46 research outputs found

    Method and Apparatus for Controlling Acoustic Signal Bandwidth in an Ultrasonic Diagnostic Imaging System

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    An ultrasonic imaging system includes a receive beam former that generates analog receive signals and a scan converter. A receive signal processing path interconnects the receive beamformer and the scan converter, and this processing path includes both an A/D converter characterized by a selectable sampling rate and at least one filter characterized by at least one filter parameter. The filter parameter is selected as a function of the sampling rate to provide enhanced image quality

    Enabling Real-Time Ultrasound Imaging of Soft Tissue Mechanical Properties by Simplification of the Shear Wave Motion Equation

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    Ultrasound based shear wave elastography (SWE) is a technique used for non-invasive characterization and imaging of soft tissue mechanical properties. Robust estimation of shear wave propagation speed is essential for imaging of soft tissue mechanical properties. In this study we propose to estimate shear wave speed by inversion of the firstorder wave equation following directional filtering. This approach relies on estimation of first-order derivatives which allows for accurate estimations using smaller smoothing filters than when estimating second-order derivatives. The performance was compared to three current methods used to estimate shear wave propagation speed: direct inversion of the wave equation (DIWE), time-to-peak (TTP) and crosscorrelation (CC). The shear wave speed of three homogeneous phantoms of different elastic moduli (gelatin by weight of 5%, 7%, and 9%) were measured with each method. The proposed method was shown to produce shear speed estimates comparable to the conventional methods (standard deviation of measurements being 0.13 m/s, 0.05 m/s, and 0.12 m/s), but with simpler processing and usually less time (by a factor of 1, 13, and 20 for DIWE, CC, and TTP respectively). The proposed method was able to produce a 2-D speed estimate from a single direction of wave propagation in about four seconds using an off-the-shelf PC, showing the feasibility of performing real-time or near real-time elasticity imaging with dedicated hardware

    Ultrasound Based Quantitative Motion Measurement using Speckle Size Estimation

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    An ultrasound system determines the relative movement in a first direction (F1) of first matter, such as blood flow, and second matter, such as an artery wall, in a subject under study (S). A beam (B1) of ultrasound waves defining a plurality of beam positions (BP1 and BP2) and beam axes (A1 and A2) are moved in scan direction having components parallel to direction F1. First and second blocks of data representing the first and second matter, respectively, are generated. A processor (20) performs an estimation of speckle size on first data to obtain a first result, and performs analysis of the second block of data to obtain a second result. The two results are analyzed to obtain a measure of the relative movement of the first and second matter

    Supraspinatus tendon micromorphology in individuals with subacromial pain syndrome

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    Study Design: Cross-sectional cohort. Introduction: Tendon collagen organization can be estimated by peak spatial frequency radius (PSFR) on ultrasound images. Characterizing PSFR can define the contribution of collagen disruption to shoulder symptoms. Purpose of the Study: The purpose of this was to characterize the (1) supraspinatus tendon PSFR in participants with sub acromial pain syndrome (SPS) and healthy controls; (2) PSFR between participants grouped on a tendon visual quality score; and (3) relationship between PSFR with patient-reported pain, function, and shoulder strength. Methods: Participants with SPS (n ¼ 20) and age, sex, and arm-dominance matched healthy controls (n ¼ 20) completed strength testing in scaption and external rotation, and patient-reported pain, and functional outcomes. Supraspinatus tendon ultrasound images were acquired, and PSFR was calculated for a region of interest 15 mm medial to the supraspinatus footprint. PSFR was compared between groups using an independent t-test and an analysis of variance to compare between 3 groups for visually qualitatively rated tendon abnormalities. Relationships between PSFR with pain, function, and strength were assessed using Pearson correlation coefficient. Results: Supraspinatus tendon PSFR was not different between groups (P ¼ .190) or tendon qualitative ratings (P ¼ .556). No relationship was found between PSFR and pain, functional loss, and strength (P \u3e .05). Conclusions: Collagen disruption (PSFR) measured via ultrasound images of the supraspinatus tendon was not different between participants with SPS or in those with visually rated tendon defects. PSFR is not related to shoulder pain, function, and strength, suggesting that supraspinatus tendon collagen disorganization may not be a contributing factor to shoulder SPS. However, collagen disruption may not be isolated to a single region of interest. Level of Evidence: 3b: case-control study

