H. Krieter et al., DOES COLLOID-INDUCED PLASMA HYPERVISCOSITY IN HEMODILUTION JEOPARDIZEPERFUSION AND OXYGENATION OF VITAL ORGANS, Acta anaesthesiologica Scandinavica, 39(2), 1995, pp. 236-244
Background and Methods. The infusion of dextran solutions is associate
d with haemodilution and, under some conditions, with a Slight increas
e in plasma viscosity. To clarify the compound effects of simultaneous
haemodilution and plasma viscosity increases on macro- and microhaemo
dynamics, we investigated the changes in arterial perfusion (radiolabe
lled microspheres, 15 mu m circle divide) and oxygenation (tissue Po-2
) Of vital organs using an animal model of plasma hyperviscosity. In n
ine splenectomized beagles plasma viscosity was increased step by step
from 1.06 (baseline) to 2.14, and 2.99 mPa's by infusion of small amo
unts (4% of total blood volume) of an ultra-high-molecular-weight dext
ran (50% w/v, mv: 500,000). Results. Despite the significant increase
in plasma viscosity, cardiac output as well as specific organ blood fl
ows in heart, brain, liver, and muscle rose steadily with each step of
viscosity, while the haematocrit declined from 0.31 to 0.24 and 0.20,
respectively. Medians of tissue Fog in liver peaked at a viscosity of
2 mPa's and returned to baseline values at 3 mPa's, whereas in non-wo
rking skeletal muscle Po-2, values were maximal at 3 mPa's. Conculsion
. These results indicate that the impact of plasma viscosity on the rh
eological properties of whole blood is completely offset by the concom
itant reduction of haematocrit, Thus, the comparatively minor changes
in plasma viscosity observed after prolonged use of clinical dextrans
and other colloids in no way compromise the perfusion and oxygenation
of vital organs.