A patient-informed approach to predict iodinated-contrast media enhancement in the liver.

Eur J Radiol

Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, Duke University, 2424 Erwin Rd, Ste. 302, Durham, NC 27705, USA; Center for Virtual Imaging Trials, Duke University, 2424 Erwin Rd, Ste. 302, Durham, NC 27705, USA; Clinical Imaging Physics Group, Duke University Health System, 2424 Erwin Rd, Ste. 302, Durham, NC 27705, USA; Graduate Program in Medical Physics, School of Medicine, Duke University, 2424 Erwin Rd, Ste. 302, Durham, NC 27705, USA; Department of Electrical and Computer Engineering, Pratt School of Engineering, Duke University, 305 Nello L. Teer Engineering Building, Box 90271, Durham, NC 27708, USA; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, 305 Nello L. Teer Engineering Building, Box 90271, Durham, NC 27708, USA; Department of Radiology, School of Medicine, Duke University, Box 3808 DUMC, Durham, NC 27710, USA; Physics Building, Science Drive Campus, Box 90305, Durham, NC 27708, USA.

Published: November 2022

Objective: To devise a patient-informed time series model that predicts liver contrast enhancement, by integrating clinical data and pharmacokinetics models, and to assess its feasibility to improve enhancement consistency in contrast-enhanced liver CT scans.

Methods: The study included 1577 Chest/Abdomen/Pelvis CT scans, with 70-30% training/validation-testing split. A Gaussian function was used to approximate the early arterial, late arterial, and the portal venous phases of the contrast perfusion curve of each patient using their respective bolus tracking and diagnostic scan data. Machine learning models were built to predict the Gaussian parameters of each patient using the patient attributes (weight, height, age, sex, BMI). Pearson's coefficient, mean absolute error, and root mean squared error were used to assess the prediction accuracy.

Results: The integration of the pharmacokinetics model with a two-layered neural network achieved the highest prediction accuracy on the test data (R = 0.61), significantly exceeding the performance of the pharmacokinetics model alone (R = 0.11). Applying the model demonstrated that adjusting the contrast administration directed by the model may reduce clinical enhancement inconsistency by up to 40 %.

Conclusions: A new model using a Gaussian function and supervised machine learning can be used to build liver parenchyma contrast enhancement prediction model. The model can have utility in clinical settings to optimize and improve consistency in contrast-enhanced liver imaging.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10777297PMC
http://dx.doi.org/10.1016/j.ejrad.2022.110555DOI Listing

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