F. Schooneman et C. Claise, THE STORAGE QUALITY OF APHERESIS PLATELETS - ANALYSIS OF RESULTS FROM7 DIFFERENT CELL SEPARATORS, Transfusion science, 17(4), 1996, pp. 559-574
Apheresis platelet concentrates (CAP) have been available for more tha
n 20 years. Now, as a result of the use of, and progress in, automatic
blood separation techniques, the quality of platelets is continually
being improved so that we currently have access to purified concentrat
es which are not contaminated by red cells and contain only very few w
hite cells. In view of the wide experience available to us, it was use
ful to monitor a number of qualitative parameters indicating platelet
activation during storage. We monitored platelet aggregation, release
of beta thromboglobulin, activation of complement and other basic para
meters in seven platelet concentrates from seven cell separators (Cobe
Spectra, MCS Haemonetics, CS3000+, Baxter, Excel Dideco, Autopheresis
C Baxter, and V50 Haemonetics). We found that in the majority of case
s aggregation was greatly reduced during storage. Release of beta thro
mboglobulin and activation of complement increased. pH remained within
acceptable limits in some cases. However, in others (MCS, Excel), a d
ecrease in pH < 6.0 was found. To conclude, although CAP, which are fr
om a single donor, reduce the risks of transfusion, they are not prote
cted from physical alteration and therefore from reduction in the clin
ical effects of transfusion. It is therefore necessary to improve the
storage conditions of these cells in the future, for example by design
ing new plastics, or adding platelet storage media. Basic biological p
arameters should also be defined, within the framework of quality assu
rance, to evaluate platelet quality. (C) 1997 Elsevier Science Ltd.