L. Bagge et al., HEMOSTASIS AT LOW HEPARIN DOSAGE DURING CARDIOPULMONARY BYPASS WITH HEPARIN-COATED CIRCUITS IN PIGS, SC CARDIOVA, 31(5), 1997, pp. 275-281
Cardiopulmonary bypass (CPB) causes activation of cascade systems. Alt
hough heparin coating of CPB circuits improves biocompatibility, the e
ffects on coagulation remain controversial. Theoretically, heparin coa
ting should permit the reduction of systemic anticoagulation during CP
B. We investigated influences on haemostatic variables in animal CPB,
comparing heparin-coated circuits and reduced systemic heparinization
(group HC) with uncoated circuits and full heparinization (group C). T
wenty pigs underwent 2-h CPB. Seven (HC, n = 4; C, n = 3) were weaned
from CPB and studied for up to 4 h. Total administered heparin was 470
+/- 6 IU/kg (mean +/- SEM) in group C and 100 +/- 0 IU/kg in group HC
. Protamine dosage was significantly reduced in group HC. In group C,
levels of prothrombin complex, factor Vm and adhesive platelets were r
educed significantly during CPB, and postoperatively there were signif
icantly lower values of prothrombin complex, fibrinogen, antithrombin
Ill, factor VIII and adhesive platelets but a significantly increased
concentration of von Willebrand factor and cumulative bleeding after 4
h. In conclusion, heparin-coated CPB circuits combined with lowered h
eparin dosage reduced coagulation factor consumption and preserved pla
telet function, possibly contributing to improved postoperative haemos
tasis.