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Published on: January 14, 2014
On the relation between aggregation, packing and the backscattered ultrasound signal for whole blood
1Institute of Biomedical Engineering, University of Toronto, Ontario, Canada.
Previous studies have shown that the backscattered ultrasound (US) power from blood depends on the manner in which red blood cells (RBCs) are packed and, in particular, on spatial variations in the red blood cell number density (i.e., the RBC concentration variance). Experimental measurements have also shown that the backscattered US power depends on the degree of RBC aggregation, and it has been hypothesized that this is primarily due to the effect of RBC aggregation on the concentration variance. An initial simulation study of the relationship between RBC aggregation and packing statistics is presented, in which the effects of hematocrit, aggregate size, shape and size distribution on concentration variance are investigated. Both two-dimensional (2-D) and 3-D samples of aggregated and disaggregated RBCs were simulated; these enabled the concentration variance to be calculated. In agreement with theoretical predictions and experimental US results, the concentration variance for disaggregated RBCs is shown to be lowest at low and high hematocrits, and to peak at intermediate hematocrits. The concentration variance is shown to be particularly sensitive to changes in aggregate size and size distribution, and less sensitive to the shape of small aggregates. The results of this study provide a foundation for relating the state of aggregation in a blood sample to the manner in which RBCs are packed and, therefore, to the backscattered US power.
Previous studies have shown that the backscattered ultrasound (US) power from blood depends on the manner in which red blood cells (RBCs) are packed and, in particular, on spatial variations in the red blood cell number density (i.e., the RBC concentration variance). Experimental measurements have also shown that the backscattered US power depends on the degree of RBC aggregation, and it has been hypothesized that this is primarily due to the effect of RBC aggregation on the concentration variance. An initial simulation study of the relationship between RBC aggregation and packing statistics is presented, in which the effects of hematocrit, aggregate size, shape and size distribution on concentration variance are investigated. Both two-dimensional (2-D) and 3-D samples of aggregated and disaggregated RBCs were simulated; these enabled the concentration variance to be calculated. In agreement with theoretical predictions and experimental US results, the concentration variance for disaggregated RBCs is shown to be lowest at low and high hematocrits, and to peak at intermediate hematocrits. The concentration variance is shown to be particularly sensitive to changes in aggregate size and size distribution, and less sensitive to the shape of small aggregates. The results of this study provide a foundation for relating the state of aggregation in a blood sample to the manner in which RBCs are packed and, therefore, to the backscattered US power.
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