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Vol. 291, Issue 3, 1308-1316, December 1999
Northwestern University Medical School, Department of
Anesthesiology, Chicago, Illinois
Recirculatory pharmacokinetic models for indocyanine green (ICG),
inulin, and antipyrine describe intravascular mixing and tissue
distribution after i.v. administration. These models characterized physiologic marker disposition in four awake, splenectomized dogs while
they were normovolemic, volume loaded (15% of estimated blood volume
added as a starch solution), and mildly and moderately hypovolemic (15 and 30% of estimated blood volume removed). ICG-determined blood
volumes increased 20% during volume loading and decreased 9 and 22%
during mild and moderate hypovolemia. Dye (ICG) dilution cardiac output
(CO) increased 31% during volume loading and decreased 27 and 38%
during mild and moderate hypovolemia. ICG-defined central and fast
peripheral intravascular circuits accommodated blood volume alterations
and the fast peripheral circuit accommodated blood flow changes.
Inulin-defined extracellular fluid volume contracted 14 and 21% during
hypovolemia. Early inulin disposition changes reflected those of ICG.
The ICG and inulin elimination clearances were unaffected by altered
blood volume. Neither antipyrine-defined total body water volume nor
antipyrine elimination clearance changed with altered blood volume. The
fraction of CO not involved in drug distribution had a significant
effect on the area under the antipyrine concentration-versus-time
relationships (AUC) in the first minutes after drug administration.
Hypovolemia increased the fraction of CO represented by nondistributive
blood flow and increased the antipyrine AUC up to 60% because
nondistributive blood flow did not change, despite decreased CO.
Volume loading resulted in a smaller (less than 20%) antipyrine AUC
decrease despite increased fast tissue distributive flow because
nondistributive flow also increased with increased CO.
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