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      Finite element simulations of smart fracture plates capable of cyclic shortening and lengthening: which stroke for which fracture?

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          Abstract

          Introduction: Bone healing can be improved by axial micromovement, as has been shown in animals and human patients with external fixators. In the development of smart fracture plates, the ideal amount of stroke for different fracture types in the different healing stages is currently unknown. It was hypothesized that the resulting strain in the fracture gap of a simple tibial shaft fracture does not vary with the amount of axial stroke in the plate, the fracture gap size, and the fracture angle.

          Methods: With finite element simulations based on body donation computed tomography data, the second invariant of the deviatoric strain tensor (J2), strain energy density, hydrostatic strain, octahedral shear strain, and percentage of the fracture gap in the “perfect healing window” were computed for different gap sizes (1–3 mm), angles (5°–60°), and plate stroke levels (0.05–0.60 mm) in three healing stages. Multiple linear regression analyses were performed.

          Results: Findings showed that an active fracture plate should deliver an axial stroke in the range of 0.10–0.45 mm. Different optimal stroke values were found for each healing phase, namely, 0.10–0.25 mm for the first, 0.10 mm for the second, and 0.35–0.45 mm for the third healing phase, depending on the fracture gap size and less on the fracture angle. J2, hydrostatic strain, octahedral shear strain and the strain energy density correlated with the fracture gap size and angle (all p < 0.001). The influence of the fracture gap size and angle on the variability (adjusted R 2) in several outcome measures in the fracture gap was shown to vary throughout healing. The contribution to the variability of the percentage of the fracture gap in the perfect healing window was greatest during the second healing phase. For J2, strain energy density, hydrostatic strain, and octahedral shear strain, the fracture gap size showed the greatest contribution in the third fracture healing phase, while the influence of fracture angle was independent of the healing phase.

          Discussion: The present findings are relevant for implant development and to design clinical studies that aim to accelerate fracture healing using axial micromovement.

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          Most cited references62

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          The biology of fracture healing.

          The biology of fracture healing is a complex biological process that follows specific regenerative patterns and involves changes in the expression of several thousand genes. Although there is still much to be learned to fully comprehend the pathways of bone regeneration, the over-all pathways of both the anatomical and biochemical events have been thoroughly investigated. These efforts have provided a general understanding of how fracture healing occurs. Following the initial trauma, bone heals by either direct intramembranous or indirect fracture healing, which consists of both intramembranous and endochondral bone formation. The most common pathway is indirect healing, since direct bone healing requires an anatomical reduction and rigidly stable conditions, commonly only obtained by open reduction and internal fixation. However, when such conditions are achieved, the direct healing cascade allows the bone structure to immediately regenerate anatomical lamellar bone and the Haversian systems without any remodelling steps necessary. In all other non-stable conditions, bone healing follows a specific biological pathway. It involves an acute inflammatory response including the production and release of several important molecules, and the recruitment of mesenchymal stem cells in order to generate a primary cartilaginous callus. This primary callus later undergoes revascularisation and calcification, and is finally remodelled to fully restore a normal bone structure. In this article we summarise the basic biology of fracture healing. Copyright © 2011 Elsevier Ltd. All rights reserved.
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            Epidemiology of Fracture Nonunion in 18 Human Bones.

            Failure of bone fracture healing occurs in 5% to 10% of all patients. Nonunion risk is associated with the severity of injury and with the surgical treatment technique, yet progression to nonunion is not fully explained by these risk factors.
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              Magnitudes of local stress and strain along bony surfaces predict the course and type of fracture healing.

              A new quantitative tissue differentiation theory which relates the local tissue formation in a fracture gap to the local stress and strain is presented. Our hypothesis proposes that the amounts of strain and hydrostatic pressure along existing calcified surfaces in the fracture callus determine the differentiation of the callus tissue. The study compares the local strains and stresses in the callus as calculated from a finite element model with histological findings from an animal fracture model. The hypothesis predicts intramembranous bone formation for strains smaller approximately +/- 5% and hydrostatic pressures smaller than +/- 0.15 MPa. Endochondral ossification is associated with compressive pressures larger than about -0.15 MPa and strains smaller than +/- 15%. All other conditions seemed to lead to connective tissue or fibrous cartilage. The hypothesis enables a better understanding of the complex tissue differentiation seen in histological images and the mechanical conditions for healing delayed healing or nonunions.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/1423648/overviewRole: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1564745/overviewRole: Role:
                URI : https://loop.frontiersin.org/people/2628752/overviewRole: Role: Role:
                Role: Role:
                URI : https://loop.frontiersin.org/people/546471/overviewRole: Role: Role: Role: Role: Role: Role:
                Journal
                Front Bioeng Biotechnol
                Front Bioeng Biotechnol
                Front. Bioeng. Biotechnol.
                Frontiers in Bioengineering and Biotechnology
                Frontiers Media S.A.
                2296-4185
                23 July 2024
                2024
                : 12
                : 1420047
                Affiliations
                [1] 1 Chair of Applied Mechanics , Saarland University , Saarbrücken, Germany
                [2] 2 Department of Trauma , Hand and Reconstructive Surgery , Departments and Institutes of Surgery , Saarland University , Homburg, Germany
                [3] 3 Werner Siemens-Endowed Chair for Innovative Implant Development (Fracture Healing) , Departments and Institutes of Surgery , Saarland University , Homburg, Germany
                Author notes

                Edited by: Chi Wu, The University of Sydney, Australia

                Reviewed by: Jingxiao Zhong, Max Planck Institute of Colloids and Interfaces, Germany

                Boyang Wan, The University of Sydney, Australia

                *Correspondence: Bergita Ganse, Bergita.ganse@ 123456uks.eu
                Article
                1420047
                10.3389/fbioe.2024.1420047
                11300273
                1bfa05b7-69e8-4e99-b9c0-f034a41c96a2
                Copyright © 2024 Roland, Diebels, Wickert, Pohlemann and Ganse.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 19 April 2024
                : 01 July 2024
                Funding
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Werner Siemens Foundation [Smart Implants 2.0]. The funding source was not involved in the study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.
                Categories
                Bioengineering and Biotechnology
                Original Research
                Custom metadata
                Biomechanics

                fracture healing,bone regeneration,computer simulation,smart implant,active implant,biomechanics,osteosynthesis,digital health

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