Key result
AI-identified pan-chamber strain dysfunction is linked to ~3.4-fold higher risk of death or HF hospitalization.
Why the study?
Clinical application of myocardial strain has largely focused on individual chambers or selected patient populations, leaving the feasibility and clinical relevance of fully automated multi-chamber strain assessment in routine practice uncertain.
Does fully automated AI-based multi-chamber myocardial strain profiling and clustering provide feasible functional characterization and incremental prognostic value for all-cause death or heart failure hospitalization in consecutive adults undergoing routine transthoracic echocardiography?
Cohort (n=8,350)
No
Does fully automated AI-based multi-chamber myocardial strain profiling and clustering provide feasible functional characterization and incremental prognostic value for all-cause death or heart failure hospitalization in consecutive adults undergoing routine transthoracic echocardiography?
Fully automated AI-derived multi-chamber strain assessment is feasible in over 90% of routine echocardiograms and identifies distinct functional phenotypes, with pan-chamber dysfunction independently predicting a more than three-fold higher risk of death or heart failure hospitalization beyond conventional echocardiographic measures.
Answers are grounded in this paper and cite their sources.
May support AI multi-chamber strain for risk stratification on routine echo; hypothesis-generating pending prospective validation.
Aims Myocardial strain enables sensitive assessment of cardiac function, but its clinical application has largely focused on individual chambers or selected patient populations. We evaluated the feasibility and clinical relevance of fully automated multi-chamber strain assessment in consecutive patients undergoing routine transthoracic echocardiography (TTE). Methods and results This retrospective study included 8,350 consecutive adults undergoing TTE. A hospital-wide artificial intelligence (AI)–based system automatically measured left ventricular (LV) global longitudinal strain (LVGLS), left atrial (LA) reservoir strain (LASr), and right ventricular (RV) free-wall strain (RVFWS). AI-derived LVGLS was available from at least one apical view in 97.1% of patients and from all three views in 94.8%; LASr and RVFWS were available in 94.1% and 94.5%, respectively, resulting in complete multi-chamber strain assessment in 90.3%. Strain measures showed modest correlations with conventional chamber-specific echocardiographic parameters and differential associations with clinical outcomes. Gaussian mixture modeling identified three distinct clusters characterized by preserved multi-chamber function, RV-dominant dysfunction, and pan-chamber dysfunction. Compared with the preserved cluster, pan-chamber dysfunction was associated with the highest risk of all-cause death or heart failure hospitalization (adjusted hazard ratio, 3.44; 95% CI, 2.43–4.88; P<0.001). Prognostic associations remained evident in patients with LV ejection fraction (LVEF) ≥50%, and cluster assignment provided incremental prognostic information beyond clinical factors, LVEF, and RV fractional area change. Conclusions Fully automated multi-chamber strain assessment was feasible in a large consecutive TTE cohort. Integrating strain across cardiac chambers may provide complementary functional characterization and identify clinically relevant clusters with prognostic information beyond conventional assessment.
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Noh et al. (2026) conducted a cohort in Consecutive adults undergoing routine transthoracic echocardiography (n=8,350). Pan-chamber dysfunction (Cluster 3) on fully automated AI-derived multi-chamber strain profiling (LVGLS, LASr, RVFWS) vs. Preserved multi-chamber strain function (Cluster 1) was evaluated on Composite of all-cause death and heart failure hospitalization (HR 3.44, 95% CI 2.43-4.88, p=<0.001). AI-identified pan-chamber strain dysfunction was associated with higher risk of all-cause death or HF hospitalization vs preserved function (HR 3.44, 95% CI 2.43-4.88; P<0.001).
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