JTCS Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Frank Redling
Hans-Reinhard Zerkowski
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Prondzinsky, R.
Right arrow Articles by Werdan, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Prondzinsky, R.
Right arrow Articles by Werdan, K.
Related Collections
Right arrow Coronary disease

J Thorac Cardiovasc Surg 2005;129:760-766
© 2005 The American Association for Thoracic Surgery


Cardiopulmonary Support and Physiology

Surgical trauma affects the proinflammatory status after cardiac surgery to a higher degree than cardiopulmonary bypass

Roland Prondzinsky, MDa,*, Axel Knüpfer, MDa, Harald Loppnow, PhDa, Frank Redling, MDb, Dirk W. Lehmann, MDc, Ina Stabenow, MDa, Rochus Witthaut, MDa, Susanne Unverzagt, PhDd, Joachim Radke, MDc, Hans-Reinhard Zerkowski, MDb, Karl Werdan, MDa

a Department of Medicine III, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany
b Department of Cardiothoracic Surgery, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany
c Department of Anesthesiology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany
d Operative Intensive Care Medicine und Coordination Centre for Clinical Trials, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany

Received for publication December 1, 2003; revisions received June 7, 2004; accepted for publication July 6, 2004.

* Address for reprints: Roland Prondzinsky, MD, Martin-Luther-University Halle-Wittenberg, Department of Internal Medicine III, Ernst-Grube-Str 40, D-06097 Halle (Saale), Germany (E-mail: roland.prondzinsky{at}medizin.uni-halle.de).

OBJECTIVES: Cytokines contribute to the development of the systemic inflammatory response syndrome or multiple-organ failure frequently observed after cardiopulmonary bypass—supported cardiac surgery. To quantify the contribution of bypass-induced versus trauma-induced inflammatory response after coronary artery bypass grafting, we examined plasma cytokine levels in 120 patients with coronary artery disease who were treated with or without cardiopulmonary bypass—assisted procedures.

METHODS: Patients were treated in accordance with one of the following protocols: (1) elective percutaneous coronary intervention without cardiopulmonary bypass (n = 69), (2) cardiopulmonary bypass—supported percutaneous coronary intervention (cardiopulmonary bypass—percutaneous coronary intervention; n = 10), and (3) cardiopulmonary bypass—supported coronary artery bypass grafting (cardiopulmonary bypass—coronary artery bypass grafting; n = 41). Cytokine levels (picograms/milliliter) were measured by enzyme-linked immunosorbent assay from plasma samples obtained at various time points.

RESULTS: Interleukin-6 was measured in blood samples from all 3 patient populations. The maximum interleukin-6 level was 13.6 ± 22.3 pg/mL in the percutaneous coronary intervention group, 170.4 ± 165.4 pg/mL in the cardiopulmonary bypass-percutaneous coronary intervention group, and 640.3 ± 285.7 pg/mL in the cardiopulmonary bypass-coronary artery bypass grafting group. Interleukin-6 levels were significantly different, and the 95% confidence intervals did not overlap. In the cardiopulmonary bypass-percutaneous coronary intervention group, bypass duration correlated well with interleukin-6 production (r = 0.915; P < .001), whereas these parameters did not correlate in patients who underwent cardiopulmonary bypass-coronary artery bypass grafting (r = 0.307; P = .054).

CONCLUSIONS: These findings support the suggestion that surgical trauma and cardiopulmonary bypass contribute to the inflammatory response after cardiac surgery, although trauma may contribute to a higher degree.





This article has been cited by other articles:


Home page
Nutr Clin PractHome page
R. A. DiMaria-Ghalili
Nutrition Risk Factors in Older Coronary Artery Bypass Graft Patients
Nutr Clin Pract, October 1, 2008; 23(5): 494 - 500.
[Abstract] [Full Text] [PDF]


Home page
PerfusionHome page
K Svennevig, T. Hoel, A. Thiara, S. Kolset, A Castelheim, T. Mollnes, F Brosstad, E Fosse, and J. Svennevig
Syndecan-1 plasma levels during coronary artery bypass surgery with and without cardiopulmonary bypass
Perfusion, May 1, 2008; 23(3): 165 - 171.
[Abstract] [PDF]


Home page
Ann. Thorac. Surg.Home page
J. Tatoulis, S. Rice, P. Davis, J. C. Goldblatt, and S. Marasco
Patterns of postoperative systemic vascular resistance in a randomized trial of conventional on-pump versus off-pump coronary artery bypass graft surgery.
Ann. Thorac. Surg., October 1, 2006; 82(4): 1436 - 1444.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
A. Haverich, S. K. Shernan, J. H. Levy, J. C. Chen, M. Carrier, K. M. Taylor, F. Van de Werf, M. F. Newman, P. X. Adams, T. G. Todaro, et al.
Pexelizumab Reduces Death and Myocardial Infarction in Higher Risk Cardiac Surgical Patients
Ann. Thorac. Surg., August 1, 2006; 82(2): 486 - 492.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
K. Ishida, F. Kimura, M. Imamaki, A. Ishida, H. Shimura, H. Kohno, M. Sakurai, and M. Miyazaki
Relation of inflammatory cytokines to atrial fibrillation after off-pump coronary artery bypass grafting.
Eur. J. Cardiothorac. Surg., April 1, 2006; 29(4): 501 - 505.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
L. Colagrande, F. Formica, F. Porta, A. Martino, F. Sangalli, L. Avalli, and G. Paolini
Reduced Cytokines Release and Myocardial Damage in Coronary Artery Bypass Patients Due to L-Arginine Cardioplegia Supplementation
Ann. Thorac. Surg., April 1, 2006; 81(4): 1256 - 1261.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
A. M. Draaisma, M. G. Hazekamp, N. Anes, P. H. Schoof, C. E. Hack, A. Sturk, and R. A.E. Dion
Phosphorylcholine Coating of Bypass Systems Used for Young Infants Does Not Attenuate the Inflammatory Response
Ann. Thorac. Surg., April 1, 2006; 81(4): 1455 - 1459.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
N. Smart, M. H. Mojet, D. S. Latchman, M. S. Marber, M. R. Duchen, and R. J. Heads
IL-6 induces PI 3-kinase and nitric oxide-dependent protection and preserves mitochondrial function in cardiomyocytes
Cardiovasc Res, January 1, 2006; 69(1): 164 - 177.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
E. M. Elmistekawy
Evaluation of surgical trauma and cardiopulmonary bypass as factors in inflammatory status after cardiac surgery
J. Thorac. Cardiovasc. Surg., October 1, 2005; 130(4): 1226 - 1226.
[Full Text] [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
Copyright © 2005 by The American Association for Thoracic Surgery.