The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle

This paper describes the process in which complex lesion geometries (specified by computer generated perfusion defects) are incorporated in the description of nonlinear finite element (FE) mechanical models used for specifying the motion of the left ventricle (LV) in the 4D extended cardiac torso (X...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of biomechanical engineering 2015-05, Vol.137 (5), p.051004-np
Hauptverfasser: Veress, Alexander I, Fung, George S. K, Lee, Taek-Soo, Tsui, Benjamin M. W, Kicska, Gregory A, Paul Segars, W, Gullberg, Grant T
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page np
container_issue 5
container_start_page 051004
container_title Journal of biomechanical engineering
container_volume 137
creator Veress, Alexander I
Fung, George S. K
Lee, Taek-Soo
Tsui, Benjamin M. W
Kicska, Gregory A
Paul Segars, W
Gullberg, Grant T
description This paper describes the process in which complex lesion geometries (specified by computer generated perfusion defects) are incorporated in the description of nonlinear finite element (FE) mechanical models used for specifying the motion of the left ventricle (LV) in the 4D extended cardiac torso (XCAT) phantom to simulate gated cardiac image data. An image interrogation process was developed to define the elements in the LV mesh as ischemic or infarcted based upon the values of sampled intensity levels of the perfusion maps. The intensity values were determined for each of the interior integration points of every element of the FE mesh. The average element intensity levels were then determined. The elements with average intensity values below a user-controlled threshold were defined as ischemic or infarcted depending upon the model being defined. For the infarction model cases, the thresholding and interrogation process were repeated in order to define a border zone (BZ) surrounding the infarction. This methodology was evaluated using perfusion maps created by the perfusion cardiac-torso (PCAT) phantom an extension of the 4D XCAT phantom. The PCAT was used to create 3D perfusion maps representing 90% occlusions at four locations (left anterior descending (LAD) segments 6 and 9, left circumflex (LCX) segment 11, right coronary artery (RCA) segment 1) in the coronary tree. The volumes and shapes of the defects defined in the FE mechanical models were compared with perfusion maps produced by the PCAT. The models were incorporated into the XCAT phantom. The ischemia models had reduced stroke volume (SV) by 18-59 ml. and ejection fraction (EF) values by 14-50% points compared to the normal models. The infarction models, had less reductions in SV and EF, 17-54 ml. and 14-45% points, respectively. The volumes of the ischemic/infarcted regions of the models were nearly identical to those volumes obtained from the perfusion images and were highly correlated (R² = 0.99).
doi_str_mv 10.1115/1.4028989
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4340187</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1685808501</sourcerecordid><originalsourceid>FETCH-LOGICAL-a461t-6f010f0c01fecfadc9ef5d399a9a6d1e5c13857970e059104d71598ef79e0c1a3</originalsourceid><addsrcrecordid>eNqNkk1v1DAQhi0EokvhwBkJ-QiHlJlNHNsXpKofsNIiOBSulnHGrKvEXuwEib_AryZhlwpuPY1m5tE7H3oZe45whojiDZ41sFZa6QdshWKtKqUFPmQrwEZVIGs8YU9KuQVAVA08ZidrUbcSpVyxXzc74pchkxv5JrqU9ynbMaTIk-efKPupLMkl-QPhUx4O_TEt1RCJb4rb0RAst7FbEJvdHyJEbvl1iGEkftXTQHHkH1JH_aI9znO35Ef-ZS7n4Hp6yh552xd6doyn7PP11c3F-2r78d3m4nxb2abFsWo9IHhwgPNK3nZOkxddrbXVtu2QhMNaCaklEAiN0HQShVbkpSZwaOtT9vagu5--DtS5Zb7tzT6HweafJtlg_u_EsDPf0g_T1A2gkrPAq6NATt8nKqMZQnHU9zZSmorBVgkFSgDeA5VtLUCv9T1QoaUEFO2Mvj6gLqdSMvm75RHM4giD5uiImX3577V35F8LzMCLA2DLQOY2TTnO35-P1Vo09W-O7LqA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1659770156</pqid></control><display><type>article</type><title>The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><source>ASME Transactions Journals (Current)</source><creator>Veress, Alexander I ; Fung, George S. K ; Lee, Taek-Soo ; Tsui, Benjamin M. W ; Kicska, Gregory A ; Paul Segars, W ; Gullberg, Grant T</creator><creatorcontrib>Veress, Alexander I ; Fung, George S. K ; Lee, Taek-Soo ; Tsui, Benjamin M. W ; Kicska, Gregory A ; Paul Segars, W ; Gullberg, Grant T</creatorcontrib><description>This paper describes the process in which complex lesion geometries (specified by computer generated perfusion defects) are incorporated in the description of nonlinear finite element (FE) mechanical models used for specifying the motion of the left ventricle (LV) in the 4D extended cardiac torso (XCAT) phantom to simulate