There has been rapid progress in research on artificial oxygen-carryin
g red blood cell substitutes composed of perfluorochemical emulsions (
PFE). PFE are capable of delivering significant amounts of oxygen to t
issues, but FDA approval is given for routine human use they must firs
t overcome concerns regarding adverse effects and then clearly demonst
rate efficacy in human trials. Infusion of the first commercial produc
t used in humans, Fluosol-DA(TM), which contained a relatively low con
centration of perfluorochemical, was associated with immediate adverse
effects in some individuals and failed to demonstrate efficacy in a p
rospective clinical trial. A second generation PFE artificial oxygen c
arrier, Oxygent-HTTM, should be more effective since it carries five-f
old more oxygen than Fluosol, does not require mixing, and is more sta
ble. Initial clinical trials of this and other second generation PFE w
ere accompanied by mild, transient flu-like side effects. PFE are also
being investigated for regional organ perfusion, tumor oxygenation pr
ior to radiotherapy, contrast imaging, and for liquid ventilation of i
nfants with respiratory distress syndrome. The development of a safe,
effective, artificial oxygen carrier at reasonable cost will have a ma
jor effect on transition practice. Since PFE have a brief intravascula
r survival they are unlikely to supplant the use of red blood cells in
treatment of anemia.