Modifiable Risk Factors for the Spread of Klebsiella pneumoniae Carbapenemase-Producing Enterobacteriaceae Among Long-Term Acute-Care Hospital Patients
Supporting Files
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6 2017
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File Language:
English
Details
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Alternative Title:Infect Control Hosp Epidemiol
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Personal Author:
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Corporate Authors:
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Description:Objective.
To identify modifiable risk factors for acquisition of Klebsiella pneumoniae carbapenemase-producing Enterobacteriaceae (KPC) colonization among long-term acute-care hospital (LTACH) patients.
Design.
Multicenter, matched case-control study.
Setting.
Four LTACHs in Chicago, Illinois.
Participants.
Each case patient included in this study had a KPC-negative rectal surveillance culture on admission followed by a KPC-positive surveillance culture later in the hospital stay. Each matched control patient had a KPC-negative rectal surveillance culture on admission and no KPC isolated during the hospital stay.
Results.
From June 2012 to June 2013, 2,575 patients were admitted to 4 LTACHs; 217 of 2,144 KPC-negative patients (10.1%) acquired KPC. In total, 100 of these patients were selected at random and matched to 100 controls by LTACH facility, admission date, and censored length of stay. Acquisitions occurred a median of 16.5 days after admission. On multivariate analysis, we found that exposure to higher colonization pressure (OR, 1.02; 95% CI, 1.01–1.04; P = .002), exposure to a carbapenem (OR, 2.25; 95% CI, 1.06–4.77; P = .04), and higher Charlson comorbidity index (OR, 1.14; 95% CI, 1.01–1.29; P = .04) were independent risk factors for KPC acquisition; the odds of KPC acquisition increased by 2% for each 1% increase in colonization pressure.
Conclusions.
Higher colonization pressure, exposure to carbapenems, and a higher Charlson comorbidity index independently increased the odds of KPC acquisition among LTACH patients. Reducing colonization pressure (through separation of KPC-positive patients from KPC-negative patients using strict cohorts or private rooms) and reducing carbapenem exposure may prevent KPC cross transmission in this high-risk patient population.
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Subjects:
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Source:Infect Control Hosp Epidemiol. 38(6):670-677
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Pubmed ID:28397615
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Pubmed Central ID:PMC8381232
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Document Type:
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Funding:
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Volume:38
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Issue:6
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Collection(s):
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Main Document Checksum:urn:sha256:1de88779db6901b404b04e42514c4093044c09365a7d54105a413e3109a5932a
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Download URL:
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File Type:
Supporting Files
File Language:
English
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