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Computational models using femur developed densitometric and density-modulus relationships have shown excellent agreement between experimental models and FEMs (Table 1).
In a previous study, Omori et al. compared the compressed displacement between experimental models and FEA models to verify the validity of the FEA models [22].
Although significant differences may exist between experimental models and the real-world clinical setting [6], the pathophysiology of the eligible septic patients in the present study may resemble that in a cecal ligation and puncture model.
The Bland and Altman limits of agreement were low and include zero for all models, indicating that there was no clinically significant difference between experimental models and that no systematic bias was apparent.
Nonetheless, greater consideration should be given to clarify inconsistencies between experimental models and population studies.
In addition, affinities and differences between experimental models and human disease need to be better defined and clarified.
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The extent of compressed displacement and the strain in the peri-implant bone were compared between the experimental models and the FEA models.
The correlation coefficient between the experimental model and the contact model was 0.925, representing a significant and strong correlation (p < 0.01).
The agreement between the experimental model and real-world tumor biology data images are surprisingly close.
The concordance between the images from the experimental model and the tumor are conclusive.
Discrepancies between experimental pain models and clinical studies including chronic pain patients are usually reported in the literature.
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between stochastic models and
between smartphone models and
between unilateral models and
between different models and
between statistical models and
between economic models and
between physical models and
between computable models and
between epidemiological models and
between conceptual models and
between classical models and
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