    Flowcell Systems for Single Molecule Detection

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    The present invention provides compounds, methods and systems for sequencing nucleic acid using single molecule detection. Using labeled NPs that exhibit charge-switching behavior, single-molecule DNA sequencing in a microchannel sorting system is realized. In operation, sequencing products are detected enabling real-time sequencing as successive detectable moieties flow through a detection channel. By electrically sorting charged molecules, the cleaved product molecules are detected in isolation without interference from unincorporated NPs and without illuminating the polymerase-DNA complex

    Flowcell Systems for Single Molecule Detection

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    The present invention provides compounds, methods and systems for sequencing nucleic acid using single molecule detection. Using labeled NPs that exhibit charge-switching behavior, single-molecule DNA sequencing in a microchannel sorting system is realized. In operation, sequencing products are detected enabling real-time sequencing as successive detectable moieties flow through a detection channel. By electrically sorting charged molecules, the cleaved product molecules are detected in isolation without interference from unincorporated NPs and without illuminating the polymerase-DNA complex

    Two-Dimensional Blood Flow Velocity Estimation Using Apparent Speckle Pattern Angle Dependence on Scan Velocity

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    An algorithm which measures the lateral component of blood flow velocity was developed in our previous studies based on the increase in speckle size due to relative motion between moving scatterers and spatial rate of scanner A-line acquisition (scan velocity). In this paper, the apparent dominant angle of the speckle pattern in a straight vessel was investigated and a new method of two-dimensional blood flow velocity estimation is introduced. Different scan velocities were used for data acquisition from blood flow traveling at an angle relative to the ultrasound beam. The apparent angle of the speckle pattern changes with different scan velocities due to mis-registration between the ultrasound beam and scatterers. The apparent angle of the speckle pattern was resolved by line-to-line cross-correlation in the fast time (axial) direction on a region-of-interest (ROI) in each blood flow image and used to spatially align the ROI. The resulting lateral speckle size within the aligned ROI was calculated. The lateral component of the blood flow is shown to be closest to the scan velocity which gives the maximum speckle size and the apparent angle of speckle pattern collected by this scan velocity is the best estimate for the actual angle of blood flow. These two components produce two dimensional blood flow velocity estimations. Blood flow data were collected from a blood flow phantom with a 50 degrees beam-to-flow angle. Nine scan velocities were used to collect data for three different actual velocities. Estimation results for the 2-D velocity magnitude (mean ± std) were 40.2 ± 10.1, 61.8 ± 9.3, and 96.8 ± 12.3 cm/s for actual velocities of 41, 65, and 98 cm/s respectively. Estimation results for the angle (actual 50 degrees for all tests) were 52.7 ± 7.8, 51.6 ± 6.2, and 53.8 ± 5.2 degrees. These results indicate a promising new way to estimate 2-D blood flow velocity

    Further Progress on Lateral Flow Estimation Using Speckle Size Variation with Scan Direction

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    Conventional blood flow velocity measurement using ultrasound is capable of resolving the axial component (i.e., that aligned with the ultrasound propagation direction) of the blood flow velocity vector. However, these Doppler-based methods are incapable of detecting blood flow in the direction normal to the ultrasound beam. In addition, these methods require repeated pulse-echo interrogation at the same spatial location. In this paper, we report additional data on a new method recently introduced. This method estimates the lateral component of blood flow within a single image frame using the observation that the speckle pattern corresponding to the blood reflectors (typically red blood cells) stretches (i.e., is “smeared”) if the blood is moving in the same direction as the electronically-controlled transducer line selection in a 2D image. The situation is analogous to the observed elongation of a subject photographed with a moving camera. Experiments were performed with a blood flow phantom and high-frequency transducer of a commercially available ultrasound machine. Data was captured through an interface allowing access to the raw beamformed data. Blood flow with velocities ranging from 50 to 110 cm/s were investigated in this paper. Previously, we showed results indicating a linear relationship between the reciprocal of the speckle stretch factor and blood flow velocity when the scan velocity is greater than the blood flow velocity [1]. When the scan velocity is 64.8 cm/s, compared with the theoretical model, fitting results based on experimental data gave us a linear relationship with average flow estimation error of 1.74±1.48 cm/s. When the scan velocity is 37.4 cm/s, the average estimation error is 0.65±0.45 cm/s. The new experiments reported here include blood flow velocities that are close to and greater than the scan velocity. Results show that the linear relationship degrades under these conditions, which we hypothesize is due to speckle decorrelation and flow gradients

