Abstract
Objectives: The objectives of this study were: (i) to describe an outbreak of multidrug-resistant Klebsiella pneumoniae in our population; (ii) to identify the potential source of this outbreak by examining antibiotic resistance trends in urocultures; (iii) to evaluate the contribution of this outbreak to resistance patterns over time in the two commonest Gram-negative blood culture isolates, namely K. pneumoniae and Escherichia coli; and (iv) to assess risk factors for multidrug resistance and the impact of this resistance on mortality and length of stay. Methods: We searched Microbiology and Patient Administration Service databases retrospectively and describe resistance trends in E. coli and K. pneumoniae bloodstream infections (BSIs) in Oxfordshire, UK, over an 11 year period. Results: An outbreak of a multidrug-resistant, CTX-M-15 extended-spectrum β-lactamase (ESBL)-producing K. pneumoniae clone was identified and shown by multilocus sequence typing to belong to a novel sequence type designated ST490. This was associated with a sporadic change in resistance rates in K. pneumoniae BSIs with rates of multidrug resistance (defined as resistance to three or more antibiotic classes) reaching 40% A case-control study showed prior antibiotic exposure as a risk factor for infection with this organism. During the same time period, rates of ESBL-producing Klebsiella spp. isolated from urocultures increased from 0.5% to almost 6%. By contrast, the rate of multidrug resistance in E. coli rose more steadily from 0% in 2000 to 10% in 2010. Conclusions: Changes in resistance rates may be associated with outbreaks of resistant clones in K. pneumoniae. Changing resistance patterns may affect important health economic issues such as length of stay.
| Original language | English |
|---|---|
| Article number | dkr246 |
| Pages (from-to) | 2126-2135 |
| Number of pages | 10 |
| Journal | Journal of Antimicrobial Chemotherapy |
| Volume | 66 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2011 |
Bibliographical note
Funding Information:D. P. W. is funded by an NIHR Clinical Lectureship. During the study B. Y., B. B. and I. C. J. W. B. were employees of Oxford Radcliffe NHS Trust and R. M. and D. C. were medical students at Oxford University engaged in project work. J. F. T., S M., D. M. L. and B. D. C. were employed by the HPA. P. B. is funded by the NIHR Biomedical Research Centre in Oxford.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- ESBLs
- MDR
- Multidrug resistance
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