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American Heart Association

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Final ID: MP306

Fully Automated vs. Human Echocardiogram Interpretation in Transthyretin Amyloid Cardiomyopathy: The SCAN-MP Study

Abstract Body (Do not enter title and authors here):
Introduction
Transthoracic echocardiography (TTE) is the standard-of-care imaging modality for management of heart failure (HF). Transthyretin amyloid cardiomyopathy (ATTR-CM) is an important cause of HF that can be difficult to identify and follow longitudinally by TTE, owing to imprecision of measurements and variability in interpretation. Analysis of standard TTE variables using Artificial Intelligence (AI) could improve precision and reproducibility while reducing interpretation time.

Aims
To assess performance of a previously validated, fully automated AI algorithm for TTE interpretation (Us2.ai) in patients with heart failure at risk for ATTR-CM. We hypothesized that AI measurements would be strongly correlated with human interpretation and identify differences between participants with and without ATTR-CM.

Methods
TTE images from participants in the prospective Screening for Cardiac Amyloidosis with Nuclear Imaging in Minority Populations (SCAN-MP) study (n = 586, 36 ATTR-CM cases) were analyzed independently by a human expert and an AI algorithm (Us2.ai). Intraclass correlation and Bland-Altman agreement between human and AI were assessed for clinically relevant TTE variables including left ventricular ejection fraction (LVEF), global longitudinal strain (GLS), maximal wall thickness (MWT), and mitral E/e’ ratio. Additionally, human and AI parameter distributions were compared between participants with and without ATTR-CM.

Results
Comparison of human and AI distributions demonstrated differences in participants with ATTR-CM for most variables, with similar magnitude and directionality (Table 1). Correlation between AI and human measurements was high for the Doppler measure E/e’ (ICC: 0.89, 95% CI: [0.86-0.90]) and moderate for LVEF [0.72 (0.27-0.86)], MWT [0.68 (0.63-0.73)], and GLS [0.64 (0.54-0.72)]. Similarly, Bland-Altman agreement was highest for E/e’, while LVEF, GLS, and MWT had relatively wider limits of agreement and greater bias. AI underestimated most parameters, including LVEF (bias AI -5.3%), MWT (bias AI -0.15cm), and E/e’ (bias AI -0.49), but overestimated GLS (bias AI +1.1%).

Conclusions
Fully automated TTE measurements were correlated with a human reference and reproduced differences between ATTR-CM cases and controls. AI TTE interpretation is a promising tool to democratize echocardiography for clinical care and research, and may be interchangeable with human readers for some measurements relevant to ATTR-CM.
  • Mcmenamin, Katie  ( Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center , Boston , Massachusetts , United States )
  • Lang, Roberto  ( University of Chicago Pritzker School of Medicine , Chicago , Illinois , United States )
  • Maurer, Mathew  ( Columbia University Irving Medical Center and New York-Presbyterian Hospital , New York , New York , United States )
  • Ruberg, Frederick  ( Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center , Boston , Massachusetts , United States )
  • Teruya, Sergio  ( Columbia University Irving Medical Center and New York-Presbyterian Hospital , New York , New York , United States )
  • Slivnick, Jeremy  ( University of Chicago Pritzker School of Medicine , Chicago , Illinois , United States )
  • Alreshq, Rabah  ( Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center , Boston , Massachusetts , United States )
  • Ullah, Ikram  ( Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center , Boston , Massachusetts , United States )
  • Fine, Denise  ( Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center , Boston , Massachusetts , United States )
  • Helmke, Stephen  ( Columbia University Irving Medical Center and New York-Presbyterian Hospital , New York , New York , United States )
  • Gallegos, Cesia  ( Yale University School of Medicine , Guilford , Connecticut , United States )
  • Miller, Edward  ( Yale University School of Medicine , Guilford , Connecticut , United States )
  • Author Disclosures:
    Katie McMenamin: DO NOT have relevant financial relationships | Roberto Lang: No Answer | Mathew Maurer: DO have relevant financial relationships ; Advisor:Pfizer:Active (exists now) ; Advisor:Intellia:Active (exists now) ; Advisor:BrigdeBio:Active (exists now) ; Advisor:AstraZeneca:Active (exists now) ; Advisor:Ionis:Active (exists now) ; Advisor:Alnylam:Active (exists now) | Frederick Ruberg: DO have relevant financial relationships ; Consultant:eMyosound:Active (exists now) ; Researcher:Anumana:Active (exists now) ; Researcher:BridgeBio:Active (exists now) ; Researcher:TriNetX:Active (exists now) ; Consultant:Attralus:Active (exists now) | Sergio Teruya: DO NOT have relevant financial relationships | Jeremy Slivnick: DO have relevant financial relationships ; Consultant:Pfizer:Past (completed) ; Consultant:GE Healthcare:Past (completed) ; Consultant:Alnylam:Past (completed) ; Consultant:BridgeBio:Past (completed) | Rabah Alreshq : DO NOT have relevant financial relationships | Ikram Ullah: No Answer | Denise Fine: DO NOT have relevant financial relationships | Stephen Helmke: No Answer | Cesia Gallegos: DO have relevant financial relationships ; Advisor:Pfizer:Past (completed) ; Advisor:Astra Zeneca:Past (completed) ; Advisor:Alnylam:Past (completed) ; Advisor:Bridge Bio:Past (completed) | Edward Miller: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Imaging Insights from Multicenter Clinical Trials

Saturday, 11/08/2025 , 10:45AM - 11:55AM

Moderated Digital Poster Session

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