 1 metal debris was found in 6.5% of patients with a TM glenoid but did not negatively influence patient-reported outcomes. Longer-term follow-up is needed and is underway. Cite this article: Bone Jt Open 2021;2(9):728–736

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

Summary Statement. In this study, excellent positioning of custom-made glenoid components was achieved using patient-specific guides. Achieving the preoperatively planned orientation of the component improved significantly and more screws were located inside the scapular bone compared to implantations without such guide. Introduction. Today's techniques for total or reverse shoulder arthroplasty are limited when dealing with severe glenoid defects. The available procedures, for instance the use of bone allografts in combination with available standard implants, are technically difficult and tend to give uncertain outcomes (Hill et al. 2001; Elhassan et al. 2008; Sears et al. 2012). A durable fixation between bone and implant with optimal fit and implant positioning needs to be achieved. Custom-made defect-filling glenoid components are a new treatment option for severe glenoid defects. Despite that the patient-specific implants are uniquely designed to fit the patient's bone, it can be difficult to achieve the preoperatively planned position of the component, resulting in less optimal screw fixation. We hypothesised that the use of a patient-specific guide would improve implant and screw positioning. The aim of this study was to evaluate the added value of a newly developed patient-specific guide for implant and screw positioning, by comparing glenoid implantations with and without such guide. Patients & Methods. Large glenoid defects, representative for the defects encountered in clinical practice, were created in ten cadaveric shoulders. A CT scan of each cadaver was taken to evaluate the defects and to generate three-dimensional models of the scapular bones. Based on these models, custom glenoid components were designed. Furthermore, a newly developed custom guide was designed for five randomly selected shoulders. New CT scans were taken after implantation to generate 3D models of the bone and the implanted component and screws. This enabled to compare the experimentally achieved and preoperatively planned reconstruction. The location and orientation of the glenoid component and screw positioning were determined and differences with the optimal preoperative planning were calculated. Results. An excellent component positioning (difference in location: 1.4±0, 7mm; difference in orientation: 2, 5±1, 2°) was achieved when using the guide compared to implantations without guidance (respectively 1, 7±0, 5mm; 5, 1±2, 3°). The guide improved component orientation significantly (P<0.1). After using the guide, all screws were positioned inside the scapular bone whereas 25% of the screws placed without guidance were positioned outside the scapular bone. Discussion/Conclusion. In this study, excellent positioning of custom-made glenoid components was achieved using patient-specific guides. Achieving the preoperatively planned orientation of the component improved significantly and more screws were located inside the scapular bone compared to implantations without such guide

Glenoid baseplate positioning for reverse total shoulder replacements (rTSR) is key for stability and longevity. 3D planning and image-derived instrumentation (IDI) are techniques for improving implant placement accuracy. This is a single-blinded randomised controlled trial comparing 3D planning with IDI jigs versus 3D planning with conventional instrumentation. Eligible patients were enrolled and had 3D pre-operative planning. They were randomised to either IDI or conventional instrumentation; then underwent their rTSR. 6 weeks post operatively, a CT scan was performed and blinded assessors measured the accuracy of glenoid baseplate position relative to the pre-operative plan. 47 patients were included: 24 with IDI and 23 with conventional instrumentation. The IDI group were more likely to have a guidewire placement within 2mm of the preoperative plan in the superior/inferior plane when compared to the conventional group (p=0.01). The IDI group had a smaller degree of error when the native glenoid retroversion was >10° (p=0.047) when compared to the conventional group. All other parameters (inclination, anterior/posterior plane, glenoids with retroversion <10°) showed no significant difference between the two groups. Both IDI and conventional methods for rTSA placement are very accurate. However, IDI is more accurate for complex glenoid morphology and placement in the superior-inferior plane. Clinically, these two parameters are important and may prevent long term complications of scapular notching or glenoid baseplate loosening. Image-derived instrumentation (IDI) is significantly more accurate in glenoid component placement in the superior/inferior plane compared to conventional instrumentation when using 3D pre-operative planning. Additionally, in complex glenoid morphologies where the native retroversion is >10°, IDI has improved accuracy in glenoid placement compared to conventional instrumentation. IDI is an accurate method for glenoid guidewire and component placement in rTSA

