An Anatomically BasedModelling of Hepatic Perfusion and Biliary Fluid Dynamics in the Human Liver for Clinical Applications

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dc.contributor.advisor Safaei, S en
dc.contributor.advisor Hunter, P en
dc.contributor.advisor Ho, H en
dc.contributor.author Ma, Renfei en
dc.date.accessioned 2020-04-29T21:25:29Z en
dc.date.issued 2019 en
dc.identifier.uri http://hdl.handle.net/2292/50498 en
dc.description.abstract This study aims to develop a computational human hepatic perfusion model to predict the pressure and flow rate inside the first few generations of anatomically based hepatic vessels. These vessels were digitised from computed tomography (CT) images of healthy living liver donors. The one-dimensional (1D) model was developed with Navier-Stokes equations and implemented in OpenCMISS, open-source software created by the Auckland Bioengineering Institute. Ultrasonic measurement of blood flow was employed to obtain inlet boundary conditions (BCs). Hepatic perfusion was modelled in the hepatic artery and portal vein with structured tree-based outflow BCs. This self-similar structured tree was used in this study in a novel manner to model the effect of the smaller hepatic arteries and arterioles and the smaller hepatic portal veins and portal venules. As these structured trees terminate at the size of the microvasculature in liver lobules, the structured tree BC has a unique advantage of enabling the proposed organ-level model to be easily connected to tissue-level models of liver lobules. Additionally, blood flow inside the hepatic vein and bile flow inside the intrahepatic bile duct were modelled with RCRWindkesselmodels. The integration of circulation in all hepatic vessels allowed the proposed model to show higher potential for clinical applications. Moreover, the proposed model was applied to predict postoperative hepatic perfusion after left hepatectomy. The resistive index and the characteristic of blood vessel self enlargement to accommodate extra blood flow were employed in a novel manner to obtain proper postoperative BCs for hepatic artery flow and portal vein flow. Additionally, as an informative application, the computational model was coupled with an advection-diffusion equation to model drug delivery phenomena in the hepatic vessels. en
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby UoA en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/nz/ en
dc.title An Anatomically BasedModelling of Hepatic Perfusion and Biliary Fluid Dynamics in the Human Liver for Clinical Applications en
dc.type Thesis en
thesis.degree.discipline Bioengineering en
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.rights.holder Copyright: The author en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.elements-id 800507 en
pubs.record-created-at-source-date 2020-04-30 en


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http://creativecommons.org/licenses/by-nc-sa/3.0/nz/ Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by-nc-sa/3.0/nz/

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