Artificial intelligence-enabled electrocardiography algorithm for detection of occlusive myocardial infarction in suspected acute coronary syndromes without ST-segment elevation in clinical practice

  • Powerful Medical
  • March 20, 2026
  • 3 min to read
European Heart Journal: Acute Cardiovascular Care supplement abstract cover — ACVC 2026 ePoster on AI-ECG detection of occlusive myocardial infarction without ST elevation (study flow, 2x2 results, AI vs human specificity and PPV)

Overview

Occlusive myocardial infarction (OMI) is often missed when the ECG shows no ST-segment elevation, even by experienced clinicians. In this prospective single-center study at Bolzano Central Hospital, Italy, the first ECG of 1,490 patients with suspected acute coronary syndrome without ST elevation was analyzed by a commercially available, CE-certified smartphone AI-ECG algorithm alongside routine clinician interpretation. Based on the ECG alone and before troponin results, the AI detected OMI with 77% sensitivity and 99% specificity (negative predictive value 98%, positive predictive value 84%). By comparison, the guideline-directed pathway reached 88% specificity and a 42% positive predictive value.

Key findings

  • On the first ECG alone, AI-ECG detected occlusive MI with 77% sensitivity and 99% specificity, before any troponin results.
  • AI-ECG reached a 98% negative predictive value and an 84% positive predictive value for occlusive MI among 1,490 patients with suspected ACS without ST elevation.
  • Specificity was 99% with AI-ECG vs 88% with the guideline-directed pathway, and positive predictive value 84% vs 42%.
  • AI-ECG flagged 108 of 1,490 patients (7%) as OMI, with 17 false positives (1%) and 27 false negatives (2%).

Published in: European Heart Journal. Acute Cardiovascular Care – presented at ACVC 2026 (ESC Acute CardioVascular Care congress), Lisbon, 20 March 2026
Presented on: 20 March 2026

Background

Accurate recognition of occlusive myocardial infarction (OMI) in acute coronary syndromes (ACS) without ST-segment elevation remains challenging, even for skilled clinicians. Artificial intelligence applied to ECG interpretation (AI-ECG) could improve diagnostic accuracy and the timing of patient management. This study assessed the performance of AI-ECG in detecting OMI based solely on automated ECG interpretation, compared with human interpretation.

Methods

In this prospective single-center study at Bolzano Central Hospital, Italy, patients with symptoms suggestive of ACS without ST elevation were enrolled and managed according to the European Society of Cardiology (ESC) NSTE-ACS pathway (serial troponin ± coronary angiography). All first ECGs at presentation were analyzed by clinicians. In parallel, the same ECGs were analyzed by a smartphone-based, commercially available, CE-certified AI-ECG algorithm and classified as AI-OMI or AI-Rule-Out. OMI was defined as TIMI flow 0–II, or TIMI III flow with troponin T >1,000 ng/L. Final diagnoses were used to assess the performance of both clinicians and AI-ECG.

Results

Of 1,490 enrolled patients, AI-ECG classified 108 (7%) as AI-OMI and 1,382 as AI-Rule-Out. Following the guideline-directed pathway, 1,207 patients were ruled out on negative or stable serial troponin values and 283 underwent coronary angiography; 118 patients had confirmed OMI. AI-ECG identified 91 true positives and 1,355 true negatives, with 17 false positives (1%) and 27 false negatives (2%), corresponding to 77% sensitivity, 99% specificity, 98% negative predictive value and 84% positive predictive value for OMI. The guideline-directed pathway achieved 88% specificity and a 42% positive predictive value.

Conclusion

The AI-ECG algorithm identified and excluded occlusive myocardial infarction in patients with suspected ACS without ST elevation more accurately than conventional expert interpretation, before troponin results were available. Its integration into routine practice may accelerate diagnosis, enable earlier treatment and promote more efficient use of medical resources.

Authors: F. Nani, L. Donazzan, M. Bonatti, A. Ruzzarin, L. Malfatti, D. Bernardi, P. Engl, R. Oberhollenzer, M. Unterhuber

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