This study examined the regional variations of cortical and cancellous bone density present in superiorly eroded glenoids. It is hypothesized that eroded regions will contain denser bone in response to localized stress. The shift in natural joint articulation may also cause bone resorption in areas opposite the erosion site. Clinical CT scans were obtained for 32 shoulders (10m/22f, mean age 72.9yrs, 56–88yrs) classified as having E2-type glenoid erosion. The glenoid was divided into four measurement regions - anterior, inferior, posterior, and superior - as well as five depth regions. Depth regions were segmented in two-millimeter increments from zero to 10 millimeters, beginning at the center of the glenoid surface. A repeated-measures multiple analysis of variance (RM-MANOVA) was performed using SPSS statistical software to look for differences and interactions between mean densities in each depth, quadrant, and between genders. A second RM-MANOVA was performed to examine effects of gender and quadrant on cortical to cancellous bone volume ratios. Significance was set at p < 0 .05. Quadrant and depth variables showed significant multivariate main effects (p 0.147 respectively). Quadrant, depth, and their interaction showed significant univariate main effects for cortical bone (p≤0.001) and cancellous bone (p < 0 .001). The lowest bone density was found to be in the inferior quadrant for cancellous bone (307±50 HU, p < 0 .001). The superior quadrant contained the highest mean density for cortical bone (895±97 HU), however it was only significantly different than in the posterior quadrant (865±97 HU, p=0.022). As for depth, it was found that cortical bone is most dense at the glenoid surface (zero to two millimeters, 892±91 HU) when compared to bone at two to eight millimeters in depth (p < 0 .02). Cancellous bone was also most dense at the surface (352±51 HU), but only compared to the eight to 10 millimeters depth (p=0.005). Cancellous bone density was found to decrease with increasing depth. For cortical-to-cancellous bone volume ratios, the inferior quadrant (0.37±0.28) had a significantly lower ratio than all other quadrants (p < 0 .001). The superoposterior region of the glenoid was found to have denser cancellous bone and a high ratio of cortical to cancellous bone, likely due to decreased formation of cancellous bone and increased formation of cortical bone, in response to localized stresses. The inferior quadrant was found to have the least dense cortical and cancellous bone, and the lowest volume of cortical bone relative to cancellous bone. Once again, this is likely due to reduction in microstrain responsible for bone adaptation via Wolff's law. The density values found in this study generally agree with the range of values found in previous studies of normal and arthritic glenoids. An important limitation of this study is the sizing of measurement regions. For a patient with a smaller glenoid, a depth measurement of two millimeters may represent a larger portion of the overall glenoid vault. Segments could be scaled for each patient based on a percentage of each individual's glenoid size

Reverse shoulder arthroplasty (RSA) is commonly used to treat patients with rotator cuff tear arthropathy. Loosening of the glenoid component remains one of the principal modes of failure and is the main complication leading to revision. For optimal RSA implant osseointegration to occur, the micromotion between the baseplate and the bone must not exceed a threshold of 150 µm. Excess micromotion contributes to glenoid loosening. This study assessed the effects of various factors on glenoid baseplate micromotion for primary fixation of RSA. A half-fractional factorial experiment design (2k-1) was used to assess four factors: central element type (central peg or screw), central element cortical engagement according to length (13.5 or 23.5 mm), anterior-posterior (A-P) peripheral screw type (nonlocking or locking), and bone surrogate density (10 or 25 pounds per cubic foot [pcf]). This created eight unique conditions, each repeated five times for 40 total runs. Glenoid baseplates were implanted into high- or low-density Sawbones™ rigid polyurethane (PU) foam blocks and cyclically loaded at 60 degrees for 1000 cycles (500 N compressive force range) using a custom designed loading apparatus. Micromotion at the four peripheral screw positions was recorded using linear variable displacement transducers (LVDTs). Maximum micromotion was quantified as the displacement range at the implant-PU interface, averaged over the last 10 cycles of loading. Baseplates with short central elements that lacked cortical bone engagement generated 373% greater maximum micromotion at all peripheral screw positions compared to those with long central elements (p < 0.001). Central peg fixation generated 360% greater maximum micromotion than central screw fixation (p < 0.001). No significant effects were observed when varying A-P peripheral screw type or bone surrogate density. There were significant interactions between central element length and type (p < 0.001). An interaction existed between central element type and level of cortical engagement. A central screw and a long central element that engaged cortical bone reduced RSA baseplate micromotion. These findings serve to inform surgical decision-making regarding baseplate fixation elements to minimize the risk of glenoid loosening and thus, the need for revision surgery

