Can patient-specific finite element models better predict fractures in metastatic bone disease than experienced clinicians?

被引:43
作者
Eggermont, F. [1 ]
Derikx, L. C. [1 ]
Verdonschot, N. [1 ,4 ]
van der Geest, I. C. M. [2 ]
de Jong, M. A. A. [1 ,5 ]
Snyers, A. [3 ]
van der Linden, Y. M. [1 ,6 ]
Tanck, E. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Orthopaed Res Lab, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Dept Orthopaed,Orthopaed Res Lab, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Dept Radiat Oncol,Orthopaed Res Lab, Nijmegen, Netherlands
[4] Lab Biomech Engn, Enschede, Netherlands
[5] Radiotherapeut Inst Friesland, Leeuwarden, Netherlands
[6] Leiden Univ, Dept Radiotherapy, Med Ctr, Leiden, Netherlands
关键词
Finite element modelling; Fracture prediction; Femur; Metastatic bone disease; CT-SCAN DATA; RANDOMIZED-TRIAL; PROXIMAL FEMUR; LESIONS; RISK; STRENGTH; RADIOTHERAPY; IMPROVES; DENSITY; STRAIN;
D O I
10.1302/2046-3758.76.BJR-2017-0325.R2
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Objectives In this prospective cohort study, we investigated whether patient-specific finite element (FE) models can identify patients at risk of a pathological femoral fracture resulting from metastatic bone disease, and compared these FE predictions with clinical assessments by experienced clinicians. Methods A total of 39 patients with non-fractured femoral metastatic lesions who were irradiated for pain were included from three radiotherapy institutes. During follow-up, nine pathological fractures occurred in seven patients. Quantitative CT-based FE models were generated for all patients. Femoral failure load was calculated and compared between the fractured and non-fractured femurs. Due to inter-scanner differences, patients were analyzed separatelyfor the three institutes. In addition, the FE-based predictions were compared with fracture risk assessments by experienced clinicians. Results In institute 1, median failure load was significantly lower for patients who sustained a fracture than for patients with no fractures. In institutes 2 and 3, the number of patients with a fracture was too low to make a clear distinction. Fracture locations were well predicted by the FE model when compared with post-fracture radiographs. The FE model was more accurate in identifying patients with a high fracture risk compared with experienced clinicians, with a sensitivity of 89% versus 0% to 33% for clinical assessments. Specificity was 79% for the FE models versus 84% to 95% for clinical assessments. Conclusion FE models can be a valuable tool to improve clinical fracture risk predictions in metastatic bone disease. Future work in a larger patient population should confirm the higher predictive power of FE models compared with current clinical guidelines.
引用
收藏
页码:430 / 439
页数:10
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