TY - JOUR
T1 - In vivo measurements of ultrasonic backscattering in blood
AU - Wang, Shyh Hau
AU - Shung, K. Kirk
N1 - Funding Information:
Manuscript received August 9, 1999; accepted August 16, 2000. This work was supported by NIH grant #HL28452. S.-H. Wang is with the Department of Biomedical Engineering, Chung Yuan Christian University, Chung Li, 32023, Taiwan (e-mail: [email protected]). K. K. Shung is with the Department of Bioengineering, The Pennsylvania State University, University Park, PA 16802.
PY - 2001/3
Y1 - 2001/3
N2 - Ultrasonic backscattering in blood including its dependence on the hematocrit, plasma proteins, shear rate, and flow disturbance, has been studied extensively theoretically and experimentally in vitro. However, much of the result has never been validated in vivo. To do so, backscattering measurements were made on pigs using a 10-MHz non-focused intravascular transducer in direct contact with blood. The probe was placed in either the abdominal aorta or the inferior vena cava. The backscattering coefficient (BSC) of blood flowing in these vessels as well as downstream from a stenosis was measured using an approach that was originally developed for measurements with focused transducers. With this approach, 6% porcine red cell saline suspensions prepared immediately after each in vivo measurement were used as the reference medium. Result from seven pigs at hematocrits ranging from 29 to 36% (31.9 ± 2.5%) demonstrated that BSC of blood in the vena cava, (4.62 ± 2.06) × 10 -5 cm-sr -1, is consistently higher than that in the aorta, (2.65±1.22) × 10 -5 cm-sr -1. The difference has been attributed to the lower shear rate and the formation of red cell aggregation in venous blood. These in vivo results are in agreement with those obtained in vitro. In response to stenoses created by ligating the aorta, backscattering of the blood measured downstream from the stenosis showed that the closer the site of measurement relative to the stenosis, the higher the backscatter, presumably resulting from the higher degree of flow disturbance. In vitro backscattering results on porcine whole blood were also acquired at 20 MHz with a Diasonics intravascular scanner.
AB - Ultrasonic backscattering in blood including its dependence on the hematocrit, plasma proteins, shear rate, and flow disturbance, has been studied extensively theoretically and experimentally in vitro. However, much of the result has never been validated in vivo. To do so, backscattering measurements were made on pigs using a 10-MHz non-focused intravascular transducer in direct contact with blood. The probe was placed in either the abdominal aorta or the inferior vena cava. The backscattering coefficient (BSC) of blood flowing in these vessels as well as downstream from a stenosis was measured using an approach that was originally developed for measurements with focused transducers. With this approach, 6% porcine red cell saline suspensions prepared immediately after each in vivo measurement were used as the reference medium. Result from seven pigs at hematocrits ranging from 29 to 36% (31.9 ± 2.5%) demonstrated that BSC of blood in the vena cava, (4.62 ± 2.06) × 10 -5 cm-sr -1, is consistently higher than that in the aorta, (2.65±1.22) × 10 -5 cm-sr -1. The difference has been attributed to the lower shear rate and the formation of red cell aggregation in venous blood. These in vivo results are in agreement with those obtained in vitro. In response to stenoses created by ligating the aorta, backscattering of the blood measured downstream from the stenosis showed that the closer the site of measurement relative to the stenosis, the higher the backscatter, presumably resulting from the higher degree of flow disturbance. In vitro backscattering results on porcine whole blood were also acquired at 20 MHz with a Diasonics intravascular scanner.
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U2 - 10.1109/58.911725
DO - 10.1109/58.911725
M3 - Article
C2 - 11370356
AN - SCOPUS:0035263379
SN - 0885-3010
VL - 48
SP - 425
EP - 431
JO - IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
JF - IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
IS - 2
ER -