• 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