Children require higher infusion rates of propofol than adults to maintain
clinical anaesthesia. We aimed to produce a manual infusion regimen capable
of maintaining a steady-state blood concentration of 3 mu g ml(-1) in chil
dren aged 3-11 years. Pharmacokinetic parameter estimates were taken from p
ublished studies of infusion data in children and used in a pharmacokinetic
simulation programme to predict likely propofol blood concentrations durin
g infusions. A variability of 5% was allowed about the target concentration
of 3 mu g ml(-1). A loading dose of 2.5 mg.kg(-1) followed by an infusion
rate of 15 mg.kg(-1).h(-1) for the first 15 min, 13 mg.kg(-1).h(-1) from 15
to 30 min, 11 mg.kg(-1).h(-1) from 30 to 60 min, 10 mg.kg(-1).h(-1) from 1
to 2 h and 9 mg.kg(-1).h(-1) from 2 to 4 h resulted in a pseudo-steady sta
te target concentration of 3 mu g.ml(-1) in children 3-11 years. We were un
able to predict similar rates by applying size models to adult data. The co
ntext sensitive half-time in children was longer than in adults, rising fro
m 10.4 min at 1 h to 19.6 min at 4 h compared to adult estimates of 6.7 min
and 9.5 min, respectively. Children require higher infusion rates than adu
lts to maintain steady state concentrations of 3 mu g.ml(-1) and have longe
r context sensitive half-times than adults. These differences tan be attrib
uted to altered pharmacokinetics in this age group.