Journal Article

An Outbreak of Infection due to β-Lactamase <i>Klebsiella pneumoniae</i> Carbapenemase 2–Producing <i>K. pneumoniae</i> in a Greek University Hospital: Molecular Characterization, Epidemiology, and Outcomes

Maria Souli, Irene Galani, Anastasia Antoniadou, Evangelos Papadomichelakis, Garyphallia Poulakou, Theofano Panagea, Sofia Vourli, Loukia Zerva, Apostolos Armaganidis, Kyriaki Kanellakopoulou and Helen Giamarellou

in Clinical Infectious Diseases

Published on behalf of Infectious Diseases Society of America

Volume 50, issue 3, pages 364-373
Published in print February 2010 | ISSN: 1058-4838
Published online February 2010 | e-ISSN: 1537-6591 | DOI: http://dx.doi.org/10.1086/649865
An Outbreak of Infection due to β-Lactamase Klebsiella pneumoniae Carbapenemase 2–Producing K. pneumoniae in a Greek University Hospital: Molecular Characterization, Epidemiology, and Outcomes

More Like This

Show all results sharing these subjects:

  • Infectious Diseases
  • Immunology
  • Public Health and Epidemiology
  • Microbiology

GO

Show Summary Details

Preview

Background. We describe the emergence and spread of Klebsiella pneumoniae carbapenemase 2 (KPC-2)–producing K. pneumoniae at a Greek University hospital.

Methods. Isolates with a carbapenem minimum inhibitory concentration >1 µg/mL and a negative EDTA-imipenem disk synergy test result were submitted to boronic acid disk test and to polymerase chain reaction (PCR) for KPC gene and sequencing. Records from patients who had KPC-2–producing K. pneumoniae isolated were retrospectively reviewed. Clinical isolates were submitted to molecular typing using pulsed-field gel electrophoresis, and the β-lactamase content was studied using isoelectric focusing and PCR.

Results. From January 2007 through December 2008, 50 patients (34 in the intensive care unit [ICU]) were colonized (n=32) or infected (n=18) by KPC-2–producing K. pneumoniae. Increasing prevalence of KPC-2–producing K. pneumoniae coincided with decreasing prevalence of metallo-β lactamase–producing isolates in our ICU. Multidrug resistance characterized the studied isolates, with colistin, gentamicin, and fosfomycin being the most active agents. Besides KPC-2, clinical isolates encoded TEM-1-like, SHV-11, SHV-12, CTX-M–15, and LEN-19 enzymes. Four different clonal types were detected; the predominant one comprised 41 single patient isolates (82%). Sporadic multiclonal cases of KPC-2–producing K. pneumoniae infection were identified from September 2007 through May 2008. The outbreak strain was introduced in February 2008 and disseminated rapidly by cross-transmission; 38 patients (76%) were identified after August 2008. Fourteen cases of bacteremia, 2 surgical site infections, 2 lower respiratory tract infections (1 bacteremic), and 1 urinary tract infection were identified. Most patients received a colistin-containing combination treatment. Crude mortality was 58.8% among ICU patients and 37.5% among non-ICU patients, but attributable mortality was 22.2% and 33.3%, respectively.

Conclusions. The emergence of KPC-2–producing K. pneumoniae in Greek hospitals creates an important challenge for clinicians and hospital epidemiologists, because it is added to the already high burden of antimicrobial resistance.

Journal Article.  4381 words.  Illustrated.

Subjects: Infectious Diseases ; Immunology ; Public Health and Epidemiology ; Microbiology

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.