Factors affecting the performance of a novel artificial intelligence-based coronary computed tomography-derived ischaemia algorithm
European Heart Journal - Imaging Methods and Practice, vol. 2, pp. qyaf033
Abstract
Abstract Aims AI-QCTischaemia is an FDA-cleared novel artificial intelligence–guided method that utilizes features from coronary computed tomography angiography (CCTA) to predict myocardial ischaemia. Objective To identify factors associated with discrepancy between AI-QCTischaemia and positron emission tomography (PET) perfusion. Methods and results Six hundred and sixty-two patients with suspected obstructive coronary artery disease (CAD) on CCTA and undergoing [15O]H2O PET were analysed using AI-QCTischaemia. Multivariable logistic regression identified factors associated with discrepancy. Perfusion homogeneity was measured by relative flow reserve. A total of 209 (32%) patients showed discrepancies: 62 (9%) exhibited normal AI-QCTischaemia but abnormal perfusion (false negative AI-QCTischaemia), whereas 147 (22%) had abnormal AI-QCTischaemia despite normal perfusion (false positive AI-QCTischaemia). False positive AI-QCTischaemia patients (vs. true positive) were more often females, older, with less typical angina, and less advanced CAD. In multivariable analysis, typical angina [OR 95% CI: 1.796 (1.015–3.179), P = 0.044], diameter stenosis per 1% increase [1.058 (1.036–1.080), P < 0.001], and percent atheroma volume per 1% increase [1.103 (1.051–1.158), P < 0.001] significantly predicted true positive, while age was inversely associated [0.955 (0.923–0.989), P = 0.010]. False-negative AI-QCTischaemia patients (vs. true negative) were more often males, smokers, with less good CCTA image quality, and more advanced CAD. However, none was significant in multivariable analysis. Furthermore, false-negative AI-QCTischaemia showed more homogenously reduced perfusion by relative flow reserve compared to true positive (median ± IQR: 0.68 ± 0.15 vs. 0.56 ± 0.23, P < 0.001) and 21 (34%) of false negative showed globally reduced perfusion. Conclusion For abnormal AI-QCTischaemia, younger age, typical angina, more severe stenosis, and more extensive atherosclerosis predicted abnormal PET perfusion. With false negative AI-QCTischaemia, perfusion abnormalities were partly explained by microvascular disease.
Authors 7
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University of Turku · Turku University Hospital · Turku PET Centre · Chulabhorn Hospital · Chulabhorn Royal Academy
Affiliation as printed
National Cyclotron and PET Centre, Chulabhorn Hospital, Chulabhorn Royal Academy , Bangkok ,
Turku PET Centre, Turku University Hospital and University of Turku , P. O. Box 52, Turku FI-20521 ,
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University of Turku · Turku University Hospital · Turku PET Centre
Affiliation as printed
Department of Clinical Physiology, Nuclear Medicine, and PET, Turku University Hospital , Turku FI-20520 ,
Turku PET Centre, Turku University Hospital and University of Turku , P. O. Box 52, Turku FI-20521 ,
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University of Turku · University Hospital of Bern · Turku University Hospital · Turku PET Centre
Affiliation as printed
Department of Cardiology, Bern University Hospital Inselspital , Bern ,
Turku PET Centre, Turku University Hospital and University of Turku , P. O. Box 52, Turku FI-20521 ,
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Leiden University Medical Center
Affiliation as printed
Department of Cardiology, Leiden University Medical Center , Leiden ,
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University of Turku · Leiden University Medical Center · Turku University Hospital
Affiliation as printed
Department of Cardiology, Leiden University Medical Center , Leiden ,
Heart Center, Turku University Hospital and University of Turku , Turku ,
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University of Turku · Turku University Hospital · Turku PET Centre
Affiliation as printed
Heart Center, Turku University Hospital and University of Turku , Turku ,
Turku PET Centre, Turku University Hospital and University of Turku , P. O. Box 52, Turku FI-20521 ,
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Juhani M. Knuuti corresponding
University of Turku · Turku University Hospital · Turku PET Centre
Affiliation as printed
Department of Clinical Physiology, Nuclear Medicine, and PET, Turku University Hospital , Turku FI-20520 ,
Turku PET Centre, Turku University Hospital and University of Turku , P. O. Box 52, Turku FI-20521 ,
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