The Xylum Clot Signature Analyzer(R) (CSA) is an automated, user-friendly,
benchtop analyzer that assesses platelet function and coagulation in nonant
icoagulated whole blood under physiological flow and temperature conditions
. From blood drawn in a single venipuncture, the CSA measures: a) the time
for platelets to occlude holes "punched" in a blood conduit (platelet hemos
tasis time or PI-IT); b) collagen-induced thrombus formation (CITF) as bloo
d flows in a channel containing a collagen fiber; and c) clotting time (CT)
. Micrographs show platelet-rich thrombi in the punched holes and on the co
llagen surface after a run. PI-IT and CITF increased at lower shear rate, s
uggesting that shear activation of platelets is involved in hole closure an
d in collagen-induced thrombus formation. In blood mixed with anti-von Will
ebrand's factor (vWF) antibodies, anti-GPIb antibodies, aurin tricarboxylic
acid (ATA), or anti-GPIIb-IIIa, PHT and CITF were prolonged, further suppo
rting the reflection of platelet function by those parameters. At low shear
rate (<1000 sec(-1)), native blood and blood treated with anti-vWF did not
have significantly different PHTs or CITFs. At high shear rate (>6000 sec(
-1)), the PHT and CITF of the anti-vWF-treated sample were significantly gr
eater than those of the untreated sample. This supports the inhibition of s
hear-induced activation of platelets by anti-vWF in the CSA. Heparin-treate
d blood showed significantly longer CT, indicating that coagulation of bloo
d under flow is inhibited by heparin. The CSA thus assess multiple aspects
of hemostasis under near-physiological conditions. (C) 1998 Elsevier Scienc
e Ltd.