The plasma supplemented modified activated clotting time for monitoring of heparinization during cardiopulmonary bypass: A pilot investigation

被引:26
作者
Koster, A
Despotis, G
Gruendel, M
Fischer, T
Praus, M
Kuppe, H
Levy, JH
机构
[1] Deutsch Herzzentrum Berlin, Dept Anesthesia, D-13353 Berlin, Germany
[2] Inst Pathobiochem & Clin Chem, Berlin, Germany
[3] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Immunol, St Louis, MO 63110 USA
[6] Emory Univ, Sch Med, Dept Cardiothorac Anesthesiol, Atlanta, GA USA
关键词
D O I
10.1097/00000539-200207000-00004
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The standard celite or kaolin activated clotting time (ACT) correlates poorly with heparin levels during cardiopulmonary bypass (CPB). We compared a modified kaolin ACT, in which plasma was supplemented, to a standard undiluted kaolin ACT for monitoring heparin levels during CPB. Fifteen patients undergoing normothermic CPB were enrolled in this prospective study. Heparin management was performed according to the Hepcon HMS results (Medtronic, Minneapolis, MN). The ACTs were performed with the ACT II device (Medtronic). Hepcon HMS calculations, standard kaolin ACTs, and plasma supplemented modified ACTs (mACTs), prepared by diluting blood samples 1:1 with human plasma (Behring, Marburg, Germany), were measured every 30 min during CPB. The data obtained were correlated to the plasma chromogenic anti-Xa activity as a reference assay for heparin levels. A total of 64, samples were evaluated. The chromogenic anti-Xa activity ranged from 0.2 to 5.5 IU/mL. The Hepcon HMS calculations ranged from 2.7-8.2 IU/mL of heparin, the standard ACT ranged from 424 to >999 s, and the mACT ranged from 210 to 801 s. The correlation to the chromogenic anti-Xa method was r = 0.43 for the standard kaolin ACT and r = 0.69 for the plasma n-LACT. The plasma mACT provided an improved correlation to chromogenically measured levels of anti-Xa activity during CPB. The improved correlation most likely results from a correction of the effects of the impairment of the coagulation system caused by hemodilution and consumption of procoagulants on extracorporeal surfaces.
引用
收藏
页码:26 / 30
页数:5
相关论文
共 16 条
[1]   Whole blood heparin concentration measurements by automated protamine titration agree with plasma anti-Xa measurements [J].
Despotis, GJ ;
Joist, JH ;
Goodnough, LT ;
Santoro, SA ;
Spitznagel, E .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1997, 113 (03) :611-613
[2]  
Despotis GJ, 1999, J CARDIOTHOR VASC AN, V13, P18
[3]   COMPARISON OF ACTIVATED COAGULATION LIME AND WHOLE-BLOOD HEPARIN MEASUREMENTS WITH LABORATORY PLASMA ANTI-XA HEPARIN CONCENTRATION IN PATIENTS HAVING CARDIAC OPERATIONS [J].
DESPOTIS, GJ ;
SUMMERFIELD, AL ;
JOIST, JH ;
GOODNOUGH, LT ;
SANTORO, SA ;
SPITZNAGEL, E ;
COX, JL ;
LAPPAS, DG .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1994, 108 (06) :1076-1082
[4]  
Despotis GJ, 1996, THROMB HAEMOSTASIS, V76, P902
[5]   Anticoagulation monitoring during cardiac surgery - A review of current and emerging techniques [J].
Despotis, GJ ;
Gravlee, G ;
Filos, K ;
Levy, J .
ANESTHESIOLOGY, 1999, 91 (04) :1122-1151
[6]  
Despotis GJ, 2001, ANESTH ANALG, V93, P28
[7]  
DESPOTIS GJ, 1995, THORAC CARDIOVASC SU, V110, P46
[8]   A quick anti-Xa-activity-based whole blood coagulation assay for monitoring unfractionated heparin during cardiopulmonary bypass: A pilot investigation [J].
Hansen, R ;
Koster, A ;
Kukucka, M ;
Mertzlufft, F ;
Kuppe, H .
ANESTHESIA AND ANALGESIA, 2000, 91 (03) :533-538
[9]   Measurement of heparin concentration in whole blood with the Hepcon/HMS device does not agree with laboratory determination of plasma heparin concentration using a chromogenic substrate for activated factor X [J].
Hardy, JF ;
Belisle, S ;
Robitaille, D ;
Perrault, J ;
Roy, M ;
Gagnon, L .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1996, 112 (01) :154-161
[10]  
Koster A, 2000, J THORAC CARDIOV SUR, V119, P1278