Abstract:Comparisons were made of the apheresis instruments Haemonetics Blood
Processor 30, IBM Blood Processor 2997 and Fenwal CS-3000, for collection of platelets
from normal donors. With each instrument the mean recovery was at least 4x10^11 platelets
per procedure, and each instrument afforded a safe and reliable collection. The Haemonetics
Blood Processor gave the lowest recovery of platelets per minute per procedure. The IBM
Blood Processor 2997 required the longest time for set-up and priming and processed 1.5
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“…The fall in platelet count that can be demonstrated immediately following mechanical cytapheresis is generally 20-30% below the preapheresis value [7,11,15]. A representative pre-and postcytapheresis value is 250 x 103/pl falling to 180 x 103/pl.…”
“…A decrease in the platelet count of donor blood varies with technique; it is influenced both by removal of platelets and by hemodilution. The fall in platelet count that can be demonstrated immediately following mechanical cytapheresis is generally 20-30% below the preapheresis value [7,11,15]. A representative pre-and postcytapheresis value is 250 x 103/pl falling to 180 x 103/pl.…”
“…The fall in platelet count that can be demonstrated immediately following mechanical cytapheresis is generally 20-30% below the preapheresis value [7,11,15]. A representative pre-and postcytapheresis value is 250 x 103/pl falling to 180 x 103/pl.…”
“…A decrease in the platelet count of donor blood varies with technique; it is influenced both by removal of platelets and by hemodilution. The fall in platelet count that can be demonstrated immediately following mechanical cytapheresis is generally 20-30% below the preapheresis value [7,11,15]. A representative pre-and postcytapheresis value is 250 x 103/pl falling to 180 x 103/pl.…”
“…The white cell residuum in platelet con centrates prepared by centrifugally based systems is typical ly comprised mainly of lymphocytes [32], as seen here. The results of the battery of in vitro platelet function assays indicate that, in general, in vitro function is well maintained over the 5-day storage period.…”
This report describes a new system for collection of platelet concentrate (PC) and cell-free plasma (PPP)
from apheresis donors. The system uses two separation devices and requires only a single venipuncture. The Plateletcell™
device separates primary platelet concentrate (PPC) from anticoagulated whole blood and the Plasmacell-C® device
separates the PPC into PC and PPP. Results of functional studies performed indicate that the separation process does not
alter viability of either the PPC, the PC, or the PPP. Platelet function after 5 days of storage is maintained. An average
yield of 3.4±0.7 x 10^11 platelets in 201 g of PC and 422 g of PPP were harvested in 71±13 min of donor time from donors with
preprocedure hematocrits averaging 42.5±2.0% and preprocedure platelet counts averaging 265±61 x 10^3/μl.
“…Thus, the donated blood could be separated into components directly at the donor, collecting the platelets and returning the residual blood components to the donor. This technique increased the amount of platelets obtained from a single donor during single apheresis up to 4 × 10 11 per PC obtained by automated apheresis (APC) [8,9]. The loss of RBC was minimized, and the frequency of platelet donations could be significantly increased.…”
Section: Establishment Of Automated Thrombocytapheresismentioning
The preparation of platelet concentrates by automated apheresis started in the early 1970s. Originally intended to increase the amount of platelets from selected (HLA compatible) donors to supply HLA-immunized patients, plateletpheresis has permanently expanded. Further development of plateletpheresis is described. Considering medical and economical perspectives, actual trends and possible future developments of plateletpheresis are discussed.
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