Journal of Shoulder and Elbow Surgery
Total shoulder arthroplasty: Glenoid component design
Introduction
Charles Neer initially described shoulder arthroplasty without resurfacing the glenoid; however, he subsequently introduced resurfacing of the glenoid because of the possibility of persistent pain, weakness, and loss of motion after hemiarthroplasty in patients with diseased and flattened glenoids.17 Although Neer’s original glenoid component underwent several modifications, the cemented, all-polyethylene, keeled component with conforming humeral and glenoid radii curvature became the glenoid implant of choice.9, 17, 18, 21, 32, 39, 40, 56
Glenoid loosening is the most common prosthesis-related cause for revision surgery after total shoulder arthroplasty, with rates ranging from 0% to 12.5%.6, 43, 60 The incidence of radiolucency at the glenoid-cement interface reported in the literature is high, ranging from 30% to 90%.5, 6 This variation is attributed to nonstandardized methods of measurement, inconsistent definitions, and limitations of conventional radiography.3, 4, 9, 11, 12, 15, 21, 39, 57Although Neer38 reported an approximately 30% incidence of radiolucent lines among 615 arthroplasties performed from 1973 to 1988, only 2 were revised for glenoid loosening. Neer postulated that the lines were the result of poor cement technique. Although the correlation between glenoid lucent lines and clinical loosening is uncertain, the association between loosening, declining patient satisfaction, and increasing shoulder pain with long-term follow-up is documented.3, 6, 9, 29, 31, 49, 51, 54 Reported survivorship of the Neer cemented, all-polyethylene glenoid component ranges from 83% to 93% at 10 years and 73% to 87% at 15 years after implantation.51, 54
Multiple factors contribute to implant stability, including glenoid preparation, soft-tissue balancing, wear debris, cellular mediators of osteoclastic bone resorption, and the availability of glenoid bone stock for prosthetic fixation. Prosthetic design considerations, such as the articular surface geometry, glenohumeral conformity, biomaterials, and the glenoid keel or peg morphology, are also critically important.33 As new components are being designed and marketed, the Neer prosthesis should be the benchmark upon which comparison studies are made. This report reviews the performance of glenoid designs, identifies factors that may influence the performance of glenoid components, and aims to provide a rationale for future changes in glenoid component design.
Section snippets
Glenoid anatomy
The normal glenoid cavity is shaped like an inverted comma. Its superior portion is narrow, and the inferior portion is broad.14 The cavity has a slightly concave articular surface covered by hyaline cartilage. The mean vertical dimension of the glenoid is 35 mm, and the mean transverse diameter is 25 mm.8, 33, 57 Saha46 found that 75% of the shoulders studied had retroverted glenoid surfaces averaging 7.4° and that 25% of the glenoid surfaces were anteverted from 2° to 10°. Regarding vertical
Anatomic versus oval
Anatomic or oval-shaped glenoid components are available (Figure 2). The anatomic glenoid may provide the advantage of avoiding internal impingement of nonarticular structures with overhanging polyethylene. However, having a smaller upper portion of the component decreases the surface area available for contact as well as the wall height. This decrease in wall height in the superior portion of the component theoretically decreases the force required for dislocation or subluxation. As shown by
Polyethylene versus alternative bearing surfaces
The generation of polyethylene wear debris may well be the factor limiting survival of contemporary designs of total shoulder implants, as has been the experience with other prosthetic joints.10, 56 Early studies have been informative, showing that the particles from shoulders are larger and more fibrillar than the particles from hips.28, 58 It remains to be seen whether polyethylene modifications will result in improved clinical outcomes.42
The use of alternative bearing surfaces in the hip and
Conclusion
The search will continue for a durable biologic fixation method for glenoid components. This is particularly important because of the decreasing age of patients requiring replacement. Future challenges for the design of glenoid components include the development of durable cementless components for routine primary total shoulder arthroplasties. This will involve the continued evaluation of metal-backed biologic ingrowth surfaces, such as fiber metal, trabecular metal, or hydroxyapatite-coated
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