gated cardiac image data. An image interrogation process was developed to define the elements in the LV mesh as ischemic or infarcted based upon the values of sampled intensity levels of the perfusion maps. The intensity values were determined for each of the interior integration points of every element of the FE mesh. The average element intensity levels were then determined. The elements with average intensity values below a user-controlled threshold were defined as ischemic or infarcted depending upon the model being defined. For the infarction model cases, the thresholding and interrogation process were repeated in order to define a border zone (BZ) surrounding the infarction. This methodology was evaluated using perfusion maps created by the perfusion cardiac-torso (PCAT) phantom an extension of the 4D XCAT phantom. The PCAT was used to create 3D perfusion maps representing 90% occlusions at four locations (left anterior descending (LAD) segments 6 and 9, left circumflex (LCX) segment 11, right coronary artery (RCA) segment 1) in the coronary tree. The volumes and shapes of the defects defined in the FE mechanical models were compared with perfusion maps produced by the PCAT. The models were incorporated into the XCAT phantom. The ischemia models had reduced stroke volume (SV) by 18-59 ml. and ejection fraction (EF) values by 14-50% points compared to the normal models. The infarction models, had less reductions in SV and EF, 17-54 ml. and 14-45% points, respectively. The volumes of the ischemic/infarcted regions of the models were nearly identical to those volumes obtained from the perfusion images and were highly correlated (R² = 0.99).</description><identifier>ISSN: 0148-0731</identifier><identifier>EISSN: 1528-8951</identifier><identifier>DOI: 10.1115/1.4028989</identifier><identifier>PMID: 25367177</identifier><language>eng</language><publisher>United States: ASME</publisher><subject>Biomechanical Phenomena ; Cardiac-Gated Single-Photon Emission Computer-Assisted Tomography ; Computer simulation ; Coronary Circulation ; Defects ; Finite Element Analysis ; Finite element method ; Heart Ventricles - diagnostic imaging ; Heart Ventricles - physiopathology ; Humans ; Imaging, Three-Dimensional ; Infarction ; Male ; Mathematical models ; Mechanical Phenomena ; Models, Cardiovascular ; Myocardial Infarction - diagnostic imaging ; Myocardial Infarction - physiopathology ; Myocardial Ischemia - diagnostic imaging ; Myocardial Ischemia - physiopathology ; Nonlinear Dynamics ; Phantoms, Imaging ; Research Papers ; Segments</subject><ispartof>Journal of biomechanical engineering, 2015-05, Vol.137 (5), p.051004-np</ispartof><rights>Copyright © 2015 by ASME 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a461t-6f010f0c01fecfadc9ef5d399a9a6d1e5c13857970e059104d71598ef79e0c1a3</citedby><cites>FETCH-LOGICAL-a461t-6f010f0c01fecfadc9ef5d399a9a6d1e5c13857970e059104d71598ef79e0c1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902,38497</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25367177$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Veress, Alexander I</creatorcontrib><creatorcontrib>Fung, George S. K</creatorcontrib><creatorcontrib>Lee, Taek-Soo</creatorcontrib><creatorcontrib>Tsui, Benjamin M. W</creatorcontrib><creatorcontrib>Kicska, Gregory A</creatorcontrib><creatorcontrib>Paul Segars, W</creatorcontrib><creatorcontrib>Gullberg, Grant T</creatorcontrib><title>The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle</title><title>Journal of biomechanical engineering</title><addtitle>J Biomech Eng</addtitle><addtitle>J Biomech Eng</addtitle><description>This paper describes the process in which complex lesion geometries (specified by computer generated perfusion defects) are incorporated in the description of nonlinear finite element (FE) mechanical models used for specifying the motion of the left ventricle (LV) in the 4D extended cardiac torso (XCAT) phantom to simulate gated cardiac image data. An image interrogation process was developed to define the elements in the LV mesh as ischemic or infarcted based upon the values of sampled intensity levels of the perfusion maps. The intensity values were determined for each of the interior integration points of every element of the FE mesh. The average element intensity levels were then determined. The elements with average intensity values below a user-controlled threshold were defined as ischemic or infarcted depending upon the model being defined. For the infarction model cases, the thresholding and interrogation process were repeated in order to define a border zone (BZ) surrounding the infarction. This