Background: The current method of determining donor- and product-relevant p
arameters from donor serum and plasma do not only involve the safety-releva
nt risk of confusing the individual samples - obtained directly from the pl
asma donor or from the plasma product - but also brings up ethical and econ
omic considerations. Material and Methods: This trial is based on the deter
mination and comparison of the parameters of total protein, IgG, ALAT, albu
min, and creatinine, obtained either from the usual serum or from plasma sa
mples which have been collected from mechanically obtained plasma. Results
and Conclusions: This trial showed that both parameter groups can be determ
ined easily and without alteration of safety-relevant factors by using the
serum or plasma collected by plasmapheresis. The anticoagulant-related plas
ma dilution can be adjusted by means of the regression functions provided s
o that all parameters may be correlated with the serum values used so far.