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Measurement of Internal Implantation Strains in Analogue Bone Using DVC
Alexander Marter1, Charles Burson-Thomas1, Alexander Dickinson1,2
1Bioengineering Science Research Group, School of Engineering, University of Southampton, Southampton SO17 1BJ, UK.
Materials (Basel, Switzerland)
|September 16, 2020
Summary
This study introduces Digital Volume Correlation (DVC) to measure strain during cementless implant surgery. DVC offers a more comprehensive understanding of bone strain compared to previous methods, aiding implant stability analysis.
Area of Science:
- Biomedical Engineering
- Orthopaedic Surgery
- Materials Science
Background:
- Cementless orthopaedic implant survivorship depends on initial stability.
- Inadequate press-fit causes micromotion, pain, and revision; excessive press-fit damages bone.
- Understanding strain generation during implantation is crucial for optimizing implant design and surgical technique.
Purpose of the Study:
- To develop and validate a Digital Volume Correlation (DVC) methodology for measuring volumetric strain during orthopaedic implant insertion.
- To compare experimental DVC measurements with Finite Element (FE) modeling predictions.
- To identify limitations and suggest improvements for future strain measurement techniques in this field.
Main Methods:
- A simplified implant model was inserted into analogue bone using a custom loading rig.
- Micro-computed tomography (micro-CT) was used to capture volumetric data.
- Digital Volume Correlation (DVC) was applied to measure full-field strain, with results compared to FE analysis.
Main Results:
- DVC successfully measured strain patterns throughout the analogue bone volume during simulated implantation.
- Correlation coefficients indicated strain localization and potential interface failure.
- FE model strain magnitudes were approximately double the experimental DVC measurements, suggesting a need for refined interface failure models.
Conclusions:
- Digital Volume Correlation (DVC) is a viable method for assessing volumetric strain during orthopaedic implant insertion.
- Discrepancies between DVC and FE models highlight the need for improved interface failure modeling, particularly accounting for bone structure behavior.
- Recommendations are provided for optimizing DVC subvolume size in future studies involving similar materials and geometries.

