Inflammatory Cascade: A Final Common Pathway for Perioperative Injury?
Herskowitz, Ahvie MD; Mangano, Dennis T. PhD, MD
Traumatic wounds, bee stings, and bacterial, viral, and parasitic infections all produce early phase reactants that lead to the efficient recruitment of targeted inflammatory cells to the affected site. Millions of years of evolution have produced dozens of molecules, primarily cytokines and growth factors, that precisely control the immune system response. The first of these early alert proteins to be discovered were the three interferons-alpha, beta, and gamma. Subsequently, during the past 2 decades, numerous proteins have been cloned and sequenced and their products used to define their precise function(s). These secreted protein mediators include cytokines (to date, interleukin (IL)-1-16), growth factors such as transforming growth factor-beta, and chemokines such as macrophage inflammatory protein-1 alpha, beta, and RANTES. Isolating the individual components of this complex communication network has enhanced our understanding of the inflammatory response and its role in acute disease. Recent findings even suggest important implications for high-risk patients undergoing surgery, particularly when subjected to postischemic reperfusion, as exemplified by a cardiopulmonary bypass (CPB) model. 
An Inflammatory Cascade Paradigm-The CPB Model
Cardiopulmonary bypass represents a unique medical condition that induces a systemic inflammatory response for which the human immune system has not yet evolved a specific response. Consequently, when confronted with the multiple insults of CPB, the magnitude of the immune system response is exaggerated, confusing, and complex. For example, the postbypass period is characterized by large fluid shifts, temperature changes, coagulation disturbances, and increased concentrations of catecholamines and stress hormones. [2,3]
* An exaggerated inflammatory response to reperfusion may be largely responsible for systemic vasodilation during rewarming, fever, postoperative bleeding, and reperfusion injury to the heart, brain, kidney, and gut, leading to either permanent organ injury or transient dysfunction. [1,4]
How might we envision the role of the inflammatory response, given this complicated sequence of events? Based on in vitro and in vivo studies, we can suggest a paradigm describing the interactive steps that likely take place during the postischemic inflammatory state after CPB. Figure 1
is one schematic representation. In this model, neutrophil-endothelial cell adhesion is central to postischemic reperfusion. 
Initially, oxygen free radicals are released from endothelial cells in reperfused organs, such as the heart and lung, leading to alterations in endothelial cells that promote early neutrophil targeting, activation of neutrophils in transit through these organs, local activation of serum complement, and induction of cytokine synthesis. Initial neutrophil attachment to the endothelium results in translocation of P-selection from intracellular vesicles to the cell membrane and initiation of platelet activating factor synthesis. These changes lead to more neutrophil adhesion, neutrophil activation, and neutrophil adhesion protein (CD11/CD18 integrin) expression via endothelial membrane-bound platelet activating factor. 
Proinflammatory cytokines such as IL-1 beta and TNF alpha, and chemokines such as IL-8, are newly synthesized, largely within endothelial cells, in reperfused organs within hours, and induce increased expression of adhesion molecules on endothelial cells and other tissue-specific cells (e.g., myocytes, pulmonary alveolar lining cells, glomerular or renal tubular epithelium). 
In turn, this results in tighter neutrophil attachment via intercellular adhesion molecule-1, transmigration of neutrophils into the interstitial space, and release of large amounts of free radicals.
Nitric oxide produced by endothelial cell nitric oxide synthase or other nitric oxide synthase isoforms may exert important controls over many of these processes by inducing vasodilation, regulating leukocyte recruitment, scavenging endothelial-generated oxygen radicals, and preventing upregulation of neutrophil CD11/CD18. However, nitric oxide production is impaired after ischemia/reperfusion, and inhibitory controls over leukocyte migration, oxygen radicals, and neutrophil adherence are mitigated.
Therefore, there are a number of potentially serious immunologic consequences associated with cardiac surgery that may lead to adverse clinical events, including: 1) the CPB circuit itself is immunogenic and induces activation of complement, platelets, and neutrophils, as well as release of proinflammatory cytokines; 2) reperfusion of ischemic organs after CPB initiates a complex interaction between these same inflammatory components, which may lead to exaggerated local, organ-based, inflammatory responses in lung, heart, kidney, brain, and gut; and 3) rewarming may further induce systemic neutrophil adhesion, sequestration, and degranulation.
