Author
Listed:
- Hans Liebl
- Eduardo Grande Garcia
- Fabian Holzner
- Peter B Noel
- Rainer Burgkart
- Ernst J Rummeny
- Thomas Baum
- Jan S Bauer
Abstract
Purpose: To experimentally validate a non-linear finite element analysis (FEA) modeling approach assessing in-vitro fracture risk at the proximal femur and to transfer the method to standard in-vivo multi-detector computed tomography (MDCT) data of the hip aiming to predict additional hip fracture risk in subjects with and without osteoporosis associated vertebral fractures using bone mineral density (BMD) measurements as gold standard. Methods: One fresh-frozen human femur specimen was mechanically tested and fractured simulating stance and clinically relevant fall loading configurations to the hip. After experimental in-vitro validation, the FEA simulation protocol was transferred to standard contrast-enhanced in-vivo MDCT images to calculate individual hip fracture risk each for 4 subjects with and without a history of osteoporotic vertebral fractures matched by age and gender. In addition, FEA based risk factor calculations were compared to manual femoral BMD measurements of all subjects. Results: In-vitro simulations showed good correlation with the experimentally measured strains both in stance (R2 = 0.963) and fall configuration (R2 = 0.976). The simulated maximum stress overestimated the experimental failure load (4743 N) by 14.7% (5440 N) while the simulated maximum strain overestimated by 4.7% (4968 N). The simulated failed elements coincided precisely with the experimentally determined fracture locations. BMD measurements in subjects with a history of osteoporotic vertebral fractures did not differ significantly from subjects without fragility fractures (femoral head: p = 0.989; femoral neck: p = 0.366), but showed higher FEA based risk factors for additional incident hip fractures (p = 0.028). Conclusion: FEA simulations were successfully validated by elastic and destructive in-vitro experiments. In the subsequent in-vivo analyses, MDCT based FEA based risk factor differences for additional hip fractures were not mirrored by according BMD measurements. Our data suggests, that MDCT derived FEA models may assess bone strength more accurately than BMD measurements alone, providing a valuable in-vivo fracture risk assessment tool.
Suggested Citation
Hans Liebl & Eduardo Grande Garcia & Fabian Holzner & Peter B Noel & Rainer Burgkart & Ernst J Rummeny & Thomas Baum & Jan S Bauer, 2015.
"In-Vivo Assessment of Femoral Bone Strength Using Finite Element Analysis (FEA) Based on Routine MDCT Imaging: A Preliminary Study on Patients with Vertebral Fractures,"
PLOS ONE, Public Library of Science, vol. 10(2), pages 1-15, February.
Handle:
RePEc:plo:pone00:0116907
DOI: 10.1371/journal.pone.0116907
Download full text from publisher
Citations
Citations are extracted by the
CitEc Project, subscribe to its
RSS feed for this item.
Cited by:
- Kevin Bethke & Virgil Andrei & Klaus Rademann, 2016.
"Decreasing the Effective Thermal Conductivity in Glass Supported Thermoelectric Layers,"
PLOS ONE, Public Library of Science, vol. 11(3), pages 1-19, March.
- Jonas A. Pramudita & Seiji Kamiya & Sadayuki Ujihashi & Hyung-Yun Choi & Masato Ito & Ryoji Watanabe & Jeff R. Crandall & Richard W. Kent, 2017.
"Estimation of conditions evoking fracture in finger bones under pinch loading based on finite element analysis,"
Computer Methods in Biomechanics and Biomedical Engineering, Taylor & Francis Journals, vol. 20(1), pages 35-44, January.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0116907. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.