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Control of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae using a computer-assisted management program to restrict third-generation cephalosporin use

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dc.contributor.authorKim, Jeong Yeon-
dc.contributor.authorSohn, Jang Wook-
dc.contributor.authorPark, Dae Won-
dc.contributor.authorYoon, Young Kyung-
dc.contributor.authorKim, Young Mi-
dc.contributor.authorKim, Min Ja-
dc.date.accessioned2021-09-09T05:43:31Z-
dc.date.available2021-09-09T05:43:31Z-
dc.date.created2021-06-10-
dc.date.issued2008-08-
dc.identifier.issn0305-7453-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/122954-
dc.description.abstractObjectives: The aim of this study was to evaluate the control of extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae and antimicrobial resistance through a computerized antibiotic control program. Methods: An ambidirectional intervention study was conducted at a 750-bed university hospital in Korea from February 2004 to April 2006. In November 2004, hospital-wide restriction of third-generation cephalosporin use was integrated into a pre-existing computerized antibiotic prescription program that included an approval system for 15 antimicrobials. The proportions of ESBL-producing K. pneumoniae and other multidrug-resistant clinical isolates were compared during three phases (9 months per phase): Phase I (pre-intervention), Phase II (intensive-intervention) and Phase III (maintenance). Results: Third-generation cephalosporin use decreased significantly from 103.2 to 84.9 antibiotic use density (AUD, defined daily dose/1000 patient-days) between Phase I and Phase II (P < 0.05), whereas use of carbapenems and beta-lactam/beta-lactamase inhibitors increased from 14.5 to 18.2 AUD and from 53.3 to 62.6 AUD, respectively. The proportion of ESBL-producing K. pneumoniae isolates increased significantly from 8.1% (47/578) in Phase I to 32.0% (188/587) in Phase II, and then decreased significantly to 20.6% (97/470) in Phase III (P < 0.05). In addition, the proportions of imipenem- or piperacillin/tazobactam-resistant Pseudomonas aeruginosa and Acinetobacter baumannii isolates decreased significantly over the same period (P < 0.05). Conclusions: The computerized antibiotic control program appears to be an effective tool for modifying antibiotic consumption, which may in turn prevent the spread of resistant pathogens.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherOXFORD UNIV PRESS-
dc.subjectINTENSIVE-CARE-UNIT-
dc.subjectRISK-FACTORS-
dc.subjectINFECTION-CONTROL-
dc.subjectESCHERICHIA-COLI-
dc.subjectTIME-SERIES-
dc.subjectRESISTANCE-
dc.subjectOUTBREAK-
dc.subjectCOLONIZATION-
dc.subjectIMPACT-
dc.subjectINTERVENTION-
dc.titleControl of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae using a computer-assisted management program to restrict third-generation cephalosporin use-
dc.typeArticle-
dc.contributor.affiliatedAuthorSohn, Jang Wook-
dc.contributor.affiliatedAuthorPark, Dae Won-
dc.contributor.affiliatedAuthorKim, Min Ja-
dc.identifier.doi10.1093/jac/dkn164-
dc.identifier.scopusid2-s2.0-47249156875-
dc.identifier.wosid000257578200030-
dc.identifier.bibliographicCitationJOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, v.62, no.2, pp.416 - 421-
dc.relation.isPartOfJOURNAL OF ANTIMICROBIAL CHEMOTHERAPY-
dc.citation.titleJOURNAL OF ANTIMICROBIAL CHEMOTHERAPY-
dc.citation.volume62-
dc.citation.number2-
dc.citation.startPage416-
dc.citation.endPage421-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaInfectious Diseases-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryInfectious Diseases-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusINTENSIVE-CARE-UNIT-
dc.subject.keywordPlusRISK-FACTORS-
dc.subject.keywordPlusINFECTION-CONTROL-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusTIME-SERIES-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusOUTBREAK-
dc.subject.keywordPlusCOLONIZATION-
dc.subject.keywordPlusIMPACT-
dc.subject.keywordPlusINTERVENTION-
dc.subject.keywordAuthorantibacterial agents-
dc.subject.keywordAuthorbacterial drug resistance-
dc.subject.keywordAuthorcephalosporins-
dc.subject.keywordAuthorbeta-lactamases-
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