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Spread of Extended‐Spectrum β‐Lactamase–ProducingKlebsiella pneumoniae: Are β‐Lactamase Inhibitors of Therapeutic Value?
Author(s) -
Lionel Piroth,
Hervé Aube,
JeanMarc Doise,
M. Vincent-Martin
Publication year - 1998
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/514643
Subject(s) - klebsiella pneumoniae , medicine , odds ratio , risk factor , intensive care unit , antibiotics , klebsiella , microbiology and biotechnology , intensive care , intensive care medicine , biology , escherichia coli , biochemistry , gene
Because of recurrent colonization by Klebsiella pneumoniae strains producing type SHV-4 extended-spectrum beta-lactamases (ESBLs), a case-control study was conducted in an intensive care unit to investigate the risk of acquisition, with special reference to antibiotic therapy and resuscitation procedures. Fifty-one patients colonized or infected by ESBL-producing K. pneumoniae (cases) were matched with 51 noncolonized patients (controls). Duration of intubation was significantly longer for cases than for controls, while duration of beta-lactamase inhibitor therapy was significantly shorter. By means of multivariate analysis, intubation was the only risk factor identified (odds ratio [OR] = 1.19), while beta-lactamase inhibitor therapy was shown to be a protective factor (OR = 0.849). During outbreaks of SHV-4 type ESBL-producing K. pneumoniae in intensive care units, preferential use of beta-lactamase inhibitors may help control the emergence and spread of these pathogens even if essential hand washing and isolation procedures are adhered to.

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