Finite element analysis of vertebroplasty in the osteoporotic T11‐L1 vertebral body: Effects of bone cement formulation

Author:

Mondal Subrata1ORCID,MacManus David B.12,Banche‐Niclot Federica3,Vitale‐Brovarone Chiara3,Fiorilli Sonia3,McCarthy Helen O.4,Dunne Nicholas15678

Affiliation:

1. School of Mechanical and Manufacturing Engineering Dublin City University Dublin 9 Ireland

2. BRAIN Lab, School of Mechanical & Materials Engineering University College Dublin Dublin 4 Ireland

3. Department of Applied Science and Technology Politecnico di Torino Turin Italy

4. School of Pharmacy Queen's University Belfast Belfast BT9 7 BL UK

5. Centre for Medical Engineering Research Dublin City University Dublin 9 Ireland

6. Department of Mechanical and Manufacturing Engineering, School of Engineering Trinity College Dublin Dublin 2 Ireland

7. Advanced Manufacturing Research Centre (I‐Form), School of Mechanical and Manufacturing Engineering Dublin City University Dublin 9 Ireland

8. Advanced Materials and Bioengineering Research Centre (AMBER) Trinity College Dublin Dublin 2 Ireland

Abstract

AbstractVertebral compression fractures are one of the most severe clinical consequences of osteoporosis and the most common fragility fracture afflicting 570 and 1070 out of 100,000 men and women worldwide, respectively. Vertebroplasty (VP), a minimally invasive surgical procedure that involves the percutaneous injection of bone cement, is one of the most efficacious methods to stabilise osteoporotic vertebral compression fractures. However, postoperative fracture has been observed in up to 30% of patients following VP. Therefore, this study aims to investigate the effect of different injectable bone cement formulations on the stress distribution within the vertebrae and intervertebral discs due to VP and consequently recommend the optimal cement formulation. To achieve this, a 3D finite element (FE) model of the T11‐L1 vertebral body was developed from computed tomography scan data of the spine. Osteoporotic bone was modeled by reducing the Young's modulus by 20% in the cortical bone and 74% in cancellous bone. The FE model was subjected to different physiological movements, such as extension, flexion, bending, and compression. The osteoporotic model caused a reduction in the average von Mises stress compared with the normal model in the T12 cancellous bone and an increment in the average von Mises stress value at the T12 cortical bone. The effects of VP using different formulations of a novel injectable bone cement were modeled by replacing a region of T12 cancellous bone with the materials. Due to the injection of the bone cement at the T12 vertebra, the average von Mises stresses on cancellous bone increased and slightly decreased on the cortical bone under all loading conditions. The novel class of bone cements investigated herein demonstrated an effective restoration of stress distribution to physiological levels within treated vertebrae, which could offer a potential superior alternative for VP surgery as their anti‐osteoclastogenic properties could further enhance the appeal of their fracture treatment and may contribute to improved patient recovery and long‐term well‐being.

Publisher

Wiley

Subject

Biomedical Engineering,Biomaterials

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