Global haemostasis was assessed on blood from patients with establishe
d blood clotting abnormalities using a hollow fibre flow device. The i
nstrument monitors pressure changes across a polyethylene fibre throug
h which non-anticoagulated whole blood is perfused. This method of ana
lysis is significant because it (1) minimizes or eliminates common pro
blems associated with routine clinical evaluations, such as sample dil
ution, completion time, and anticoagulant artifacts, (2) rapidly (unde
r 90 min) and accurately calculates in vitro bleeding time (IVBT) and
whole blood clotting time (WBCT), (3) presents a reliable means of dis
tinguishing coagulation defects from platelet dysfunction, and (4) red
uces the need for a series of screening tests to a single test that re
quires a small amount of non-anticoagulated whole blood. Using this te
chnology, global haemostasis of normal volunteers was studied using bl
ood samples spiked with PPACK and prostacyclin. Blood from patients wi
th acquired factor VIII deficiency and Glanzmann's thrombasthenia and
from those receiving Coumadin therapy were also studied. The hollow fi
bre device detailed haemostatic abnormalities of both congenital and t
herapeutic conditions.