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The Annals of Thoracic Surgery, Vol 55, 389-394, Copyright © 1993 by The Society of Thoracic Surgeons
A Markewitz, E Faist, S Lang, S Endres, L Hultner and B Reichart
The object of this prospective, randomized trial was to study the
dysregulation effects of cardiopulmonary bypass on the synthesis pattern of
interleukin-1, tumor necrosis factor, and interleukin-6, which have been
identified as the key mediators of acute phase response. In addition, the
counterregulation achieved by administration of indomethacin, which blocks
the downregulating mediator prostaglandin E2, or indomethacin combined with
thymopentin, which enhances T- lymphocytic reactivity, was investigated.
Sixty patients who had undergone open heart operations were included in the
study. These patients were divided into three groups: group A (n = 20)
received both indomethacin and thymopentin, and group C (n = 20) served as
control. In control patients interleukin-1 and tumor necrosis factor
synthesis were suppressed postoperatively. This effect was significantly
counteracted by indomethacin with no further improvement by adding
thymopentin. Interleukin-6 synthesis increased in all groups. Although
indomethacin treatment alone had little effect on this phenomenon,
additional administration of thymopentin significantly reduced elevated
interleukin-6 synthesis. Corresponding differences in clinical outcome
could not be detected due to small patient numbers. This study was,
however, able to demonstrate that an immunomodulatory therapy can influence
alterations in immune mechanisms after cardiopulmonary bypass.
ARTICLES
Regulation of acute phase response after cardiopulmonary bypass by immunomodulation
Department of Cardiac Surgery, University of Munich, Germany.
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