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Pharmacokinetic models in clinical practice: What model to use for DCE-MRI of the breast?

机译:临床实践中的药物动力学模型:乳腺的DCE-MRI使用哪种模型?

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Pharmacokinetic modeling is increasingly used in DCE-MRI high risk breast cancer screening. Several models are available. The most common models are the standard and extended Tofts, the shutter-speed, and the Brix model. Each model and the meaning of its parameters is explained. It was investigated which models can be used in a clinical setting by simulating a range of sampling rates and noise levels representing different MRI acquisition schemes. In addition, an investigation was performed on the errors introduced in the estimates of the pharmacokinetic parameters when using a physiologically less complex model, i.e. the standard Tofts model, to fit curves generated with more complex models. It was found that the standard Tofts model is the only model that performs within an error margin of 20% on parameter estimates over a range of sampling rates and noise levels. This still holds when small complex physiological effects are present.
机译:药代动力学建模越来越多地用于DCE-MRI高风险乳腺癌筛选。有几种型号可用。最常见的模型是标准和延长的Tofts,快门速度和Brix模型。解释每个模型和其参数的含义。通过模拟代表不同MRI采集方案的采样率和噪声水平,研究了哪种型号可以在临床环境中使用。此外,在使用生理学上更少的复杂模型时,对药代动力学参数估计中引入的误差进行了研究,即标准TOFT模型,以更复杂的模型产生的曲线。发现标准Tofts模型是唯一在一系列采样率和噪声水平的参数估计的误差余量内执行的唯一模型。当存在小复杂的生理效果时,这仍然存在。

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