The problem of respiratory motion has proved a serious obstacle in developing techniques to acquire images or guide interventions in abdominal and thoracic organs. Motion models offer a possible solution to these problems, and as a result the field of respiratory motion modelling has become an active one over the past 15 years. A motion model can be defined as a process that takes some surrogate data as input and produces a motion estimate as output. Many techniques have been proposed in the literature, differing in the data used to form the models, the type of model employed, how this model is computed, the type of surrogate data used as input to the model in order to make motion estimates and what form this output should take. In addition, a wide range of different application areas have been proposed. In this paper we summarise the state of the art in this important field and in the process highlight the key papers that have driven its advance. The intention is that this will serve as a timely review and comparison of the different techniques proposed to date and as a basis to inform future research in this area.
Training a fully convolutional network for pixel-wise (or voxelwise) image segmentation normally requires a large number of training images with corresponding ground truth label maps. However, it is a challenge to obtain such a large training set in the medical imaging domain, where expert annotations are time-consuming and difficult to obtain. In this paper, we propose a semi-supervised learning approach, in which a segmentation network is trained from both labelled and unlabelled data. The network parameters and the segmentations for the unlabelled data are alternately updated. We evaluate the method for short-axis cardiac MR image segmentation and it has demonstrated a high performance, outperforming a baseline supervised method. The mean Dice overlap metric is 0.92 for the left ventricular cavity, 0.85 for the myocardium and 0.89 for the right ventricular cavity. It also outperforms a state-ofthe-art multi-atlas segmentation method by a large margin and the speed is substantially faster.
The problem of providing surgical navigation using image overlays on the operative scene can be split into four main tasks-calibration of the optical system; registration of preoperative images to the patient; tracking of the display system and patient and display using a suitable visualisation scheme. To achieve a convincing result in the magnified view through the operating microscope high alignment accuracy is required. We have simulated our entire system to establish the major sources of error. We have improved each of the stages involved. The microscope calibration process has been automated. We have introduced bone-implanted markers for registration and incorporated a locking acrylic dental stent (LADS) for patient tracking and/or registration. These improvements have significantly increased the alignment accuracy of our overlays. LADS repositioning on volunteers showed a mean target registration error of 0.7mm. Phantom accuracy is 0.3-0.5mm and clinical overlay errors were 0.5-1.0mm on the bone fiducials and 0.5-4mm on target structures. We have improved the graphical representation of the stereo overlays. The resulting system provides 3D surgical navigation for microscope-assisted guided interventions (MAGI).
Respiratory motion models have potential application for estimating and correcting the effects of motion in a wide range of applications, for example in PET-MR imaging. Given that motion cycles caused by breathing are only approximately repeatable, an important quality of such models is their ability to capture and estimate the intra- and inter-cycle variability of the motion. In this paper we propose and describe a technique for free-form nonrigid respiratory motion correction in the thorax. Our model is based on a principal component analysis of the motion states encountered during different breathing patterns, and is formed from motion estimates made from dynamic 3-D MRI data. We apply our model using a data-driven technique based on a 2-D MRI image navigator. Unlike most previously reported work in the literature, our approach is able to capture both intra- and inter-cycle motion variability. In addition, the 2-D image navigator can be used to estimate how applicable the current motion model is, and hence report when more imaging data is required to update the model. We also use the motion model to decide on the best positioning for the image navigator. We validate our approach using MRI data acquired from 10 volunteers and demonstrate improvements of up to 40.5% over other reported motion modelling approaches, which corresponds to 61% of the overall respiratory motion present. Finally we demonstrate one potential application of our technique: MRI-based motion correction of real-time PET data for simultaneous PET-MRI acquisition.
Magnetic resonance imaging (MRI) has been commonly used for guiding and planning image guided interventions since it provides excellent soft tissue visualization of anatomy and allows motion modeling to predict the position of target tissues during the procedure. However, MRI-based motion modeling remains challenging due to the difficulty of acquiring multiple motion-free 3-D respiratory phases with adequate contrast and spatial resolution. Here, we propose a novel retrospective respiratory gating scheme from a 3-D undersampled high-resolution MRI acquisition combined with fast and robust image registrations to model the nonrigid deformation of the liver. The acquisition takes advantage of the recently introduced golden-radial phase encoding (G-RPE) trajectory. G-RPE is self-gated, i.e., the respiratory signal can be derived from the acquired data itself, and allows retrospective reconstructions of multiple respiratory phases at any arbitrary respiratory position. Nonrigid motion modeling is applied to predict the liver deformation of an average breathing cycle. The proposed approach was validated on 10 healthy volunteers. Motion model accuracy was assessed using similarity-, surface-, and landmark-based validation methods, demonstrating precise model predictions with an overall target registration error of TRE = 1.70 ± 0.94 mm which is within the range of the acquired resolution.
Advances in medical imaging and image processing are paving the way for personalised cardiac biomechanical modelling. Models provide the capacity to relate kinematics to dynamics and—through patient-specific modelling—derived material parameters to underlying cardiac muscle pathologies. However, for clinical utility to be achieved, model-based analyses mandate robust model selection and parameterisation. In this paper, we introduce a patient-specific biomechanical model for the left ventricle aiming to balance model fidelity with parameter identifiability. Using non-invasive data and common clinical surrogates, we illustrate unique identifiability of passive and active parameters over the full cardiac cycle. Identifiability and accuracy of the estimates in the presence of controlled noise are verified with a number of in silico datasets. Unique parametrisation is then obtained for three datasets acquired in vivo. The model predictions show good agreement with the data extracted from the images providing a pipeline for personalised biomechanical analysis.
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