# Detection and prognostic stratification of left ventricular systolic dysfunction in left bundle branch block using an artificial intelligence–enabled electrocardiography

**Authors:** Soo Youn Lee, Ah-Hyun Yoo, Sora Kang, Jong-Hwan Jang, Yong-Yeon Jo, Jeong Min Son, Min Sung Lee, Ga In Han, Joon-myoung Kwon, Hak Seung Lee, Kyung-Hee Kim

PMC · DOI: 10.1186/s44348-026-00066-9 · Journal of Cardiovascular Imaging · 2026-02-16

## TL;DR

An AI model accurately detects heart dysfunction in patients with left bundle branch block and predicts their future health risks.

## Contribution

An AI-ECG model is shown to effectively detect LVSD and stratify long-term cardiovascular risk in LBBB patients.

## Key findings

- The AiTiALVSD model achieved high sensitivity (0.979) in detecting LVSD in LBBB patients.
- High-risk patients had significantly higher hazards for mortality and hospitalization compared to low-risk patients.
- The model's performance metrics include an AUROC of 0.930 and AUPRC of 0.913.

## Abstract

Left bundle branch block (LBBB) significantly increases the risk of left ventricular systolic dysfunction (LVSD) due to cardiac dyssynchrony. Although artificial intelligence–enabled electrocardiography (AI-ECG) models show promise in detecting LVSD, their performance in LBBB patients remains underexplored. We hypothesized that an AI-ECG model clinically validated for detecting LVSD would accurately detect LVSD and predict future clinical outcomes in LBBB patients.

In this retrospective multicenter study, 5,689 expert-validated LBBB ECGs collected from 2,813 patients between 2016 and 2024 were analyzed using a previously developed and validated AI-ECG model. LVSD was defined as an ejection fraction of ≤ 40%. Model performance was assessed using the area under the receiver operating characteristic curve (AUROC), the area under the precision-recall curve (AUPRC), sensitivity, and specificity. Patients were stratified into high- and low-risk groups based on a threshold that achieved 90% sensitivity. A Kaplan–Meier analysis was used to compare clinical outcomes.

Among the 2,813 LBBB patients (mean age, 70.7 years; male sex, 43.7%), hypertension and a history of heart failure were common. The AiTiALVSD model showed strong diagnostic performance for LVSD (AUROC, 0.930 [95% CI, 0.924–0.937]; AUPRC, 0.913 [95% CI, 0.902–0.923]; sensitivity, 0.979; specificity, 0.473). During the mean follow-up of 4.1 years, high-risk patients had significantly higher hazards than low-risk patients for all-cause mortality (adjusted hazard ratio [HR], 1.87; 95% CI, 1.53–2.28), implantable cardioverter defibrillator/cardiac resynchronization therapy implantation (adjusted HR, 15.2; 95% CI, 7.51–30.77), and cardiovascular hospitalization (adjusted HR, 1.11; 95% CI, 0.96–1.28).

AiTiALVSD effectively detects LVSD and stratifies long-term cardiovascular risk in LBBB patients, supporting its clinical utility for early detection and patient management.

The online version contains supplementary material available at 10.1186/s44348-026-00066-9.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** myocardial strain abnormalities (MESH:D013180), AI (MESH:C538142), LV dysfunction (MESH:D018487), aortic stenosis (MESH:D001024), MR (MESH:D008944), conduction disease (MESH:D004194), ventricular dysfunction (MESH:D018754), chronic kidney disease (MESH:D051436), diabetes (MESH:D003920), LBBB (MESH:D002037), cardiac dyssynchrony (MESH:D006331), tricuspid regurgitation (MESH:D014262), heart failure (MESH:D006333), systolic impairment (MESH:D000092244), in ventricular function (MESH:D014693), hypertension (MESH:D006973), conduction abnormalities (MESH:D054537), ischemic heart disease (MESH:D017202), atrial fibrillation (MESH:D001281), ST-T abnormalities (MESH:D001260)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12914959