Abstract:The performance of deep learning (DL) methods for the analysis of cine cardiovascular magnetic resonance (CMR) is typically assessed in terms of accuracy, overlooking precision. In this work, uncertainty estimation techniques, namely deep ensemble, test-time augmentation, and Monte Carlo dropout, are applied to a state-of-the-art DL pipeline for cardiac functional biomarker estimation, and new distribution-based metrics are proposed for the assessment of biomarker precision. The model achieved high accuracy (average Dice 87%) and point estimate precision on two external validation scan-rescan CMR datasets. However, distribution-based metrics showed that the overlap between scan/rescan confidence intervals was >50% in less than 45% of the cases. Statistical similarity tests between scan and rescan biomarkers also resulted in significant differences for over 65% of the cases. We conclude that, while point estimate metrics might suggest good performance, distributional analyses reveal lower precision, highlighting the need to use more representative metrics to assess scan-rescan agreement.
Abstract:Automatic quantification of intramyocardial motion and strain from tagging MRI remains an important but challenging task. We propose a method using implicit neural representations (INRs), conditioned on learned latent codes, to predict continuous left ventricular (LV) displacement -- without requiring inference-time optimisation. Evaluated on 452 UK Biobank test cases, our method achieved the best tracking accuracy (2.14 mm RMSE) and the lowest combined error in global circumferential (2.86%) and radial (6.42%) strain compared to three deep learning baselines. In addition, our method is $\sim$380$\times$ faster than the most accurate baseline. These results highlight the suitability of INR-based models for accurate and scalable analysis of myocardial strain in large CMR datasets.