Publication:
Intestinal Colonization of Preterm Neonates with Carbapenem Resistant Enterobacteria at Hospital Discharge

dc.contributor.authorMijac, Vera (6507998440)
dc.contributor.authorBrkic, Snezana (57193991713)
dc.contributor.authorMilic, Marija (58539378400)
dc.contributor.authorSiljic, Marina (55428134900)
dc.contributor.authorCirkovic, Valentina (7102074128)
dc.contributor.authorPerovic, Vladimir (14054540500)
dc.contributor.authorMarkovic, Milos (7101935774)
dc.contributor.authorCirkovic, Ivana (16309091000)
dc.contributor.authorStanojevic, Maja (57828665700)
dc.date.accessioned2025-07-02T11:57:16Z
dc.date.available2025-07-02T11:57:16Z
dc.date.issued2023
dc.description.abstractOur aim was to investigate gut colonization with carbapenem-resistant Enterobacterales (CRE) in the population of preterm neonates at discharge from a tertiary care center in Serbia. The study included 350 randomly selected neonates/infants discharged in the period April 2018–May 2019. CRE colonization was present in 88/350 (25.1%) of patients. Klebsiella pneumoniae producing KPC and OXA-48 carbapenemase were detected in 45 and 42 subjects, respectively, while NDM producing Escherichia coli was identified in one patient only. All OXA-48 strains harbored blaCTX-M-15, while both blaTEM and blaSHV were present in all but one KPC-producing strain. CRE isolates exhibited a multidrug resistance pattern with uniform fluoroquinolone resistance, universal susceptibility to colistin, and variable susceptibility to aminoglycosides. Administration of carbapenems was common (~50%) and it was strongly associated with colonization, as well as the combinational therapeutic regimens that included meropenem, contrary to ampicillin–sulbactam/colistin therapy and prolonged course of the initial therapy (ampicillin/amikacin ≥ 7 days). Other risk factors for CRE carriage were level of immaturity, admission to neonatal intensive care unit, prolonged hospitalization and invasive procedures. Although the rate of clinically and/or laboratory proven systemic infections was significantly higher among colonized patients, CRE infection was confirmed in one patient only (1.1%) that was colonized with NDM E. coli. Clonal relatedness of CRE isolates was high, with seven and eight clusters detected among KPC (N = 30) and OXA-48 (N = 37) producing strains, respectively. The follow up of the 31 KPC-colonized patients after discharge from hospital revealed common decolonization within one month (~68%). In conclusion, our results demonstrated a high rate of CRE colonization that is most likely related to carbapenem consumption and lack of screening as important infection prevention practice. © 2023 by the authors.
dc.identifier.urihttps://doi.org/10.3390/antibiotics12020284
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85148856326&doi=10.3390%2fantibiotics12020284&partnerID=40&md5=a6329b9ff5815844150a9eff81d83634
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/11886
dc.subjectcarbapenem resistant Enterobacterales
dc.subjectcarbapenemases
dc.subjectcolonization
dc.subjectduration of carriage
dc.subjectpreterm neonates
dc.titleIntestinal Colonization of Preterm Neonates with Carbapenem Resistant Enterobacteria at Hospital Discharge
dspace.entity.typePublication

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