Clinical Investigation of the Perioperative Inflammatory Response
Clearly, the clinical implication of the perioperative inflammatory response may be enormous and, therefore, warrants serious investigation. Four stages of this investigatory process can be postulated. The first stage, which consists of observational studies, has been addressed during the past decade, and has demonstrated complement activation and cytokine/chemokine release, as well as increased concentrations of neutrophils, endotoxin, and elastases, during and after CPB. [8-12]
Although these descriptive results are of interest, the critical challenge for investigators is to establish the true significance of these findings by determining whether a relation between these inflammatory markers and adverse clinical outcome exists, and, if it does, whether this relation is associative or causal (the second stage of investigation). If, in fact, the second stage studies find that no relations exist, then one questions the rationale for further substantive research. However, if an associative relation can be discerned (or even perhaps a causal relation), then there is potential for discovering therapeutic agents that may mitigate the CPB inflammatory response (the third stage of investigation). Finally, if these investigations yield such agents, and if these are proven safe, then pursuit of large-scale outcome trials (the fourth stage of investigation) is warranted, to establish the efficacy and cost-effectiveness of these novel therapeutic agents.
Currently, it appears that we are at the second stage of investigation of CPB-induced inflammatory response, and preliminary studies have been encouraging, because they suggest a relation between CPB-induced mediators and both early and late hemodynamic effects, as well as more important surrogates of injury, such as myocardial ischemia and dysfunction. 
Also, these investigators postulate that the early effects are mediated through regulation of nitric oxide homeostasis, and the later effects by alteration of the vascular endothelium. These findings are important, but are limited because only surrogates of outcome have been investigated, and not adverse outcome itself.
The Current Study
In the current issue of Anesthesiology, Journois and colleagues 
focus our attention on the potential role of inflammatory mediators modulating specific clinical end-points, including postoperative pulmonary oxygen exchange, bleeding, and body temperature fluctuations after bypass. The results of this preliminary study suggest beneficial effects of high-volume, zero-fluid balance ultrafiltration (z-BUF) during the rewarming period of CPB in children. The use of z-BUF was associated with reduced perioperative blood loss, time to extubation, and postoperative alveolar-arterial oxygen gradient, and suggest potential association between these events and reduction in plasma levels of proinflammatory mediators. Immediately after z-BUF, TNF alpha, C3a, and myeloperoxidase, a surrogate marker for neutrophil degranulation, were reduced; and, at 24 h, plasma levels of proinflammatory cytokines IL-1 beta and IL-6, the neutrophil chemoattractant IL-8, neutrophil counts, and myeloperoxidase levels also were decreased. Although this is a preliminary study in which an association is suggested, and although there are a number of limitations in this study's design, the findings are suggestive and potentially important.
Journois et al.'s 
finding of a significant reduction in time to extubation and postoperative alveolar-arterial oxygen gradient suggests diminished post-CPB pulmonary injury. Postoperative blood loss may have resulted from multiple factors, such as a direct or indirect effect on platelet function, a reduction in capillary leak typically induced by proinflammatory cytokines and complement, or inhibition in cytokine-induced coagulopathy and fibrinolysis. Inhibition of sustained and increased levels of cytokines may have blunted the typical central actions of cytokines that produce fever. 
However, three factors are important to consider:
1. A direct cause-and-effect relation between the measured inflammatory mediators and improvements in clinical endpoints cannot be proven;
2. Whether the broad removal of multiple inflammatory mediators is necessary for clinical benefit is unclear. Significant reductions in post-CPB pulmonary injury were demonstrated previously experimentally either with pharmacologic inhibition of complement 
or the use of a complement-deficient model. 
In addition, in previous studies, researchers suggested that mechanical removal of neutrophils alone may confer protection from postischemic injury. 
3. Neutrophils, cytokines, and other inflammatory mediators are necessary for wound healing and, because CPB is known to induce a state of immunosuppression, the indiscriminate removal of inflammatory mediators may be detrimental. For example, proinflammatory cytokines may play a beneficial role in preconditioning of ischemic tissues, 
and may confer protection from ischemic injury in certain patients.
An additional intriguing finding by Journois and colleagues is the elimination of IL-10 in the immediate post-CPB period. Interleukin-10 is a potent antiinflammatory cytokine that inhibits the release of TNF alpha and IL-8 by activated macrophages and neutrophils, which are induced during and after CPB. [11,12]
Accordingly, as Journois and colleagues acknowledge, the elimination of, or reduction in, cytokine levels may not a priori lead to desired antiinflammatory effects.
