随机数字人现在正在参加计算机成像试验——生成数字队列的方法和工具

IF 5 Q1 ENGINEERING, BIOMEDICAL Progress in biomedical engineering (Bristol, England) Pub Date : 2023-10-18 DOI:10.1088/2516-1091/ad04c0
Aldo Badano, MIguel Lago, Elena Sizikova, Jana Delfino, Shuyue Guan, Mark A Anastasio, Berkman Sahiner
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引用次数: 2

摘要

随机临床试验通常被视为判断医疗干预质量的最高证据标准,但它远非完美。计算机成像试验是一种计算机研究,旨在通过完全通过计算机模拟收集这些信息来确定医疗设备的性能。评估新技术的硅片试验的好处包括节省大量资源和时间,将受试者风险降至最低,能够研究在物理世界中无法实现的设备,允许对新技术进行快速有效的调查,并确保来自所有相关子群体的代表。为了进行计算机试验,需要人类的数字表示。我们回顾了获取数字人体用于计算机成像研究的方法和工具的最新发展。首先,我们介绍了数字人体模型的术语和分类。其次,我们调查了产生健康状态的数字人类和产生疾病病例的可用方法,并简要讨论了增强方法的作用。最后,我们讨论了采样数字队列的方法,并了解与选择特定患者分布相关的权衡和潜在的研究偏差。
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The stochastic digital human is now enrolling for in silico imaging trials – Methods and tools for generating digital cohorts
Abstract Randomized clinical trials, while often viewed as the highest evidentiary bar by which to judge the quality of a medical intervention, are far from perfect. In silico imaging trials are computational studies that seek to ascertain the performance of a medical device by collecting this information entirely via computer simulations. The benefits of in silico trials for evaluating new technology include significant resource and time savings, minimization of subject risk, the ability to study devices that are not achievable in the physical world, allow for the rapid and effective investigation of new technologies and ensure representation from all relevant subgroups. To conduct in silico trials, digital representations of humans are needed. We review the latest developments in methods and tools for obtaining digital humans for in silico imaging studies. First, we introduce terminology and a classification of digital human models. Second, we survey available methodologies for generating digital humans with healthy status and for generating diseased cases and discuss briefly the role of augmentation methods. Finally, we discuss approaches for sampling digital cohorts and understanding the trade-offs and potential for study bias associated with selecting specific patient distributions.
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CiteScore
9.40
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