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William P. Segars

Publications and source records attributed to William P. Segars.

7 recordsLinked to original sources

Modality-agnostic, patient-specific digital twins modeling temporally varying digestive motion

Objective: Clinical implementation of deformable image registration (DIR) requires voxel-based spatial accuracy metrics such as manually identified landmarks, which are challenging to implement for highly mobile gastrointestinal (GI) organs. To address this, patient-specific digital twins (DT) modeling temporally varying motion were created to assess the accuracy of DIR methods. Approach: 21 motion phases simulating digestive GI motion as 4D sequences were generated from static 3D patient scans using published analytical GI motion models through a semi-automated pipeline. Eleven datasets, including six T2w FSE MRI (T2w MRI), two T1w 4D golden-angle stack-of-stars, and three contrast-enhanced CT scans. The motion amplitudes of the DTs were assessed against real patient stomach motion amplitudes extracted from independent 4D MRI datasets. The generated DTs were then used to assess six different DIR methods using target registration error, Dice similarity coefficient, and the 95th percentile Hausdorff distance using summary metrics and voxel-level granular visualizations. Finally, for a subset of T2w MRI scans from patients treated with MR-guided radiation therapy, dose distributions were warped and accumulated to assess dose warping errors, including evaluations of DIR performance in both low- and high-dose regions for patient-specific error estimation. Main results: Our proposed pipeline synthesized DTs modeling realistic GI motion, achieving mean and maximum motion amplitudes and a mean log Jacobian determinant within 0.8 mm and 0.01, respectively, similar to published real-patient gastric motion data. It also enables the extraction of detailed quantitative DIR performance metrics and rigorous validation of dose mapping accuracy. Significance: The pipeline enables rigorously testing DIR tools for dynamic, anatomically complex regions enabling granular spatial and dosimetric accuracies.

cs.CV

TransMorph: Transformer for unsupervised medical image registration

In the last decade, convolutional neural networks (ConvNets) have been a major focus of research in medical image analysis. However, the performances of ConvNets may be limited by a lack of explicit consideration of the long-range spatial relationships in an image. Recently Vision Transformer architectures have been proposed to address the shortcomings of ConvNets and have produced state-of-the-art performances in many medical imaging applications. Transformers may be a strong candidate for image registration because their substantially larger receptive field enables a more precise comprehension of the spatial correspondence between moving and fixed images. Here, we present TransMorph, a hybrid Transformer-ConvNet model for volumetric medical image registration. This paper also presents diffeomorphic and Bayesian variants of TransMorph: the diffeomorphic variants ensure the topology-preserving deformations, and the Bayesian variant produces a well-calibrated registration uncertainty estimate. We extensively validated the proposed models using 3D medical images from three applications: inter-patient and atlas-to-patient brain MRI registration and phantom-to-CT registration. The proposed models are evaluated in comparison to a variety of existing registration methods and Transformer architectures. Qualitative and quantitative results demonstrate that the proposed Transformer-based model leads to a substantial performance improvement over the baseline methods, confirming the effectiveness of Transformers for medical image registration.

eess.IV

MRXCAT-CDTI: A Numerical Cardiac Diffusion Tensor Imaging Phantom

Magnetic Resonance cardiac diffusion tensor imaging (cDTI) and cardiac intravoxel incoherent motion imaging enables probing of in vivo myofiber architecture and myocardial perfusion surrogates. To study the impact of experimental parameters such as resolution, off-resonances and heart-rate variations, we propose a numerical open-source framework called MRXCAT-CDTI. It allows simulating diffusion and perfusion contrast for spin-echo (SE) and stimulated echo acquisition mode (STEAM) cDTI sequences. The Fourier encoder supports in-plane and/or through-slice off-resonance effects, as well as T2* effects during single-shot image encoding. Optional lesions are included to mimic ischemic and infarcted myocardial regions. MRXCAT-CDTI allows assessing realistic influences on data acquisition, and how these affect the data encoding process and subsequent data processing. As an example, heart-rate variations lead to differences in partial saturation and relaxation of magnetization that end up in errors of 9 to 30% for cDTI angle metrics if not accounted for. For SE echo-planar cDTI, in-plane off-resonance effects more adversely affect cDTI metrics compared to through-slice off-resonances. With this work we propose an open-source MRXCAT-CDTI numerical simulation framework that offers realistic image encoding effects found in cardiac diffusion and perfusion data to systematically study influences of data encoding, reconstruction, and post-processing to promote reproducible research.

physics.med-ph

Quality or Quantity: Toward a Unified Approach for Multi-organ Segmentation in Body CT

