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Machine Learning for Myocardial Infarction Compared With Guideline-Recommended Diagnostic Pathways.
Jasper Boeddinghaus1,2, Dimitrios Doudesis2,3, Pedro Lopez-Ayala1
1Cardiovascular Research Institute Basel (CRIB) and Department of Cardiology (J.B., P.L.-A., L.K., K.W., T.N., R.B., I.S., M.R.G., C.M.), University Hospital Basel, University of Basel, Switzerland.
The Collaboration for the Diagnosis and Evaluation of Acute Coronary Syndrome (CoDE-ACS) tool accurately identifies myocardial infarction (MI) probability using machine learning, outperforming guideline-recommended pathways. This tool consistently identifies more low-risk patients, improving early diagnosis of MI.
Area of Science:
- Cardiology
- Medical Informatics
- Machine Learning in Healthcare
Background:
- Acute Coronary Syndrome (ACS) diagnosis relies on clinical assessment and cardiac troponin measurements.
- Current diagnostic pathways for myocardial infarction (MI) use fixed time points and thresholds, which may not be optimal.
- The Collaboration for the Diagnosis and Evaluation of Acute Coronary Syndrome (CoDE-ACS) is a machine learning tool for MI probability assessment.
Purpose of the Study:
- To evaluate the diagnostic performance of the CoDE-ACS tool at different serial cardiac troponin measurement time points.
- To compare CoDE-ACS performance with guideline-recommended diagnostic pathways for MI.
- To assess the effectiveness of CoDE-ACS in identifying low- and high-probability scores for type 1 MI.
Main Methods:
- A prospective study enrolled 4105 patients with suspected MI across 12 sites in 5 countries.
- Serial high-sensitivity cardiac troponin I measurements were taken at 0, 1, and 2 hours.
- Diagnostic performance was assessed for CoDE-ACS against European Society of Cardiology (ESC) and High-STEACS pathways.
Main Results:
- CoDE-ACS identified 56% of patients as low probability at presentation (NPV 99.7%, sensitivity 99.0%), ruling out more patients than ESC 0-hour and High-STEACS pathways.
- At 1 or 2 hours, CoDE-ACS identified 65%-68% as low probability (NPV 99.7%) and 18%-19% as high probability (PPV 64.9%-68.8%).
- Guideline pathways identified fewer low-risk patients (49%-71%) with varying PPVs and NPVs, leaving more patients for further observation.
Conclusions:
- CoDE-ACS demonstrates consistent performance irrespective of serial troponin measurement timing.
- The tool identifies a greater proportion of low-probability patients compared to guideline-recommended pathways.
- Prospective evaluation is needed to determine if probability-guided care improves early MI diagnosis.
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