A. Degasperi et al., PHARMACOKINETIC PROFILE OF THE INDUCTION DOSE OF PROPOFOL IN PATIENTSWITH SEVERE BURNS, Clinical drug investigation, 14(4), 1997, pp. 314-320
The pharmacokinetics of propofol were studied in nine severely burnt p
atients undergoing general anaesthesia with enflurane/fentanyl for esc
arectomy. All patients received an intravenous bolus dose of propofol
2 mg/kg, and blood concentrations of propofol were measured over the s
ubsequent 12 hours using high performance liquid chromatography with f
luorescent detection. Propofol blood concentrations, showing a very ra
pid initial decline and a long terminal elimination phase, were best f
itted by a triexponential function describing a 3-compartment open mam
illary model with rapid distribution from the central compartment, ext
ensive redistribution and elimination from the central compartment. Wh
en compared with nonburnt normal controls, the patients with burns sho
wed lower propofol blood concentrations, lower baseline albumin blood
levels (p less than or equal to 0.001), smaller areas under the concen
tration-time curve (p less than or equal to 0.001), larger volumes of
distribution (p less than or equal to 0.001), and higher total body cl
earance (p less than or equal to 0.001). Pathophysiological systemic r
esponses to the burn injury and particularly the presence of oedema an
d changes in albumin concentrations were probably responsible for the
significant alterations in the disposition kinetics of propofol in the
patients with burns.