E. Ovrum et al., COMPLETE HEPARIN-COATED CARDIOPULMONARY BYPASS AND LOW HEPARIN DOSE REDUCE COMPLEMENT AND GRANULOCYTE ACTIVATION, European journal of cardio-thoracic surgery, 10(1), 1996, pp. 54-60
Complete heparin-coated extracorporeal circuits, including cardiotomy
reservoir, have recently become available for routine cardiac surgery.
The effects on complement and granulocyte activation using a heparin-
coated circuit in combination with reduced systemic heparinization (ac
tivated clotting time (ACT) > 250 s) were studied in 33 patients under
going elective first time myocardial revascularization. The patients w
ere prospectively randomized either to a heparin-coated group (Group H
, n = 17), or to a control group (Group C, n = 16)treated with an iden
tical uncoated circuit and full heparin dose (ACT > 480 s). During car
diopulmonary bypass (CPB) the C3 activation products C3b, iC3b, and C3
c (C3bc) and the terminal SC5b-9 complement complex (TCC) increased ma
rkedly in both groups compared to baseline, but to a much lesser exten
t in the heparin-coated group. The maximal increase of C3bc during the
operation was a median of 28 arbitrary units (AU)/ml in the heparin-c
oated group, compared to 45 AU/ml in the nr control group (P = 0.01).
Similarly, in Group H the maximal increase of TCC was significantly lo
wer (median 0.8 AU/ml) than the levels recognized in Group C(median 1.
9 AU/ml) (P < 0.0001). The release of the granulocyte activation enzym
es lactoferrin and myeloperoxidase also increased during CPB in both g
roups compared to baseline level. The maximal increase of lactoferrin
concentration was a median of 229 mu g/l in Group H and significantly
lower than 647 mu g/l in the control group (P = 0.0002). As for myelop
eroxidase, there were no significant intergroup differences. In conclu
sion, a complete heparin-coated circuit and low systemic heparinizatio
n for CPB in coronary artery surgery were associated with reduced acti
vation of the complement system and less release of lactoferrin. The r
esults indicate improved biocompatibility of this option for extracorp
oreal circulation.