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Published on: January 7, 2019
Carbapenemase-producing Klebsiella pneumoniae
Elizabeth Robilotti1, Stan Deresinski1
1Department of Medicine, Division of Infectious Diseases, Stanford University School of Medicine 300 Pasteur Drive, Stanford, CA 94305 USA.
Abstract:
The continuing emergence of infections due to multidrug resistant bacteria is a serious public health problem. Klebsiella pneumoniae, which commonly acquires resistance encoded on mobile genetic elements, including ones that encode carbapenemases, is a prime example. K. pneumoniae carrying such genetic material, including both blaKPC and genes encoding metallo-β-lactamases, have spread globally. Many carbapenemase-producing K. pneumoniae are resistant to multiple antibiotic classes beyond β-lactams, including tetracyclines, aminoglycosides, and fluoroquinolones. The optimal treatment, if any, for infections due to these organisms is unclear but, paradoxically, appears to often require the inclusion of an optimally administered carbapenem.
Insights
Multidrug resistant bacteria, like Klebsiella pneumoniae, pose a significant public health threat. Infections caused by carbapenemase-producing K. pneumoniae may paradoxically require carbapenem antibiotics for optimal treatment.
Area of Science:
- Microbiology
- Infectious Diseases
- Public Health
Background:
- Emergence of multidrug resistant (MDR) bacteria is a global public health crisis.
- Klebsiella pneumoniae is a key pathogen, frequently acquiring resistance via mobile genetic elements.
- Carbapenemase-producing K. pneumoniae strains have spread worldwide.
Purpose of the Study:
- To highlight the challenge of treating infections caused by MDR Klebsiella pneumoniae.
- To discuss the complex resistance mechanisms and treatment strategies for carbapenemase-producing K. pneumoniae.
Main Methods:
- Review of current literature on multidrug resistant Klebsiella pneumoniae.
- Analysis of resistance mechanisms, including carbapenemase genes (blaKPC, metallo-β-lactamases).
- Examination of antibiotic resistance profiles beyond beta-lactams (tetracyclines, aminoglycosides, fluoroquinolones).
Main Results:
- Klebsiella pneumoniae frequently harbors genes for carbapenemases on mobile genetic elements.
- These strains exhibit resistance to multiple antibiotic classes.
- Optimal treatment for these infections remains challenging and may paradoxically involve carbapenems.
Conclusions:
- Carbapenemase-producing Klebsiella pneumoniae represents a critical threat due to extensive antibiotic resistance.
- Treatment strategies require careful consideration, potentially including carbapenems.
- Further research is needed to establish definitive optimal therapies.
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