David Bradway

In vivo visualization of abdominal malignancies with acoustic radiation force elastography

The utility of acoustic radiation force impulse (ARFI) imaging for real-time visualization of abdominal malignancies was investigated. Nine patients presenting with suspicious masses in the liver (n = 7) or kidney (n = 2) underwent combined sonography/ARFI imaging. Images were acquired of a total of 12 tumors in the nine patients. In all cases, boundary definition in ARFI images was improved or equivalent to boundary definition in B-mode images. Displacement contrast in ARFI images was superior to echo contrast in B-mode images for each tumor. The mean contrast for suspected hepatocellular carcinomas (HCCs) in B-mode images was 2.9 dB (range: 1.5-4.2) versus 7.5 dB (range: 3.1-11.9) in ARFI images, with all HCCs appearing more compliant than regional cirrhotic liver parenchyma. The mean contrast for metastases in B-mode images was 3.1 dB (range: 1.2-5.2) versus 9.3 dB (range: 5.7-13.9) in ARFI images, with all masses appearing less compliant than regional non-cirrhotic liver parenchyma. ARFI image contrast (10.4 dB) was superior to B-mode contrast (0.9 dB) for a renal mass. To our knowledge, we present the first in vivo images of abdominal malignancies in humans acquired with the ARFI method or any other technique of imaging tissue elasticity.

In Vivo Guidance and Assessment of Liver Radio-Frequency Ablation with Acoustic Radiation Force Elastography

The initial results from clinical trials investigating the utility of acoustic radiation force impulse (ARFI) imaging for use with radio-frequency ablation (RFA) procedures in the liver are presented. To date, data have been collected from 6 RFA procedures in 5 unique patients. Large displacement contrast was observed in ARFI images of both pre-ablation malignancies (mean 7.5 dB, range 5.7-11.9 dB) and post-ablation thermal lesions (mean 6.2 dB, range 5.1-7.5 dB). In general, ARFI images provided superior boundary definition of structures relative to the use of conventional sonography alone. Although further investigations are required, initial results are encouraging and demonstrate the clinical promise of the ARFI method for use in many stages of RFA procedures.

Intracardiac acoustic radiation force impulse imaging: A novel imaging method for intraprocedural evaluation of radiofrequency ablation lesions

BACKGROUND Arrhythmia recurrence after cardiac radiofrequency ablation (RFA) for atrial fibrillation has been linked to conduction through discontinuous lesion lines. Intraprocedural visualization and corrective ablation of lesion line discontinuities could decrease postprocedure atrial fibrillation recurrence. Intracardiac acoustic radiation force impulse (ARFI) imaging is a new imaging technique that visualizes RFA lesions by mapping the relative elasticity contrast between compliant-unablated and stiff RFA-treated myocardium. OBJECTIVE To determine whether intraprocedure ARFI images can identify RFA-treated myocardium in vivo. METHODS In 8 canines, an electroanatomical mapping-guided intracardiac echo catheter was used to acquire 2-dimensional ARFI images along right atrial ablation lines before and after RFA. ARFI images were acquired during diastole with the myocardium positioned at the ARFI focus (1.5 cm) and parallel to the intracardiac echo transducer for maximal and uniform energy delivery to the tissue. Three reviewers categorized each ARFI image as depicting no lesion, noncontiguous lesion, or contiguous lesion. For comparison, 3 separate reviewers confirmed RFA lesion presence and contiguity on the basis of functional conduction block at the imaging plane location on electroanatomical activation maps. RESULTS Ten percent of ARFI images were discarded because of motion artifacts. Reviewers of the ARFI images detected RFA-treated sites with high sensitivity (95.7%) and specificity (91.5%). Reviewer identification of contiguous lesions had 75.3% specificity and 47.1% sensitivity. CONCLUSIONS Intracardiac ARFI imaging was successful in identifying endocardial RFA treatment when specific imaging conditions were maintained. Further advances in ARFI imaging technology would facilitate a wider range of imaging opportunities for clinical lesion evaluation.

Safety Assessment of Advanced Imaging Sequences I: Measurements

A method for rapid measurement of intensities (Ispta), mechanical index (MI), and probe surface temperature for any ultrasound scanning sequence is presented. It uses the scanners sampling capability to give an accurate measurement of the whole imaging sequence for all emissions to yield the true distributions. The method is several orders of magnitude faster than approaches using an oscilloscope, and it also facilitates validating the emitted pressure field and the scanners emission sequence software. It has been implemented using the experimental synthetic aperture real-time ultrasound system (SARUS) scanner and the Onda AIMS III intensity measurement system (Onda Corporation, Sunnyvale, CA, USA). Four different sequences have been measured: a fixed focus emission, a duplex sequence containing B-mode and flow emissions, a vector flow sequence with B-mode and flow emissions in 17 directions, and finally a SA duplex flow sequence. A BK8820e (BK Medical, Herlev, Denmark) convex array probe is used for the first three sequences and a BK8670 linear array probe for the SA sequence. The method is shown to give the same intensity values within 0.24% of the AIMS III Soniq 5.0 (Onda Corporation, Sunnyvale, CA, USA) commercial intensity measurement program. The approach can measure and store data for a full imaging sequence in 3.8-8.2 s per spatial position. Based on Ispta, MI, and probe surface temperature, the method gives the ability to determine whether a sequence is within U.S. FDA limits, or alternatively indicate how to scale it to be within limits.

