{"id":{"repo_id":"uwo","oai_identifier":"oai:uwo.scholaris.ca:20.500.14721/32511"},"canonical_url":"https://search.dev.ndltd.org/etd/uwo/oai:uwo.scholaris.ca:20.500.14721/32511","repository":{"repo_id":"uwo","name":"Western University","base_url":"https://uwo.scholaris.ca/server/oai/request"},"display":{"title":"Multi-scale computational modeling of coronary blood flow: application to fractional flow reserve.","abstract":"Introduction. Fractional flow reserve (FFR) is presently an invasive coronary clinical index. Non-invasive CT imaging combined with computational coronary flow modelling may reduce the patient’s burden of undergoing invasive testing. Research statement. The ability to obtain information of the hemodynamic significance of detected lesions would streamline decision making in escalation to invasive angiography. Methods. A reduced order (lumped parameter) model of the coronary vasculature was further developed. The model was used in the assessment of the roles of structure and function on the FFR. Sophisticated methods were used to elicit numerical solutions. Further, CT imaging (n = 10) provided multiple porcine geometries based upon algorithms encoded within an existing scientific platform. Results. It was found that the length of large vessel stenosis and presence of microvascular disease are primary regulators of FFR. Further, the CT data provided a basis to investigate relationships between coronary geometry (structure) and blood flow (function) attributes. Discussion. The presented model, upon personalization, may compliment and streamline ongoing imaging efforts by guiding FFR assessment. It is likely to assist in preliminary data generation for future projects. The computational geometries will contribute to an open source service that will be made available to our University’s researchers.","abstract_html":"Introduction. Fractional flow reserve (FFR) is presently an invasive coronary clinical index. Non-invasive CT imaging combined with computational coronary flow modelling may reduce the patient’s burden of undergoing invasive testing. Research statement. The ability to obtain information of the hemodynamic significance of detected lesions would streamline decision making in escalation to invasive angiography. Methods. A reduced order (lumped parameter) model of the coronary vasculature was further developed. The model was used in the assessment of the roles of structure and function on the FFR. Sophisticated methods were used to elicit numerical solutions. Further, CT imaging (n = 10) provided multiple porcine geometries based upon algorithms encoded within an existing scientific platform. Results. It was found that the length of large vessel stenosis and presence of microvascular disease are primary regulators of FFR. Further, the CT data provided a basis to investigate relationships between coronary geometry (structure) and blood flow (function) attributes. Discussion. The presented model, upon personalization, may compliment and streamline ongoing imaging efforts by guiding FFR assessment. It is likely to assist in preliminary data generation for future projects. The computational geometries will contribute to an open source service that will be made available to our University’s researchers.","abstract_has_math":false,"creators":["Joseph, Jermiah"],"institution":"The University of Western Ontario","degree_name":"M Sc","degree_level":null,"degree_discipline":"Medical Biophysics","degree_department":null,"school":null,"contributors":[],"advisors":["McIntyre, Christopher W.","Goldman, Daniel."],"committee_chairs":[],"committee_members":[],"year":2022,"date_issued":"2022-09-23","date_published":"2022-09-23","updated_at":"2026-07-27T21:56:18Z","subjects":["Keywords: Computational fluid dynamics","coronary vasculature","lumped parameter modelling","data driven modelling."],"languages":["en_ca"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/20.500.14721/32511","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["McIntyre, Christopher W.","Goldman, Daniel."]},{"key":"dc:creator","label":"Author","values":["Joseph, Jermiah"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2025-07-10T19:31:35Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2025-07-10T19:31:35Z"]},{"key":"dc:date.issued","label":"Date","values":["2022-09-23"]},{"key":"dc:publisher","label":"Institution","values":["The University of Western Ontario"]},{"key":"dc:type","label":"Dc Type","values":["thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Medical Biophysics"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M Sc"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Keywords: Computational fluid dynamics","coronary vasculature","lumped parameter modelling","data driven modelling."]