乳房切除术后乳房重建中组织扩张过程中人体皮肤变形和生长的预测模型。

IF 1.7 4区 医学 Q4 BIOPHYSICS
Joel Laudo, Tianhong Han, Joanna Ledwon, Ariel Figueroa, Arun/Kumar Gosain, Taeksang Lee, Adrian Buganza Tepole
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引用次数: 0

摘要

使用组织扩张器进行乳房重建是乳房切除术后的主要治疗选择。虽然皮肤生长是对慢性超生理拉伸的反应,但个体患者因素,如乳房形状、体积、皮肤预张力和机械特性,会产生独特的变形和生长模式。在治疗前无法预测皮肤的生长和变形常常导致并发症和次优的美学结果。个性化预测模拟为这些挑战提供了一个有希望的解决方案。我们提出了一个管道预测计算模型的皮肤生长在组织扩张。在治疗开始时,我们收集3D照片并创建初始有限元(FE)模型。我们的框架考虑了治疗方案、机械性能和生物参数的不确定性。这些不确定性是由外科医生的输入、现有的机械特性文献和先前对猪的生物参数模型的研究得出的。通过在治疗过程中纵向收集三维照片,并通过贝叶斯框架整合数据,我们可以系统地减少预测中的不确定性。使用蒙特卡罗方法对校准的个性化模型进行采样,这需要数千个模型评估。为了克服直接评估有限元模型的计算限制,我们使用高斯过程替代模型。我们期望在不久的将来,这个管道可以用来指导患者的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive Modeling of Human Skin Deformation and Growth During Tissue Expansion In Post-Mastectomy Breast Reconstruction.

Breast reconstruction using tissue expanders is the primary treatment option following mastectomy. Although skin growth in response to chronic supra-physiological stretch is well-established, individual patient factors such as breast shape, volume, skin pre-strain, and mechanical properties, create unique deformation and growth patterns. The inability to predict skin growth and deformation prior to treatment often leads to complications and suboptimal aesthetic outcomes. Personalized predictive simulations offer a promising solution to these challenges. We present a pipeline for predictive computational models of skin growth in tissue expansion. At the start of treatment, we collect 3D photos and create an initial finite element (FE) model. Our framework accounts for uncertainties in treatment protocols, mechanical properties, and biological parameters. These uncertainties are informed by surgeon input, existing literature on mechanical properties, and prior research on porcine models for biological parameters. By collecting 3D photos longitudinally during treatment, and integrating the data through a Bayesian framework, we can systematically reduce uncertainty in the predictions. Calibrated personalized models are sampled using Monte Carlo methods, which require thousands of model evaluations. To overcome the computational limitations of directly evaluating the FE model, we use Gaussian process surrogate models. We anticipate that this pipeline can be used to guide patient treatment in the near future.

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来源期刊
CiteScore
3.40
自引率
5.90%
发文量
169
审稿时长
4-8 weeks
期刊介绍: Artificial Organs and Prostheses; Bioinstrumentation and Measurements; Bioheat Transfer; Biomaterials; Biomechanics; Bioprocess Engineering; Cellular Mechanics; Design and Control of Biological Systems; Physiological Systems.
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