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AI Evaluation of Stenosis on Coronary CTA, Comparison With Quantitative Coronary Angiography and Fractional Flow Reserve: A CREDENCE Trial Substudy

Authors
 William F Griffin  ;  Andrew D Choi  ;  Joanna S Riess  ;  Hugo Marques  ;  Hyuk-Jae Chang  ;  Jung Hyun Choi  ;  Joon-Hyung Doh  ;  Ae-Young Her  ;  Bon-Kwon Koo  ;  Chang-Wook Nam  ;  Hyung-Bok Park  ;  Sang-Hoon Shin  ;  Jason Cole  ;  Alessia Gimelli  ;  Muhammad Akram Khan  ;  Bin Lu  ;  Yang Gao  ;  Faisal Nabi  ;  Ryo Nakazato  ;  U Joseph Schoepf  ;  Roel S Driessen  ;  Michiel J Bom  ;  Randall Thompson  ;  James J Jang  ;  Michael Ridner  ;  Chris Rowan  ;  Erick Avelar  ;  Philippe Généreux  ;  Paul Knaapen  ;  Guus A de Waard  ;  Gianluca Pontone  ;  Daniele Andreini  ;  James P Earls 
Citation
 JACC-CARDIOVASCULAR IMAGING, Vol.16(2) : 193-205, 2023-02 
Journal Title
JACC-CARDIOVASCULAR IMAGING
ISSN
 1936-878X 
Issue Date
2023-02
MeSH
Artificial Intelligence ; Atherosclerosis* ; Computed Tomography Angiography / methods ; Constriction, Pathologic ; Coronary Angiography / methods ; Coronary Artery Disease* / diagnostic imaging ; Coronary Stenosis* / diagnostic imaging ; Female ; Fractional Flow Reserve, Myocardial* ; Humans ; Male ; Myocardial Ischemia* ; Predictive Value of Tests ; Retrospective Studies ; Severity of Illness Index
Keywords
artificial intelligence ; atherosclerosis ; coronary CTA ; coronary artery disease ; coronary computed tomography ; fractional flow reserve ; quantitative coronary angiography
Abstract
Background: Clinical reads of coronary computed tomography angiography (CTA), especially by less experienced readers, may result in overestimation of coronary artery disease stenosis severity compared with expert interpretation. Artificial intelligence (AI)-based solutions applied to coronary CTA may overcome these limitations. Objectives: This study compared the performance for detection and grading of coronary stenoses using artificial intelligence–enabled quantitative coronary computed tomography (AI-QCT) angiography analyses to core lab–interpreted coronary CTA, core lab quantitative coronary angiography (QCA), and invasive fractional flow reserve (FFR). Methods: Coronary CTA, FFR, and QCA data from 303 stable patients (64 ± 10 years of age, 71% male) from the CREDENCE (Computed TomogRaphic Evaluation of Atherosclerotic DEtermiNants of Myocardial IsChEmia) trial were retrospectively analyzed using an Food and Drug Administration–cleared cloud-based software that performs AI-enabled coronary segmentation, lumen and vessel wall determination, plaque quantification and characterization, and stenosis determination. Results: Disease prevalence was high, with 32.0%, 35.0%, 21.0%, and 13.0% demonstrating ≥50% stenosis in 0, 1, 2, and 3 coronary vessel territories, respectively. Average AI-QCT analysis time was 10.3 ± 2.7 minutes. AI-QCT evaluation demonstrated per-patient sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of 94%, 68%, 81%, 90%, and 84%, respectively, for ≥50% stenosis, and of 94%, 82%, 69%, 97%, and 86%, respectively, for detection of ≥70% stenosis. There was high correlation between stenosis detected on AI-QCT evaluation vs QCA on a per-vessel and per-patient basis (intraclass correlation coefficient = 0.73 and 0.73, respectively; P < 0.001 for both). False positive AI-QCT findings were noted in in 62 of 848 (7.3%) vessels (stenosis of ≥70% by AI-QCT and QCA of <70%); however, 41 (66.1%) of these had an FFR of <0.8. Conclusions: A novel AI-based evaluation of coronary CTA enables rapid and accurate identification and exclusion of high-grade stenosis and with close agreement to blinded, core lab–interpreted quantitative coronary angiography. (Computed TomogRaphic Evaluation of Atherosclerotic DEtermiNants of Myocardial IsChEmia [CREDENCE]; NCT02173275) © 2023 The Authors
Files in This Item:
T202302531.pdf Download
DOI
10.1016/j.jcmg.2021.10.020
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Chang, Hyuk-Jae(장혁재) ORCID logo https://orcid.org/0000-0002-6139-7545
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/194177
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