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Considerations for reporting finite element analysis studies in biomechanics
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Simulation-based medicine and the development of complex computer models of biological structures is becoming ubiquitous for advancing biomedical engineering and clinical research. Finite element analysis (FEA) has been widely used in the last few decades to understand and predict biomechanical phenomena. Modeling and simulation approaches in biomechanics are highly interdisciplinary, involving novice and skilled developers in all areas of biomedical engineering and biology. While recent advances in model development and simulation platforms offer a wide range of tools to investigators, the decision making process during modeling and simulation has become more opaque. Hence, reliability of such models used for medical decision making and for driving multiscale analysis comes into question. Establishing guidelines for model development and dissemination is a daunting task, particularly with the complex and convoluted models used in FEA. Nonetheless, if better reporting can be established, researchers will have a better understanding of a model's value and the potential for reusability through sharing will be bolstered. Thus, the goal of this document is to identify resources and considerate reporting parameters for FEA studies in biomechanics. These entail various levels of reporting parameters for model identification, model structure, simulation structure, verification, validation, and availability. While we recognize that it may not be possible to provide and detail all of the reporting considerations presented, it is possible to establish a level of confidence with selective use of these parameters. More detailed reporting, however, can establish an explicit outline of the decision-making process in simulation-based analysis for enhanced reproducibility, reusability, and sharing.
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Each entity and activity in the final set has already been mentioned for provenance, modeling or documentation purposes, or experiment design of simulation studies, but they have not all been used together.
“Each entity and activity has already been mentioned for provenance, modeling or documentation purposes, or experiment design of simulation studies [1, 3–5, 8, 20, 21, 60–63], but they have not all been used together.”
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Self-citation
Metadata
- Authors
- Erdemir, A., Guess, T. M., Halloran, J., Tadepalli, S. C., & Morrison, T. M.
- Affiliations
- Cleveland Clinic (US)
- University of Missouri–Kansas City (US)
- University of Washington (US)
- United States Food and Drug Administration (US)
- Venue
- Journal of Biomechanics
- Publisher
- Elsevier BV
- Published
- 2012-02
- Volume
- 45
- Issue
- 4
- Pages
- 625-633
- ISSN
- 0021-9290 (ISSN-L)
- PMC
- PMC3278509
- OpenAlex
- W2039126460
- Cited by
- 234
- References
- 21
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 17 · 2023: 22 · 2022: 32 · 2021: 25 · 2020: 19 · 2019: 8 · 2018: 11 · 2017: 15 · 2016: 10 · 2015: 8 · 2014: 16 · 2013: 14 · 2012: 7
- FWCI
- 8.21
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Biomechanics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation (09–1078, CBET-0821459, CMMI-1039524, CMS-0506297)
- National Institutes of Health (R01EB006735, R01EB009643, R01HD037433)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Elasticity and Material Modeling
- Physical Sciences › Engineering › Biomedical Engineering › Anatomy and Medical Technology
- Physical Sciences › Computer Science › Information Systems › Research Data Management Practices
- Keywords
- finite element analysis, biomechanics, reporting guidelines, model verification, model validation, model reuse, model sharing, reproducibility, multiscale modeling
- MeSH terms
- Animals, Biomechanical Phenomena, Biomedical Engineering, Humans, Models, Biological, Finite Element Analysis
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