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Enterobacter cloacae sepsis outbreak in a newborn unit caused by contaminated total parenteral nutrition solution

Objective: The study aimed to investigate an outbreak caused by Enterobacter cloacae in a neonate intensive care unit. Design: A descriptive study of an outbreak of sepsis in high-risk neonates was used. Setting: The study was set in a tertiary care university teaching hospital. Patients: The patien...

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Bibliographic Details
Published in:American journal of infection control 2000-06, Vol.28 (3), p.258-261
Main Authors: Tresoldi, Antonia Teresinha, Padoveze, Maria Clara, Trabasso, Plínio, Veiga, Janice Ferreira Silva, Marba, Sergio Tadeu M., von Nowakonski, Angela, Branchini, Maria Luíza Moretti
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Language:English
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Summary:Objective: The study aimed to investigate an outbreak caused by Enterobacter cloacae in a neonate intensive care unit. Design: A descriptive study of an outbreak of sepsis in high-risk neonates was used. Setting: The study was set in a tertiary care university teaching hospital. Patients: The patients were 11 neonates infected with Enterobacter cloacae whose symptoms and signs of sepsis developed during a 16-hour period. All but one neonate received parenteral nutrition. Isolates from blood cultures, in-use parenteral nutrition solutions, and control aliquots of parenteral nutrition solution were typed by pulsed-field gel electrophoresis. Results:Enterobacter cloacae was found in the refrigerated aliquots of parenteral nutrition solution, in blood cultures from infected newborns, and from in-use parenteral nutrition solutions. All these strains of Enterobacter cloacae had the same antibiotic susceptibility pattern and the same genomic DNA profile. The strain isolated from the one patient who did not receive parenteral nutrition presented a different susceptibility profile and genotype. Conclusion: The source of the nosocomial sepsis was the parenteral nutrition solution in 10 neonates. This contamination apparently occurred during preparation of the parenteral solution. (AJIC Am J Infect Control 2000;28:258-61)
ISSN:0196-6553
1527-3296
DOI:10.1067/mic.2000.105286