Biocompatibility of Heparin‐Coated Circuits in Pediatric Cardiopulmonary Bypass
- 1 July 1997
- journal article
- clinical trial
- Published by Wiley in Artificial Organs
- Vol. 21 (7) , 836-840
- https://doi.org/10.1111/j.1525-1594.1997.tb03753.x
Abstract
In this study, we evaluated the biocompatibility of heparin‐coated circuits in pediatric cardiopulmonary bypass (CPB). Eight patients were divided into 2 groups: the control group (Group C) and heparin‐coated group (Group H). In Group H, CPB circuits, including the arterial pump, oxygenator, and cannulas were heparin‐coated. Before, during, and after CPB, blood samples were obtained to assess the platelet counts (Plat), α2‐plasmin plas‐minogen inhibitor complex (PIC), thrombin‐antithrombin III complex (TAT), C3 activation products (C3a), inter‐leukin (IL)‐6, IL‐8, and polymorphonuclear neutrophil leukocyte (PMN) elastase. There was no significant difference in Plat, PIC, or TAT between groups. Group H showed significantly low levels of C3a (during and after CPB), PMN elastase (during CPB), and IL‐6 (after CPB). These data demonstrated that in pediatric CPB, heparin‐coated CPB circuits reduced the activation of complements and the production of PMN elastase and IL‐6, suggesting the superior biocompatibility of the heparin‐coated circuits.Keywords
This publication has 32 references indexed in Scilit:
- Attenuation of cardiopulmonary bypass–derived inflammatory reactions reduces myocardial reperfusion injury in cardiac operationsThe Journal of Thoracic and Cardiovascular Surgery, 1996
- Normothermia Has Beneficial Effects in Cardiopulmonary Bypass Attenuating Inflammatory ReactionsAsaio Journal, 1995
- Heparin-coated cardiopulmonary bypass circuits: Hemostatic alterations and postoperative blood lossThe Annals of Thoracic Surgery, 1994
- Heparin-coated circuits reduce the inflammatory response to cardiopulmonary bypassThe Annals of Thoracic Surgery, 1993
- Heparin-coating of extracorporea circuits reduces thrombin formation in patients undergoing cardiopulmonary bypassPerfusion, 1991
- Reduced Granulocyte Activation with a Heparin–Coated Device in an In Vitro Model of Cardiopulmonary BypassArtificial Organs, 1991
- C5a-mediated release of interleukin 6 by human monocytesClinical Immunology and Immunopathology, 1990
- Effects of Protamine Administration after Cardiopulmonary Bypass on Complement, Blood Elements, and the Hemodynamic StateThe Annals of Thoracic Surgery, 1986
- A New Non-Thrombogenic Surface Prepared by Selective Covalent Binding of Heparin Via a Modified Reducing Terminal ResidueBiomaterials, Medical Devices, and Artificial Organs, 1983
- Complement and Leukocyte-Mediated Pulmonary Dysfunction in HemodialysisNew England Journal of Medicine, 1977