Abstract 4364391: Artificial Intelligence-Powered Electrocardiogram to Detect Acute Coronary Obstruction in Patients with Suspected Acute Coronary Syndrome

Background: ST-elevation on a 12-lead ECG helps identify occlusion myocardial infarction (OMI) requiring emergent invasive coronary angiography (ICA) and revascularization. However, ~25% of non-ST-elevation myocardial infarctions have OMI on ICA, highlighting the need for improved risk assessment. Methods: This multicenter, retrospective study analyzed consecutive adults with suspected high-risk non-ST-elevation acute coronary syndrome (NSTE-ACS) from 2022 to 2024, using the Minneapolis Heart Institute Level 2 Protocol within the PROGRESS-CATH registry. Eligible patients underwent a 12-lead ECG before urgent ICA referral based on criteria such as ST depression, anterior T-wave inversion, positive biomarkers, unstable arrhythmias, clinical instability, or ischemia on stress testing. STEMI (Level 1) patients were excluded. The FDA-cleared OMI AI ECG model (Powerful Medical, Slovakia) assessed OMI risk, which was validated via ICA. OMI was defined as an angiographic culprit lesion with TIMI-0-2 flow or TIMI-3/unknown flow with elevated cardiac troponin (cTn) or new regional wall motion abnormality. Results: Among 172 patients with suspected NSTE-ACS, 76 (44%) were classified as high-risk of OMI by the AI model, while 96 (56%) were categorized as non-OMI. Among the 76 patients with high-risk of OMI by AI, 65 (86%) had OMI confirmed by the ICA, whereas 11 (15%) did not have a culprit lesion. Patients in the AI-based OMI and non-OMI groups had comparable demographic characteristics. Institutional treatment protocols ensured similar management across both groups. Time intervals between admission and first ECG (21 [10-29] vs. 14 [7.3-60] minutes; p=0.93), first cTn measurement (42 [32-57] vs. 56 [26-98] minutes; p=0.78), and presentation to the catheterization laboratory (194 [64-850] vs. 250 [68-778] minutes; p=0.80) were comparable. In-hospital mortality was higher in the OMI group (8 patients, 10.5%) compared with the non-OMI group (2 patients, 2.1%) (OR 5.52; 95% CI 1.14-26.82; p=0.03). After a mean follow-up period of 442 days, there was higher mortality in the OMI group (HR 3.18; 95% CI 1.05-10.1; p=0.04). Conclusion: AI-enhanced detection of OMI among patients without ST-elevation facilitates the rapid detection of patients at high risk for mortality that may require prompt revascularization and may outperform standard 12-lead ECG risk-stratification.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4364391
Primary Topic
ECG Monitoring and Analysis
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article
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article

Abstract 4364391: Artificial Intelligence-Powered Electrocardiogram to Detect Acute Coronary Obstruction in Patients with Suspected Acute Coronary Syndrome

Emmanouil S. Brilakis, Pedro Carvalho, Bavana Rangan, Sandeep Jalli et al.
Circulation
ECG Monitoring and Analysis
article

Abstract 4364391: Artificial Intelligence-Powered Electrocardiogram to Detect Acute Coronary Obstruction in Patients with Suspected Acute Coronary Syndrome

Emmanouil S. Brilakis, Pedro Carvalho, Bavana Rangan, Sandeep Jalli, D S Pollmann, William R. Belzer, Olga Mastrodemos, Eleni Kladou, Deniz Mutlu, Özgür Selim Ser, Dimitrios Strepkos, Michaella Alexandrou, Yader Sandoval, Hans C. Helseth
article en

Abstract

Background: ST-elevation on a 12-lead ECG helps identify occlusion myocardial infarction (OMI) requiring emergent invasive coronary angiography (ICA) and revascularization. However, ~25% of non-ST-elevation myocardial infarctions have OMI on ICA, highlighting the need for improved risk assessment. Methods: This multicenter, retrospective study analyzed consecutive adults with suspected high-risk non-ST-elevation acute coronary syndrome (NSTE-ACS) from 2022 to 2024, using the Minneapolis Heart Institute Level 2 Protocol within the PROGRESS-CATH registry. Eligible patients underwent a 12-lead ECG before urgent ICA referral based on criteria such as ST depression, anterior T-wave inversion, positive biomarkers, unstable arrhythmias, clinical instability, or ischemia on stress testing. STEMI (Level 1) patients were excluded. The FDA-cleared OMI AI ECG model (Powerful Medical, Slovakia) assessed OMI risk, which was validated via ICA. OMI was defined as an angiographic culprit lesion with TIMI-0-2 flow or TIMI-3/unknown flow with elevated cardiac troponin (cTn) or new regional wall motion abnormality. Results: Among 172 patients with suspected NSTE-ACS, 76 (44%) were classified as high-risk of OMI by the AI model, while 96 (56%) were categorized as non-OMI. Among the 76 patients with high-risk of OMI by AI, 65 (86%) had OMI confirmed by the ICA, whereas 11 (15%) did not have a culprit lesion. Patients in the AI-based OMI and non-OMI groups had comparable demographic characteristics. Institutional treatment protocols ensured similar management across both groups. Time intervals between admission and first ECG (21 [10-29] vs. 14 [7.3-60] minutes; p=0.93), first cTn measurement (42 [32-57] vs. 56 [26-98] minutes; p=0.78), and presentation to the catheterization laboratory (194 [64-850] vs. 250 [68-778] minutes; p=0.80) were comparable. In-hospital mortality was higher in the OMI group (8 patients, 10.5%) compared with the non-OMI group (2 patients, 2.1%) (OR 5.52; 95% CI 1.14-26.82; p=0.03). After a mean follow-up period of 442 days, there was higher mortality in the OMI group (HR 3.18; 95% CI 1.05-10.1; p=0.04). Conclusion: AI-enhanced detection of OMI among patients without ST-elevation facilitates the rapid detection of patients at high risk for mortality that may require prompt revascularization and may outperform standard 12-lead ECG risk-stratification.

CirculationVol. 152(Suppl_3)
Minneapolis Heart Institute Foundation (US)
Openalex Percentile: Top 51%
ECG Monitoring and Analysis
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