Propofol is an intravenous anaesthetic which is chemically unrelated t
o other iv anaesthetics. Most anaesthetists are now becoming familiar
with propofol's pharmacokinetic and pharmacodynamic properties. It has
proved to be a reliable drug that can be used safely for induction an
d maintenance of anaesthesia for most surgical Procedures and unlike o
ther anaesthetic agents, it can especially be extended into the postop
erative setting or intensive care unit for sedation. Propofol's greate
st attributes are its pharmacokinetic properties which result in a rap
id, clear emergence and lack of cumulative effects even after prolonge
d administration. Compared with other iv anaesthetics, the induction d
ose of propofol has a relatively higher incidence Of respiratorY depre
ssion, short-lived apnoea and blood pressure reduction that may occasi
onally be marked. possible mechanisms for the hypotension may relate t
o (1) its action on peripheral vasculature (vasodilatation), (2) decre
ased myocardial contractility, (3) resetting of the baroreflex activit
y and (4) inhibition of the sympathetic nervous system outflow. In vit
ro studies indicate that propofol depresses the unmunological reaction
to bacterial challenge as well as the chemotactic activity. Clinical
studies, in cardiac surgery, have demonstrated that propofol, in assoc
iation with an opioid, is a logical anaesthetic choice. Propofol is ab
out to receive approval for continuous iv sedation. Comparative studie
s of propofol and midazolam have clearly demonstrated the superiority
of propofol in terms of rapid recovery and precise control of the leve
l of sedation.