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Risk Factors for Klebsiella Infections among Hospitalized Patients with Preexisting Colonization

dc.contributor.authorRao, K
dc.contributor.authorPatel, A
dc.contributor.authorSun, Y
dc.contributor.authorVornhagen, J
dc.contributor.authorMotyka, J
dc.contributor.authorCollingwood, A
dc.contributor.authorTeodorescu, A
dc.contributor.authorBaang, JH
dc.contributor.authorZhao, L
dc.contributor.authorKaye, KS
dc.contributor.authorBachman, MA
dc.contributor.editorD’Orazio, Sarah EF
dc.coverage.spatialUnited States
dc.date.accessioned2022-08-26T19:22:39Z
dc.date.available2022-08-26T19:22:39Z
dc.date.issued2021-05-01
dc.identifier.issn2379-5042
dc.identifier.issn2379-5042
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/34160237
dc.identifier.urihttps://hdl.handle.net/2027.42/174137en
dc.description.abstractKlebsiella commonly colonizes the intestinal tract of hospitalized patients and is a leading cause of health care-associated infections. Colonization is associated with subsequent infection, but the factors determining this progression are unclear. A cohort study was performed, in which intensive care and hematology/oncology patients with Klebsiella colonization based on rectal swab culture were enrolled and monitored for infection for 90 days after a positive swab. Electronic medical records were analyzed for patient factors associated with subsequent infection, and variables of potential significance in a bivariable analysis were used to build a final multivariable model. Concordance between colonizing and infecting isolates was assessed by wzi capsular gene sequencing. Among 2,087 hospitalizations from 1,978 colonized patients, 90 cases of infection (4.3%) were identified. The mean time to infection was 20.6 6 24.69 (range, 0 to 91; median, 11.5) days. Of 86 typed cases, 68 unique wzi types were identified, and 69 cases (80.2%) were colonized with an isolate of the same type prior to infection. Based on multivariable modeling, overall comorbidities, depression, and low albumin levels at the time of rectal swab collection were independently associated with subsequent Klebsiella infection (i.e., cases). Despite the high diversity of colonizing strains of Klebsiella, there is high concordance with subsequent infecting isolates, and progression to infection is relatively quick. Readily accessible data from the medical record could be used by clinicians to identify colonized patients at an increased risk of subsequent Klebsiella infection.
dc.format.mediumPrint-Electronic
dc.languageeng
dc.publisherAmerican Society for Microbiology
dc.relation.haspartARTN e00500-21
dc.rightsLicence for published version: Creative Commons Attribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectKlebsiella
dc.subjectcohort study
dc.subjectinfection risk
dc.subjectintestinal colonization
dc.subjectmultivariable model
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectCohort Studies
dc.subjectComorbidity
dc.subjectDepression
dc.subjectFemale
dc.subjectHematologic Neoplasms
dc.subjectHumans
dc.subjectIntensive Care Units
dc.subjectKlebsiella Infections
dc.subjectKlebsiella pneumoniae
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectRectum
dc.subjectRisk Factors
dc.titleRisk Factors for Klebsiella Infections among Hospitalized Patients with Preexisting Colonization
dc.typeArticle
dc.identifier.pmid34160237
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/174137/2/Risk Factors for Klebsiella Infections among Hospitalized Patients with Preexisting Colonization.pdf
dc.identifier.doi10.1128/mSphere.00132-21
dc.identifier.doihttps://dx.doi.org/10.7302/5868
dc.identifier.sourcemSphere
dc.description.versionPublished version
dc.date.updated2022-08-26T19:22:37Z
dc.identifier.orcid0000-0002-9213-7850
dc.identifier.orcid0000-0002-5925-4289
dc.identifier.orcid0000-0003-2051-1732
dc.identifier.orcid0000-0003-2507-6987
dc.description.filedescriptionDescription of Risk Factors for Klebsiella Infections among Hospitalized Patients with Preexisting Colonization.pdf : Accepted version
dc.identifier.volume6
dc.identifier.issue3
dc.identifier.startpagee0013221
dc.identifier.name-orcidRao, K; 0000-0002-9213-7850
dc.identifier.name-orcidPatel, A
dc.identifier.name-orcidSun, Y
dc.identifier.name-orcidVornhagen, J
dc.identifier.name-orcidMotyka, J
dc.identifier.name-orcidCollingwood, A
dc.identifier.name-orcidTeodorescu, A
dc.identifier.name-orcidBaang, JH; 0000-0002-5925-4289
dc.identifier.name-orcidZhao, L
dc.identifier.name-orcidKaye, KS; 0000-0003-2051-1732
dc.identifier.name-orcidBachman, MA; 0000-0003-2507-6987
dc.working.doi10.7302/5868en
dc.owningcollnameInternal Medicine, Department of


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Licence for published version: Creative Commons Attribution 4.0 International
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