# AI Applications in Electrocardiography for Ischemic and Structural Heart Disease: A Review of the Current State

**Authors:** Eugene J. Kim, Dhir Gala, Mohammed Ayyad, Manaal Pramanik, Amgad N. Makaryus

PMC · DOI: 10.3390/jcm15010316 · Journal of Clinical Medicine · 2026-01-01

## TL;DR

This paper reviews how AI improves ECG analysis for heart disease detection, offering more accurate and faster diagnosis.

## Contribution

The paper highlights novel AI applications in ECG for detecting ischemic and structural heart diseases with high accuracy.

## Key findings

- AI-augmented ECG algorithms detect myocardial infarction with high accuracy.
- AI models can identify subtle ECG patterns linked to left ventricular dysfunction and aortic stenosis.
- Concerns remain about AI generalizability and bias in training data.

## Abstract

Cardiovascular disease is the leading cause of morbidity and mortality worldwide, with ischemic and structural heart diseases being key contributors. While the 12-lead electrocardiogram (ECG) is a common low-cost diagnostic test, its interpretation is limited by human variability. Through machine learning with large diverse ECG data sets and artificial intelligence (AI) algorithms, ECG analysis can be automated for pattern recognition with higher accuracy. AI-augmented ECG algorithms have been demonstrated to be able to detect myocardial infarction with high accuracy and reduce door-to-balloon coronary intervention times. Similar models can be utilized to detect subtle ECG waveforms suggestive of current or future asymptomatic left ventricular dysfunction, aortic stenosis, and hypertrophic cardiomyopathy. Despite these promising results, there is concern for generalizability and bias or errors in training data. As AI systems evolve to multimodal integration, AI-augmented ECG has the potential to redefine cardiovascular diagnostics and enable earlier detection, risk stratification, and precision-guided interventions.

## Linked entities

- **Diseases:** ischemic heart disease (MONDO:0024644), myocardial infarction (MONDO:0005068), aortic stenosis (MONDO:0042981), hypertrophic cardiomyopathy (MONDO:0005045)

## Full-text entities

- **Diseases:** left ventricular dysfunction (MESH:D018487), aortic stenosis (MESH:D001024), myocardial infarction (MESH:D009203), Heart Disease (MESH:D006331), Cardiovascular disease (MESH:D002318), hypertrophic cardiomyopathy (MESH:D002312), Ischemic (MESH:D002545)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12786525/full.md

## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786525/full.md

---
Source: https://tomesphere.com/paper/PMC12786525