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Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
Prospective validation of current quantitative electrocardiographic criteria for ST-elevation myocardial infarction
Petra Hillinger1, Ivo Strebel2, Roger Abächerli3
1Department of Cardiology & Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Switzerland; Department of Anesthesia and Intensive Care Medicine, University Hospital Innsbruck, University of Innsbruck, Austria.
Insights
Current Electrocardiogram (ECG) criteria for ST-elevation myocardial infarction (STEMI) show suboptimal diagnostic performance. Automated analysis revealed low sensitivity and positive predictive value for STEMI diagnosis in the emergency department.
Area of Science:
- Cardiology
- Medical Diagnostics
- Emergency Medicine
Background:
- Rapid diagnosis of ST-elevation myocardial infarction (STEMI) is crucial for timely reperfusion therapy.
- STEMI diagnosis often relies on Electrocardiogram (ECG) criteria.
Purpose of the Study:
- To evaluate the diagnostic accuracy of current guideline-recommended ECG criteria for STEMI.
- To assess the performance of automated ECG analysis in identifying STEMI.
Main Methods:
- Prospective, multicenter diagnostic study involving adult patients with suspected myocardial infarction (MI).
- Objective quantification of ST-segment elevation using automated software analysis of digital 12-lead ECGs.
- Comparison of ECG criteria against final adjudicated diagnoses by cardiologists.
Main Results:
- Only 35% of final STEMI cases were correctly identified by current ECG criteria (Sensitivity 35%, PPV 54%).
- Suboptimal diagnostic performance was attributed to timing, measurement points, borderline ST-segment elevation, and inferoposterior MI location.
- High Negative Predictive Value (NPV 97.8%) indicates current criteria are good at ruling out STEMI.
Conclusions:
- Current guideline-recommended ECG criteria for STEMI exhibit suboptimal diagnostic performance when applied to a single ECG at emergency department presentation.
- Automated ECG analysis highlights limitations in current criteria, necessitating further research for improved STEMI detection.
Background:
Rapid and reliable diagnosis of ST-elevation myocardial infarction (STEMI) as a surrogate for acute coronary occlusion is critical for early reperfusion therapy.
Objectives:
We aimed to examine the diagnostic performance of current guideline-recommended Electrocardiogram (ECG) STEMI criteria.
Methods:
In a prospective diagnostic multicenter study, we objectively quantified the extent of ST-segment elevation in all ECG leads using an automated software-based analysis of the digital 12-lead-ECG in adult patients presenting to the emergency department (ED) with suspected myocardial infarction (MI). Classification according to current guideline-recommended ECG criteria for STEMI at ED presentation was compared against a final diagnosis adjudicated by two independent cardiologists after reviewing all available medical records including serial ECGs, cardiac imaging and coronary angiograms.
Results:
Among 2486 patients, 52 (2%) were found to have significant ST-segment elevation on ECG at ED presentation according to current guideline-recommended ECG criteria for STEMI. Eighty-one (3%) patients received a final adjudicated diagnosis of STEMI. Only 35% (28 of 81) of all patients with a final diagnosis of STEMI were correctly identified (PPV 54% (95% CI 41-66%), sensitivity 35% (95% Cl 24-46%), NPV 97.8% (95% CI 97.5-98.1%). Four reasons for missing STEMIs emerged: timing (significant STE at an earlier/later time point) in 25%, incorrect measurement points in 30%, non or borderline-significant STE in 36% and inferoposterior MI localisation in 9%.
Conclusions:
A computerized analysis of current guideline-recommended ECG criteria for STEMI showed suboptimal diagnostic performance when applied to a single 12‑lead ECG performed at ED presentation.
Clinical Trial Registration:
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00470587.
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