Maintenance and restoration of intravascular volume are essential tasks of
critical care management to achieve sufficient organ function and to avoid
multiple organ failure in critically ill patients. Inadequate intravascular
volume followed by impaired renal perfusion is the predominate cause of ac
ute renal failure. Crystalloid solutions are the first choice to correct fl
uid and electrolyte deficits in these patients. However, in case of major h
ypovolemia, particularly in situations of increased capillary permeability,
colloid solutions are indicated to achieve sufficient tissue perfusion. Wh
ereas albumin should be avoided for correction of intravascular hypovolemia
, synthetic colloids can restore intravascular volume and stabilize hemodyn
amic conditions. In addition to a faster, more effective and prolonged rest
oration of intravascular volume, colloid solutions are able to improve micr
ocirculation. Of the synthetic colloids, hydroxyethyl starch (HES) solution
s with a low in vivo molecular weight, such as HES 200/0.5, offer the best
risk/benefit ratio. These solutions are safe with respect to effects on coa
gulation, platelets, reticuloendothelial system, and renal function, if use
d below their upper dosage limits. For patients with acute renal dysfunctio
n, daily monitoring of renal function is necessary if colloids are required
to stabilize hemodynamic conditions. In these patients, measurement of the
colloidal osmotic pressure and adequate amounts of crystalloid solutions w
ill reduce the risk of hyperoncotic renal failure. Of all colloids, gelatin
and HES solutions with low in vivo molecular weight are preferred in these
cases. In the very specific situation of kidney transplantation. colloid s
olutions should be administered in a restricted manner to organ donors and
kidney recipients.