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Jeremy J. Dahl

Publications and source records attributed to Jeremy J. Dahl.

8 recordsLinked to original sources

MBFormer: Microbubble Transformer for 3D Time-Series Data Processing to Improve Bound Bubble Detection in Nonde-structive Ultrasound Molecular Imaging

Development of nondestructive ultrasound molecular imaging (UMI) is essential for early cancer detection through real-time screening using clinical ultrasound systems. Current techniques face challenges in accurately detecting targeted microbubbles (MBs) bound to specific biomarkers, primarily due to false-positive detections of unbound free-floating MBs. We propose a transformer model for time-series video processing to improve the differentiation of bound MBs. We propose a hierarchical transformer, termed MBFormer (microbubble transformer), featuring a positional-embedding-free encoder and a lightweight decoder. Leveraging attention within 3D spatio-temporal data to effectively capture stationary signals from bound MBs while suppressing nonstationary signals from unbound MBs. Since MBs appears as relatively small textures compared with conventional segmentation targets in medical imaging, such as organs and tumors, we optimized the model with two hierarchical layers, each with an attention block, to process ultrasound video data. The network outputs the molecular signal amplitude to visualize fine MB textures. Performance was evaluated using an in vivo breast cancer model, compared against a prior CNN-based UMI method and SegFormer3D baseline, a representative 3D transformer. MBFormer (AUC = 0.943) outperformed both CNN (AUC = 0.897) and SegFormer3D (AUC = 0.766) in detecting bound MBs. The CNN showed residual molecular signal from free MBs in the cardiac chambers, whereas SegFormer3D failed to detect fine MB textures. Overall, MBFormer demonstrated enhanced detection of bound MBs while suppressing free MBs and achieved a frame rate of 16.7 to 18.1 FPS, demonstrating its potential for real-time application. We anticipate that this transformer-based UMI model can facilitate real-time, free-hand nondestructive UMI in clinical systems.

physics.med-ph↗

A 2D autocorrelation-based frequency estimator reflecting spatial tissue distribution to improve Ultrasound H-scan tissue characterization

H-scan is a promising quantitative ultrasound technique that estimates the frequency content of backscattered signals and maps the estimated frequencies onto a red/blue color scale to reflect underlying tissue properties. Although it relies on matched filters tuned to different frequencies, the broad spectral bandwidth of ultrasound produces noisy, granular displays. Here, we introduce an adaptive frequency estimator designed to suppress the noise within homogeneous regions while preserving sharpness across tissue boundaries. The method combines 2D autocorrelation with a matched filter. In the first stage, a matched-filter-based estimation yields an a priori map of the spatial distribution of frequencies. The local heterogeneity of these estimates then defines a 2D weighting function that guides a second estimation stage. Drawing on the concept of Loupas's blood velocity estimator, we apply autocorrelation over a 2D spatial kernel to recover the axial frequency components, employing a weighted summation that accounts for the spatial frequency distribution within the kernel. We benchmarked the proposed estimator against conventional approaches, including the short-time Fourier transform, the H-scan matched filter, and standard autocorrelation, using both Field II simulations and in vivo data from human subjects with hepatic steatosis. In simulation, our adaptive estimator reduced the noisy texture in homogeneous regions while retaining clear boundary delineation, whereas the other estimators could achieve only one of these objectives. Applied to the in vivo human liver, the estimator improved H-scan image quality by lowering noise and enhancing the discrimination of steatotic liver from adjacent gallbladder and skin layers.

physics.med-ph↗

Lens-Aware Differentiable Beamforming for In Vivo Distributed Aberration Correction with Curvilinear Transducers

We previously introduced ultrasound autofocusing, an iterative model-based aberration correction technique that estimates local sound speed and incorporates it into beamforming to correct image distortion from heterogeneous media. In this work, we extend ultrasound autofocusing to curvilinear arrays and introduce advancements to the underlying model. A differentiable bent-ray tracing approach accounts for refraction through the transducer lens, while a new adaptive-grid initialization accounts for changes in speckle position with sound speed. The method is validated in silico and in calibrated sound speed phantoms. Our distributed aberration-correction method is then applied to a first large-scale in vivo evaluation comprising 313 liver acquisitions from 76 high-BMI human subjects. In images containing anechoic regions, contrast and CNR improved by $1.38 \pm 1.60$ dB (+18.0%) and $0.09 \pm 0.14$ (+10.2%), respectively. Improvements were also observed in speckle brightness (+20.3%), coherence factor (+13.1%), lag-one coherence (+2.7%), common-midpoint correlation coefficient (+0.7%), and common-midpoint phase error (-9.1%; lower is better), with all metric improvements statistically significant. Target structure and visibility also improved significantly. These results demonstrate the potential of ultrasound autofocusing for clinically applicable distributed aberration correction.

physics.med-ph↗

A Wavefield Correlation Approach to Improve Sound Speed Estimation in Ultrasound Autofocusing

In pulse-echo ultrasound, aberration often degrades image quality when beamforming does not account for wavefront distortions. To address this issue, local sound speed estimators have been developed in the past decade for distributed aberration correction. Recently, methods based on iterative optimization have improved sound speed accuracy with respect to earlier approaches. However, the accuracy of these newer methods is limited by media with reverberation clutter and by the straight-ray model of wave propagation. To address these challenges, we propose using wavefield correlation (WFC) beamforming when performing sound speed optimization. WFC, an ultrasound adaptation of reverse time migration, correlates simulated forward-propagated transmit wavefields and backwards-propagated receive wavefields in order to reconstruct images. This process more accurately models wave propagation in heterogeneous media and can decrease diffuse clutter due to its spatiotemporal matched filtering effect. We implement herein a WFC beamformer using an auto-differentiation software and estimate the sound speed map by optimizing a regularized common-midpoint phase focusing criterion using gradient descent. This approach is compared to a previous method relying on delay and sum (DAS) with straight-ray time delay calculations on a variety of simulated, phantom, and in vivo data with large sound speed variations and clutter. Results show that using WFC decreases sound speed estimation error, leading to improvements in resolution and contrast in the corrected image. In particular, these promising results have potential to improve pulse-echo imaging for challenging clinical scenarios.

