| Literature DB >> 30076041 |
Matthaios Papadimitriou-Olivgeris1, Christina Bartzavali2, Aikaterini Spyropoulou2, Anastasia Lambropoulou2, Nektarios Sioulas3, Sophia Vamvakopoulou2, Georgios Karpetas3, Iris Spiliopoulou2, Theofanis Vrettos3, Evangelos D Anastassiou2, Fotini Fligou3, Myrto Christofidou2, Markos Marangos4.
Abstract
A matched 1:2 case-control study was conducted among critically ill patients in order to identify the risk factors of colistin or tigecycline-resistant carbapenemase-producing Klebsiella pneumoniae (ColR-Kp, TigR-Kp) bacteraemia. MIC to colistin and tigecycline were determined by Etest. From 224 bacteraemic patients, 46.4% and 29.5% were resistant to colistin and tigecycline, respectively. PCR revealed that 199 isolates carried the blaKPC gene. PCR revealed that no isolate carried the mcr-1 gene. Risk factors for ColR-Kp bacteraemia as compared to patients with bacteraemia by a colistin-susceptible isolate or patients without carbapenemase-producing K. pneumoniae bacteraemia were colistin or tigecycline administration and tracheostomy, while TigR-Kp bacteraemia as compared to either patients with bacteraemia by tigecycline-susceptible isolate or patients without carbapenemase-producing K. pneumoniae bacteraemia were colistin or tigecycline administration, number of comorbidities and prior bacteraemia by a Gram-negative pathogen. Administration of colistin and tigecycline predisposed to development of bacteraemia by either ColR-Kp or TigR-Kp.Entities:
Keywords: Intensive care unit; KPC; Mcr-1; NDM; PFGE; Resistance epidemiology
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Year: 2018 PMID: 30076041 DOI: 10.1016/j.diagmicrobio.2018.06.001
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803