Three-Dimensional Blood Vessel Segmentation and Centerline Extraction based on Two-Dimensional Cross-Section Analysis

被引:15
作者
Kumar, Rahul Prasanna [1 ,2 ]
Albregtsen, Fritz [2 ,3 ]
Reimers, Martin [2 ]
Edwin, Bjorn [1 ,4 ]
Lango, Thomas [5 ]
Elle, Ole Jakob [1 ,2 ]
机构
[1] Oslo Univ Hosp, Intervent Ctr, N-0372 Oslo, Norway
[2] Univ Oslo, Dept Informat, N-0373 Oslo, Norway
[3] Oslo Univ Hosp, Inst Canc Genet & Informat, N-0372 Oslo, Norway
[4] Univ Oslo, Fac Med, N-0372 Oslo, Norway
[5] SINTEF, Med Technol, MTFS, N-7034 Trondheim, Norway
关键词
Blood vessel segmentation; Centerline extraction; Vessel tracking; Multi-scale analysis and circle enhancement filter; ACTIVE CONTOUR MODELS; ALGORITHMS; SNAKES;
D O I
10.1007/s10439-014-1184-4
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The segmentation of tubular tree structures like vessel systems in volumetric datasets is of vital interest for many medical applications. In this paper we present a novel, semi-automatic method for blood vessel segmentation and centerline extraction, by tracking the blood vessel tree from a user-initiated seed point to the ends of the blood vessel tree. The novelty of our method is in performing only two-dimensional cross-section analysis for segmentation of the connected blood vessels. The cross-section analysis is done by our novel single-scale or multi-scale circle enhancement filter, used at the blood vessel trunk or bifurcation, respectively. The method was validated for both synthetic and medical images. Our validation has shown that the cross-sectional centerline error for our method is below 0.8 pixels and the Dice coefficient for our segmentation is 80% +/- A 2.7%. On combining our method with an optional active contour post-processing, the Dice coefficient for the resulting segmentation is found to be 94% +/- A 2.4%. Furthermore, by restricting the image analysis to the regions of interest and converting most of the three-dimensional calculations to two-dimensional calculations, the processing was found to be more than 18 times faster than Frangi vesselness with thinning, 8 times faster than user-initiated active contour segmentation with thinning and 7 times faster than our previous method.
引用
收藏
页码:1223 / 1234
页数:12
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