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dc.contributor.authorCarson, JM
dc.contributor.authorRoobottom, C
dc.contributor.authorAlcock, R
dc.contributor.authorNithiarasu, P
dc.date.accessioned2021-11-04T10:34:25Z
dc.date.issued2019-11
dc.identifier.issn1069-8299
dc.identifier.issn2040-7947
dc.identifier.othere3255
dc.identifier.urihttp://hdl.handle.net/10026.1/18210
dc.description.abstract

<jats:title>Abstract</jats:title><jats:p>In this work, we estimate the diagnostic threshold of the instantaneous wave‐free ratio (iFR) through the use of a one‐dimensional haemodynamic framework. To this end, we first compared the computed fractional flow reserve (cFFR) predicted from a 1D computational framework with invasive clinical measurements. The framework shows excellent promise and utilises minimal patient data from a cohort of 52 patients with a total of 66 stenoses. The diagnostic accuracy of the cFFR model was 75.76<jats:italic>%</jats:italic>, with a sensitivity of 71.43<jats:italic>%</jats:italic>, a specificity of 77.78<jats:italic>%</jats:italic>, a positive predictive value of 60<jats:italic>%</jats:italic>, and a negative predictive value of 85.37<jats:italic>%</jats:italic>. The validated model was then used to estimate the diagnostic threshold of iFR. The model determined a quadratic relationship between cFFR and the ciFR. The iFR diagnostic threshold was determined to be 0.8910 from a receiver operating characteristic curve that is in the range of 0.89 to 0.9 that is normally reported in clinical studies.</jats:p>

dc.format.extente3255-
dc.format.mediumPrint
dc.languageen
dc.language.isoen
dc.publisherJohn Wiley and Sons
dc.subjectcoronary arteries
dc.subjectFFR
dc.subjecthaemodynamic modelling
dc.subjectiFR
dc.titleComputational instantaneous wave‐free ratio (IFR) for patient‐specific coronary artery stenoses using 1D network models
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000508184800001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue11
plymouth.volume35
plymouth.publication-statusPublished
plymouth.journalInternational Journal for Numerical Methods in Biomedical Engineering
dc.identifier.doi10.1002/cnm.3255
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2019-08-21
dc.rights.embargodate2021-11-5
dc.identifier.eissn2040-7947
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1002/cnm.3255
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2019-11
rioxxterms.typeJournal Article/Review


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