Literature DB >> 2353183

Inflammatory system activation during cardiopulmonary bypass as an indicator of biocompatibility: a randomized comparison of bubble and membrane oxygenators.

L Nilsson1, U Nilsson, P Venge, O Johansson, H Tydén, T Aberg, S O Nyström.   

Abstract

As the exposure of blood to foreign material during cardiopulmonary bypass (CPB) leads to triggering of inflammatory systems, the inflammatory response was used as an indicator of the biocompatibility of oxygenators. Activation of complement and neutrophil granulocytes during CPB was studied in 96 patients undergoing coronary bypass, with randomized comparisons between four different oxygenators, two of bubble and two of membrane type. Seven patients undergoing thoracotomy without CPB served as controls. During CPB there was significant complement activation, measured as changes in the ratio C3d/C3, with no demonstrable difference between the bubble and membrane oxygenator groups. Such change was not seen in the controls. Neutrophil granulocytes released significant amounts of the granule proteins lactoferrin and myeloperoxidase during CPB, but not during thoracotomy without CPB. The plasma concentrations of lactoferrin and myeloperoxidase were significantly lower in the membrane oxygenator groups, possibly indicating better biocompatibility. The strong inflammatory response with both oxygenator types, however, indicates that presently used CPB devices have unsatisfactory biocompatibility.

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Year:  1990        PMID: 2353183     DOI: 10.3109/14017439009101824

Source DB:  PubMed          Journal:  Scand J Thorac Cardiovasc Surg        ISSN: 0036-5580


  3 in total

1.  Complement activation and bioincompatibility. The terminal complement complex for evaluation and surface modification with heparin for improvement of biomaterials.

Authors:  T E Mollnes; V Videm; J Riesenfeld; P Garred; J L Svennevig; E Fosse; K Hogasen; M Harboe
Journal:  Clin Exp Immunol       Date:  1991-10       Impact factor: 4.330

2.  Triiodothyronine supplementation and cytokines during cardiopulmonary bypass in infants and children.

Authors:  James R Priest; April Slee; Aaron K Olson; Dolena Ledee; Fionnuala Morrish; Michael A Portman
Journal:  J Thorac Cardiovasc Surg       Date:  2012-06-27       Impact factor: 5.209

3.  Evidence for iC3 generation during cardiopulmonary bypass as the result of blood-gas interaction.

Authors:  M Pekna; L Nilsson; K Nilsson-Ekdahl; U R Nilsson; B Nilsson
Journal:  Clin Exp Immunol       Date:  1993-03       Impact factor: 4.330

  3 in total

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