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en_ca"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/20.500.14721/32511"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["The thesis cover page in the PDF document includes references to Western University’s previous institutional repository platform, known as Scholarship@Western, and links to that platform (beginning with ir.lib.uwo.ca). In citing or referring to this thesis, use the DOI or handle from this page instead. Sample citation: Author name, \"Thesis title.\" (Year). Western University Open Repository. https://doi.org/10.71858/123456."]},{"key":"dc:description.abstract","label":"Abstract","values":["Introduction. Fractional flow reserve (FFR) is presently an invasive coronary clinical index. Non-invasive CT imaging combined with computational coronary flow modelling may reduce the patient’s burden of undergoing invasive testing. Research statement. The ability to obtain information of the hemodynamic significance of detected lesions would streamline decision making in escalation to invasive angiography. Methods. A reduced order (lumped parameter) model of the coronary vasculature was further developed. The model was used in the assessment of the roles of structure and function on the FFR. Sophisticated methods were used to elicit numerical solutions. Further, CT imaging (n = 10) provided multiple porcine geometries based upon algorithms encoded within an existing scientific platform. Results. It was found that the length of large vessel stenosis and presence of microvascular disease are primary regulators of FFR. Further, the CT data provided a basis to investigate relationships between coronary geometry (structure) and blood flow (function) attributes. Discussion. The presented model, upon personalization, may compliment and streamline ongoing imaging efforts by guiding FFR assessment. It is likely to assist in preliminary data generation for future projects. The computational geometries will contribute to an open source service that will be made available to our University’s researchers."]},{"key":"dc:title","label":"Title","values":["Multi-scale computational modeling of coronary blood flow: application to fractional flow reserve."]}]}],"canonical_facts":{"dc:contributor.advisor":["McIntyre, Christopher W.","Goldman, Daniel."],"dc:creator":["Joseph, Jermiah"],"dc:date.accessioned":["2025-07-10T19:31:35Z"],"dc:date.available":["2025-07-10T19:31:35Z"],"dc:date.issued":["2022-09-23"],"dc:description":["The thesis cover page in the PDF document includes references to Western University’s previous institutional repository platform, known as Scholarship@Western, and links to that platform (beginning with ir.lib.uwo.ca). In citing or referring to this thesis, use the DOI or handle from this page instead. Sample citation: Author name, \"Thesis title.\" (Year). Western University Open Repository. https://doi.org/10.71858/123456."],"dc:description.abstract":["Introduction. Fractional flow reserve (FFR) is presently an invasive coronary clinical index. Non-invasive CT imaging combined with computational coronary flow modelling may reduce the patient’s burden of undergoing invasive testing. Research statement. The ability to obtain information of the hemodynamic significance of detected lesions would streamline decision making in escalation to invasive angiography. Methods. A reduced order (lumped parameter) model of the coronary vasculature was further developed. The model was used in the assessment of the roles of structure and function on the FFR. Sophisticated methods were used to elicit numerical solutions. Further, CT imaging (n = 10) provided multiple porcine geometries based upon algorithms encoded within an existing scientific platform. Results. It was found that the length of large vessel stenosis and presence of microvascular disease are primary regulators of FFR. Further, the CT data provided a basis to investigate relationships between coronary geometry (structure) and blood flow (function) attributes. Discussion. The presented model, upon personalization, may compliment and streamline ongoing imaging efforts by guiding FFR assessment. It is likely to assist in preliminary data generation for future projects. The computational geometries will contribute to an open source service that will be made available to our University’s researchers."],"dc:identifier.uri":["https://hdl.handle.net/20.500.14721/32511"],"dc:language.iso":["en_ca"],"dc:publisher":["The University of Western Ontario"],"dc:subject":["Keywords: Computational fluid dynamics","coronary vasculature","lumped parameter modelling","data driven modelling."],"dc:title":["Multi-scale computational modeling of coronary blood flow: application to fractional flow reserve."],"dc:type":["thesis"],"thesis:degree_discipline":["Medical Biophysics"],"thesis:degree_name":["M Sc"]},"updated_at":"2026-07-27T21:56:18Z"}