The data presented by Journois et al. suggest that the cumulative effect of mechanically removing inflammatory mediators during CPB by their ultrafiltration method may be clinically beneficial in pediatric cardiac surgery patients, and warrants further study. Understanding the inflammatory cascade during and after CPB will be important in forming the basis for new therapies and in designing rational clinical trials to definitively test the safety and efficacy of hemofiltration in the setting of CPB. If larger controlled studies confirm and expand on the beneficial clinical effects of hemofiltration, and continue to demonstrate that hemofiltration is safe, a positive impact on postcardiac surgical morbidity and mortality may result. From a cautionary perspective, it is important to note that modulation of the human immune response has always been difficult, and often dangerous. Therefore, future clinical trials likely will need to focus on a relatively homogeneous clinical population and contain rigorous measures of safety, before multicenter trials in the broad population are undertaken. Perhaps, though, cardiac surgery offers both a unique window into the workings of immune system and a unique opportunity to modulate it. Because the human immune system has only dealt with CPB for less than two generations, we may be able to create a more perfect balance between appropriate wound healing and a systemic immune response gone awry.
The authors thank the investigators at The Johns Hopkins Hospital involved in grant #P50-HL52315, entitled "SCOR in Ischemic Heart Disease," for their studies that elucidate the postischemic inflammatory response.
Ahvie Herskowitz, M.D., Director of Research, Ischemia Research and Education Foundation, 250 Executive Park Boulevard, Suite 3400, San Francisco, California 94134.
Dennis T. Mangano, Ph.D., M.D., Veterans Affairs Medical Center, San Francisco, California.
* Plunkett JJ, Reeves JD, Ngo L, Bellows W, Shafer SL, Roach G, Howse J, Leung JM, Herskowitz A, Mangano DT, McSPI Research Group: Endocrine stress response following myocardial myocardial revascularization: Modulation by continuous sedation with propofol. [Unpublished data.]
1. Mangano DT: Myocardial stunning: An overview. J Cardiac Surg 1993; 8:204-13.
2. Mangano DT: Perioperative cardiac morbidity. Anesthesiology 1990; 72:153-84.
3. Siliciano D, Mangano DT: Postoperative myocardial ischemia: Mechanisms and therapies, Opioids in Anesthesia. Edited by Estafanous FG. Boston, Butterworth Publishers, 1990, pp 164-77.
4. Hennein HA, Ebba H, Rodriguez JL, Merrick SH, Keith FM, Bronstein MH, Leung JM, Mangano DT, Greenfield LJ, Rankin JS: Relationship of the proinflammatory cytokines to myocardial ischemia and dysfunction after uncomplicated coronary revascularization. J Thorac Cardiovasc Surg 1994; 108:626-35.
5. Lefer DJ, Shandelya SM, Serrano CV JR, Becker LC, Kuppusamy P, Zweier JL: Cardioprotective actions of a monoclonal antibody CD-18 in myocardial ischemia-reperfusion. Circulation 1993; 88:1779-87.
6. von Asmuth EJ, Buurman WA: Endothelial cell associated platelet-activating factor (PAF), a costimulatory intermediate in TNF-alpha-induced H202 release by adherent neutrophil leukocytes. J Immunol 1995; 154:1383-90.
7. Herskowitz A, Choi S, Ansari AA, Wesselingh S: Cytokine mRNA expression in postischemic/reperfused myocardium. Am J Pathol 1995; 146:419-28.
8. Journois D, Ouard P, Greeley WJ, Mauriat P, Vouhe P, Safran D: Hemofiltration during cardiopulmonary bypass in pediatric cardiac surgery. Effects on hemostasis, cytokines and complement components. Anesthesiology 1994; 81:1181-9.
9. Gillinov AM, Redmond JM, Winkelstein JA, Zehr KJ, Herskowitz A, Cameron DE: Complement and neutrophil activation during cardiopulmonary bypass: A study in the complement-deficient dog. Ann Thorac Surg 1994; 57:345-52.
10. Wilson TC, Gardner TJ, DiNatale JM, Gillinov AM, Curtis WE, Cameron DE: Temporary leukocyte depletion reduces ventricular dysfunction during prolonged postischemic reperfusion. J Thorac Cardiovasc Surg 1993; 106:805-10.
