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BMJ 2017;356:j254 doi: 10.1136/bmj.

j254 (Published 16 January 2017) Page 1 of 2

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Woman dies after infection with bacteria resistant to


all antibiotics available in US
Michael McCarthy
Seattle

A woman in the US died of septic shock last year after becoming approximately 80% remained susceptible to at least one
infected with carbapenem resistant Enterobacteriaceae (CRE) aminoglycoside and nearly 90% were susceptible to tigecycline,”
that were resistant to all antimicrobial drugs available in the they wrote.
US. In this case the isolate had a relatively low fosfomycin MIC of
The bacterium, a Klebsiella pneumoniae, was found to be 16 micrograms/mL, but, although intravenous fosfomycin is
resistant to 26 antibiotics, including all aminoglycosides and available in some other countries including the UK, it is
polymyxins tested, and intermediately resistant to tigecycline. approved in the US only as an oral treatment for uncomplicated
The case was described in the 13 January issue of the US Centers cystitis.
for Disease Control and Prevention’s (CDC) Morbidity and After CRE infection was identified the patient was placed in a
Mortality Weekly Report.1 It involved a woman in her 70s living single room under contact precautions. Testing of patients
in Washoe County, Nevada, who had lived in India for an currently admitted to the same unit where she was treated has
extended period. In the previous two years she had been not detected additional CRE; nor has ongoing surveillance in
repeatedly admitted to hospital in India after fracturing her right Washoe County, which was initiated in 2010.
femur and subsequently developing osteomyelitis of the right Paul Hoskisson, of the University of Strathclyde in Glasgow,
femur and hip. Her last admission in India was in June 2016. Scotland, said that the case report highlighted the importance
She returned to the US in early August and was admitted to of infection control measures, such as testing drug susceptibility,
hospital on 19 August with a diagnosis of systemic inflammatory isolation of infected patients, and knowledge of a patient’s
response syndrome thought to be due to an infected right hip medical history. “Drug resistant infections are a global problem,
seroma. She developed septic shock and died in early September. and the movement of people around the world can lead to the
After CRE had been detected an isolate was sent to the CDC, dissemination of drug resistant bacteria,” he said.
where the presence of New Delhi metallo-β-lactamase (NDM)
was confirmed. NDM is an enzyme that confers resistance to a bmj.com Clinical Review: Antibiotic resistance in Enterobacteriaceae:
broad range of β-lactam antibiotics, including those of the mechanisms and clinical implications (BMJ 2016;352:h6420, doi:10.
carbapenem family. The strain was first identified in 2009 in a 1136/bmj.h6420)
Swedish patient of Indian origin who had developed a urinary
1 Chen L, Todd R, Kiehlbauch J, Walters M, Kallen A. Notes from the field: pan-resistant
tract infection while travelling in New Delhi, India.2 New Delhi metallo-beta-lactamase-producing Klebsiella pneumoniae—Washoe County,
Because the isolate in the Nevada case had a high minimum Nevada, 2016. MMWR Morb Mortal Wkly Rep 2017;66:33.
doi:10.15585/mmwr.mm6601a7.28081065
inhibitory concentration (MIC) to colistin, the isolate was also 2 Yong D, Toleman MA, Giske CG. Characterization of a new metallo-beta-lactamase gene,
tested for the mcr-1 gene, which confers plasma mediated bla(NDM-1), and a novel erythromycin esterase gene carried on a unique genetic structure
in Klebsiella pneumoniae sequence type 14 from India. Antimicrob Agents Chemother
resistance to colistin, but the results were negative. 2009;53:5046-54. doi:10.1128/AAC.00774-09.19770275
The report’s authors noted that CRE isolates tested by CDC are Published by the BMJ Publishing Group Limited. For permission to use (where not already
rarely resistant to all antimicrobials: “Among >250 CRE isolate granted under a licence) please go to http://group.bmj.com/group/rights-licensing/
permissions
reports collected as part of the Emerging Infections Program,

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BMJ 2017;356:j254 doi: 10.1136/bmj.j254 (Published 16 January 2017) Page 2 of 2

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[Image: Branden Camp/PA]

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