    Lateral Blood Flow Velocity Estimation Based on Ultrasound Speckle Size Change With Scan Velocity

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    Conventional (Doppler-based) blood flow velocity measurement methods using ultrasound are capable of resolving the axial component (i.e., that aligned with the ultrasound propagation direction) of the blood flow velocity vector. However, these methods are incapable of detecting blood flow in the direction normal to the ultrasound beam. In addition, these methods require repeated pulse-echo interrogation at the same spatial location. A new method has been introduced which estimates the lateral component of blood flow within a single image frame using the observation that the speckle pattern corresponding to blood reflectors (typically red blood cells) stretches (i.e., is smeared) if the blood is moving in the same direction as the electronically-controlled transducer line selection in a 2-D image. The situation is analogous to the observed distortion of a subject photographed with a moving camera. The results of previous research showed a linear relationship between the stretch factor (increase in lateral speckle size) and blood flow velocity. However, errors exist in the estimation when used to measure blood flow velocity. In this paper, the relationship between speckle size and blood flow velocity is investigated further with both simulated flow data and measurements from a blood flow phantom. It can be seen that: 1) when the blood flow velocity is much greater than the scan velocity (spatial rate of A-line acquisition), the velocity will be significantly underestimated because of speckle decorrelation caused by quick blood movement out of the ultrasound beam; 2) modeled flow gradients increase the average estimation error from a range between 1.4% and 4.4%, to a range between 4.4% and 6.8%; and 3) estimation performance in a blood flow phantom with both flow gradients and random motion of scatterers increases the average estimation error to between 6.1% and 7.8%. Initial attempts at a multiple-scan strategy for estimating flow by a least-squares model suggest the possibility of increased accuracy using multiple scan velocities

    Two-Dimensional Blood Flow Velocity Estimation Using Ultrasound Speckle Pattern Dependence on Scan Direction and A-Line Acquisition Velocity

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    We have previously investigated the change of apparent lateral speckle size caused by the direction and spatial rate of scanner A-line acquisition (scan velocity). An algorithm which measures the lateral component of blood flow velocity was developed based on the increase in speckle size resulting from relative motion between moving scatterers and the scan velocity. In this paper, the change of the apparent dominant angle of the speckle pattern in a straight vessel was investigated and a new method of two-dimensional blood flow velocity estimation is introduced. Different scan velocities were used for data acquisition from blood flow traveling at an angle relative to the ultrasound beam. The apparent angle of the speckle pattern changes with different scan velocities because of misregistration between the ultrasound beam and scatterers. The apparent angle of the speckle pattern was resolved by line-to-line cross-correlation in the fast-time (axial) direction on a region-of-interest (ROI) in each blood flow image and used to spatially align the ROI. The resulting lateral speckle size within the aligned ROI was calculated. The lateral component of the blood flow is shown to be closest to the scan velocity which gives the maximum speckle size and the apparent angle of speckle pattern collected by this scan velocity is the best estimate for the actual angle of blood flow. These two components produce two-dimensional blood flow velocity estimations. This method was studied through both computer simulation and experiments with a blood flow phantom. Nine scan velocities were used to collect blood flow data with velocities ranging from 33 to 98 cm/s and four beam-to-flow angles. In simulated plug blood flow, the mean bias of angle estimation is below 2% with an average standard deviation of 3.6%. In simulated parabolic blood flow, the angle of blood flow is overestimated because of speckle decorrelation caused by flow gradients and the estimation bias increases with decreasing beam-to-flow angle, which has an average value of 8.8% and standard deviation of 10%. Because of the complexity of flow profiles in the blood flow phantom, the angle of blood flow is also overestimated and the mean bias is increased by a factor of two compared with simulated parabolic flow. For the velocity estimation results, the mean bias is below 5% with an average standard deviation of 4.6% in the simulated plug blood flow. In the simulated parabolic flow and blood flow phantom, the velocity is underestimated because of speckle decorrelation. The mean bias of velocity estimation in the simulated parabolic flow is −6% with an average standard deviation of 11.2%. In the blood flow phantom, the mean bias of the velocity estimation is −5% with a higher average standard deviation of 21.5%. This method can resolve the angle and amplitude of two-dimensional blood flow simultaneously. The accuracy of the estimation can be further improved by using more scanning velocities
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