11. Tabardel Y, Duchateau J, Schmartz D, Marecaux G, Shahla M, Barvais L, Leclerc JL, Vincent JL: Corticosteroids increase blood interleukin-10 levels during cardiopulmonary bypass in men. Surgery 1996; 19:76-80.
12. Seghaye M, Duchateau J, Bruniaux J, Demontox S, Bosson C, Serraf A, Lecronier G, Mokhfi E, Planche C: Interleukin-10 release related to cardiopulmonary bypass in infants undergoing cardiac operations. J Thorac Cardiovasc Surg 1996; 111:545-53.
13. Journois D, Israel-Biet D, Pouard P, Rolland B, Silvester W, Vouhe P, Safran D: High volume, zero-balanced hemofiltration to reduce delayed inflammatory response to cardiopulmonary bypass in children. Anesthesiology 1996; 85:965-76.
14. Stribjos PJ, Hardwick AJ, Relton JK, Carey F, Rothwell NJ: Inhibition of central actions of cytokines on fever and thermogenesis by lipocortin-1 involves CRF. Am J Physiol 1992; 263:E632-6.
15. Gillinov AM, DeValeria PA, Winkelstein JA, Ilson I, Curtis WE, Shaw D, Yeh CG, Rudolph AR, Baumgartner WA, Herskowitz A, Cameron DE: Complement inhibition with soluble complement receptor type 1 in cardiopulmonary bypass. Ann Thorac Surg 1993; 55:619-24.
16. Brown JM, White CW, Terada LS, Grosso MA, Shanley PF, Mulvin DW, Banerjee A, Whitman GJR, Harken AH, Repine JE: Interleukin 1 pretreatment decreases ischemia/reperfusion injury. Proc Natl Acad Sci U S A 1990; 87:5026-30.
This article has been cited 40 time(s).
American Journal of Physiology-Heart and Circulatory PhysiologyCompromised regulation of tissue perfusion and arteriogenesis limit, in an AT(1)R-independent fashion, recovery of ischemic tissue in Cx40(-/-) miceAmerican Journal of Physiology-Heart and Circulatory Physiology
Anesthesia and AnalgesiaThe ECLIPSE trials: Comparative studies of clevidipine to nitroglycerin, sodium nitroprusside, and nicardipine for acute hypertension treatment in cardiac surgery patientsAnesthesia and Analgesia
Nutrition in Clinical PracticeNutrition Risk Factors in Older Coronary Artery Bypass Graft PatientsNutrition in Clinical Practice
Anesthesia and Analgesia
Intraoperative cytokine release during coronary artery bypass grafting surgery
Anesthesia and Analgesia, 86(4):
Anesthesia and AnalgesiaThe hemodynamic effects of methylene blue when administered at the onset of cardiopulmonary bypassAnesthesia and Analgesia
Texas Heart Institute Journal
Peritoneal dialysis - An adjunct to pediatric postcardiotomy fluid management
Texas Heart Institute Journal, 24(4):
The effects of preoperative therapy with angiotensin-converting enzyme inhibitors on clinical outcome after cardiovascular surgery
Annals of Thoracic Surgery
Inhibition by dipyridamole of neutrophil adhesion to vascular endothelium during coronary bypass surgery
Annals of Thoracic Surgery, 67(5):
Anaesthesia Pain Intensive Care and Emergency Medicine - Apice 15
Fast track cardiac surgery - The Italian multicenter study on steroids in coronary bypass surgery
Anaesthesia Pain Intensive Care and Emergency Medicine - Apice 15, ():
StrokeLower endotoxin immunity predicts increased cognitive dysfunction in elderly patients after cardiac surgeryStroke
Journal of Cardiothoracic and Vascular Anesthesia
Con: The use of modified ultrafiltration during pediatric cardiovascular surgery is not a benefit
Journal of Cardiothoracic and Vascular Anesthesia, 12(4):
Anesthesia and AnalgesiaPulse pressure and risk of adverse outcome in coronary bypass surgeryAnesthesia and Analgesia
Canadian Journal of Anaesthesia-Journal Canadien D Anesthesie
Factors influencing MAC reduction after cardiopulmonary bypass in dogs
Canadian Journal of Anaesthesia-Journal Canadien D Anesthesie, 44():
Clinical and Experimental Immunology
Perioperative serum levels of tumour-necrosis-factor alpha (TNF-alpha), IL-1 beta, IL-6, IL-10 and soluble IL-2 receptor in patients undergoing cardiac surgery with cardiopulmonary bypass without and with correction for haemodilution
Clinical and Experimental Immunology, 118(2):
Annals of Thoracic Surgery
A Target for Perioperative Blood Pressure During Cardiac Operations
Annals of Thoracic Surgery, 89(2):
Blood levels of corticosteroid-binding globulin, total cortisol and unbound cortisol in patients undergoing coronary artery bypass grafting surgery with cardiopulmonary bypass
International Heart Journal
Single or double aortic clamping safer in terms of cerebral outcome during coronary bypass surgery?
