The effects of hypertonic fluid administration on the gene expression of inflammatory mediators in circulating leucocytes in patients with septic shock: a preliminary study
Objective This study was designed to investigate the effect of hypertonic fluid administration on inflammatory mediator gene expression in patients with septic shock. Design and setting Prospective, randomized, controlled, double-blind clinical study in a 15-bed mixed intensive care unit in a tertia...
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Veröffentlicht in: | Annals of intensive care 2011-11, Vol.1 (1), p.44-8, Article 44 |
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Sprache: | eng |
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Zusammenfassung: | Objective
This study was designed to investigate the effect of hypertonic fluid administration on inflammatory mediator gene expression in patients with septic shock.
Design and setting
Prospective, randomized, controlled, double-blind clinical study in a 15-bed mixed intensive care unit in a tertiary referral teaching hospital.
Interventions
Twenty-four patients, who met standard criteria for septic shock, were randomized to receive a bolus of hypertonic fluid (HT, 250 ml 6% HES/7.2% NaCl) or isotonic fluid (IT, 500 ml 6% HES/0.9% NaCl) administered over 15 minutes. Randomization and study fluid administration was within 24 hours of ICU admission for all patients. This trial is registered with ANZCTR.org.au as ACTRN12607000259448.
Results
Blood samples were taken immediately before and 4, 8, 12, and 24 hours after fluid administration. Real-time reverse transcriptase polymerase chain reaction (RT rtPCR) was used to quantify mRNA expression of different inflammatory mediators in peripheral leukocytes. In the HT group, compared with the IT group, levels of gene expression of MMP9 and L-selectin were significantly suppressed (
p
= 0.0002 and
p
= 0.007, respectively), and CD11b gene expression tended to be elevated (
p
= NS). No differences were found in the other mediators examined.
Conclusions
In septic shock patients, hypertonic fluid administration compared with isotonic fluid may modulate expression of genes that are implicated in leukocyte-endothelial interaction and capillary leakage.
The study was performed at the Intensive Care Department, Waikato Hospital, and at the Molecular Genetics Laboratory, University of Waikato, Hamilton, New Zealand.
Trial registration
Australia and New Zealand Clinical Trials Register (ANZCTR):
ACTRN12607000259448 |
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ISSN: | 2110-5820 2110-5820 |
DOI: | 10.1186/2110-5820-1-44 |