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Updated: Mar 29, 2026

Ultrasonic Assessment of Myocardial Microstructure
Published on: January 14, 2014
Machine learning for detection of regional wall motion abnormalities on transthoracic echocardiography: A systematic
Thomas Koh1, Raunak Desai2, Krishnaa Sivapalan3
1Department of Cardiology, Division of Specialist Medical Services, Gold Coast Hospital and Health Services, Southport, QLD 4215, Australia; School of Medicine and Dentistry, Griffith University, Southport, QLD 4215, Australia.
Background:
Regional wall motion abnormality (RWMA) assessment is fundamental in transthoracic echocardiography (TTE) for diagnosing ischaemic heart disease, yet visual interpretation is subjective and variable. Machine-learning (ML) models may offer a more objective and reproducible RWMA evaluation, but their diagnostic accuracy has not been comprehensively synthesized.
Objective:
To systematically evaluate the diagnostic performance of ML algorithms for detecting RWMA on TTE.
Methods:
PubMed (MEDLINE) and EMBASE were searched from inception to 7 December 2025 for studies applying ML to RWMA detection using two-dimensional TTE. The primary outcomes were C-statistics, sensitivity and specificity of ML models.
Results:
Eight studies comprising ≈36,000 echocardiographic examinations were included. RWMA prevalence ranged from 9 % to 75 %, with ground truth definitions primarily based on expert consensus. Reported C-statistics ranged between 0.67-0.99, reflecting substantial heterogeneity (I² = 98 %). The pooled C-statistic was 0.88 (95 % CI 0.81-0.95). Internally validated models demonstrated a pooled C-statistic of 0.90 (95 % CI 0.82-0.97), and externally validated models 0.88 (95 % CI 0.84-0.92). Across studies reporting diagnostic data, pooled sensitivity and specificity were 0.83 (95 % CI 0.64-0.93) and 0.84 (95 % CI 0.75-0.91) respectively.
Conclusions:
ML models demonstrate good diagnostic performance for RWMA detection on TTE, approaching the accuracy of human readers in existing studies. However, marked heterogeneity, limited external validation, and methodological limitations currently restrict clinical readiness. Future research should prioritize multicentre external validation, improved reference standards, and adherence to TRIPOD-AI framework to support safe clinical integration.
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