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The Annals of Thoracic Surgery, Vol 57, 376-382, Copyright © 1994 by The Society of Thoracic Surgeons
DP Taggart, S Sundaram, C McCartney, A Bowman, H McIntyre, JM Courtney and DJ Wheatley
Endotoxin activates complement and white blood cells and all are implicated
in the pathologic effects of cardiopulmonary bypass (CPB). We investigated
if reduction in intestinal bacterial load with a laxative and/or pulsatile
perfusion to improve bowel circulation during CPB reduced endotoxemia and
complement and white blood cell activation. Sixty patients were randomized
to four groups in a 2 x 2 factorial structure: group 1 (no laxative,
nonpulsatile perfusion); group 2 (laxative, nonpulsatile perfusion); group
3 (no laxative, pulsatile perfusion); and group 4 (laxative, pulsatile
perfusion). Plasma concentrations of endotoxin, C3a and C5a, and
granulocyte elastase (GE) were measured before anesthesia, skin incision,
and heparin administration; during CPB (1, 30, 60, 90, and 120 minutes and
after protamine administration); and after CPB at 3, 6, 12, 24, and 48
hours and 7 days. In all groups there was a small increase in the
concentration of endotoxin (overall from 6 ng/L before CPB to 11 ng/L at 90
to 120 minutes; p < 0.001) and significant increases in C3a, C5a, and GE
levels but no significant differences among the groups. Endotoxin levels
did not correlate with activation of complement or white blood cells. There
was a weak correlation between duration of CPB and levels of C3a (r = 0.14;
p < 0.03) and GE (r = 0.25; p = 0.001) but not endotoxin or C5a. There
was a general correlation between levels of C3a and GE but not in
individual patients. In conclusion, CPB results in statistically
significant increases in endotoxin, C3a, C5a, and GE during CPB.(ABSTRACT
TRUNCATED AT 250 WORDS)
ARTICLES
Endotoxemia, complement, and white blood cell activation in cardiac surgery: a randomized trial of laxatives and pulsatile perfusion
Department of Cardiac Surgery, Royal Infirmary Glasgow, United Kingdom.
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