Dj. Murray et al., HEPARIN DETECTION BY THE ACTIVATED COAGULATION TIME - A COMPARISON OFTHE SENSITIVITY OF COAGULATION TESTS AND HEPARIN ASSAYS, Journal of cardiothoracic and vascular anesthesia, 11(1), 1997, pp. 24-28
Citations number
23
Categorie Soggetti
Anesthesiology,"Peripheal Vascular Diseas","Cardiac & Cardiovascular System
Objective: Laboratory and point-of-care coagulation tests are frequent
ly obtained to determine the presence of heparin after surgical proced
ures. The objective of this study was (1) to compare the sensitivity o
f the activated coagulation time (ACT), activated partial thromboplast
in time (aPTT), protamine titration (Hepcon; HMS Medtronic, Hemotec, E
nglewood, CO), and thromboelastography (TEG) with heparin anticoagulat
ion and (2) to determine how frequently residual heparin is present in
the 24-hour period after heparin neutralization in cardiopulmonary by
pass (CPB) patients. Design: A prospective study. Setting: A tertiary
care university teaching center that performs more than 15,000 surgica
l procedures per year. Participants: Vascular surgical (n = 17) and CP
B (n = 29). Interventions: In vascular surgical patients, coagulation
tests (ACT, protamine titration [Hepcon], and TEG) were obtained befor
e and 90 minutes after heparin (50 to 60 U/kg IV) and compared with he
parin concentration determined by factor Xa inhibition assay. In cardi
ac surgical patients, ACT and heparin concentrations were measured aft
er anesthesia induction, during CPB, after protamine neutralization, a
nd 3 as well as 6 hours after CPB. In addition to heparin concentratio
ns and ACT measures, platelet counts, fibrinogen levels, and bleeding
times were determined before and 3 and 24 hours after CPB. Measurement
s and Main Results: Ninety minutes after heparin, significant heparin
concentrations were present in all vascular surgical patients, but ACT
was elevated in only 4 of 17 patients. Protamine titration (Hepcon) c
orrelated with the factor Xa inhibitory assay for heparin (r(2) = 0.76
). All 17 patients had an abnormal TEG (mean ''R'' time = 81 +/- 39 mi
nutes) and a marked elevation of aPTT (135 +/- 35 sec [normal 22 to 33
seconds]) 90 minutes after heparin. In CPB patients, ACT did not corr
elate with heparin assays. After protamine neutralization of heparin i
n CPB patients, ACT returned to baseline despite the presence of hepar
in in 3 of 29 patients (0.22, 0.18, and 0.33 U/mL). Conclusions: ACT w
as less Sensitive to residual heparin anticoagulation than aPTT, TEG,
and whole blood heparin assay. The whole blood heparin assay (Hepcon)
provided sensitive and specific data about the presence of residual he
parin. Despite the limitation of ACT in detecting heparin, the investi
gators found that residual heparin was not common in the period after
uncomplicated CPB. Copyright (C) 1997 by W.B. Saunders Company.