1995 has brought several novelties into the field of thrombocytapheres
is. The most important is the presentation by Baxter of the Amicus CFC
apparatus that, in a two-vein collection time of 51-53 min, collects
3.93-4.13 x 10(11) platelets contaminated by 0.2 x 10(6) white blood c
ells (WBC) with an efficiency of 72-74%. Similar results are obtained
in 55 min, in single-needle procedures, with a collection efficiency o
f 70.7%, a total yield of 4.3 x 10(11) and a contamination of 0.9 x 10
(6) WBC. Presently the machine cannot collect red blood cells (RBC), a
long with platelets, as does the DFC Haemonetics MCS3p. With this mach
ine in mandatory single-needle procedures lasting 80-85 min, approxima
tely 4.5 x 10(11) platelets can be collected with a WBC contamination
of 3.1 x 10(6). Along with the platelet cells (PC), with the SDP PRC p
rotocol at the end of each pass it is possible to collect aliquots of
plasma red blood cells (PRBC) (10-50 mL) with a haematocrit of 65%. De
pending on the number of passes and on the donor's body weight (BW), f
rom 1 to 2 U/PRBC containing approximately 55 g of haemoglobin (Hb) ea
ch can be obtained. This method not only costs less but alsoimmunologi
cal and viral risks for the patients are more efficiently addressed si
nce it is possible to reduce the number of allogeneic exposures in the
same transfusion event. PRBC can also be collected with the Fresenius
AS104 and the Dideco Excel apparatuses. Dideco is presently using the
''Genova'' separation chamber, which can collect an average of 4.8 x
10(11) platelets contaminated with 0.5 x 10(6) WBC, in approximately 5
5 min. The ACD-A-to-blood ratio may be as low as 1/20 since the very l
ast belts and lines are coated with non-thrombogenic substances. There
fore, there is no alteration of the quality of the platelets as evalua
ted with monoclonal antibodies (MoAbs) anti-CD 62, 63, 36 and 51, no e
xtra haemorrhagic risk for the donors and citrate reactions and microa
ggregate formation are totally eliminated. In 1995 there has also been
some rejuvenation of the older cell separators. The CS3000+ uses the
TN6/PLT 30 combination of separation collection chambers. Platelets ar
e collected in only 30 mt of plasma, and non-plasma solutions containi
ng acetate can be used for their resuspension. The Fresenius AS204 is
ready for better-quality combined platelet collection, and RBC-PC coll
ection with Cobe Spectra is under evaluation along with the leucocyte
reduction system that apparently brings leucocyte contamination down t
o 0.35 x 10(5). This interest in thrombocytapheresis is also the resul
t of the challenge that thrombopoietin phase I and II trials have prom
oted. (C) 1997 Elsevier Science Ltd.