A Spatiotemporal-Based Scheme for Efficient Registration-Based Segmentation of Thoracic 4-D MRI

被引:10
|
作者
Yang, Y. [1 ]
Van Reeth, E. [1 ]
Poh, C. L. [1 ]
Tan, C. H. [2 ]
Tham, I. W. K. [3 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[2] Tan Tock Seng Hosp, Dept Diagnost Radiol, Singapore 308433, Singapore
[3] Natl Univ Canc Inst, Dept Radiat Oncol, Singapore 119228, Singapore
基金
英国医学研究理事会;
关键词
Cancer; four-dimensional (4-D); image registration; image segmentation; magnetic resonance imaging (MRI); LUNG; IMAGES; TRACKING;
D O I
10.1109/JBHI.2013.2282183
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Dynamic three-dimensional (3-D) (four-dimensional, 4-D) magnetic resonance (MR) imaging is gaining importance in the study of pulmonary motion for respiratory diseases and pulmonary tumor motion for radiotherapy. To perform quantitative analysis using 4-D MR images, segmentation of anatomical structures such as the lung and pulmonary tumor is required. Manual segmentation of entire thoracic 4-D MRI data that typically contains many 3-D volumes acquired over several breathing cycles is extremely tedious, time consuming, and suffers high user variability. This requires the development of new automated segmentation schemes for 4-D MRI data segmentation. Registration-based segmentation technique that uses automatic registration methods for segmentation has been shown to be an accurate method to segment structures for 4-D data series. However, directly applying registration-based segmentation to segment 4-D MRI series lacks efficiency. Here we propose an automated 4-D registration-based segmentation scheme that is based on spatiotemporal information for the segmentation of thoracic 4-DMR lung images. The proposed scheme saved up to 95% of computation amount while achieving comparable accurate segmentations compared to directly applying registration-based segmentation to 4-D dataset. The scheme facilitates rapid 3-D/4-D visualization of the lung and tumormotion and potentially the tracking of tumor during radiation delivery.
引用
收藏
页码:969 / 977
页数:9
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