International Heart Journal, 47(2):
Annals of Thoracic Surgery
Platelet-rich plasma harvest in redo CABG - Reply
Annals of Thoracic Surgery, 63(6):
Journal of Endocrinological Investigation
Persistent endocrine stress response in patients undergoing cardiac surgery
Journal of Endocrinological Investigation, 21(1):
Perfusion-UkInflammatory cytokines in pediatric cardiac surgery and variable effect of the hemofiltration processPerfusion-Uk
Journal of the American College of CardiologyGenetic variants in P-selectin and C-reactive protein influence susceptibility to cognitive decline after cardiac surgeryJournal of the American College of Cardiology
Journal of Thoracic and Cardiovascular SurgeryEfficacy and safety of the cyclooxygenase 2 inhibitors parecoxib and valdecoxib in patients undergoing coronary artery bypass surgeryJournal of Thoracic and Cardiovascular Surgery
Annals of Thoracic SurgeryBalancing the benefit and risk of oral antiplatelet agents in coronary artery bypass surgeryAnnals of Thoracic Surgery
Chinese Medical Journal
Postoperative neuropsychological change and its underlying mechanism in patients undergoing coronary artery bypass grafting
Chinese Medical Journal, 120():
Clinical and Experimental Immunology
Perioperative cytokine release during coronary artery bypass grafting in patients of different ages
Clinical and Experimental Immunology, 114(1):
Journal of Cardiothoracic and Vascular AnesthesiaPerturbations in laboratory values after coronary artery bypass graft surgery with cardiopulmonary bypassJournal of Cardiothoracic and Vascular Anesthesia
Journal of Cardiothoracic and Vascular AnesthesiaPerioperative beta-blockade and late cardiac outcomes: A complementary hypothesisJournal of Cardiothoracic and Vascular Anesthesia
Canadian Journal of Anaesthesia-Journal Canadien D Anesthesie
Ischaemia-reperfusion: time to increase our awareness during anaesthesia
Canadian Journal of Anaesthesia-Journal Canadien D Anesthesie, 45(3):
European Journal of Cardio-Thoracic Surgery
Neutrophil-endothelial cells modulation in diabetic patients undergoing coronary artery bypass grafting
European Journal of Cardio-Thoracic Surgery, 14(4):
Clinical and Experimental Immunology
Inter-individual differences in cytokine release in patients undergoing cardiac surgery with cardiopulmonary bypass
Clinical and Experimental Immunology, 125(1):
New England Journal of Medicine
Aspirin and mortality from coronary bypass surgery
New England Journal of Medicine, 347():
Acta Anaesthesiologica Scandinavica
No impact of a leucocyte depleting arterial line filter on patient recovery after cardiopulmonary bypass
Acta Anaesthesiologica Scandinavica, 45(5):
Heart and Vessels
Predictive risk factors for delayed extubation in patients undergoing coronary artery bypass grafting
Heart and Vessels, 15(5):
Acta Anaesthesiologica Scandinavica
Effects of a leucocyte depleting arterial line filter on perioperative proteolytic enzyme and oxygen free radical release in patients undergoing aortocoronary bypass surgery
Acta Anaesthesiologica Scandinavica, 43(4):
British Journal of Anaesthesia
Effects of hemodilution on cortisol and transcortin levels in patients undergoing cardiac surgery - preliminary results
British Journal of Anaesthesia, 82():
Interleukin-8 secretion following cardiopulmonary bypass in children as a marker of early postoperative morbidity
Paediatric Anaesthesia, 12(2):
Cardiopulmonary bypass. Complement. Chemokines. Cytokines. Endothelium. Leukocytes. Ultrafiltration.
© 1996 American Society of Anesthesiologists, Inc.
Publication of an advertisement in Anesthesiology Online does not constitute endorsement by the American Society of Anesthesiologists, Inc. or Lippincott Williams & Wilkins, Inc. of the product or service being advertised.