4.5 Article Proceedings Paper

A computer reconstruction of the entire coronary arterial tree based on detailed morphometric data

期刊

ANNALS OF BIOMEDICAL ENGINEERING
卷 33, 期 8, 页码 1015-1026

出版社

SPRINGER
DOI: 10.1007/s10439-005-5758-z

关键词

Strahler system; diameter-defined Strahler system; vascular reconstruction; growth algorithm; design rules

资金

  1. NHLBI NIH HHS [2 R01 HL055554-06, R01 HL67159-03] Funding Source: Medline

向作者/读者索取更多资源

A rigorous analysis of blood flow must be based on the branching pattern and vascular geometry of the full vascular circuit of interest. It is experimentally difficult to reconstruct the entire vascular circuit of any organ because of the enormity of the vessels. The objective of the present study was to develop a novel method for the reconstruction of the full coronary vascular tree from partial measurements. Our method includes the use of data on those parts of the tree that are measured to extrapolate the data on those parts that are missing. Specifically, a two-step approach was employed in the reconstruction of the entire coronary arterial tree down to the capillary level. Vessels > 40 mu m were reconstructed from cast data while vessels < 40 mu m were reconstructed from histological data. The cast data were reconstructed one-bifurcation at a time while histological data were reconstructed one-sub-tree at a time by cutting and pasting of data from measured to missing vessels. The reconstruction algorithm yielded a full arterial tree down to the first capillary bifurcation with 1.9, 2.04 and 1.15 million vessel segments for the right coronary artery (RCA), left anterior descending (LAD) and left circumflex (LCx) trees, respectively. The node-to-node connectivity along with the diameter and length of every vessel segment was determined. Once the full tree was reconstructed, we automated the assignment of order numbers, according to the diameter-defined Strahler system, to every vessel segment in the tree. Consequently, the diameters, lengths, number of vessels, segments-per-element ratio, connectivity and longitudinal matrices were determined for every order number. The present model establishes a morphological foundation for future analysis of blood flow in the coronary circulation.

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