R. M. Arthur, J. W. Trobaugh, Y. Guo, W. L. Straube and E. G. Moros, "Change in Ultrasonic Backscattered Energy for Temperature Imaging: Factors Affecting Temperature Accuracy and Spatial Resolution" 32nd International Symposium on Ultrasonic Imaging and Tissue Characterization, Arlington, Virginia, 16-18 May 2007.
Abstract
Ultrasound is an
attractive modality for non-invasive temperature imaging to enhance the ability
to target tumor heating at therapeutic levels.
Previously, we measured monotonic changes in ultrasonic backscattered energy (CBE)
in vitro in 2D and in 3D for multiple porcine, bovine and turkey tissues and in
vivo in living normal murine tissue with implanted tumors (HT29 colon cancer
line) on nude-mouse preparations. Measured changes were consistent with
predictions for certain sub-wavelength scatterers and with results from
simulations for images of populations of temperature-dependent scatterers.
Application of temperature imaging to monitoring of tumor heating requires
accurate temperature estimation over small volumes, e.g., to within 0.5oC
for tissue volumes of 1cm3, requiring consistent and predictable
measurements of the temperature dependence of CBE. Using simulation studies, we
have studied the impact of various factors on the variation of measurable CBE
with temperature. In these simulations, we represented the imaging system by its
point-spread function and the tissue medium by discrete scatterers with a
variable range of temperature dependence. Images were simulated to represent
temperatures from 37 to 50oC by changing the scatterer amplitudes
according to curves predicted previously for single scatterers, and CBE was
computed for regions based on the means and standard deviation for CBE over all
pixels in the region. CBE computed from simulation showed the same monotonic
increase and decrease as in experimental results and covered ranges similar to
both prediction and experiment. We used multiple simulations to characterize
temperature-dependent CBE statistically and found that the region size, type and
distribution of scatterers in a population, and image signal-to-noise ratio (SNR)
all had a significant impact, i.e., each could change the mean and/or standard
deviation of the temperature-dependent CBE by 0.5-1dB resulting in potential
temperature estimation errors of 1-2oC. With a consistent scatterer
population and image SNR, however, a region size equivalent to a 1cm3 tissue
volume produced estimation error less than 0.5oC. We are currently
conducting 3D in vitro heating experiments with turkey tissue to apply these
simulation findings to experimental measurements and investigate temperature
accuracy and spatial resolution. 2D images are acquired with a Terason 3000 (Teratech
Corp., Burlington, MA), laptop-based, phased-array system using a 7-MHz linear
probe (model 12L5). 3D images are generated by translating the probe in the
elevation dimension using a stepper motor system and are acquired at
temperatures from 37.0 to 50.0oC in 0.5oC steps. Apparent
motion in the images is compensated using a 3D non-rigid motion-compensation
algorithm. The 3D motion field is approximated as varying linearly over the
tissue volume and is estimated by maximizing the 3D normalized cross-correlation
using standard optimization techniques available in MatlabŪ. Initial CBE
measurements are consistent with previous results. We expect that by using a
consistent region size and accounting for SNR, CBE can be calibrated in this
tissue to provide estimation of temperature to 0.5oC for a 1cm3
volume.
Support: R21-CA90531,
R01-CA107558 and the Wilkinson Trust at Washington University, St. Louis.