Acoustic Radiation Force Impulse Imaging (ARFI) on an IVUS Circular Array

Our long-term goal is the detection and characterization of vulnerable plaque in the coronary arteries of the heart using intravascular ultrasound (IVUS) catheters. Vulnerable plaque, characterized by a thin fibrous cap and a soft, lipid-rich necrotic core is a precursor to heart attack and stroke. Early detection of such plaques may potentially alter the course of treatment of the patient to prevent ischemic events. We have previously described the characterization of carotid plaques using external linear arrays operating at 9 MHz. In addition, we previously modified circular array IVUS catheters by short-circuiting several neighboring elements to produce fixed beamwidths for intravascular hyperthermia applications. In this paper, we modified Volcano Visions 8.2 French, 9 MHz catheters and Volcano Platinum 3.5 French, 20 MHz catheters by short-circuiting portions of the array for acoustic radiation force impulse imaging (ARFI) applications. The catheters had an effective transmit aperture size of 2 mm and 1.5 mm, respectively. The catheters were connected to a Verasonics scanner and driven with pushing pulses of 180 V p-p to acquire ARFI data from a soft gel phantom with a Young’s modulus of 2.9 kPa. The dynamic response of the tissue-mimicking material demonstrates a typical ARFI motion of 1 to 2 microns as the gel phantom displaces away and recovers back to its normal position. The hardware modifications applied to our IVUS catheters mimic potential beamforming modifications that could be implemented on IVUS scanners. Our results demonstrate that the generation of radiation force from IVUS catheters and the development of intravascular ARFI may be feasible.

Contrast in Intracardiac Acoustic Radiation Force Impulse Images of Radiofrequency Ablation Lesions

We have previously shown that intracardiac acoustic radiation force impulse (ARFI) imaging visualizes tissue stiffness changes caused by radiofrequency ablation (RFA). The objectives of this in vivo study were to (1) quantify measured ARFI-induced displacements in RFA lesion and unablated myocardium and (2) calculate the lesion contrast (C) and contrast-to-noise ratio (CNR) in two-dimensional ARFI and conventional intracardiac echo images. In eight canine subjects, an ARFI imaging-electroanatomical mapping system was used to map right atrial ablation lesion sites and guide the acquisition of ARFI images at these sites before and after ablation. Readers of the ARFI images identified lesion sites with high sensitivity (90.2%) and specificity (94.3%) and the average measured ARFI-induced displacements were higher at unablated sites (11.23 ± 1.71 µm) than at ablated sites (6.06 ± 0.94 µm). The average lesion C (0.29 ± 0.33) and CNR (1.83 ± 1.75) were significantly higher for ARFI images than for spatially registered conventional B-mode images (C = −0.03 ± 0.28, CNR = 0.74 ± 0.68).

Intracardiac acoustic radiation force impulse (ARFI) and shear wave imaging in pigs with focal infarctions

Four pigs, three with focal infarctions in the apical intraventricular septum (IVS) and/or left ventricular free wall (LVFW), were imaged with an intracardiac echocardiography (ICE) transducer. Custom beam sequences were used to excite the myocardium with focused acoustic radiation force (ARF) impulses and image the subsequent tissue response. Tissue displacement in response to the ARF excitation was calculated with a phase-based estimator, and transverse wave magnitude and velocity were each estimated at every depth. The excitation sequence was repeated rapidly, either in the same location to generate 40 Hz M-modes at a single steering angle, or with a modulated steering angle to synthesize 2-D displacement magnitude and shear wave velocity images at 17 points in the cardiac cycle. Both types of images were acquired from various views in the right and left ventricles, in and out of infarcted regions. In all animals, acoustic radiation force impulse (ARFI) and shear wave elasticity imaging (SWEI) estimates indicated diastolic relaxation and systolic contraction in noninfarcted tissues. The M-mode sequences showed high beat-to-beat spatio-temporal repeatability of the measurements for each imaging plane. In views of noninfarcted tissue in the diseased animals, no significant elastic remodeling was indicated when compared with the control. Where available, views of infarcted tissue were compared with similar views from the control animal. In views of the LVFW, the infarcted tissue presented as stiff and non-contractile compared with the control. In a view of the IVS, no significant difference was seen between infarcted and healthy tissue, whereas in another view, a heterogeneous infarction was seen to be presenting itself as non-contractile in systole.

