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The rate of bloodstream infection is high in infants with short bowel syndrome: relationship with small bowel bacterial overgrowth, enteral feeding, and inflammatory and immune responses.
Cole, Conrad R; Frem, Juliana C; Schmotzer, Brian; Gewirtz, Andrew T; Meddings, Jonathan B; Gold, Benjamin D; Ziegler, Thomas R.
Afiliación
  • Cole CR; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA. Electronic address: crcole@emory.edu.
  • Frem JC; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR.
  • Schmotzer B; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.
  • Gewirtz AT; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA.
  • Meddings JB; Department of Medicine, University of Alberta, Edmonton, Canada.
  • Gold BD; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Ziegler TR; Department of Medicine, Emory University School of Medicine, Atlanta, GA.
J Pediatr ; 156(6): 941-947.e1, 2010 Jun.
Article en En | MEDLINE | ID: mdl-20171649
ABSTRACT

OBJECTIVE:

This pilot study in parenteral nutrition-dependent infants with short bowel syndrome (SBS) evaluated the impact of feeding route and intestinal permeability on bloodstream infection (BSI), small bowel bacterial overgrowth (SBBO), and systemic immune responses, as well as fecal calprotectin as a biomarker for SBBO. STUDY

DESIGN:

Ten infants (ages 4.2-15.4 months) with SBS caused by necrotizing enterocolitis were evaluated. Nutritional assessment, breath hydrogen testing, intestinal permeability, fecal calprotectin, serum flagellin- and lipopolysaccharide-specific antibody titers, and proinflammatory cytokine concentrations (tumor necrosis factor-alpha [TNF-alpha], interleukin-1 beta, -6, and -8) were performed at baseline and at 60 and 120 days. Healthy, age-matched control subjects (n = 5) were recruited.

RESULTS:

BSI incidence was high (80%), and SBBO was common (50%). SBBO increased the odds for BSI (>7-fold; P = .009). Calprotectin levels were higher in children with SBS and SBBO versus those without SBBO and healthy control subjects (P < .05). Serum TNF-alpha, was elevated at baseline versus controls. Serum TNF-alpha and interleukin-1 beta, -6, and -8 levels diminished with increased enteral nutrition. Anti-flagellin and anti-lipopolysaccharide immunoglobulin G levels in children with SBS were lower versus control subjects and rose over time.

CONCLUSION:

In children with SBS, SBBO increases the risk for BSI, and systemic proinflammatory response decreases with increasing enteral feeding and weaning parenteral nutrition.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Intestino Corto / Sepsis / Intestino Delgado Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Año: 2010 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Intestino Corto / Sepsis / Intestino Delgado Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Año: 2010 Tipo del documento: Article