1. An Artificial Intelligence Algorithm for Detection of Severe Aortic Stenosis: A Clinical Cohort Study.
- Author
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Strom JB, Playford D, Stewart S, and Strange G
- Abstract
Background: Identifying individuals with severe aortic stenosis (AS) at high risk of mortality remains challenging using current clinical imaging methods., Objectives: The purpose of this study was to evaluate an artificial intelligence decision support algorithm (AI-DSA) to augment the detection of severe AS within a well-resourced health care setting., Methods: Agnostic to clinical information, an AI-DSA trained to identify echocardiographic phenotype associated with an aortic valve area (AVA)<1 cm
2 using minimal input data (excluding left ventricular outflow tract measures) was applied to routine transthoracic echocardiograms (TTE) reports from 31,141 U.S. Medicare beneficiaries at an academic medical center (2003-2017)., Results: Performance of AI-DSA to detect the phenotype associated with an AVA<1 cm2 was excellent (sensitivity 82.2%, specificity 98.1%, negative predictive value 9.2%, c-statistic = 0.986). In addition to identifying clinical severe AS cases, AI-DSA identified an additional 1,034 (3.3%) individuals with guideline-defined moderate AS but with a similar clinical and TTE phenotype to those with severe AS with low rates of aortic valve replacement (6.6%). Five-year mortality was 75.9% in those with known severe AS, 73.5% in those with a similar phenotype to severe AS, and 44.6% in those without severe AS. The AI-DSA continued to perform well to identify severe AS among those with a depressed left ventricular ejection fraction. Overall rates of aortic valve replacement remained low, even in those with an AVA<1 cm2 (21.9%)., Conclusions: Without relying on left ventricular outflow tract measurements, an AI-DSA used echocardiographic reports to reliably identify the phenotype of severe AS. These results suggest possible utility for this AI-DSA to enhance detection of severe AS individuals at risk for adverse outcomes., Competing Interests: This work was supported by Echo IQ Pty Ltd. Dr Stewart is supported by the 10.13039/501100000925National Health and Medical Research Council of Australia (GNT1135894). Dr Strom is supported by the 10.13039/100000002National Institutes of Health (1K23HL144907, R01AG063937), 10.13039/100006520Edwards Lifesciences, Ultromics, HeartSciences, Anumana, and EchoIQ. Unrelated to this work, Dr Strom has served on the Scientific Advisory Board for Edwards Lifesciences and EchoIQ and has received consulting fees from Bracco Diagnostics, General Electric Healthcare, and Lantheus Medical Imaging. Prof Strange has received consulting fees from Edwards, Medtronic, and Echo IQ and has received speaker fees from Edwards, Medtronic, Abbott, and Echo IQ. Prof Playford has received consulting fees from Edwards, Medtronic, and Echo IQ. Prof Stewart has received consulting fees from Echo IQ., (© 2024 The Authors.)- Published
- 2024
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