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This article is part of the supplement: International Symposium on the Pathophysiology of Cardiopulmonary Bypass

Meeting abstract

Nerve growth factor levels rise following cardiopulmonary bypass in children: a novel mediator in the systemic inflammatory response syndrome?

M Codispoti, K Sedowofia, R Pandey, N McIntosh and PS Mankad

Department of Cardiac Surgery, Royal Hospital for Sick Children, Sciennes Road, Edinburgh EH9 1LF, UK

from International Symposium on the Pathophysiology of Cardiopulmonary Bypass
Aachen, Germany. 12 December 1998

Critical Care 1999, 3(Suppl A):P12doi:10.1186/cc323

Published: 2 March 1999

© 1999 Current Science Ltd

Objectives

Nerve growth factor (NGF) plays a crucial role in the differentiation and survival of sympathetic neurones, including the ones represented in the cardiovascular system. NGF has also been reported to be an intermediary product in various inflammatory reactions. The aim of this study was to investigate whether cardiopulmonary bypass (CPB) has any effects on NGF release and to determine the time course of any changes in its release.

Methods

Twelve consecutive children undergoing elective cardiac surgery were recruited for the purposes of this study. The plasma levels of NGF, interleukin 6 (IL-6) and interleukin-8 (IL-8) were measured by enzyme-linked immunosorbent assay (ELISA). Samples were obtained from the patients at the following time points: induction of anaesthesia, end of CPB, and at 1, 2 and 24h following CPB.

Results

There was a highly significant increase in the release of NGF following CPB, reaching its highest concentration at 2 h following CPB. The pattern of release was very similar to that observed for IL-6 and IL-8. The results are summarised in the Table.

Conclusions

NGF is released following CPB in paediatric patients, with a similar pattern to the one observed for known mediators of the systemic inflammatory response to CPB. Further studies, both in paediatric and adult patients, are needed to elucidate the role of NGF in the pathophysiology of the body response to CPB and to evaluate its clinical impact.

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