BACKGROUND: The current requirements for the preparation of fresh-frozen pl
asma within 8 hours of whole-blood collection were designed to maintain clo
tting factor activities. These requirements, however, limit the production
of fresh-frozen plasma in a large blood center. There are few data on the e
ffect of the extension of CPD whole-blood storage to 24 hours on clotting f
actor activity.
STUDY DESIGN AND METHODS: A 500-mL unit of whole blood was collected from 1
0 volunteer donors. At 1 hour after collection, a plasma sample was separat
ed by centrifugation, and each unit was equally divided into 2 half-units,
with 1 half-unit stored at 4 degrees C (range, 1-6 degrees C) and I half-un
it stored at 22 degrees C (range, 20-24 degrees C) for 8 hours after collec
tion. Each half-unit was then placed at 4 degrees C for further storage for
16 hours. At 8 and 24 hours after collection, plasma samples were separate
d from each half-unit. All plasma samples were frozen at -18 degrees C. Fac
tors V, VII, VIII, and X; fibrinogen; antithrombin III; protein C; and prot
ein S were measured.
RESULTS: No significant changes were noted in factors V,VII, and X; fibrino
gen; antithrombin III; protein C; and protein S over the 24-hour storage pe
riod. Factor VIII in both half-units was significantly reduced, by 13 perce
nt, from the baseline sample as compared to the level in the 8-hour storage
sample (p<0.05). Factor VIII was further reduced by 15 to 20 percent after
the 24-hour storage period (p<0.05).
CONCLUSION: The coagulation factor activity for all factors measured, with
the exception of factor VIII, showed no significant change over the 24-hour
storage period. Factor VIII was significantly decreased by 13 percent in 8
-hour storage and by an additional 15 to 20 percent in 24-hour storage. For
clinical situations not requiring the replacement of factor VIII only, 24-
hour frozen plasma has properties comparable to those of fresh-frozen plasm
a.