Organ segmentation of medical images is a key step in virtual imaging trials. However, organ segmentation datasets are limited in terms of quality (because labels cover only a few organs) and quantity (since case numbers are limited). In this study, we explored the tradeoffs between quality and quantity. Our goal is to create a unified approach for multi-organ segmentation of body CT, which will facilitate the creation of large numbers of accurate virtual phantoms. Initially, we compared two segmentation architectures, 3D-Unet and DenseVNet, which were trained using XCAT data that is fully labeled with 22 organs, and chose the 3D-Unet as the better performing model. We used the XCAT-trained model to generate pseudo-labels for the CT-ORG dataset that has only 7 organs segmented. We performed two experiments: First, we trained 3D-UNet model on the XCAT dataset, representing quality data, and tested it on both XCAT and CT-ORG datasets. Second, we trained 3D-UNet after including the CT-ORG dataset into the training set to have more quantity. Performance improved for segmentation in the organs where we have true labels in both datasets and degraded when relying on pseudo-labels. When organs were labeled in both datasets, Exp-2 improved Average DSC in XCAT and CT-ORG by 1. This demonstrates that quality data is the key to improving the model's performance.

eess.IV

Development of the Lymphatic System in the 4D XCAT Phantom

Purpose: The XCAT phantom allows for highly sophisticated multimodality imaging research. It includes a complete set of organs, muscle, bone, soft tissue, while also accounting for age, sex, and body mass index (BMI), which allows phantom studies to be performed at a population scale. At the same time, the XCAT phantom does not currently include the lymphatic system, critical for evaluating bulky nodal malignancies in lymphoma. We aimed to incorporate a full lymphatic system into the XCAT phantom and to generate realistic simulated images via guidance from lymphoma patient studies. Methods: A template lymphatic system was extended based on known anatomy was used to define 276 lymph nodes and corresponding vessels using non-uniform rational basis spline (NURBS) surfaces. Lymph node properties were modified using the Rhinoceros 3D viewing software. The XCAT general parameter script was used to input organ concentrations and generate binary files with uptake and attenuation information. Results: Lymph nodes can be scaled, stretched, and translated within the intuitive Rhinoceros interface, to allow for realistic simulation of different lymph node pathologies. Bulky, heterogeneous PMBCL tumours were generated in the mediastinum using expanded lymph nodes. Our results suggest that optimized thresholding provides better accuracy for determining total metabolic tumour volume (TMTV) of PMBCL tumours, while the gradient method was most accurate for total lesion glycolysis (TLG). Conclusions: An upgraded XCAT phantom with a fully simulated lymphatic system was created. Distributed to the research community, the XCAT phantom with the new lymphatic system has the potential of enabling studies to optimize image quality and quantitation, towards improved assessment of lymphoma including predictive modeling (e.g. improved TMTV and radiomics research).

physics.med-ph

Generation of annotated multimodal ground truth datasets for abdominal medical image registration

Sparsity of annotated data is a major limitation in medical image processing tasks such as registration. Registered multimodal image data are essential for the diagnosis of medical conditions and the success of interventional medical procedures. To overcome the shortage of data, we present a method that allows the generation of annotated multimodal 4D datasets. We use a CycleGAN network architecture to generate multimodal synthetic data from the 4D extended cardiac-torso (XCAT) phantom and real patient data. Organ masks are provided by the XCAT phantom, therefore the generated dataset can serve as ground truth for image segmentation and registration. Realistic simulation of respiration and heartbeat is possible within the XCAT framework. To underline the usability as a registration ground truth, a proof of principle registration is performed. Compared to real patient data, the synthetic data showed good agreement regarding the image voxel intensity distribution and the noise characteristics. The generated T1-weighted magnetic resonance imaging (MRI), computed tomography (CT), and cone beam CT (CBCT) images are inherently co-registered. Thus, the synthetic dataset allowed us to optimize registration parameters of a multimodal non-rigid registration, utilizing liver organ masks for evaluation. Our proposed framework provides not only annotated but also multimodal synthetic data which can serve as a ground truth for various tasks in medical imaging processing. We demonstrated the applicability of synthetic data for the development of multimodal medical image registration algorithms.

eess.IV

iPhantom: a framework for automated creation of individualized computational phantoms and its application to CT organ dosimetry

Objective: This study aims to develop and validate a novel framework, iPhantom, for automated creation of patient-specific phantoms or digital-twins (DT) using patient medical images. The framework is applied to assess radiation dose to radiosensitive organs in CT imaging of individual patients. Method: From patient CT images, iPhantom segments selected anchor organs (e.g. liver, bones, pancreas) using a learning-based model developed for multi-organ CT segmentation. Organs challenging to segment (e.g. intestines) are incorporated from a matched phantom template, using a diffeomorphic registration model developed for multi-organ phantom-voxels. The resulting full-patient phantoms are used to assess organ doses during routine CT exams. Result: iPhantom was validated on both the XCAT (n=50) and an independent clinical (n=10) dataset with similar accuracy. iPhantom precisely predicted all organ locations with good accuracy of Dice Similarity Coefficients (DSC) >0.6 for anchor organs and DSC of 0.3-0.9 for all other organs. iPhantom showed less than 10% dose errors for the majority of organs, which was notably superior to the state-of-the-art baseline method (20-35% dose errors). Conclusion: iPhantom enables automated and accurate creation of patient-specific phantoms and, for the first time, provides sufficient and automated patient-specific dose estimates for CT dosimetry. Significance: The new framework brings the creation and application of CHPs to the level of individual CHPs through automation, achieving a wider and precise organ localization, paving the way for clinical monitoring, and personalized optimization, and large-scale research.

physics.med-ph