Background. Stemless prostheses are recognized to be an effective solution for anatomic total shoulder arthroplasty (TSA) while providing bone preservation and shortest operating time. Reverse shoulder arthroplasty (RSA) with stemless has not showed the same effectiveness, as clinical and biomechanical performances strongly depend on the design. The main concern is related to stability and bone response due to the changed biomechanical conditions; few studies have analyzed these effects in anatomic designs through Finite Element Analysis (FEA), however there is currently no study analyzing the reverse configuration. Additionally, most of the studies do not consider the effect of changing the neck-shaft angle (NSA) resection of the humerus nor the proper assignment of spatial bone properties to the bone models used in the simulations. The aim of this FEA study is to analyze bone response and primary stability of the SMR
In the past century several shoulder reconstruction systems with different types of prostheses and fixation methods have been developed to improve shoulder arthroplasty, especially to cover a wide range of pathologies and revision situations. The aim of this prospective trial was to report clinical and radiological mid-term results of a stemless humeral head replacement with metaphyseal hollow screw fixation. A consecutive series of 147 shoulders in 138 patients (84 female, 54 male; mean age of 67 years, range 40–84) undergoing stemless humeral head arthroplasty were considered for this single-centre trial. We prospectively followed 120 shoulders (40 hemi- and 80 total-arthroplasties) for an average of five years or until a reoperation. Patient's clinical and functional outcome was evaluated according to the Constant score and active range of motions (ROM) was measured. Patient's satisfaction with the treatment was evaluated. Additionally, operating times and complications were recorded. Radiological assessment for radiolucencies or implant migration was performed. The mean Constant score significantly increased from 35 points preoperatively to 62 points at the last follow-up (p<0.001). All subcomponents (pain, daily activity, ROM, strength) of the Constant score were significantly (p<0.001) higher at follow-up. Active flexion improved from 90° to 150° (p<0.001), active abduction from 78° to 120° (p<0.001), and active external rotation from 20° to 40° (p<0.001) between preoperative and last clinical assessment. Furthermore, 54% of the patients were very satisfied, 34% satisfied, and 12% unsatisfied. Operating times of the new
Introduction. The new era of shoulder arthroplasty is moving away from long stemmed, cemented humeral components to cementless, stemless and metaphyseal fixed implants and to humeral resurfacing. The early clinical results and functional outcome of stemless shoulder arthroplasty is presented. Methods. A retrospective single-surgeon series of stemless shoulder prostheses implanted from 2011 to 2013 at our institution was evaluated. Perioperative complications, Theatre time and length of hospital stay (LOS) were recorded. Postoperative radiographic and clinical evaluation including measurement of joint mobility, the Oxford Shoulder Score (OSS), and Disabilities of the Arm, Shoulder and Hand (DASH) score by independent evaluators were made. Results. A total of 23 stemless shoulder arthroplasty were implanted in 22 patients. Mean age was 57.8 years. Mean follow up was 22 months (8–45). Symptomatic primary gleno-humeral osteoarthritis was the main indication for implantation (83%). None of the patients experienced periprosthetic fractures, glenoid notching, and implant loosening/migration. Mean OSS (44 ± 6.0) and mean DASH score (11 ± 6.5). Mean operative time was (88 ± 16.0 min) and mean length of hospital stay (1.1 ± 0.82 day). Active shoulder motion improved by (mean): 30° (95% CI 10–45) external rotation, 67° (95% CI 30- 100) forward elevation and 54° (95% CI 35- 90) Abduction. Conclusion. The implantation of
Introduction: The Motus (Osteo) total knee replacement design is an uncemented,
Summary Statement. The current biomecahnical study demonstrated that the stemless peripheral leg humeral component prototype and central screw humeral component prototype achieved similar initial fixation as stemmed Global Advantage humeral component in terms of resultant micromotion in total shoulder arthroplasty. Introduction. A stemless humeral component may offer a variety of advantages over its stemmed counterpart, e.g. easier implantation, preservation of humeral bone stock, fewer humeral complications, etc. However, the initial fixation of a stemless humeral component typically depends on cementless metaphyseal press-fit, which could pose some challenges to the initial stability. Long-term success of cementless implants is highly related to osseous integration, which is affected by initial implant-bone interface motion. 1. The purpose of the study was to biomechanically compare micromotion at the implant-bone interface of three humeral components in total shoulder arthroplasty. Patients & Methods. Three humeral components were evaluated: Global Advantage, a central screw prototype, and a peripheral leg prototype. All components were the smallest sizes available. Global Advantage is a stemmed design. Both central screw prototype and peripheral leg prototype are stemless designs. Five specimens were tested for each design. Composite analogue humeral models were utilized to simulate the humeral bone. The cortical wall had a thickness of 3 mm and a density of 481 kg/m. 3. , while the cancellous density was 80 kg/m. 3. The model was custom fabricated to accommodate 40 mm humeral component and had a 45° resected surface and a square base to facilitate test setup. Each humeral component was implanted per its surgical technique. The construct was clamped in a vise with the humeral shaft angled at 27°. A MTS test system was employed to conduct the test. A sinusoidal compressive load from 157 N to 1566 N (2BW) was applied to the humeral component at 1 Hz for 100 cycles. The implant-bone interface micromotion was measured with a digital image correlation system which had a resolution of less than 1 micron. The micromotion measurement was transformed to 2 components: 1 was parallel and the other perpendicular to the humeral resection surface. Peak-valley micromotion from the last 10 cycles were averaged and utilised for data analyses. A one-way ANOVA and post-hoc Tukey tests were performed to compare the micromotion of different designs (α=0.05). Results. Micromotion of Global Advantage parallel to the resection (X-Axis) was significantly less than that of central screw prototype and peripheral leg prototype. Micromotion of peripheral leg prototype perpendicular to the resection (Y-Axis) was significantly less than Global Advantage and central screw prototype. There was no significant difference between different designs in resultant micromotion. Discussion/Conclusion. Clinical studies have shown that current