11 models found
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11 public code
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11 public weights
Reinforcement-learning-based unsupervised domain adaptation framework for spatio-temporal (2D+time) echocardiography segmentation, extending the authors' earlier RL4Seg work to full-length video sequences. RL4Seg3D uses a sliding-window approach supporting high-resolution, full-sized inputs, and fuses multiple reward mechanisms to improve segmentation reliability without requiring additional expert annotations in the target domain. Trained and evaluated on a large dataset of over 30,000 echocardiography videos, it outperforms baselines and foundation models on overall segmentation accuracy as well as echocardiography-specific metrics including anatomical/temporal validity and mitral-valve-commissure landmark precision, and supports test-time optimization via calibrated uncertainty estimates.
Model ID: 0159
The original U-Net baseline segmentation network introduced alongside the CAMUS (Cardiac Acquisitions for Multi-structure Ultrasound Segmentation) dataset, one of the largest fully open-access, expert-annotated 2D echocardiography benchmarks. The network segments the left ventricle endocardium (LVEndo), left ventricle epicardium/myocardium (LVEpi), and left atrium (LA) from apical 2-chamber and 4-chamber echo views at end-diastole (ED) and end-systole (ES). In the original ten-fold cross-validation benchmark comparing U-Net, U-Net++, Stacked Hourglass, Anatomically Constrained Neural Networks, and classical methods, the U-Net variant (18M parameters) achieved the best overall accuracy, reaching Dice scores of 0.939 (ED) / 0.916 (ES) for LVEndo and 0.954 (ED) / 0.945 (ES) for LVEpi, approaching inter-observer variability. A pretrained checkpoint of this baseline U-Net is distributed via the University of Sherbrooke's vitalab CASTOR project as part of a broader library for building anatomically-constrained cardiac segmentation pipelines.
Model ID: 0115
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Subject Count: 500
Deep learning platform for fully automatic segmentation and phenotyping of coronary intravascular ultrasound (IVUS) pullbacks, packaged with a desktop GUI and CLI. A convolutional encoder-decoder network delineates the internal (lumen) and external elastic lamina borders on each cross-sectional IVUS frame; downstream rule-based analysis derives lumen area, plaque area, plaque burden, automatically flags lesions with plaque burden exceeding 40%, and reports minimum lumen area and maximum plaque burden along the pullback. Also supports end-diastolic gating and manual contour editing. Trained on 305 clinical IVUS pullbacks (270 train / 35 validation) from Philips and Boston Scientific catheters at Emory University; downstream evaluations have applied DeepIVUS to tasks such as automated detection of stent underexpansion.
Model ID: 0104
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Subject Count: 305
nnU-Net-based segmentation network that detects and delineates stenotic lesions directly from X-ray coronary angiography frames, developed for the ARCADE (MICCAI 2023) stenosis-detection challenge. A companion model (YOLO-Angio, same team) handles vessel-tree segmentation; StenUNet focuses specifically on pixel-wise localization of stenotic regions. Placed 3rd overall among ARCADE challenge entrants with an F1 score of 0.5348 on the hold-out test set, within 0.0005 of the 2nd-place team.
Model ID: 0101
U-Net-variant segmentation model that identifies and quantifies coronary artery calcium (CAC) directly from routine non-gated, non-contrast chest CT scans -- the kind ordered for lung-cancer screening or unrelated indications rather than a dedicated cardiac scan -- so that the tens of millions of such scans performed annually can be opportunistically screened for cardiovascular risk without any extra imaging. Predicted calcium masks are combined with the CT's Hounsfield units to compute an Agatston-equivalent score. Trained on 446 expert-segmented scans from 98 medical centers across the U.S. Department of Veterans Affairs national health system (capturing substantial heterogeneity in scanners and protocols) and benchmarked against 795 patients with a paired same-year gated CAC study: nongated AI-CAC differentiates zero-vs-nonzero and <100-vs->=100 Agatston categories with 89.4% (F1 0.93) and 87.3% (F1 0.89) accuracy respectively, and its score stratifies 10-year all-cause mortality (CAC 0 vs. >400: 25.4% vs. 60.2%, hazard ratio 3.49) and composite stroke/MI/death risk (33.5% vs. 63.8%, hazard ratio 3.00). In a simulated opportunistic-screening run across 8,052 low-dose CT scans, cardiologists confirmed 99.2% of patients flagged with AI-CAC >400 would benefit from lipid-lowering therapy. Code and trained model weights are both public under an MIT license.
Model ID: 0099
Multimodal cardiac MRI foundation model that fuses 3D+T cine CMR (short-axis and long-axis views) with tabular patient health records (demographics, metabolic, and lifestyle factors) from 42,000 UK Biobank participants. Two-stage self-supervised pretraining -- masked-image reconstruction, then imaging-tabular contrastive alignment -- produces representations that transfer to whole-heart segmentation, cardiac phenotype/physiological-feature regression, and cardiac/metabolic disease classification within one unified framework.
Model ID: 0062
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Subject Count: 74,916
Fully automated deep learning workflow for characterizing cardiac mechanics from balanced steady-state free-precession (bSSFP) cine cardiac MRI. It decouples two convolutional networks—a segmentation net (CarSON) and a 3D motion-estimation net (CarMEN)—to derive left- and right-ventricular volumes plus global and regional myocardial strain and strain rate without manual tracing. Trained and validated on healthy and cardiovascular-disease subjects and shown to be robust across MRI vendors, with excellent intra-scanner repeatability for strain. Developed at Massachusetts General Hospital and the Harvard-MIT Division of Health Sciences and Technology.
Model ID: 0056
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Subject Count: 150
Foundation model for cine cardiac MRI, self-supervised via masked autoencoding on nearly 75,000 UK Biobank scans. Uses a Vision Transformer with a convolutional stem, unified across long-axis and short-axis views. Fine-tuned checkpoints are released for ventricle and myocardium segmentation, ejection-fraction regression, cardiovascular disease classification, and landmark localization across several public benchmark datasets (ACDC, M&Ms, M&Ms2, EMIDEC, and others).
Model ID: 0003
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Subject Count: 74,916
End-to-end pipeline for apical-4-chamber echocardiogram videos that segments the left ventricle, estimates ejection fraction on a beat-to-beat basis, and classifies cardiomyopathy with reduced ejection fraction. Combines a DeepLabV3-ResNet50 segmentation model with a 3D CNN (R2+1D/R3D/MC3) initialized on the Kinetics-400 video dataset. Trained on the public EchoNet-Dynamic dataset released alongside it, and one of the most widely reused open echocardiography models since its 2020 Nature publication. Developed by Stanford University.
Model ID: 0036
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Subject Count: 10,030
Segments coronary vessels from invasive X-ray angiography images and automatically quantifies the degree of stenosis along the extracted centerlines. Combines MedSAM, a Segment-Anything-style vision model, with a Mamba-based VM-UNet segmentation branch for efficient long-range feature modeling. Trained and evaluated on the ARCADE, DCA1, and GH angiography datasets by researchers at Ocean University of China and Shandong University.
Model ID: 0001
Long-standing toolbox for automated segmentation of the ventricles and atria and derivation of cardiac imaging phenotypes from short- and long-axis cine cardiac MRI. Built on a fully convolutional network trained per slice, and widely reused across UK Biobank cardiac imaging studies since its 2018 publication. Developed at Imperial College London.
Model ID: 0006
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Subject Count: 74,916