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European Journal of Cardio-Thoracic Surgery, Vol 8, 315-322, Copyright © 1994 by European Association for Cardio-thoracic Surgery
P Kallis, JA Tooze, S Talbot, D Cowans, DH Bevan and T Treasure
The present recommendation is that aprotinin should be started before
cardiac surgery, but as bleeding is only a problem in a minority, most
patients are treated unnecessarily. In a prospective, randomised,
double-blind trial we have studied the use of aprotinin, given only to the
minority of patients who bled significantly post-operatively and who had
not received prophylactic aprotinin. Sixty patients, who bled in excess of
400 ml in the first 3 h post-operatively were randomised to receive either
aprotinin (2 x 10(6) KIU loading dose followed by an infusion of 0.5 x
10(6) KIU/h for 4 h) or placebo, in addition to conventional treatment. The
demographic characteristics and the surgical procedures performed were
similar in the two groups. Haematological variables were measured (A)
before and (B) at the end of the infusion. Three patients were re-explored
for excessive bleeding in each group and one patient died in each group.
The patients in the aprotinin group bled significantly less and had higher
haemoglobin levels on discharge than the patients in the placebo group. The
tissue plasminogen activator antigen decreased and the fibrinogen level
increased in the aprotinin group. In addition, aprotinin increased the
number of surface GPIb platelet receptors as estimated by flow cytometry
(36% versus 5%, P < 0.01) and maintained the platelet von Willebrand
Factor activity (vWF). There was no significant difference in D-dimers,
fibrin(ogen) degradation products, plasma vWF activity and antigen,
platelet vWF antigen, platelet aggregation (to collagen, arachidonic acid,
platelet activating factor and ristocetin), platelet count or transfusion
of blood products between the two groups.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Aprotinin inhibits fibrinolysis, improves platelet adhesion and reduces blood loss. Results of a double-blind randomized clinical trial
Harefield Hospital, Middlesex, UK.
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