Cardiopulmonary bypass in man: Role of the intestine in a self-limiting inflammatory response with demonstrable bacterial translocation

被引:52
作者
Rossi, M
Sganga, G
Mazzone, M
Valenza, V
Guarneri, S
Portale, G
Carbone, L
Gatta, L
Pioli, C
Sanguinetti, M
Montalto, M
Glieca, F
Fadda, G
Schiavello, R
Silveri, NG
机构
[1] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Dept Anesthesia,ENEA,Sect Toxicol & Biomed, Unit Cardiac Anesthesia Surg & Med, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Dept Microbiol, I-00168 Rome, Italy
[3] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Dept Nucl Med, I-00168 Rome, Italy
[4] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Dept Cardiac Surg, I-00168 Rome, Italy
关键词
D O I
10.1016/S0003-4975(03)01520-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Cardiopulmonary bypass provokes a systemic inflammatory reaction that, in 1% to 2% of all cases, leads to multiorgan disfunction. The aim of this study was to evaluate the possible role of the intestine in the pathogenesis and development of this reaction. Methods. Eleven selected patients scheduled for elective coronary artery bypass graft surgery were enrolled in a open, prospective clinical study. Gastric tonometry, chromium-labeled test and double sugar intestinal absorption tests, polymerase chain reaction microbial DNA test, and measurement of cytokines and transcriptional factor (nuclear factor kappaB) activation were performed. Results. During the postoperative period, gastric pH remained stable (range, 7.2 to 7.3). The partial pressure for carbon dioxide gradient between the gastric mucosa and arterial blood increased significantly (from 1 to 23 mm Hg), peaking in the sixth postoperative hour. Interleukin 6 increased significantly over basal levels, peaking 3 hours after cardiopulmonary bypass (96.3 versus 24 pg/mL). Nuclear factor kappaB never reached levels higher than those observed after lipopolysaccharide stimulation. Escherichia coli translocation was documented in 10 patients: in eight cases from removal of aortic cross-clamps and in two cases from the first postoperative hour. With respect to basal value (6.4%), the urine collection revealed a significant increase in excretion of the radioisotope during the first 24 hours after surgery (39.1%), although there were no significant variations with the double sugar test. Conclusions. The results obtained showed a correlation between the damage of the gastrointestinal mucosa, subsequent increased permeability, E coli bacteremia, and the activation of a self-limited inflammatory response in the absence of significant macrocirculatory changes and postoperative complications. (C) 2004 by The Society of Thoracic Surgeons.
引用
收藏
页码:612 / 618
页数:7
相关论文
共 25 条
[1]   ASSOCIATION BETWEEN GASTRIC INTRAMUCOSAL PH AND SPLANCHNIC ENDOTOXIN, ANTIBODY TO ENDOTOXIN, AND TUMOR-NECROSIS-FACTOR-ALPHA CONCENTRATIONS IN PATIENTS UNDERGOING CARDIOPULMONARY BYPASS [J].
ANDERSEN, LW ;
LANDOW, L ;
BAEK, L ;
JANSEN, E ;
BAKER, S .
CRITICAL CARE MEDICINE, 1993, 21 (02) :210-217
[2]   Schemes against ischemia; solutions for reperfusion (injury)? [J].
Barie, PS .
CRITICAL CARE MEDICINE, 1999, 27 (04) :684-685
[3]   Automated detection of gastric luminal partial pressure of carbon dioxide during cardiovascular surgery using the Tonocap [J].
Bennett-Guerrero, E ;
Panah, MH ;
Bodian, CA ;
Methikalam, BJ ;
Alfarone, JR ;
DePerio, M ;
Mythen, MG .
ANESTHESIOLOGY, 2000, 92 (01) :38-45
[4]  
BJARNASON I, 1983, LANCET, V1, P323
[5]   Sir Isaac Newton, sepsis, SIRS, and CARS [J].
Bone, RC .
CRITICAL CARE MEDICINE, 1996, 24 (07) :1125-1128
[6]   MULTIPLE ORGAN FAILURE - PATHOPHYSIOLOGY AND POTENTIAL FUTURE THERAPY [J].
DEITCH, EA .
ANNALS OF SURGERY, 1992, 216 (02) :117-134
[7]   Inflammatory response to cardiopulmonary bypass [J].
Edmunds, LH .
ANNALS OF THORACIC SURGERY, 1998, 66 (05) :S12-S16
[8]   EVALUATION OF MANNITOL, LACTULOSE AND CR-51 LABELED ETHYLENEDIAMINETETRA-ACETATE AS MARKERS OF INTESTINAL PERMEABILITY IN MAN [J].
ELIA, M ;
BEHRENS, R ;
NORTHROP, C ;
WRAIGHT, P ;
NEALE, G .
CLINICAL SCIENCE, 1987, 73 (02) :197-204
[9]  
FELTIS BA, 2000, CURR OPIN CRIT CARE, V6, P117
[10]   Mechanisms of disease: Acute-phase proteins and other systemic responses to inflammation [J].
Gabay, C ;
Kushner, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (06) :448-454