Background A heparin/protamine titration system for measurement of heparin
levels (Hepcon) is promising for efficient anticoagulation during cardiopul
monary bypass (CPB).
Methods. Fifty-seven patients subjected to CPB were divided into two groups
, control (n=24) and Hepcon groups (n=33), The Hepcon group was further div
ided into three subgroups according to perfusion temperature. For the contr
ol group, conventional administration of an anticoagulant (300 IU/kg of hep
arin) and reversal protocol (heparin 1: protamine 1) was performed. For the
Hepcon group, a heparin dose-response assay directed the initial dose of h
eparin, Hepcon also determined the dose of protamine by the titration. The
initial dose of heparin in the control group (300 IU/kg) was statistically
less than that of Hepcon group (360+/-80 IU/kg).
Results. In the Hepcon group, the sensitivity to heparin was correlated wit
h coagulation time (r=-0.78) and antithrombin III levels (r=0.70), and indi
vidual difference of sensitivity resulted in a wide range of dosage (160 to
490 IU/kg). A strong correlation was observed between plasma and whole blo
od concentration of heparin (r=0.86). However, they did not correlate with
ACT values. Perfusion temperature didn't affect the heparin level, but did
the ACT value. In the Hepcon group, the dose of protamine was significantly
less and adverse events were rare.
Conclusions. In conclusion, whole blood heparin measurements correlated wel
l with plasma heparin concentration. Protamine titration of heparin reduced
the dose of protamine and decreased the chance of adverse reactions.