Literature DB >> 2896731

The bacterial flora of neonates in intensive care-monitoring and manipulation.

D A Goldmann1.   

Abstract

Unlike healthy babies, newborns hospitalized in the neonatal intensive care unit (NICU) are colonized with bacterial flora that reflects their exposure to pathogens in the NICU, not bacterial acquired from mother in the perinatal period. For example, nosocomial Gram-negative bacilli, such as klebsiella, enterobacter, and citrobacter but not Escherichia coli tend to colonize the gastrointestinal tract. Colonization with Gram-negative bacilli generally is a prerequisite for nosocomial infection with these pathogens, but surveillance cultures may not be a cost effective approach to predicting which babies will ultimately become ill. However, screening cultures to detect the emergence of antibiotic-resistant Gram-negative bacilli facilitate containment and guide empiric antibiotic therapy, and surveillance cultures are necessary to detect colonized babies when nosocomial Gram-negative bacilli become epidemic in the NICU. Such cultures are inexpensive and easy to perform if appropriate selective media are used. Surveillance cultures to detect coagulase-negative staphylococci, which numerous investigators claim are increasingly important NICU pathogens, are of little value since colonization is virtually universal in the first week of life. Documentation of colonization with group B streptococci or Staphylococcus aureus also cannot be justified on a routine basis. Screening for methicillin-resistant S. aureus, however, may be indicated since early detection of these strains can limit dissemination in the NICU. Research aimed at restoring colonization resistance with elements of normal bacterial flora or preventing colonization by nosocomial pathogens is in its infancy.

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Year:  1988        PMID: 2896731     DOI: 10.1016/0195-6701(88)90209-5

Source DB:  PubMed          Journal:  J Hosp Infect        ISSN: 0195-6701            Impact factor:   3.926


  8 in total

1.  Importance of the environment and the faecal flora of infants, nursing staff and parents as sources of gram-negative bacteria colonizing newborns in three neonatal wards.

Authors:  B Fryklund; K Tullus; B Berglund; L G Burman
Journal:  Infection       Date:  1992 Sep-Oct       Impact factor: 3.553

2.  Factors influencing the presence of faecal lactobacilli in early infancy.

Authors:  M A Hall; C B Cole; S L Smith; R Fuller; C J Rolles
Journal:  Arch Dis Child       Date:  1990-02       Impact factor: 3.791

Review 3.  Pathogenesis of infections related to intravascular catheterization.

Authors:  D A Goldmann; G B Pier
Journal:  Clin Microbiol Rev       Date:  1993-04       Impact factor: 26.132

4.  Enteral feeding of premature infants with Lactobacillus GG.

Authors:  M R Millar; C Bacon; S L Smith; V Walker; M A Hall
Journal:  Arch Dis Child       Date:  1993-11       Impact factor: 3.791

5.  Carbohydrate fermentation by gut microflora in preterm neonates.

Authors:  V Walker; G A Mills; M A Hall; J A Lowes
Journal:  Arch Dis Child       Date:  1989-10       Impact factor: 3.791

6.  Similar Strains of Coagulase-Negative Staphylococci Found in the Gastrointestinal Tract and Bloodstream of Bacteremic Neonates.

Authors:  Jennifer O Adeghate; Emese Juhász; Miklós Á Iván; Júlia Pongrácz; Katalin Kristóf
Journal:  Can J Infect Dis Med Microbiol       Date:  2020-07-21       Impact factor: 2.471

Review 7.  Healthcare-associated infections in neonatal units: lessons from contrasting worlds.

Authors:  S Srivastava; N Shetty
Journal:  J Hosp Infect       Date:  2007-03-12       Impact factor: 3.926

Review 8.  Neonate Bloodstream Infections in Organization for Economic Cooperation and Development Countries: An Update on Epidemiology and Prevention.

Authors:  Jadwiga Wójkowska-Mach; Agnieszka Chmielarczyk; Magdalena Strus; Ryszard Lauterbach; Piotr Heczko
Journal:  J Clin Med       Date:  2019-10-21       Impact factor: 4.241

  8 in total

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