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A novel method for noninvasive quantification of fractional flow reserve based on the custom function
Boundary condition settings are key risk factors for the accuracy of noninvasive quantification of fractional flow reserve (FFR) based on computed tomography angiography (i.e., FFR(CT)). However, transient numerical simulation-based FFR(CT) often ignores the three-dimensional (3D) model of coronary...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498765/ https://www.ncbi.nlm.nih.gov/pubmed/37711442 http://dx.doi.org/10.3389/fbioe.2023.1207300 |
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author | Zhang, Honghui Song, Xiaorui Wu, Rile Li, Na Hou, Qianwen Xie, Jinjie Hou, Yang Qiao, Aike |
author_facet | Zhang, Honghui Song, Xiaorui Wu, Rile Li, Na Hou, Qianwen Xie, Jinjie Hou, Yang Qiao, Aike |
author_sort | Zhang, Honghui |
collection | PubMed |
description | Boundary condition settings are key risk factors for the accuracy of noninvasive quantification of fractional flow reserve (FFR) based on computed tomography angiography (i.e., FFR(CT)). However, transient numerical simulation-based FFR(CT) often ignores the three-dimensional (3D) model of coronary artery and clinical statistics of hyperemia state set by boundary conditions, resulting in insufficient computational accuracy and high computational cost. Therefore, it is necessary to develop the custom function that combines the 3D model of the coronary artery and clinical statistics of hyperemia state for boundary condition setting, to accurately and quickly quantify FFR(CT) under steady-state numerical simulations. The 3D model of the coronary artery was reconstructed by patient computed tomography angiography (CTA), and coronary resting flow was determined from the volume and diameter of the 3D model. Then, we developed the custom function that took into account the interaction of stenotic resistance, microcirculation resistance, inlet aortic pressure, and clinical statistics of resting to hyperemia state due to the effect of adenosine on boundary condition settings, to accurately and rapidly identify coronary blood flow for quantification of FFR(CT) calculation (FFR(U)). We tested the diagnostic accuracy of FFR(U) calculation by comparing it with the existing methods (CTA, coronary angiography (QCA), and diameter-flow method for calculating FFR (FFR(D))) based on invasive FFR of 86 vessels in 73 patients. The average computational time for FFR(U) calculation was greatly reduced from 1–4 h for transient numerical simulations to 5 min per simulation, which was 2-fold less than the FFR(D) method. According to the results of the Bland-Altman analysis, the consistency between FFR(U) and invasive FFR of 86 vessels was better than that of FFR(D). The area under the receiver operating characteristic curve (AUC) for CTA, QCA, FFR(D) and FFR(U) at the lesion level were 0.62 (95% CI: 0.51–0.74), 0.67 (95% CI: 0.56–0.79), 0.85 (95% CI: 0.76–0.94), and 0.93 (95% CI: 0.87–0.98), respectively. At the patient level, the AUC was 0.61 (95% CI: 0.48–0.74) for CTA, 0.65 (95% CI: 0.53–0.77) for QCA, 0.83 (95% CI: 0.74–0.92) for FFR(D), and 0.92 (95% CI: 0.89–0.96) for FFR(U). The proposed novel method might accurately and rapidly identify coronary blood flow, significantly improve the accuracy of FFR(CT) calculation, and support its wide application as a diagnostic indicator in clinical practice. |
format | Online Article Text |
id | pubmed-10498765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104987652023-09-14 A novel method for noninvasive quantification of fractional flow reserve based on the custom function Zhang, Honghui Song, Xiaorui Wu, Rile Li, Na Hou, Qianwen Xie, Jinjie Hou, Yang Qiao, Aike Front Bioeng Biotechnol Bioengineering and Biotechnology Boundary condition settings are key risk factors for the accuracy of noninvasive quantification of fractional flow reserve (FFR) based on computed tomography angiography (i.e., FFR(CT)). However, transient numerical simulation-based FFR(CT) often ignores the three-dimensional (3D) model of coronary artery and clinical statistics of hyperemia state set by boundary conditions, resulting in insufficient computational accuracy and high computational cost. Therefore, it is necessary to develop the custom function that combines the 3D model of the coronary artery and clinical statistics of hyperemia state for boundary condition setting, to accurately and quickly quantify FFR(CT) under steady-state numerical simulations. The 3D model of the coronary artery was reconstructed by patient computed tomography angiography (CTA), and coronary resting flow was determined from the volume and diameter of the 3D model. Then, we developed the custom function that took into account the interaction of stenotic resistance, microcirculation resistance, inlet aortic pressure, and clinical statistics of resting to hyperemia state due to the effect of adenosine on boundary condition settings, to accurately and rapidly identify coronary blood flow for quantification of FFR(CT) calculation (FFR(U)). We tested the diagnostic accuracy of FFR(U) calculation by comparing it with the existing methods (CTA, coronary angiography (QCA), and diameter-flow method for calculating FFR (FFR(D))) based on invasive FFR of 86 vessels in 73 patients. The average computational time for FFR(U) calculation was greatly reduced from 1–4 h for transient numerical simulations to 5 min per simulation, which was 2-fold less than the FFR(D) method. According to the results of the Bland-Altman analysis, the consistency between FFR(U) and invasive FFR of 86 vessels was better than that of FFR(D). The area under the receiver operating characteristic curve (AUC) for CTA, QCA, FFR(D) and FFR(U) at the lesion level were 0.62 (95% CI: 0.51–0.74), 0.67 (95% CI: 0.56–0.79), 0.85 (95% CI: 0.76–0.94), and 0.93 (95% CI: 0.87–0.98), respectively. At the patient level, the AUC was 0.61 (95% CI: 0.48–0.74) for CTA, 0.65 (95% CI: 0.53–0.77) for QCA, 0.83 (95% CI: 0.74–0.92) for FFR(D), and 0.92 (95% CI: 0.89–0.96) for FFR(U). The proposed novel method might accurately and rapidly identify coronary blood flow, significantly improve the accuracy of FFR(CT) calculation, and support its wide application as a diagnostic indicator in clinical practice. Frontiers Media S.A. 2023-08-30 /pmc/articles/PMC10498765/ /pubmed/37711442 http://dx.doi.org/10.3389/fbioe.2023.1207300 Text en Copyright © 2023 Zhang, Song, Wu, Li, Hou, Xie, Hou and Qiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Zhang, Honghui Song, Xiaorui Wu, Rile Li, Na Hou, Qianwen Xie, Jinjie Hou, Yang Qiao, Aike A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title | A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title_full | A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title_fullStr | A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title_full_unstemmed | A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title_short | A novel method for noninvasive quantification of fractional flow reserve based on the custom function |
title_sort | novel method for noninvasive quantification of fractional flow reserve based on the custom function |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498765/ https://www.ncbi.nlm.nih.gov/pubmed/37711442 http://dx.doi.org/10.3389/fbioe.2023.1207300 |
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