Feasibility of Swept Synthetic Aperture Ultrasound Imaging

Ultrasound image quality is often inherently limited by the physical dimensions of the imaging transducer. We hypothesize that, by collecting synthetic aperture data sets over a range of aperture positions while precisely tracking the position and orientation of the transducer, we can synthesize large effective apertures to produce images with improved resolution and target detectability. We analyze the two largest limiting factors for coherent signal summation: aberration and mechanical uncertainty. Using an excised canine abdominal wall as a model phase screen, we experimentally observed an effective arrival time error ranging from 18.3 ns to 58 ns (root-mean-square error) across the swept positions. Through this clutter-generating tissue, we observed a 72.9% improvement in resolution with only a 3.75 dB increase in side lobe amplitude compared to the control case. We present a simulation model to study the effect of calibration and mechanical jitter errors on the synthesized point spread function. The relative effects of these errors in each imaging dimension are explored, showing the importance of orientation relative to the point spread function. We present a prototype device for performing swept synthetic aperture imaging using a conventional 1-D array transducer and ultrasound research scanner. Point target reconstruction error for a 44.2 degree sweep shows a reconstruction precision of 82.8 and 17.8 in the lateral and axial dimensions respectively, within the acceptable performance bounds of the simulation model. Improvements in resolution, contrast and contrast-to-noise ratio are demonstrated in vivo and in a fetal phantom.

6B-6 Transthoracic Cardiac Acoustic Radiation Force Impulse Imaging: A Feasibility Study

We describe new non-invasive techniques for visualizing local variations of stiffness in cardiac tissue through the use of transthoracic acoustic radiation force impulse (ARFI) imaging. Custom M-mode and two-dimensional ARFI sequences were implemented on the Siemens SONOLINE Antares scanner, and a porcine model was used to demonstrate the feasibility of transthoracic cardiac ARFI. The hearts of two live 20 kg Sinclair pigs were imaged through intercostal and subcostal acoustic windows, using M-mode and two-dimensional B-mode imaging. An abdominal low-frequency (2.2 MHz) probe was used with an extended radiation force pulse length (320 mus) to produce tissue displacements at depths up to 7 cm. Quadratic motion filters were used to separate ARFI displacements from cardiac and respiratory physiological motion artifacts. During M-mode imaging, matched ECG signals were acquired to enable registration to the cardiac cycle. M-mode ARFI displacement images reflect the expected myocardial stiffness changes through the cardiac cycle. During two-dimensional ARFI imaging, ECG gating was used during image acquisition, and while the images show local variations in displacement, some noise and artifacts remain. These preliminary results indicate the feasibility of real-time imaging of cardiac stiffness in vivo.

Feasibility and safety of transthoracic cardiac acoustic radiation force impulse imaging methods

This work examines clinical feasibility of using noninvasive transthoracic echocardiography techniques to visualize temporal variations of stiffness through the cardiac cycle using acoustic radiation force impulse (ARFI) imaging. Custom M-mode ARFI sequences were implemented on a Verasonics Research Platform using a Philips/ATL P4-2 phased-array echocardiography transducer. The research systems robust power supply, full parallel-receive capability, and programmable interface enabled sustained excitations, rapid data acquisition, and real-time processing and display of images in the clinic. An extended radiation force pulse length of 480 μs was used to produce tissue displacements up to 12μm around a region of excitation focused at 3 cm. Quadratic motion filters were used to separate ARFI excitation-induced displacements from intrinsic cardiac and respiratory physiological motion artifacts. Acoustic intensity and face heating measurements, as well as finite element method tissue focal heating simulations, were completed. These measurements and simulations calibrated the sequences with respect to the FDA acoustic exposure limits for intensity, mechanical index (MI) and tissue heating. Tests were conducted in phantom and animal models in preparation for the clinical trial. A series of 7 healthy volunteers were scanned in accordance with an approved Duke University Medical Center Institutional Review Board (IRB) protocol. Measurements were acquired from the apical 4 chamber view of the apex, at power levels with MIs ranging from 1.9-3.0. During each M-mode ARFI acquisition, the matched ECG signal was acquired, enabling registration with cardiac cycle. The M-mode ARFI displacement images reflect the expected myocardial stiffness changes through the cardiac cycle, with greatest displacements in diastole and lowest in systole. In the 7 volunteers, the mean displacements throughout the cardiac cycle rose with increasing transmit power level. The ratio of diastolic-to-systolic displacement was examined as a possible indicator of myocardial health. In this study, the measured ratios were in range up to 3.1:1 for the 7 patients, showing agreement with previous ratios reported by an animal studies using transthoracic, intracardiac and epicardial imaging methods. These preliminary clinical results support the feasibility of real-time imaging of cardiac stiffness in vivo using transthoracic ARFI imaging.