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Ann Thorac Surg 1999;68:1751-1755
© 1999 The Society of Thoracic Surgeons


Original Articles

IL-6 and IL-8 levels after cardiopulmonary bypass are not affected by surface coating

Stephen B. Horton, BSa, Warwick W. Butt, MDb, Richard J. Mullaly, BSa, Clarke A. Thuys, BSa, Eve B. O’Connor, CCPa, Keith Byron, PhDc, Andrew D. Cochrane, FRACSa, Christian P. Brizard, MDa, Tom R. Karl, MDa

a Cardiac Surgical Unit, Royal Children’s Hospital, Melbourne, Australia
b Intensive Care Unit, Royal Children’s Hospital, Melbourne, Australia
c Pathology Department, Royal Melbourne Hospital, Melbourne, Australia

Address reprint requests to Dr Karl, Cardiac Surgical Unit, Royal Children’s Hospital, Flemington Rd, Parkville, 3052 Victoria, Australia
e-mail: cardiac{at}cryptic.rch.unimelb.edu.au

Background. Contact of blood with the surfaces of the cardiopulmonary bypass (CPB) circuit has been implicated as a cause of the inflammatory response. We undertook a prospective randomized trial of 200 pediatric patients, all with a calculated total bypass flow of less than 2.3 L/min (< 0.96 L/m2/min).

Methods. Patients were randomly assigned to 1 of 4 CPB groups: (1) Nonheparin-bonded circuit with no albumin preprime; (2) Nonheparin-bonded circuit with albumin preprime; (3) Heparin-bonded circuit with no albumin preprime; (4) Heparin-bonded circuit with albumin preprime. Measurements of cytokines, (interleukin [IL]-6, IL-8) and blood cell counts were made prebypass and 6 and 24 hours after institution of cardiopulmonary bypass.

Results. Analysis of variance showed no significant difference in any of the clinical or biochemical characteristics of the 4 groups. The interaction between heparin-bonded oxygenators and albumin preprime was not significant. No important differences in IL-6 or IL-8 concentrations were noted after CPB using either heparin or nonheparin-bonded oxygenators with albumin or albumin free preprime using two-way analysis of variance.

Conclusions. Albumin preprime and heparin-bonding do not attenuate the inflammatory response component attributable to the concentration of these markers.




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