FASTR-SCANN (Fully Automated Segmental Relaxometry using Synthetic Contrast Augmentation with Neural Networks) / U-NetSCANN
2026-01-24https://doi.org/10.1148/atlas.1769272958014
20
Overview
Schema Version
https://atlas.rsna.org/schemas/2025-11/model.json
Name
FASTR-SCANN (Fully Automated Segmental Relaxometry using Synthetic Contrast Augmentation with Neural Networks) / U-NetSCANN
Link
https://pubmed.ncbi.nlm.nih.gov/36523641/
Indexing
Keywords: cardiac MRI, T1 mapping, extracellular volume, MOLLI, STONE sequence, myocardial segmentation, U-Net, deep learning, synthetic contrast augmentation
Content: CA, MR
SNOMED: 50920009, 85898001, 399020009, 233873004, 22298006, 414545008, 16573007
Author(s)
Nitish Bhatt
Venkat Ramanan
Ady Orbach
Labonny Biswas
Matthew Ng
Fumin Guo
Xiuling Qi
Lancia Guo
Laura Jimenez-Juan
Idan Roifman
Graham A. Wright
Nilesh R. Ghugre
Organization(s)
University of Toronto
Sunnybrook Research Institute
Sunnybrook Health Sciences Centre
St Michael’s Hospital
Version
1.0
License
Text: © 2022 by the Radiological Society of North America, Inc.
Contact
ac.otnorotu.liam@ttahb.hsitin
Funding
Ontario Research Fund (Canada) (ORF-RE7–21); Natural Sciences and Engineering Research Council (NSERC) Discovery Program (RGPIN-2019–06367); N.R.G. supported by the Heart and Stroke Foundation of Canada National New Investigator award.
Ethical review
The Research Ethics Board of Sunnybrook Health Sciences Center approved the study; all patients provided written informed consent.
Date
Updated: 2022-10-19
Published: 2022-11-02
Created: 2021-11-24
References
[1] Bhatt N, Ramanan V, Orbach A, Biswas L, Ng M, Guo F, Qi X, Guo L, Jimenez-Juan L, Roifman I, Wright GA, Ghugre NR. "A Deep Learning Segmentation Pipeline for Cardiac T1 Mapping Using MRI Relaxation–based Synthetic Contrast Augmentation". Radiology: Artificial Intelligence. 2022 Nov;4(6):e210294.. 2022-11-02. doi:10.1148/ryai.210294. PMID: 36523641. PMCID: PMC9745444.
Model
Architecture
Convolutional Neural Network (U-Net) with synthetic contrast augmentation at multiple inversion times and label voting aggregation.
Clinical benefit
Automated segmentation of cardiac T1 maps and computation of segmental/global native T1, postcontrast T1, and extracellular volume to reduce manual effort and variability.
Degree of automation
Fully automated segmentation and quantification pipeline.
Indications for use
Automated analysis of cardiac MRI T1 mapping studies (native and postcontrast) for patients across various cardiac abnormalities to obtain LV/RV segmentation, RV insertion point, and segmental/global T1 and ECV values in clinical research or clinical imaging settings.
Input
Cardiac MRI T1-weighted image series (multiple inversion times) used to reconstruct T1 maps; native and postcontrast series (e.g., MOLLI) and native STONE for external testing; hematocrit for ECV when available.
Limitations
Evaluated only at 1.5T and on MOLLI and STONE sequences; findings may not generalize to other field strengths or sequences. Possible registration errors during T1 reconstruction and absence of additional registration between native and postcontrast maps for ECV; however, agreement with experts was strong. Failure cases included thin myocardial wall, artifacts/partial volume, and dilated myocardium. RV insertion point localization showed larger inter-method distances than interobserver variability.
Output
CDEs: RDE218, RDE2204, RDE215, RDE226, RDE2205, RDE223, RDE217, RDE216
Description: Segmentation masks for LV myocardium, LV blood pool, and RV blood pool; automatic RV insertion point; AHA 17-segment assignments; per-segment and global T1 (native and postcontrast) and extracellular volume values.
Reproducibility
Performance validated with fivefold cross-validation, internal test set with two expert readers, and an external multi-center/multi-vendor/sequence dataset (generalization demonstrated).
Use
Intended: Image segmentation
Out-of-scope: Other
Excluded: Decision support, Artifact reduction
User
Intended: Physician, Subspecialist diagnostic radiologist, Researcher