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Biomedical subjects

J C Lacefield

Publications and source records attributed to J C Lacefield.

3 recordsLinked to original sources

Volume measurement variability in three-dimensional high-frequency ultrasound images of murine liver metastases.

The identification and quantification of tumour volume measurement variability is imperative for proper study design of longitudinal non-invasive imaging of pre-clinical mouse models of cancer. Measurement variability will dictate the minimum detectable volume change, which in turn influences the scheduling of imaging sessions and the interpretation of observed changes in tumour volume. In this paper, variability is quantified for tumour volume measurements from 3D high-frequency ultrasound images of murine liver metastases. Experimental B16F1 liver metastases were analysed in different size ranges including less than 1 mm3, 1-4 mm3, 4-8 mm3 and 8-70 mm3. The intra- and inter-observer repeatability was high over a large range of tumour volumes, but the coefficients of variation (COV) varied over the volume ranges. The minimum and maximum intra-observer COV were 4% and 14% for the 1-4 mm3 and <1 mm3 tumours, respectively. For tumour volumes measured by segmenting parallel planes, the maximum inter-slice distance that maintained acceptable measurement variability increased from 100 to 600 microm as tumour volume increased. Comparison of free breathing versus ventilated animals demonstrated that respiratory motion did not significantly change the measured volume. These results enable design of more efficient imaging studies by using the measured variability to estimate the time required to observe a significant change in tumour volume.

Algorithms↗

Time-shift estimation and focusing through distributed aberration using multirow arrays.

The effects of element height on time-shift estimation and transmit focus compensation are demonstrated experimentally. Multirow ultrasonic transducer arrays were emulated by combining adjacent elements of a 3.0-MHz, 0.6-mm pitch, two-dimensional array to define larger virtual elements. Pulse-echo data were acquired through tissue-mimicking distributed aberrators, and time-shift maps estimated from those data were used for transmit focus compensation. Compensated beams formed by arrays with fine row pitches were similar, but focus restoration was significantly less effective for "1.75-D" arrays with a coarse row pitch. For example, when focus compensation was derived from strongly aberrated random scattering data [70-ns nominal rms arrival time fluctuation with 7 mm FWHM (full-width at half-maximum) correlation length], the mean -20 dB lateral beamwidths were 5.2 mm for f/2.0 arrays with 0.6- and 1.8-mm row pitches and 9.5 mm for an f/2.0 array with 5.4-mm pitch. Time-shift maps estimated from random scattering data acquired with 5.4-mm pitch arrays included large discontinuities caused by low correlation of signals received on vertically and diagonally adjacent emulated elements. The results indicate that multirow arrays designed for use with aberration correction should have element dimensions much less than 75% of the correlation length of the aberration and perhaps as small as 25 to 30% of the correlation length.

Scattering, Radiation↗

Angular scatter ultrasound imaging of wavelength scale targets.

A bistatic ultrasound imaging system is demonstrated that uses two 32-element linear phased array transducers oriented at an angle of 40 degrees to one another. The system simultaneously acquires and displays in real time one conventional backscatter image and one "angular scatter" image formed using side-scattered echoes from the same B-mode sector region. Experiments are presented that show differences in the magnitudes of backscatter and angular scatter signals acquired from three nylon monofilaments with diameters less than one wavelength and from soft tissue structures in vivo. The relative magnitudes of angular scatter signals from the monofilaments are qualitatively consistent with a theoretical analysis of acoustic scattering from elastic cylinders. Larger tissue features are more clearly defined in angular scatter images. This result is attributed to the orientation of specularly reflecting surfaces and the expected influence of scattering angle on the system's sensitivity to different scatterer spacings.

Acoustics↗