3D late gadolinium enhanced (LGE) CMR images of left atrial (LA) scar tissue can be used to stratify patients with atrial fibrillation and to guide subsequent ablation therapy. This requires a segmentation of the LA anatomy (usually from an anatomical acquisition) and a further segmentation of the scar tissue within the LA (from a 3D LGE acquisition). We propose a deep learning based framework incorporating multiview information and attention mechanism to solve both LA anatomy and scar segmentations simultaneously from a single 3D LGE acquisition. Compared to existing methods, we show improved segmentation accuracy (mean Dice=93%/87% for LA/scar).
Atrial fibrillation (AF) is the most common arrhythmia of clinical significance and the incidence is increasing fast as the population ages [1]. It affects quality of life and is associated with an increased risk of stroke and heart failure. Visualization and quantification of left atrial (LA) and scar tissue using 3D late gadolinium enhanced (LGE) CMR can provide clinical information for patient stratification and ablation therapy guidance and can also be used to predict outcome. These require accurate segmentation of the LA anatomy (usually from an anatomical acquisition, e.g., 3D b-SSFP or MRA [2,3]) and a further delineation of scar tissue within the LA (from a 3D LGE acquisition). In this study, we propose an automated deep learning based framework to accomplish these two segmentations simultaneously from a single 3D LGE acquisition. This reduces overall study duration and avoids registration errors using two acquisitions.
With ethical approval, from 2011 to 2018, 202 CMR studies were carried out in patients presenting with long-standing persistent AF on a Siemens Magnetom Avanto 1.5T scanner. Transverse navigator-gated 3D LGE CMR [4,5] was performed using an inversion prepared segmented gradient echo sequence (TE/TR=2.2ms/5.2ms, resolution: (1.4–1.5)×(1.4–1.5)×4mm3 reconstructed into (0.7–0.75)×(0.7–0.75)×2mm3) 15 minutes after gadolinium administration (Gadovist—gadobutrol, 0.1mmol/kg body weight) [6]. A dynamic inversion time (TI) was designed to null the signal from normal myocardium [7]. Prior to contrast agent administration, coronal navigator-gated 3D b-SSFP (TE/TR=1ms/2.3ms, resolution: (1.6–1.8)×(1.6–1.8)×3.2mm3 reconstructed into (0.8–0.9)×(0.8–0.9)×1.6mm3) data were acquired. Both LGE and b-SSFP data were acquired during free-breathing using a prospective crossed-pairs navigator positioned over the dome of the right hemi-diaphragm with navigator acceptance window size of 5mm and CLAWS respiratory motion control [6,8]. Navigator artefact (from the navigator-restore pulse) in the LGE acquisition was reduced by introducing a navigator-restore delay of 100 ms [6,8]. For our proposed method, only the LGE CMR data are required, and the b-SSFP data are used for some comparison studies.
Based on image quality scored by a senior cardiac MRI physicist, 190 out of 202 cases were retrospectively entered into this study. Manual segmentations of the LA anatomy (with proximal pulmonary veins) and scar were performed by a cardiac MRI physicist with consensus from a senior radiologist and were used as the ground truth for training and evaluation.
Our deep learning framework (Figure 1) used multiview information to mimic the inspection process of reporting clinicians who step through 2D axial slices to find correlated information while also using complementary information from orthogonal views. In addition, attention mechanism was used to enforce the network to focus on the scar regions, and therefore improve the delineation. Our segmentations were compared with the manually-delineated ground truths using Dice scores. For the LA anatomy segmentation, we also compared our method with the whole heart segmentation (WHS) [9], U-Net [10,11] and V-Net [12,13] based methods. For the scar delineation, we compared with both unsupervised learning based methods [3] and also U-Net and V-Net based methods [10–13].
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