Cardiopulmonary bypass induced inflammation: pathophysiology and treatment. An update

Cardiac surgery with cardiopulmonary bypass (CPB) induces an acute phase reaction that has been implicated in the pathogenesis of several postoperative complications. Recent data indicate that a complex sequence of events leads to the final activation of leukocytes and endothelial cells (EC), which...

Full description

Saved in:
Bibliographic Details
Published inEuropean journal of cardio-thoracic surgery Vol. 21; no. 2; pp. 232 - 244
Main Authors Paparella, D., Yau, T.M., Young, E.
Format Journal Article
LanguageEnglish
Published Germany Elsevier Science B.V 01.02.2002
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cardiac surgery with cardiopulmonary bypass (CPB) induces an acute phase reaction that has been implicated in the pathogenesis of several postoperative complications. Recent data indicate that a complex sequence of events leads to the final activation of leukocytes and endothelial cells (EC), which is responsible for cell dysfunction in different organs. Activation of the contact system, endotoxemia, ischemia and reperfusion injury and surgical trauma are all potential triggers of inflammation following CPB. Different pro- and anti-inflammatory mediators (cytokines, adhesion molecules) are involved and their release is mediated by intracellular transcription factors (nuclear factor-kB, NF-kB). In this review, we examine recent advances in the understanding of the pathophysiology of the CPB-induced acute phase reaction and evaluate the different pharmacological, technical and surgical strategies used to reduce its effects. Emphasis is given to the central role of transcription factor NF-kB in the complex mechanism of the inflammatory reaction and to the effects of compounds such as heparin and glycosaminoglycans, phosphodiesterase inhibitors and protease inhibitors whose role as anti-inflammatory agent has only recently been recognized.
Bibliography:ark:/67375/HXZ-VN7XKX12-7
istex:3C67D8221934CE1A438F808F3C3E89E9A4B04985
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:1010-7940
1873-734X
DOI:10.1016/S1010-7940(01)01099-5