Parallel beamforming is frequently used to increase the acquisition rate of medical ultrasound imaging. However, such imaging systems will not be spatially shift invariant due to significant variation across adjacent beams. This paper investigates a few methods of parallel beamforming that aims at eliminating this flaw and restoring the shift invariance property. The beam-to-beam variations occur because the transmit and receive beams are not aligned. The underlying idea of the main method presented here is to generate additional synthetic transmit beams (STB) through interpolation of the received, unfocused signal at each array element prior to beamforming. Now each of the parallel receive beams can be aligned perfectly with a transmit beam-synthetic or real-thus eliminating the distortion caused by misalignment. The proposed method was compared to the other compensation methods through a simulation study based on the ultrasound simulation software Field II. The results have been verified with in vitro experiments. The simulations were done with parameters similar to a standard cardiac examination with two parallel receive beams and a transmit-line spacing corresponding to the Rayleigh criterion, wavelength times f-number ( f#).From the results presented, it is clear that straightforward parallel beamforming reduces the spatial shift invariance property of an ultrasound imaging system. The proposed method of using synthetic transmit beams seems to restore this important property, enabling higher acquisition rates without loss of image quality. Manuscript
We have examined the effect of incorporating tissue anisotropy in simulated ultrasound images of the heart. In simulation studies, the cardiac muscle (myocardium) is usually modeled as a cloud of uncorrelated point scatterers. Although this approach successfully generates a realistic speckle pattern, it fails to reproduce any effects of image anisotropy seen in real ultrasound images. We hypothesize that some of this effect is caused by the varying orientation of anisotropic myocardial structures relative to the ultrasonic beam and that this can be taken into account in simulations by imposing an angle dependent correlation of the scatterer points. Ultrasound images of a porcine heart were obtained in vitro, and the dominating fiber directions were estimated from the insonification angles that gave rise to the highest backscatter intensities. A cylindrical sample of the myocardium was then modeled as a grid of point scatterers correlated in the principal directions of the muscle fibers, as determined experimentally. Ultrasound images of the model were simulated by using a fast k-space based convolution approach, and the results were compared with the in vitro recordings. The simulated images successfully reproduced the insonification dependent through-wall distribution of backscatter intensities in the myocardial sample, as well as a realistic speckle pattern.
Most available ultrasound imaging simulation methods are based on the spatial impulse response approach. The execution speed of such a simulation is of the order of days for one heart-sized frame using desktop computers. For some applications, the accuracy of such rigorous simulation approaches is not necessary. This work outlines a much faster 3-D ultrasound imaging simulation approach that can be applied to tasks like simulating 3-D ultrasound images for speckletracking. The increased speed of the proposed simulation method is based primarily on the approximation that the point spread function is set to be spatially invariant, which is a reasonably good approximation when using polar coordinates for simulating images from phased arrays with constant aperture. Ultrasound images are found as the convolution of the PSF and an object of sparsely distributed scatterers. The scatterers are passed through an anti-aliasing filter before insertion into a regular beam-space grid to reduce the bandwidth and significantly reduce the amount of data. A comparison with the well-established simulation software package Field II has been made. A simulation of a cyst image using the same input object was found to be in the order of 7000 times slower than the presented method. Following these considerations, the proposed simulation method can be a rapid and valuable tool for working with 3-D ultrasound imaging and in particular 3-D speckle-tracking.
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