Antimicrobial Resistance and Infection Control | |
Differences in risk-factor profiles between patients with ESBL-producing Escherichia coli and Klebsiella pneumoniae: a multicentre case-case comparison study | |
Joshua T Freeman3  Joseph Rubin4  Gary N McAuliffe1  Gisele Peirano4  Sally A Roberts3  Dragana Drinković2  Johann DD Pitout4  | |
[1] Department of Clinical Microbiology, Auckland District Health Board, Auckland City Hospital, Auckland, New Zealand | |
[2] Department of Clinical Microbiology, Waitemata District Health Board, Auckland, New Zealand | |
[3] Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand | |
[4] Division of Microbiology, Calgary Laboratory Services, Departments of Pathology & Laboratory Medicine, Microbiology Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada | |
关键词: Risk factors; Bacteraemia; Escherichia coli; Klebsiella pneumoniae; ESBL; | |
Others : 1084081 DOI : 10.1186/2047-2994-3-27 |
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received in 2014-01-23, accepted in 2014-08-08, 发布年份 2014 | |
【 摘 要 】
Background
Generic epidemiological differences between extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli (ESBL-EC) and Klebsiella pneumoniae (ESBL-KP), are poorly defined. Nonetheless, defining such differences and understanding their basis could have strategic implications for infection control policy and practice.
Methods
Between 2009 and 2011 patients with bacteraemia due to ESBL-EC or ESBL-KP across all three acute hospitals in the city of Auckland, New Zealand, were eligible for inclusion. Recognised risk factors for ESBL bacteraemia were compared between species in a retrospective case-case study design using multivariate logistic regression. Representative isolates underwent ESBL gene characterisation and molecular typing.
Results
170 patients and 176 isolates were included in the study (92 patients with ESBL-EC, 78 with ESBL-KP). 92.6% had CTX-Ms. 39% of EC were ST131 while 51% of KP belonged to 3 different STs (i.e. ST20, ST48 & ST1087). Specific sequence types were associated with specific hospitals for ESBL-KP but not ESBL-EC. Variables positively associated with ESBL-EC on multivariate analysis were: community acquired infection (odds ratio [OR] 7.9; 95% CI: 2.6-23.9); chronic pulmonary disease (OR 5.5; 95% CI: 1.5-20.1); and high prevalence country of origin (OR 4.3; 95% CI: 1.6-11.6). Variables negatively associated with ESBL-EC were previous transplant (OR 0.06; 95% CI: 0.007-0.6); Hospital 2 (OR 0.3; 95% CI: 0.1-0.7) and recent ICU admission (OR 0.3; 95% CI: 0.07-0.9).
Conclusions
Differences in risk profiles between patients with ESBL-EC and ESBL-KP suggest fundamental differences in transmission dynamics. Understanding the biological basis for these differences could have implications for infection control practice. Tailoring of infection control measures according to ESBL species may be indicated in some instances.
【 授权许可】
2014 Freeman et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
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20150113144249986.pdf | 210KB | download |
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