DocumentCode
2748599
Title
Sickle cell blood flow in the microcirculation
Author
Berger, S.A. ; Carlson, B.E.
Author_Institution
Dept. of Bioengineering, California Univ., Berkeley, CA, USA
Volume
2
fYear
2004
fDate
1-5 Sept. 2004
Firstpage
5057
Lastpage
5060
Abstract
The clinical symptomology, as well as the subclinical sequela, of sickle-cell (S-C) disease, or anemia, is thought to be largely the consequence of abnormal events in the capillaries, resulting primarily from theological changes SC erythrocytes undergo when deoxygenated. A model of the flow of such RBCs in a single capillary was formulated taking into account the principal characteristics of the disease. This has been extended to a microcirculatory bed, generated in a pseudo-random manner. S-C disease is characterized by episodic painful and debilitating clinical events, called S-C "crisis". These studies, undertaken to evaluate possible causative mechanisms, suggest that the pressure available to drive the S-C RBCs through the microcirculation might be the control parameter.
Keywords
blood; capillarity; cellular biophysics; diseases; haemorheology; anemia; capillaries; clinical symptomology; episodic debilitating clinical events; episodic painful clinical events; erythrocytes; microcirculation; sickle cell blood flow; subclinical sequela; Blood flow; Cells (biology); Diseases; Lungs; Polymers; Pressure control; Production; Red blood cells; Rheology; Viscosity; Sickle-cell disease; microcirculatory flow;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology Society, 2004. IEMBS '04. 26th Annual International Conference of the IEEE
Conference_Location
San Francisco, CA
Print_ISBN
0-7803-8439-3
Type
conf
DOI
10.1109/IEMBS.2004.1404398
Filename
1404398
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