Anatomically- and computationally-informed hepatic contrast perfusion simulations for use in virtual clinical trials

被引:7
作者
Sauer, Thomas J. [1 ,2 ]
Abadi, Ehsan [1 ]
Segars, Paul [1 ,2 ,3 ]
Samei, Ehsan [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Duke Univ, Med Ctr, Dept Radiol, Carl E Ravin Adv Imaging Labs, Durham, NC 27706 USA
[2] Duke Univ, Med Phys Grad Program, Durham, NC 27706 USA
[3] Duke Univ, Med Ctr, Dept Biomed Engn, Durham, NC 27706 USA
[4] Duke Univ, Med Ctr, Clin Imaging Phys Grp, Durham, NC 27706 USA
[5] Duke Univ, Dept Elect & Comp Engn, Durham, NC 27706 USA
[6] Duke Univ, Dept Phys, Durham, NC 27706 USA
来源
MEDICAL IMAGING 2019: PHYSICS OF MEDICAL IMAGING | 2019年 / 10948卷
关键词
liver modeling; tissue modeling; phantom development; XCAT; contrast perfusion; LIVER; CT; BODY; LUNG;
D O I
10.1117/12.2513465
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study modeled a framework for virtual human liver phantoms, focusing primarily on the intricate vascular networks that comprise the liver. Large vasculature was segmented from clinical liver perfusion images to ascertain a general starting point for the vascular networks of the liver that would be common among a healthy population. Clinical imaging methods cannot currently resolve the vast majority of the vasculature of the liver, and at the limiting resolution, modeling techniques continued the structure of the existing vasculature according to empirically known properties of blood vessel formation. Such advances in virtual phantom modeling enable simulation work in CT liver imaging, as clinical CT liver imaging is not ideally performed without contrast and multi-phasic acquisitions taking place over the course of the contrast's perfusion. The total amount of contrast in each organ in the body as a function of time is known from prior work, and the complete vascular network of the liver allows this information to be translated into an organ-specific contrast-concentration as a function of time. The ability to simulate this physiology is necessary for liver perfusion imaging, as pathologies typically impede or otherwise alter healthy perfusion patterns. The perfusion simulated here was in good agreement with known patterns of perfusion. Thus, virtual clinical trials can be performed with a dynamic model of the liver containing a fully integrated and realistic vascular network.
引用
收藏
页数:9
相关论文
共 18 条
  • [1] Abadi E, 2018, IEEE T MED IMAGING, P1
  • [2] Modeling "Textured" Bones in Virtual Human Phantoms
    Abadi, Ehsan
    Segars, William P.
    Sturgeon, Gregory M.
    Harrawood, Brian
    Kapadia, Anuj
    Samei, Ehsan
    [J]. IEEE TRANSACTIONS ON RADIATION AND PLASMA MEDICAL SCIENCES, 2019, 3 (01) : 47 - 53
  • [3] Modeling Lung Architecture in the XCAT Series of Phantoms: Physiologically Based Airways, Arteries and Veins
    Abadi, Ehsan
    Segars, William P.
    Sturgeon, Gregory M.
    Roos, Justus E.
    Ravin, Carl E.
    Samei, Ehsan
    [J]. IEEE TRANSACTIONS ON MEDICAL IMAGING, 2018, 37 (03) : 693 - 702
  • [4] APPLICATIONS OF LAGGED NORMAL DENSITY CURVE AS A MODEL FOR ARTERIAL DILUTION CURVES
    BASSINGT.JB
    ACKERMAN, FH
    WOOD, EH
    [J]. CIRCULATION RESEARCH, 1966, 18 (04) : 398 - &
  • [5] The tree of convective heat streams: its thermal insulation function and the predicted 3/4-power relation between body heat loss and body size
    Bejan, A
    [J]. INTERNATIONAL JOURNAL OF HEAT AND MASS TRANSFER, 2001, 44 (04) : 699 - 704
  • [6] Bejan A., 2013, Convective heat transfer
  • [7] Constrained diffusion-limited aggregation in 3 dimensions
    Bourke, Paul
    [J]. COMPUTERS & GRAPHICS-UK, 2006, 30 (04): : 646 - 649
  • [8] LIVER MORPHOLOGY
    ELIAS, H
    [J]. BIOLOGICAL REVIEWS, 1955, 30 (03) : 263 - 310
  • [9] Elias H., 1969, Morphology of the liver
  • [10] DETECTION OF FOCAL HEPATIC MASSES - PROSPECTIVE EVALUATION WITH CT, DELAYED CT, CT DURING ARTERIAL PORTOGRAPHY, AND MR IMAGING
    HEIKEN, JP
    WEYMAN, PJ
    LEE, JKT
    BALFE, DM
    PICUS, D
    BRUNT, EM
    FLYE, MW
    [J]. RADIOLOGY, 1989, 171 (01) : 47 - 51