methodology was evaluated using perfusion maps created by the perfusion cardiac-torso (PCAT) phantom an extension of the 4D XCAT phantom. The PCAT was used to create 3D perfusion maps representing 90% occlusions at four locations (left anterior descending (LAD) segments 6 and 9, left circumflex (LCX) segment 11, right coronary artery (RCA) segment 1) in the coronary tree. The volumes and shapes of the defects defined in the FE mechanical models were compared with perfusion maps produced by the PCAT. The models were incorporated into the XCAT phantom. The ischemia models had reduced stroke volume (SV) by 18-59 ml. and ejection fraction (EF) values by 14-50% points compared to the normal models. The infarction models, had less reductions in SV and EF, 17-54 ml. and 14-45% points, respectively. The volumes of the ischemic/infarcted regions of the models were nearly identical to those volumes obtained from the perfusion images and were highly correlated (R² = 0.99).</description><subject>Biomechanical Phenomena</subject><subject>Cardiac-Gated Single-Photon Emission Computer-Assisted Tomography</subject><subject>Computer simulation</subject><subject>Coronary Circulation</subject><subject>Defects</subject><subject>Finite Element Analysis</subject><subject>Finite element method</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Heart Ventricles - physiopathology</subject><subject>Humans</subject><subject>Imaging, Three-Dimensional</subject><subject>Infarction</subject><subject>Male</subject><subject>Mathematical models</subject><subject>Mechanical Phenomena</subject><subject>Models, Cardiovascular</subject><subject>Myocardial Infarction - diagnostic imaging</subject><subject>Myocardial Infarction - physiopathology</subject><subject>Myocardial Ischemia - diagnostic imaging</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>Nonlinear Dynamics</subject><subject>Phantoms, Imaging</subject><subject>Research Papers</subject><subject>Segments</subject><issn>0148-0731</issn><issn>1528-8951</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhwBkJ-QiHlJlNHNsXpKofsNIiOBSulnHGrKvEXuwEib_AryZhlwpuPY1m5tE7H3oZe45whojiDZ41sFZa6QdshWKtKqUFPmQrwEZVIGs8YU9KuQVAVA08ZidrUbcSpVyxXzc74pchkxv5JrqU9ynbMaTIk-efKPupLMkl-QPhUx4O_TEt1RCJb4rb0RAst7FbEJvdHyJEbvl1iGEkftXTQHHkH1JH_aI9znO35Ef-ZS7n4Hp6yh552xd6doyn7PP11c3F-2r78d3m4nxb2abFsWo9IHhwgPNK3nZOkxddrbXVtu2QhMNaCaklEAiN0HQShVbkpSZwaOtT9vagu5--DtS5Zb7tzT6HweafJtlg_u_EsDPf0g_T1A2gkrPAq6NATt8nKqMZQnHU9zZSmorBVgkFSgDeA5VtLUCv9T1QoaUEFO2Mvj6gLqdSMvm75RHM4giD5uiImX3577V35F8LzMCLA2DLQOY2TTnO35-P1Vo09W-O7LqA</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Veress, Alexander I</creator><creator>Fung, George S. K</creator><creator>Lee, Taek-Soo</creator><creator>Tsui, Benjamin M. W</creator><creator>Kicska, Gregory A</creator><creator>Paul Segars, W</creator><creator>Gullberg, Grant T</creator><general>ASME</general><general>American Society of Mechanical Engineers</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7TB</scope><scope>7U5</scope><scope>F28</scope><scope>L7M</scope><scope>5PM</scope></search><sort><creationdate>20150501</creationdate><title>The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle</title><author>Veress, Alexander I ; Fung, George S. K ; Lee, Taek-Soo ; Tsui, Benjamin M. W ; Kicska, Gregory A ; Paul Segars, W ; Gullberg, Grant T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a461t-6f010f0c01fecfadc9ef5d399a9a6d1e5c13857970e059104d71598ef79e0c1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biomechanical Phenomena</topic><topic>Cardiac-Gated Single-Photon Emission Computer-Assisted Tomography</topic><topic>Computer simulation</topic><topic>Coronary Circulation</topic><topic>Defects</topic><topic>Finite Element Analysis</topic><topic>Finite element method</topic><topic>Heart Ventricles - diagnostic imaging</topic><topic>Heart Ventricles - physiopathology</topic><topic>Humans</topic><topic>Imaging, Three-Dimensional</topic><topic>Infarction</topic><topic>Male</topic><topic>Mathematical models</topic><topic>Mechanical Phenomena</topic><topic>Models, Cardiovascular</topic><topic>Myocardial Infarction - diagnostic imaging</topic><topic>Myocardial Infarction - physiopathology</topic><topic>Myocardial Ischemia - diagnostic imaging</topic><topic>Myocardial Ischemia - physiopathology</topic><topic>Nonlinear Dynamics</topic><topic>Phantoms, Imaging</topic><topic>Research Papers</topic><topic>Segments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Veress, Alexander I</creatorcontrib><creatorcontrib>Fung, George S. K</creatorcontrib><creatorcontrib>Lee, Taek-Soo</creatorcontrib><creatorcontrib>Tsui, Benjamin