Induction of monocyte tissue factor procoagulant activity during coronary artery bypass surgery is reduced with heparin-coated extracorporeal circuit

被引:37
作者
Barstad, RM
Ovrum, E
Ringdal, MA
Oystese, R
Hamers, MJAG
Veiby, OP
Rolfsen, T
Stephens, RW
Sakariassen, KS
机构
[1] OSLO HEART CTR, OSLO, NORWAY
[2] UNIV OSLO, ELECT MICROSCOPY UNIT BIOL SCI, OSLO, NORWAY
关键词
extracorporeal circulation; heparin-coating; monocytes; tissue factor;
D O I
10.1111/j.1365-2141.1996.tb08989.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The possible activation of monocytes to express tissue factor procoagulant activity (TF-PCA) during CPB (cardiopulmonary bypass) was investigated, 22 patients undergoing myocardial revascularization were randomly assigned to two groups, In group C, heparin-coated circuits (Duraflo II) and reduced systemic heparinization (ACT > 250 s) were used, In group NC, non-coated circuits and standard heparin administration (ACT > 480 s) were used. Adherent monocytes retrieved from the oxygenators immediately after bypass arrest showed a 2-3-fold increase in TF-PCA when compared to circulating cells pre-CPB (P < 0.01). When cell PCA was expressed as percent change from pre-CPB (baseline) values, circulating monocytes in group NC at CPB-arrest showed a 2-fold increase in PCA compared to group C (P < 0.05). Moreover, the percent increase in PCA of oxygenator-retrieved monocytes was 7-fold in group NC and 2-fold in group C (P < 0.008 and P < 0.004, respectively). Thus, heparin-coating of the extracorporeal circuit reduced induction of adherent cell TF-PCA by 70% (P < 0.05). Thus, monocyte TF-PCA may cause activation of the extrinsic coagulation pathway during CPB surgery, It is apparent that heparin-coating enhanced biocompatibility of extracorporeal circuits, Reduced systemic heparinization in group C proved to be safe. However, further reduction of heparin administration map not be advisable, since monocytes were still activated in the coated oxygenator.
引用
收藏
页码:517 / 525
页数:9
相关论文
共 42 条
  • [1] ALTIERI DC, 1993, BLOOD, V81, P569
  • [2] RETINOIC ACID REDUCES INDUCTION OF MONOCYTE TISSUE FACTOR AND TISSUE FACTOR FACTOR VIIA-DEPENDENT ARTERIAL THROMBUS FORMATION
    BARSTAD, RM
    HAMERS, MJAG
    STEPHENS, RW
    SAKARIASSEN, KS
    [J]. BLOOD, 1995, 86 (01) : 212 - 218
  • [3] PROCOAGULANT HUMAN MONOCYTES MEDIATE TISSUE FACTOR FACTOR VIIA-DEPENDENT PLATELET-THROMBUS FORMATION WHEN EXPOSED TO FLOWING NONANTICOAGULATED HUMAN BLOOD
    BARSTAD, RM
    HAMERS, MJAG
    KIERULF, P
    WESTVIK, AB
    SAKARIASSEN, KS
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (01) : 11 - 16
  • [4] BIOCOMPATIBILITY OF EXTRACORPOREAL-CIRCULATION WITH AUTOOXYGENATION
    BOCHENEK, A
    RELIGA, Z
    KOKOT, F
    WNUKWOJNAR, AM
    WOJNAR, J
    WNUK, R
    GALLERT, G
    SKIBA, J
    [J]. EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 1992, 6 (08) : 397 - 402
  • [5] BOISCLAIR MD, 1993, BLOOD, V82, P3350
  • [6] BOISCLAIR MD, 1993, BLOOD COAGUL FIBRIN, V4, P1007, DOI 10.1097/00001721-199304060-00017
  • [7] DECREASED BLOOD-LOSS AFTER CARDIOPULMONARY BYPASS USING HEPARIN-COATED CIRCUIT AND 50-PERCENT REDUCTION OF HEPARIN DOSE
    BOROWIEC, J
    THELIN, S
    BAGGE, L
    HULTMAN, J
    HANSSON, HE
    [J]. SCANDINAVIAN JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1992, 26 (03): : 177 - 185
  • [8] ISOLATION OF LYMPHOCYTES, GRANULOCYTES AND MACROPHAGES
    BOYUM, A
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1976, : 9 - 15
  • [9] ROLE OF FACTOR-XII IN THROMBIN GENERATION AND FIBRINOLYSIS DURING CARDIOPULMONARY BYPASS
    BURMAN, JF
    CHUNG, HI
    LANE, DA
    PHILIPPOU, H
    ADAMI, A
    LINCOLN, JCR
    [J]. LANCET, 1994, 344 (8931) : 1192 - 1193
  • [10] INFLAMMATORY RESPONSE TO CARDIOPULMONARY BYPASS
    BUTLER, J
    ROCKER, GM
    WESTABY, S
    [J]. ANNALS OF THORACIC SURGERY, 1993, 55 (02) : 552 - 559