TY - JOUR
T1 - The finite cell method for bone simulations
T2 - Verification and validation
AU - Ruess, Martin
AU - Tal, David
AU - Trabelsi, Nir
AU - Yosibash, Zohar
AU - Rank, Ernst
N1 - Funding Information:
Acknowledgments We would like to thank Prof. Charles Milgrom from the Hadassah Hospital, Jerusalem for the femur and his help with the CT scans and experiments. The authors gratefully acknowledge the generous support of the Technische Universität München—Institute for Advanced Study and International Graduate School of Science and Engineering, funded by the German Excellence Initiative, which made this research possible.
PY - 2012/3
Y1 - 2012/3
N2 - Standard methods for predicting bone's mechanical response from quantitative computer tomography (qCT) scans aremainly based on classical h-version finite element methods (FEMs). Due to the low-order polynomial approximation, the need for segmentation and the simplified approach to assign a constant material property to each element in h-FE models, these often compromise the accuracy and efficiency of h-FE solutions. Herein, a non-standard method, the finite cellmethod (FCM), is proposed for predicting the mechanical response of the human femur. The FCM is free of the above limitations associated with h-FEMs and is orders of magnitude more efficient, allowing its use in the setting of computational steering. This non-standard method applies a fictitious domain approach to simplify the modeling of a complex bone geometry obtained directly from a qCT scan and takes into consideration easily the heterogeneous material distribution of the various bone regions of the femur. The fundamental principles and properties of theFCM are briefly described in relation to bone analysis, providing a theoretical basis for the comparison with the p-FEM as a reference analysis and simulation method of high quality. Both p-FEM and FCM results are validated by comparison with an in vitro experiment on a fresh-frozen femur.
AB - Standard methods for predicting bone's mechanical response from quantitative computer tomography (qCT) scans aremainly based on classical h-version finite element methods (FEMs). Due to the low-order polynomial approximation, the need for segmentation and the simplified approach to assign a constant material property to each element in h-FE models, these often compromise the accuracy and efficiency of h-FE solutions. Herein, a non-standard method, the finite cellmethod (FCM), is proposed for predicting the mechanical response of the human femur. The FCM is free of the above limitations associated with h-FEMs and is orders of magnitude more efficient, allowing its use in the setting of computational steering. This non-standard method applies a fictitious domain approach to simplify the modeling of a complex bone geometry obtained directly from a qCT scan and takes into consideration easily the heterogeneous material distribution of the various bone regions of the femur. The fundamental principles and properties of theFCM are briefly described in relation to bone analysis, providing a theoretical basis for the comparison with the p-FEM as a reference analysis and simulation method of high quality. Both p-FEM and FCM results are validated by comparison with an in vitro experiment on a fresh-frozen femur.
KW - Bone mechanics
KW - Ficitious domain method
KW - High-order FEM
KW - Human femur
UR - http://www.scopus.com/inward/record.url?scp=84861094879&partnerID=8YFLogxK
U2 - 10.1007/s10237-011-0322-2
DO - 10.1007/s10237-011-0322-2
M3 - מאמר
AN - SCOPUS:84861094879
VL - 11
SP - 425
EP - 437
JO - Biomechanics and Modeling in Mechanobiology
JF - Biomechanics and Modeling in Mechanobiology
SN - 1617-7959
IS - 3-4
ER -