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Clostridium difficile stool shedding in infants hospitalized in two neonatal intensive care units is lower than previous point prevalence estimates using molecular diagnostic methods.
Hines, Andrea Green; Freifeld, Alison; Zhao, Xing; Berry, Ann Anderson; Willett, Lynne; Iwen, Peter C; Simonsen, Kari A.
Afiliação
  • Hines AG; Adult Infectious Diseases, University of Nebraska Medical Center, Omaha, NE, USA.
  • Freifeld A; Pediatric Infectious Diseases, University of Nebraska Medical Center, Omaha, NE, USA.
  • Zhao X; Adult Infectious Diseases, University of Nebraska Medical Center, Omaha, NE, USA.
  • Berry AA; Pediatric Infectious Diseases, University of Nebraska Medical Center, Omaha, NE, USA.
  • Willett L; Neonatology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Iwen PC; Neonatology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Simonsen KA; Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
BMC Pediatr ; 18(1): 137, 2018 04 13.
Article em En | MEDLINE | ID: mdl-29653526
ABSTRACT

BACKGROUND:

The point prevalence of Clostridium difficile stool shedding in hospitalized infants from two neonatal intensive care units (NICUs) was examined utilizing standard clinical testing compared with duplex PCR to identify toxigenic and non-toxigenic C. difficile strains.

METHODS:

All infants from the two NICUs affiliated with a single academic medical center were eligible for inclusion. Stool collection was blinded to patient characteristics and occurred during a one week period at each NICU and repeated with a second weeklong collection 6 months later to increase sample size. Stools were tested for C. difficile using EIA (GDH/toxin A/B) with samples testing +/+ or +/- subsequently evaluated by Loop-Mediated Isothermal Amplification (LAMP) and by duplex PCR amplification of tcdB and tpi (housekeeping) genes. Cytotoxicity assays were performed on all samples positive for C. difficile by any modality.

RESULTS:

Eighty-four stools were collected from unique infants for evaluation. EIA results showed 6+/+ [7.1%], 7 +/- [8.3%], and 71 -/- [84.5%] samples. All 6 EIA +/+ were confirmed as toxigenic C. difficile by LAMP; 6/7 EIA +/- were negative by LAMP with one identified as invalid. Duplex PCR concurred with LAMP in all 6 stools positive for toxigenic C. difficile. PCR identified 2 EIA -/- stools positive for tpi, indicating shedding of non-toxigenic C. difficile. Cytotoxicity assay was positive in 4/6 duplex PCR positive samples and negative for all stools that were EIA +/- but negative by molecular testing.

CONCLUSIONS:

C. difficile blinded point prevalence in infants from two NICUs was 7.1% by molecular methods; and lower than expected based on historical incidence estimates. In house duplex PCR had excellent concordance with clinically available LAMP and EIA tests, and added detection of non-toxigenic C. difficile strain shedding. Evolving NICU care practices may be influencing the composition of infant gut microbiota and reducing the point prevalence of C. difficile shedding in NICU patient stools.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Unidades de Terapia Intensiva Neonatal / Clostridioides difficile / Infecções por Clostridium / Fezes Tipo de estudo: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: BMC Pediatr Assunto da revista: PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Unidades de Terapia Intensiva Neonatal / Clostridioides difficile / Infecções por Clostridium / Fezes Tipo de estudo: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: BMC Pediatr Assunto da revista: PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos