|
|
||||||||
J Thorac Cardiovasc Surg 1995;110:768-0773
© 1995 Mosby, Inc.
CARDIOPULMONARY BYPASS, |
Helsinki, Finland, and Uppsala, Sweden
Supported by the Foundation for Pediatric Research, Academy of Finland,and the Sigrid Jusélius Foundation.
Received for publication Oct. 27, 1994. Accepted for publication Feb. 13, 1995. Address for reprints: Eero J. Personen, MD, Children's Hospital, Stenbackinkatu 11, 00290 Helsinki, Finland.
Abstract
Studies on free radical generation during cardiopulmonary bypass have focused mainly on the heart and the lungs. However, low pumping pressure, nonpulsatile perfusion, and hypothermia affect the entire circulation, resulting in decreased splanchnic blood flow, increased intestinal permeability, and endotoxemia. To evaluate regional phenomena, we studied 16 children undergoing cardiopulmonary bypass. Free radical production, granulocyte activation, and hypoxanthine metabolism were assessed separately in the circulations drained by the inferior and superior venae cavae, as well as in the oxygenator. Three minutes after the onset of cardiopulmonary bypass, significant gradients between the inferior vena cava and the arterial line of the oxygenator existed in malondialdehyde (+0.60±0.12µmol/L, lactoferrin (+18.21±7.65µg/L), myeloperoxidase (+53.75±16.50µg/L), hypoxanthine (-0.62±0.15µmol/L), and urate (+8.87±4.03µmol/L). These gradients decreased in parallel with decreasing body temperature. Except for a transient gradient in malondialdehyde at 3 minutes after the onset of cardiopulmonary bypass (+0.23±0.08µmol/L), no changes were detected between the superior vena cava and the arterial line. In the oxygenator, granulocyte activation was observed only after aortic declamping. We conclude that during cardiopulmonary bypass, significant free radical generation, granulocyte activation, hypoxanthine elimination, and urate production take place in the region drained by the inferior vena cava. In the oxygenator, granulocyte activation occurs only after aortic declamping. (J THORACCARDIOVASCSURG1995;110: 768-73)
This article has been cited by other articles:
![]() |
C. J. McMahon, D. J. Penny, D. P. Nelson, A. M. Ades, S. Al Maskary, M. Speer, J. Katkin, E. D. McKenzie, C. D. Fraser Jr, MD, and A. C. Chang Preterm Infants With Congenital Heart Disease and Bronchopulmonary Dysplasia: Postoperative Course and Outcome After Cardiac Surgery Pediatrics, August 1, 2005; 116(2): 423 - 430. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. B. Andrasi, A. Blazovics, G. Szabo, C. F. Vahl, and S. Hagl Poly(ADP-ribose) polymerase inhibitor PJ-34 reduces mesenteric vascular injury induced by experimental cardiopulmonary bypass with cardiac arrest Am J Physiol Heart Circ Physiol, June 1, 2005; 288(6): H2972 - H2978. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.-U. Sack, B. Reidenbach, R. Dollner, A. Schledt, M. M. Gebhard, and S. Hagl Influence of steroids on microvascular perfusion injury of the bowel induced by extracorporeal circulation Ann. Thorac. Surg., October 1, 2001; 72(4): 1321 - 1326. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. A. Hennein Inflammation After Cardiopulmonary Bypass: Therapy for the Postpump Syndrome Seminars in Cardiothoracic and Vascular Anesthesia, September 1, 2001; 5(3): 236 - 255. [Abstract] [PDF] |
||||
![]() |
A. Belboul, D. Roberts, R. Borjesson, and J. Johnsson Oxygen free radical generation in healthy blood donors and cardiac patients: the protective effect of allopurinol Perfusion, January 1, 2001; 16(1): 59 - 65. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |