Basic Study for Size Estimation of Red Blood Cell Aggregates by Analyzing Ultrasonic Backscattering Properties Considering Ultrasonic Propagation Attenuation
“…We have studied a noninvasive and quantitative method for measuring the RBC aggregate size using a high-frequency focused ultrasound transducer. [26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface.…”
Section: Introductionmentioning
confidence: 99%
“…[26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface. The reflection characteristics at the posterior wall might have a frequency dependence, which caused errors in the size estimation results, because a high-frequency ultrasound around 30 MHz was used.…”
We have studied a noninvasive and quantitative method for measuring the aggregate size of red blood cells (RBCs). In our previous study, the scattering power spectrum obtained from the vascular lumen was fitted to the reference scattering spectra calculated from the scattering spectrum of a single-sphere scatterer. In this paper, we propose a method for calculating the reference scattering spectra by summing the scattering spectra for numerous scatterers in the ultrasound focal region. By applying this method to the size estimation of microparticles simulating RBC aggregates, the estimated sizes are found to be close to the true values. In in vivo measurements, the estimated sizes at rest are equivalent to the size of a single sphere with the same volume as an RBC, and those during avascularization are larger than those at rest, which is reasonable. The proposed method has the potential to accurately estimate the size of RBC aggregates.
“…We have studied a noninvasive and quantitative method for measuring the RBC aggregate size using a high-frequency focused ultrasound transducer. [26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface.…”
Section: Introductionmentioning
confidence: 99%
“…[26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface. The reflection characteristics at the posterior wall might have a frequency dependence, which caused errors in the size estimation results, because a high-frequency ultrasound around 30 MHz was used.…”
We have studied a noninvasive and quantitative method for measuring the aggregate size of red blood cells (RBCs). In our previous study, the scattering power spectrum obtained from the vascular lumen was fitted to the reference scattering spectra calculated from the scattering spectrum of a single-sphere scatterer. In this paper, we propose a method for calculating the reference scattering spectra by summing the scattering spectra for numerous scatterers in the ultrasound focal region. By applying this method to the size estimation of microparticles simulating RBC aggregates, the estimated sizes are found to be close to the true values. In in vivo measurements, the estimated sizes at rest are equivalent to the size of a single sphere with the same volume as an RBC, and those during avascularization are larger than those at rest, which is reasonable. The proposed method has the potential to accurately estimate the size of RBC aggregates.
“…We have studied a noninvasive and quantitative method for measuring blood properties. [28][29][30][31][32][33][34][35][36][37] Saito et al assumed that RBCs aggregate as a single-sphere scatterer and estimated the size from the scattering characteristics extracted by normalizing the power spectrum measured from the vessel lumen with that from the rear wall using a focused ultrasound transducer. [28][29][30][31][32] We also examined the relationship between RBC aggregation using ultrasound and blood glucose level.…”
Section: Introductionmentioning
confidence: 99%
“…[28][29][30][31][32][33][34][35][36][37] Saito et al assumed that RBCs aggregate as a single-sphere scatterer and estimated the size from the scattering characteristics extracted by normalizing the power spectrum measured from the vessel lumen with that from the rear wall using a focused ultrasound transducer. [28][29][30][31][32] We also examined the relationship between RBC aggregation using ultrasound and blood glucose level. Sakaki et al compared the blood glucose levels with the parameters determined from changes in the scattering power spectra of the echoes from the vascular lumen before and after avascularization.…”
Noninvasive measurement of the degree of red blood cell (RBC) aggregation is useful for evaluating blood properties. In the present paper, we proposed a method to estimate the size of RBC aggregates without using the power spectrum of the posterior wall by introducing a reference scattering spectrum. The reference power spectra were calculated using the power spectrum measured for an ultrafine wire with a hemispherical tip. They were applied to the size estimation of microparticles simulating RBC aggregates. The estimated sizes were close to the true values, which shows that the calculated reference power spectra were suitable for accurate size estimation. The proposed method was also applied to in vivo measurements, and the estimated sizes between at rest and in RBCs aggregated by avascularization were successfully differentiated. This demonstrates that the proposed method will be useful for estimating the size of RBC aggregates.
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