British Journal of Anaesthesia, Vol 82, Issue 6 890-899, Copyright © 1999 by The Board of Management and Trustees of the British Journal of Anaesthesia
R. N. Upton and G. L. Ludbrook
We describe a six-compartment kinetic and dynamic physiological model of
induction of anaesthesia with thiopental. The model included an accurate
account of initial drug distribution by representing the inter-
relationships between initial vascular mixing, lung kinetics and cardiac
output, and the use of the brain as the target organ for anaesthesia
(two-compartment sub-model with slight membrane limitation). It also
accounted for thiopental-induced reductions in cerebral blood flow and
cardiac output. Parameters for the model were estimated using hybrid
modelling from an extensive in vivo data set collected in sheep.
Simulations were used to compare the properties of the thiopental model
with an analogous previously published model of propofol. Differences in
the blood:brain equilibrium half-lives of thiopental (1.22 min) and
propofol (4.32 min) contributed to significant differences in the predicted
optimal rate of bolus injection of each agent for inducing anaesthesia in
sheep.
LABORATORY INVESTIGATIONS
A model of the kinetics and dynamics of induction of anaesthesia in sheep: variable estimation for thiopental and comparison with propofol
Department of Anaesthesia and Intensive Care, Royal Adelaide Hospital, University of Adelaide, North Terrace, Adelaide, SA 5005, Australia
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