physics.med-ph↗

Wave-Equation Migration Velocity Analysis for Multistatic Synthetic Aperture Ultrasound

Sound speed heterogeneities can create aberrations in B-mode ultrasound images by inducing tissue-dependent delays and diffractive effects that conventional beamforming does not incorporate. By using the Fourier split-step method to simulate pressure fields in heterogenous sound speed media, reverse-time migration (RTM) can reconstruct the B-mode image by cross-correlating transmitted and received pressure fields. As a result, RTM is differentiable with respect to sound speed. This enables the reconstruction of the sound speed profile that minimizes the aberration in the B-mode image. In seismic imaging, this form of diffraction tomography, known as wave-equation migration velocity analysis, can roughly be understood as a type of full-waveform inversion (FWI) that acts in the image domain rather than errors in the received channel data. This is the first work applying WEMVA to medical pulse-echo ultrasound imaging. Phantom experiments show dramatic improvements in image quality with measured improvements in point target resolution from 1.22$\pm$1.01 to 0.32$\pm$0.07 mm and lesion contrast from 3.05 to 4.39 dB.

physics.med-ph↗

Ultrasound Autofocusing: Common Midpoint Phase Error Optimization via Differentiable Beamforming

In ultrasound imaging, propagation of an acoustic wavefront through heterogeneous media causes phase aberrations that degrade the coherence of the reflected wavefront, leading to reduced image resolution and contrast. Adaptive imaging techniques attempt to correct this phase aberration and restore coherence, leading to improved focusing of the image. We propose an autofocusing paradigm for aberration correction in ultrasound imaging by fitting an acoustic velocity field to pressure measurements, via optimization of the common midpoint phase error (CMPE), using a straight-ray wave propagation model for beamforming in diffusely scattering media. We show that CMPE induced by heterogeneous acoustic velocity is a robust measure of phase aberration that can be used for acoustic autofocusing. CMPE is optimized iteratively using a differentiable beamforming approach to simultaneously improve the image focus while estimating the acoustic velocity field of the interrogated medium. The approach relies solely on wavefield measurements using a straight-ray integral solution of the two-way time-of-flight without explicit numerical time-stepping models of wave propagation. We demonstrate method performance through in silico simulations, in vitro phantom measurements, and in vivo mammalian models, showing practical applications in distributed aberration quantification, correction, and velocity estimation for medical ultrasound autofocusing.

physics.med-ph↗

Enhancing Ultrasound Molecular Imaging: Toward Real-Time RPCA-Based Filtering to Differentiate Bound and Free Microbubbles

Ultrasound molecular imaging (UMI) is an advanced imaging modality that shows promise in detecting cancer at early stages. It uses microbubbles as contrast agents, which are functionalized to bind to cancer biomarkers overexpressed on endothelial cells. A major challenge in UMI is isolating bound microbubble signal, which represents the molecular imaging signal, from that of free-floating microbubbles, which is considered background noise. In this work, we propose a fast GPU-based method using robust principal component analysis (RPCA) to distinguish bound microbubbles from free-floating ones. We explore the method using simulations and measure the accuracy using the Dice coefficient and RMS error as functions of the number of frames used in RPCA reconstruction. Experiments using stationary and flowing microbubbles in tissue-mimicking phantoms were used to validate the method. Additionally, the method was applied to data from ten transgenic mouse models of breast cancer development, injected with B7-H3-targeted microbubbles, and two mice injected with non-targeted microbubbles. The results showed that RPCA using 20 frames achieved a Dice score of 0.95 and a computation time of 0.2 seconds, indicating that 20 frames is potentially suitable for real-time implementation. On in vivo data, RPCA using 20 frames achieved a Dice score of 0.82 with DTE, indicating good agreement between the two, given the limitations of each method.

physics.med-ph↗

Investigating Pulse-Echo Sound Speed Estimation in Breast Ultrasound with Deep Learning

Ultrasound is an adjunct tool to mammography that can quickly and safely aid physicians with diagnosing breast abnormalities. Clinical ultrasound often assumes a constant sound speed to form B-mode images for diagnosis. However, the various types of breast tissue, such as glandular, fat, and lesions, differ in sound speed. These differences can degrade the image reconstruction process. Alternatively, sound speed can be a powerful tool for identifying disease. To this end, we propose a deep-learning approach for sound speed estimation from in-phase and quadrature ultrasound signals. First, we develop a large-scale simulated ultrasound dataset that generates quasi-realistic breast tissue by modeling breast gland, skin, and lesions with varying echogenicity and sound speed. We developed a fully convolutional neural network architecture trained on a simulated dataset to produce an estimated sound speed map from inputting three complex-value in-phase and quadrature ultrasound images formed from plane-wave transmissions at separate angles. Furthermore, thermal noise augmentation is used during model optimization to enhance generalizability to real ultrasound data. We evaluate the model on simulated, phantom, and in-vivo breast ultrasound data, demonstrating its ability to accurately estimate sound speeds consistent with previously reported values in the literature. Our simulated dataset and model will be publicly available to provide a step towards accurate and generalizable sound speed estimation for pulse-echo ultrasound imaging.

cs.CV↗