Microbial translocation in neonates and infants receiving long-term parenteral nutrition
A. Pierro, H. K. van Saene, S. C. Donnell, J. Hughes, C. Ewan, A. J. Nunn and D. A. Lloyd
Department of Paediatric Surgery, Institute of Child Health, London, England.
OBJECTIVE: To explore whether episodes of endogenous septicemias due to
microbial translocation are clinically relevant in neonates and infants who
are receiving long-term parenteral nutrition (PN). DESIGN: Prospective
observational cohort study of 2 years. SETTING: Neonates and infants who
underwent surgical procedures and required PN because of gastrointestinal
abnormalities. MEASUREMENTS: Surveillance cultures of the oropharynx and
gut were obtained at the first of PN and thereafter twice each week. These
cultures were processed for all microorganisms, except for
coagulase-negative staphylococci, in a semiquantitative manner to detect
overgrowth. A blood sample was taken for culture from both the central
venous line and peripheral vein on clinical indication only. Microbial
translocation was diagnosed when the microorganisms that were isolated from
the blood sample were also carried in the throat and/or rectum within the 2
weeks preceding the episode of septicemia. MAIN RESULTS: Of 94 infants, 10
(11%) experienced 24 episodes of septicemia (ie, 7.3 septicemic episodes
per 1000 days of PN). Six infants experienced 15 episodes of microbial
translocation due to enteric microorganisms, including Escherichia coli,
Klebsiella, Candida species, and enterococci. Microbial translocation
occurred after a median of 58 days of PN (range, 32 to 286 days). The
enteric organisms that caused septicemia were always present in the throat
and/or rectum and in high concentrations ( > 10(5) colony-forming units
per gram [ie, overgrowth]) in 60% of the translocation episodes. All but
one episode occurred in infants with an abnormal serum bilirubin level (
> 17 mumol/L [0.99 mg/dl]). CONCLUSIONS: In neonates and infants who are
receiving PN, septicemia may be a gut-related phenomenon.
Detectable serum flagellin and lipopolysaccharide and upregulated anti-flagellin and lipopolysaccharide immunoglobulins in human short bowel syndrome
Ziegler et al.
Am. J. Physiol. Regul. Integr. Comp. Physiol. 2008;294:R402-R410.
ABSTRACT
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Kansagra et al.
Am. J. Physiol. Gastrointest. Liver Physiol. 2003;285:G1162-G1170.
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Deplancke et al.
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