Basic Science
Augmented wedge-shaped glenoid component for the correction of glenoid retroversion: a finite element analysis

https://doi.org/10.1016/j.jse.2013.06.008Get rights and content

Background

This study undertook a computational analysis of a wedged glenoid component for correction of retroverted glenoid arthritic deformity to determine whether a wedge-shaped glenoid component design with a built-in correction for version reduces excessive stresses in the implant, cement, and glenoid bone. Recommendations for correcting retroversion deformity are asymmetric reaming of the anterior glenoid, bone grafting of the posterior glenoid, or a glenoid component with posterior augmentation. Eccentric reaming has the disadvantages of removing normal bone, reducing structural support for the glenoid component, and increasing the risk of bone perforation by the fixation pegs. Bone grafting to correct retroverted deformity does not consistently generate successful results.

Methods

Finite element models of 2 scapulae models representing a normal and an arthritic retroverted glenoid were implanted with a standard glenoid component (in retroversion or neutral alignment) or a wedged component. Glenohumeral forces representing in vivo loading were applied and stresses and strains computed in the bone, cement, and glenoid component.

Results

The retroverted glenoid components generated the highest compressive stresses and decreased cyclic fatigue life predictions for trabecular bone. Correction of retroversion by the wedged glenoid component significantly decreased stresses and predicted greater bone fatigue life. The cement volume estimated to survive 10 million cycles was the lowest for the retroverted components and the highest for neutrally implanted glenoid components and for wedged components.

Conclusion

A wedged glenoid implant is a viable option to correct severe arthritic retroversion, reducing the need for eccentric reaming and the risk for implant failure.

Section snippets

Materials and methods

Two whole scapula bone models were selected from CT scan data sets: 1 from a normal, healthy scapula with neutral glenoid alignment (55-year-old man) and 1 from an osteoarthritic scapula with 17° retroversion (62-year-old man). Surface meshes were generated for both cortical and cancellous bone layers using Mimics 3-dimensional image segmentation software (Materialise, Leuven, Belgium). These surface meshes were converted to solid 4-node tetrahedral element meshes with HyperMesh (Altair

Stress on bone model structures

The retroverted glenoid components of both normal and arthritic models generated the highest minimal principal stresses (23 and 24 MPa, respectively), with stress distributed posteriorly toward the edge of the glenoid face. As determined from the bone strength assigned to our models, these stress values were high enough to place the cortical bone of the scapula neck at risk for single cycle failure. Correction of glenoid retroversion by the wedged-glenoid component decreased stress magnitudes

Discussion

Most patients requiring total shoulder arthroplasty have an arthritic glenoid deformity that results in retroversion.8, 12 Implanting the glenoid component without correcting moderate to severe retroversion can have adverse biomechanical effects. The 3 options for correcting retroversion deformity are asymmetric reaming of the anterior glenoid, bone grafting of the posterior glenoid, and implanting a specialized glenoid component with posterior augmentation. Eccentric reaming to correct

Conclusion

Our study indicates that an appropriately wedged glenoid implant is an option to correct severe arthritic retroversion and to reduce the risk for implant or bone failure without the need for eccentric reaming. This study is a biomechanical analysis and therefore requires appropriate clinical studies for validation.

Disclaimer

The authors, their immediate families, and any research foundations with which they are affiliated have not received any financial payments or other benefits from any commercial entity related to the subject of this article.

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Investigational Review Board approval was obtained for the use of de-identified clinical CT scans.

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