M. W</creatorcontrib><creatorcontrib>Kicska, Gregory A</creatorcontrib><creatorcontrib>Paul Segars, W</creatorcontrib><creatorcontrib>Gullberg, Grant T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biomechanical engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Veress, Alexander I</au><au>Fung, George S. K</au><au>Lee, Taek-Soo</au><au>Tsui, Benjamin M. W</au><au>Kicska, Gregory A</au><au>Paul Segars, W</au><au>Gullberg, Grant T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle</atitle><jtitle>Journal of biomechanical engineering</jtitle><stitle>J Biomech Eng</stitle><addtitle>J Biomech Eng</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>137</volume><issue>5</issue><spage>051004</spage><epage>np</epage><pages>051004-np</pages><issn>0148-0731</issn><eissn>1528-8951</eissn><abstract>This paper describes the process in which complex lesion geometries (specified by computer generated perfusion defects) are incorporated in the description of nonlinear finite element (FE) mechanical models used for specifying the motion of the left ventricle (LV) in the 4D extended cardiac torso (XCAT) phantom to simulate gated cardiac image data. An image interrogation process was developed to define the elements in the LV mesh as ischemic or infarcted based upon the values of sampled intensity levels of the perfusion maps. The intensity values were determined for each of the interior integration points of every element of the FE mesh. The average element intensity levels were then determined. The elements with average intensity values below a user-controlled threshold were defined as ischemic or infarcted depending upon the model being defined. For the infarction model cases, the thresholding and interrogation process were repeated in order to define a border zone (BZ) surrounding the infarction. This methodology was evaluated using perfusion maps created by the perfusion cardiac-torso (PCAT) phantom an extension of the 4D XCAT phantom. The PCAT was used to create 3D perfusion maps representing 90% occlusions at four locations (left anterior descending (LAD) segments 6 and 9, left circumflex (LCX) segment 11, right coronary artery (RCA) segment 1) in the coronary tree. The volumes and shapes of the defects defined in the FE mechanical models were compared with perfusion maps produced by the PCAT. The models were incorporated into the XCAT phantom. The ischemia models had reduced stroke volume (SV) by 18-59 ml. and ejection fraction (EF) values by 14-50% points compared to the normal models. The infarction models, had less reductions in SV and EF, 17-54 ml. and 14-45% points, respectively. The volumes of the ischemic/infarcted regions of the models were nearly identical to those volumes obtained from the perfusion images and were highly correlated (R² = 0.99).</abstract><cop>United States</cop><pub>ASME</pub><pmid>25367177</pmid><doi>10.1115/1.4028989</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0148-0731
ispartof Journal of biomechanical engineering, 2015-05, Vol.137 (5), p.051004-np
issn 0148-0731
1528-8951
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4340187
source MEDLINE; Alma/SFX Local Collection; ASME Transactions Journals (Current)
subjects Biomechanical Phenomena
Cardiac-Gated Single-Photon Emission Computer-Assisted Tomography
Computer simulation
Coronary Circulation
Defects
Finite Element Analysis
Finite element method
Heart Ventricles - diagnostic imaging
Heart Ventricles - physiopathology
Humans
Imaging, Three-Dimensional
Infarction
Male
Mathematical models
Mechanical Phenomena
Models, Cardiovascular
Myocardial Infarction - diagnostic imaging
Myocardial Infarction - physiopathology
Myocardial Ischemia - diagnostic imaging
Myocardial Ischemia - physiopathology
Nonlinear Dynamics
Phantoms, Imaging
Research Papers
Segments
title The Direct Incorporation of Perfusion Defect Information to Define Ischemia and Infarction in a Finite Element Model of the Left Ventricle
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T08%3A12%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Direct%20Incorporation%20of%20Perfusion%20Defect%20Information%20to%20Define%20Ischemia%20and%20Infarction%20in%20a%20Finite%20Element%20Model%20of%20the%20Left%20Ventricle&rft.jtitle=Journal%20of%20biomechanical%20engineering&rft.au=Veress,%20Alexander%20I&rft.date=2015-05-01&rft.volume=137&rft.issue=5&rft.spage=051004&rft.epage=np&rft.pages=051004-np&rft.issn=0148-0731&rft.eissn=1528-8951&rft_id=info:doi/10.1115/1.4028989&rft_dat=%3Cproquest_pubme%3E1685808501%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1659770156&rft_id=info:pmid/25367177&rfr_iscdi=true