Patients receiving reverse total shoulder arthroplasty (RTSA) often have osseous erosions because of glenohumeral arthritis, leading to increased surgical complexity. Glenoid implant fixation is a primary predictor of the success of RTSA and affects micromotion at the bone-implant interface. Augmented implants which incorporate specific geometry to address superior erosion are currently available, but the clinical outcomes of these implants are still considered short-term. The objective of this study was to investigate micromotion at the glenoid-baseplate interface for a standard, 3 mm and 6 mm lateralized baseplates, half-wedge, and full-wedge baseplates. It was hypothesized that the mechanism of load distribution from the baseplate to the glenoid will differ between implants, and these varying mechanisms will affect overall baseplate micromotion. Clinical CT scans of seven shoulders (mean age 69 years, 10°-19° glenoid inclinations) that were classified as having E2-type glenoid erosions were used to generate 3D scapula models using MIMICS image processing software (Materialise, Belgium) with a 0.75 mm mesh size. Each scapula was then repeatedly virtually reconstructed with the five implant types (standard,3mm,6mm lateralized, and half/full wedge; Fig.1) positioned in neutral version and inclination with full backside contact. The reconstructed scapulae were then imported into ABAQUS (SIMULIA, U.S.) finite element software and loads were applied simulating 15°,30°,45°,60°,75°, and 90° of abduction based on published instrumented in-vivo implant data. The micromotion normal and tangential to the bone surface, and effective load transfer area were recorded for each implant and abduction angle. A repeated measures ANOVA was used to perform statistical analysis. Maximum normal micromotion was found to be significantly less when using the standard baseplate (5±4 μm), as opposed to the full-wedge (16±7 μm, p=0.004), 3 mm lateralized (10±6 μm, p=0.017), and 6 mm lateralized (16±8 μm, p=0.007) baseplates (Fig.2). The half-wedge baseplate (11±7 μm) also produced significantly less micromotion than the full-wedge (p=0.003), and the 3 mm lateralized produced less micromotion than the full wedge (p=0.026) and 6 mm lateralized (p=0.003). Similarly, maximum tangential micromotion was found to be significantly less when using the standard baseplate (7±4 μm), as opposed to the half-wedge (12±5 μm, p=0.014), 3 mm lateralized (10±5 μm, p=0.003), and 6 mm lateralized (13±6 μm, p=0.003) baseplates (Fig.2). The full wedge (11±3 μm), half-wedge, and 3 mm lateralized baseplate also produced significantly less micromotion than the 6 mm lateralized (p=0.027, p=012, p=0.02, respectively). Both normal and tangential micromotion were highest at the 30° and 45° abduction angles (Fig.2). The effective load transfer area (ELTA) was lowest for the full wedge, followed by the half wedge, 6mm, 3mm, and standard baseplates (Fig.3) and increased with abduction angle. Glenoid baseplates with reduced lateralization and flat backside geometries resulted in the best outcomes with regards to normal and tangential micromotion. However, these types of implants are not always feasible due to the required amount of bone removal, and medialization of the bone-implant interface. Future work should study the acceptable levels of bone removal for patients with E-type glenoid erosion and the corresponding best implant selections for such cases. For any figures or tables, please contact the authors directly

In an effort to address the relatively high rate of glenoid component lucent lines, loosening and failure, tantalum/trabecular metal glenoid implant fixation has evolved as it has in hip and knee arthroplasty. Trabecular metal-anchored glenoid implants used in a consecutive patient case series have demonstrated a lower failure rate than traditional all polyethylene cemented glenoids. Although the radiographs of some patients demonstrated small focal areas of lucency, none have become loose, and only two have actually demonstrated glenoid component failure due to a fracture 6 years after the index procedure. One with glenoid loosening was due to polyethylene wear from a massive cuff tear occurring 8 years after the index procedure. Most patients experienced significant improvements in shoulder range of motion and reduction in pain. Trabecular metal-anchored glenoids when carefully implanted do not produce excessive failure rates, but rather result in functional improvements while decreasing operative time

Glenoid exposure is the name of the game in total shoulder arthroplasty. I can honestly say that it took me more than 5 years but less than 10 to feel confident exposing any glenoid, regardless of the degree of bone deformity and the severity of soft-tissue contracture. This lecture represents the synthesis of my experience exposing some of the most difficult glenoids. The basic principles are performing extensive soft-tissue release, minimizing the anteroposterior dimension of the humerus by osteophyte excision, making an accurate humeral neck cut, having a plethora of glenoid retractors, and knowing where to place them. The ten tips, in reverse order of importance are: 10.) Tilt the table away from operative side—this helps face the surface of the glenoid, especially in cases of posterior wear, toward the surgeon. 9.) Have multiple glenoid retractors—these include a large Darrach, a reverse double-pronged Bankart, one or two blunt Homans, small and large Fukudas. 8.) Remove all humeral osteophytes before attempting to retract the humerus posteriorly to expose the glenoid—this helps to decrease the overall anteroposterior dimension of the humerus and allows for maximum posterior displacement of the humerus. 7.) Make an accurate humeral neck cut—even 5mm of extra humeral bone will make glenoid exposure difficult. 6.) Optimal humeral position—it has been taught that abduction, external rotation, and extension is the optimal position. It may vary with each case. Therefore, experiment with humeral rotation to find the position that allows maximum visualization. This is often the position that makes the cut surface of the humerus parallel to the surface of the glenoid. 5.) Optimal retractor placement—my typical retractor placement is a Fukuda on the posterior lip of the glenoid, a reverse double-pronged Bankart on the anterior neck of the scapula, and a blunt Homan posterosuperiorly. Occasionally, a second blunt Homan anteroinferiorly is helpful, particularly in muscular males with a large pectoralis major. 4.) Laminar spreader for lateral humeral displacement—this can be helpful for posterior capsulorrhaphy or for posterior glenoid bone grafting. 3.) Maximal humeral capsular release—the release of the anterior capsule from the humerus must go well past the 6 o'clock position and up the posterior surface of the humerus. This aides in humeral exposure but also allows for more posterior displacement of the humerus during glenoid exposure. 2.) Anteroinferior capsular release or excision—extensive anteroinferior release or excision (my preference), allows for maximal posterior humeral displacement and also restores external rotation. 1.) Posterior or posteroinferior capsular release—release of the posteroinferior corner of the capsule from the glenoid results in a noticeable increase in posterior humeral retractability. In cases without substantial posterior subluxation, extensive release of the entire posterior capsule is performed