Abstract 4373195: A Novel Framework for End-Diastolic and End-Systolic Frame Localization in Contrast and Non-Contrast Echocardiography Without Manual Annotations

Background: End-diastolic (ED) and end-systolic (ES) frames are critical for left ventricular (LV) volume measurements in echocardiography but show high inter- and intra-observer variability. Deep learning (DL) methods have emerged for ED/ES detection; however, these typically rely on manually annotated reference frames and often fail to generalize across different image types, such as contrast and non-contrast echocardiographic views. Methods: A fully automated novel framework was developed for localizing ED/ES frames in both contrast and non-contrast cine loops without the use of manual annotations. The process begins with the YOLO (v12) object detection DL model to identify the LV as a region of interest (ROI); alternatively, a fixed bounding box or no localization step may be used. The largest ROI is selected to crop the cine loop. Robust principal component analysis is then applied to decompose the cine into a low-rank matrix, followed by singular value decomposition to extract the top three left singular vectors ( U ). Pseudo-periodic cardiac cycles are identified in each U using the Spectral Dominance Ratio. Zero-crossings and their variances are computed, and the U with the lowest variance (with at least two cycles) is chosen to represent the cardiac cycle. A peak detection algorithm is used to identify local extrema corresponding to the ED/ES frames. Results: The method was validated using a UAB dataset (N=984; 912 contrast, 72 non-contrast) and the publicly available EchoNet-Dynamic dataset (N=10,030, non-contrast) for external validation. The YOLO model was trained exclusively on the UAB dataset (1394 images for training, 298 images for validation, and 300 images for testing). On the UAB test set, the model achieved a mean Average Precision (mAP50) of 0.994 and mAP50-95 of 0.717. Mean absolute errors (MAE) in the UAB dataset were 2.65 ± 2.95 frames (median 2) for ED and 1.58 ± 1.49 frames (median 1) for ES. In the EchoNet dataset, the MAE was 3.75 ± 4.02 frames (median 2) for ED and 2.72 ± 2.81 frames (median 2) for ES. The framework excluded 5 UAB and 115 EchoNet cases due to only one cardiac cycle in the U . Conclusion: A robust and generalizable framework has been presented for localizing ED/ES frames without reliance on manually labeled training data. This approach supports both contrast and non-contrast images and can function with or without DL-based ROI detection, offering a scalable fully automated solution for echocardiographic analysis.

Authors

Institutions

Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4373195
Primary Topic
Cardiovascular Function and Risk Factors
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 4373195: A Novel Framework for End-Diastolic and End-Systolic Frame Localization in Contrast and Non-Contrast Echocardiography Without Manual Annotations

Akhil Pampana, Garima Arora, Cynthia Li, Pankaj Arora et al.
Circulation
Cardiovascular Function and Risk Factors
article

Abstract 4373195: A Novel Framework for End-Diastolic and End-Systolic Frame Localization in Contrast and Non-Contrast Echocardiography Without Manual Annotations

Akhil Pampana, Garima Arora, Cynthia Li, Pankaj Arora, Nehal Vekariya, Krishin Yerabolu, Abdulla Shahid, Samira Patel, Neeraj Kummaragunta, Priyank Baria
article en

Abstract

Background: End-diastolic (ED) and end-systolic (ES) frames are critical for left ventricular (LV) volume measurements in echocardiography but show high inter- and intra-observer variability. Deep learning (DL) methods have emerged for ED/ES detection; however, these typically rely on manually annotated reference frames and often fail to generalize across different image types, such as contrast and non-contrast echocardiographic views. Methods: A fully automated novel framework was developed for localizing ED/ES frames in both contrast and non-contrast cine loops without the use of manual annotations. The process begins with the YOLO (v12) object detection DL model to identify the LV as a region of interest (ROI); alternatively, a fixed bounding box or no localization step may be used. The largest ROI is selected to crop the cine loop. Robust principal component analysis is then applied to decompose the cine into a low-rank matrix, followed by singular value decomposition to extract the top three left singular vectors ( U ). Pseudo-periodic cardiac cycles are identified in each U using the Spectral Dominance Ratio. Zero-crossings and their variances are computed, and the U with the lowest variance (with at least two cycles) is chosen to represent the cardiac cycle. A peak detection algorithm is used to identify local extrema corresponding to the ED/ES frames. Results: The method was validated using a UAB dataset (N=984; 912 contrast, 72 non-contrast) and the publicly available EchoNet-Dynamic dataset (N=10,030, non-contrast) for external validation. The YOLO model was trained exclusively on the UAB dataset (1394 images for training, 298 images for validation, and 300 images for testing). On the UAB test set, the model achieved a mean Average Precision (mAP50) of 0.994 and mAP50-95 of 0.717. Mean absolute errors (MAE) in the UAB dataset were 2.65 ± 2.95 frames (median 2) for ED and 1.58 ± 1.49 frames (median 1) for ES. In the EchoNet dataset, the MAE was 3.75 ± 4.02 frames (median 2) for ED and 2.72 ± 2.81 frames (median 2) for ES. The framework excluded 5 UAB and 115 EchoNet cases due to only one cardiac cycle in the U . Conclusion: A robust and generalizable framework has been presented for localizing ED/ES frames without reliance on manually labeled training data. This approach supports both contrast and non-contrast images and can function with or without DL-based ROI detection, offering a scalable fully automated solution for echocardiographic analysis.

CirculationVol. 152(Suppl_3)
University of Alabama at Birmingham (US)
Openalex Percentile: Top 50%
Cardiovascular Function and Risk Factors
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.