计算机视觉
运动估计
微气泡
翻译(生物学)
人工智能
图像分辨率
计算机科学
运动补偿
迭代重建
运动(物理)
数据集
超声波
生物医学工程
物理
声学
化学
工程类
信使核糖核酸
基因
生物化学
作者
Sevan Harput,Kirsten Christensen-Jeffries,Jemma Brown,Yuanwei Li,Katherine J. Williams,Alun H. Davies,Robert J. Eckersley,Christopher Dunsby,Meng‐Xing Tang
出处
期刊:IEEE Transactions on Ultrasonics Ferroelectrics and Frequency Control
[Institute of Electrical and Electronics Engineers]
日期:2018-04-09
卷期号:65 (5): 803-814
被引量:147
标识
DOI:10.1109/tuffc.2018.2824846
摘要
The structure of microvasculature cannot be resolved using conventional ultrasound (US) imaging due to the fundamental diffraction limit at clinical US frequencies. It is possible to overcome this resolution limitation by localizing individual microbubbles through multiple frames and forming a superresolved image, which usually requires seconds to minutes of acquisition. Over this time interval, motion is inevitable and tissue movement is typically a combination of large- and small-scale tissue translation and deformation. Therefore, super-resolution (SR) imaging is prone to motion artifacts as other imaging modalities based on multiple acquisitions are. This paper investigates the feasibility of a two-stage motion estimation method, which is a combination of affine and nonrigid estimation, for SR US imaging. First, the motion correction accuracy of the proposed method is evaluated using simulations with increasing complexity of motion. A mean absolute error of 12.2 was achieved in simulations for the worst-case scenario. The motion correction algorithm was then applied to a clinical data set to demonstrate its potential to enable in vivo SR US imaging in the presence of patient motion. The size of the identified microvessels from the clinical SR images was measured to assess the feasibility of the two-stage motion correction method, which reduced the width of the motion-blurred microvessels to approximately 1.5-fold.
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