Morris, P.D., Silva Soto, D.A. orcid.org/0000-0002-2229-6194, Feher, J.F.A. et al. (6 more authors) (2017) Fast Virtual Fractional Flow Reserve Based Upon Steady-State Computational Fluid Dynamics Analysis: Results From the VIRTU-Fast Study. JACC: Basic to Translational Science, 2 (4). pp. 434-446. ISSN 2452-302X
Abstract
Objectives (i) Develop and validate a method which computes fractional flow reserve (FFR) in <5 minutes on a personal computer; (ii) perform a sensitivity analysis of the physiological parameters which determine FFR. Background Percutaneous coronary intervention (PCI) guided by FFR is superior to standard assessment but remains underused. Computed, ‘virtual’ FFR (vFFR), may increase uptake of physiological guidance but is slow to compute with computational fluid dynamics (CFD) modelling. Methods Seventy-three 3-D arterial geometries were segmented from 20 patients undergoing PCI and FFR. The trans-lesional pressure drop was represented as a quadratic function of flow based upon paired steady-state analyses. Coronary microvascular impedance was determined from invasive pressure measurements. vFFR was computed using a novel pseudo-transient analysis protocol. Results were compared with fully transient CFD analysis and the clinically-measured FFR. Model sensitivity analysis was performed with the Sobol decomposition method. Results The newly developed computational protocol executed in a mean time of 189 seconds (SD 34s), whereas transient analysis took >26h. Mean error was <1%. Intraclass correlation coefficient between virtual and measured values was 0.99 (P<0.0001). Physiological lesion significance (FFR≤0.80) was discerned with 100% accuracy. Sensitivity analysis demonstrated that coronary microvascular resistance (CMVR) was the dominant influence upon vFFR. Conclusions Given an accurate value for CMV resistance, vFFR can be accurately computed from coronary angiography in <4 min. Transient physiological results can be approximated without performing time-consuming transient CFD analysis. vFFR is influenced less by geometric accuracy than by the accuracy of the representation of the distal CMV resistance.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2017 THE AUTHORS. PUBLISHED BY ELSEVIER ON BEHALF OF THE AMERICAN COLLEGE OF CARDIOLOGY FOUNDATION. THIS IS AN OPEN ACCESS ARTICLE UNDER THE CC BY LICENSE ( http://creativecommons.org/licenses/by/4.0/ ) . |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Infection, Immunity and Cardiovascular Disease The University of Sheffield > Sheffield Teaching Hospitals |
Funding Information: | Funder Grant number WELLCOME TRUST (THE) HICF-R6-365 BRITISH HEART FOUNDATION FS/12/85/29869 WELLCOME TRUST (THE) UNSPECIFIED BRITISH HEART FOUNDATION FS/16/48/32306 NATIONAL INSTITUTE FOR HEALTH RESEARCH II-LB-0216-20006 |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 06 Oct 2017 14:41 |
Last Modified: | 07 Nov 2018 13:21 |
Published Version: | https://doi.org/10.1016/j.jacbts.2017.04.003 |
Status: | Published |
Publisher: | Elsevier |
Refereed: | Yes |
Identification Number: | 10.1016/j.jacbts.2017.04.003 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:122162 |