TY - JOUR
T1 - Computational efficient method for assessing the influence of surgical variability on primary stability of a contemporary femoral stem in a cohort of subjects
AU - Al-Dirini, Rami M.A.
AU - Martelli, Saulo
AU - Taylor, Mark
PY - 2020/8
Y1 - 2020/8
N2 - Finite element (FE) modelling can provide detailed information on implant stability; however, its computational cost limits the possibility of completing large numerical analyses into the effect of surgical variability in a cohort of patients. The aim of this study was to develop an efficient surrogate model for a cohort of patients implanted using a common cementless hip stem. FE models of implanted femora were generated from computed tomography images for 20 femora (11 males, 9 females; 50–80 years; 52–116 kg). An automated pipeline generated FE models for 61 different unique scenarios that span the femur-specific range of implant positions. Peak hip contact and muscle forces for stair climbing were scaled to the donors’ body weight and applied to the models. A cohort-specific surrogate for implant micromotion was constructed from Gaussian process models trained using data from FE simulations representing the median and extreme implant positions for each femur. A convergence study confirmed suitability of the sampling method for cohorts with 10+ femora. The final model was trained using data from the 20 femora. Results showed very good agreement between the FE and the surrogate predictions for a total of 1036 alignment scenarios [root mean squared error (RMSE) < 20 µm; Rvalidation2 = 0.81]. The total time required for the surrogate model to predict the micromotion range associated with surgical variability was approximately one-eighth of the corresponding full FE analysis. This confirms that the developed model is an accurate yet computationally cheaper alternative to full FE analysis when studying the implant robustness in a cohort of 10+ femora.
AB - Finite element (FE) modelling can provide detailed information on implant stability; however, its computational cost limits the possibility of completing large numerical analyses into the effect of surgical variability in a cohort of patients. The aim of this study was to develop an efficient surrogate model for a cohort of patients implanted using a common cementless hip stem. FE models of implanted femora were generated from computed tomography images for 20 femora (11 males, 9 females; 50–80 years; 52–116 kg). An automated pipeline generated FE models for 61 different unique scenarios that span the femur-specific range of implant positions. Peak hip contact and muscle forces for stair climbing were scaled to the donors’ body weight and applied to the models. A cohort-specific surrogate for implant micromotion was constructed from Gaussian process models trained using data from FE simulations representing the median and extreme implant positions for each femur. A convergence study confirmed suitability of the sampling method for cohorts with 10+ femora. The final model was trained using data from the 20 femora. Results showed very good agreement between the FE and the surrogate predictions for a total of 1036 alignment scenarios [root mean squared error (RMSE) < 20 µm; Rvalidation2 = 0.81]. The total time required for the surrogate model to predict the micromotion range associated with surgical variability was approximately one-eighth of the corresponding full FE analysis. This confirms that the developed model is an accurate yet computationally cheaper alternative to full FE analysis when studying the implant robustness in a cohort of 10+ femora.
KW - Efficient models
KW - Machine learning
KW - Micromotion
KW - Primary stability
UR - http://www.scopus.com/inward/record.url?scp=85074638797&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/FT180100338
UR - http://purl.org/au-research/grants/ARC/DP180103146
U2 - 10.1007/s10237-019-01235-0
DO - 10.1007/s10237-019-01235-0
M3 - Article
C2 - 31637534
AN - SCOPUS:85074638797
SN - 1617-7959
VL - 19
SP - 1283
EP - 1295
JO - Biomechanics and Modeling in Mechanobiology
JF - Biomechanics and Modeling in Mechanobiology
IS - 4
ER -