L. Bagge et al., HEMOSTASIS AT LOW HEPARIN DOSAGE DURING CARDIOPULMONARY BYPASS WITH HEPARIN-COATED CIRCUITS IN PIGS (VOL 31, PG 275, 1997), SC CARDIOVA, 31(6), 1997, pp. 3
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 VIII and adhesive platelets were
reduced significantly during CPB, and postoperatively there were sign
ificantly lower values of prothrombin complex, fibrinogen, antithrombi
n III, factor VIII and adhesive platelets but a significantly increase
d concentration of von Willebrand factor and cumulative bleeding after
4 h. In conclusion, heparin-coated CPB circuits combined with lowered
heparin dosage reduced coagulation factor consumption and preserved p
latelet function, possibly contributing to improved postoperative haem
ostasis.