| Literature DB >> 31007339 |
Grace J Gang1, Kailun Cheng1, Xueqi Guo1, J Webster Stayman1.
Abstract
Model-based reconstruction (MBR) algorithms in CT have demonstrated superior dose-image quality tradeoffs compared to traditional analytical methods. However, the nonlinear and data-dependent nature of these algorithms pose significant challenges for performance evaluation and parameter optimization. To address these challenges, this work presents an analysis framework for quantitative and predictive modeling of image properties in general nonlinear MBR algorithms. We propose to characterize the reconstructed appearance of arbitrary stimuli by the generalized system response function that accounts for dependence on the imaging conditions, reconstruction parameters, object, and the stimulus itself (size, contrast, location). We estimate this nonlinear function using a multilayer perceptron neural network by providing input and output pairs that samples the range of imaging parameters of interest. The feasibility of this approach was demonstrated for predicting the appearance of a spiculated lesion reconstructed by a penalized-likelihood objective with a Huber penalty in a physical phantom as a function of its location and reconstruction parameters β and δ. The generalized system response functions predicted from the trained neural network show good agreement with those computed from mean reconstructions, proving the ability of the framework in mapping out the nonlinear function for combinations of imaging parameters not present in the training data. We demonstrated utility of the framework to achieve desirable (e.g., non-blocky) lesion appearance in arbitrary locations in the phantom without the need for performing actual reconstructions. The proposed prediction framework permits efficient and quantifiable performance evaluations to provide robust control and understanding of image properties for general classes of nonlinear MBR algorithms.Entities:
Year: 2019 PMID: 31007339 PMCID: PMC6469864 DOI: 10.1117/12.2513485
Source DB: PubMed Journal: Proc SPIE Int Soc Opt Eng ISSN: 0277-786X