Publication:
Rapid molecular detection of gastrointestinal pathogens and its role in antimicrobial stewardship

dc.contributor.coauthorKeske, Şiran
dc.contributor.coauthorPalaoğlu, Erhan
dc.contributor.departmentN/A
dc.contributor.departmentDepartment of Industrial Engineering
dc.contributor.kuauthorZabun, Burak
dc.contributor.kuauthorAksoy, Kahraman
dc.contributor.kuauthorCan, Füsun
dc.contributor.kuauthorErgönül, Önder
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.otherDepartment of Industrial Engineering
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokid110398
dc.date.accessioned2024-11-09T13:24:10Z
dc.date.issued2018
dc.description.abstractWe aimed to detect the etiological agents of acute diarrhea by a molecular gastrointestinal pathogen test (MGPT) and to assess the impact of MGPT on antimicrobial stewardship programs (ASP). This is a prospective observational study and was conducted between 1 January 2015 and 30 June 2017. We included consequent patients who had acute diarrhea. At the end of 2015, we implemented ASP in acute diarrhea cases and compared the outcomes in the pre-ASP and post-ASP periods. An FDA-cleared multiplexed gastrointestinal PCR panel system, the BioFire FilmArray (Idaho Technology, Salt Lake City, UT), which detects 20 pathogens in stool, was used. In 499 out of 699 patients (71%), at least one pathogen was detected. Among 314 adults with positive MGPT, 101 (32%) enteropathogenic Escherichia coli (EPEC), 71 (23%) enteroaggregative E. coli (EAEC), 68 (22%) enterotoxigenic E. coli (ETEC), 55 (18%) Shiga toxin-producing E. coli (STEC) (17%) Norovirus, 48 (15%) Campylobacter, 21 (7%) Salmonella, and 20 (6%) Clostridium difficile strains were detected. Among 185 children, 55 (30%) EPEC, 37 (20%) C. difficile, 32 (17%) Norovirus, 29 (16%) EAEC, 22 (12%) STEC, 21 (11%) ETEC, 21 (11%) Campylobacter, 20 (11%) Salmonella, and 16 (5%) Rotavirus strains were detected. Inappropriate antibiotic use decreased in the post-ASP period compared with the pre-ASP period among inpatients (42.9% and 25.8%, respectively; P = 0.023). Using MGPT in clinical practice significantly decreased the unnecessary use of antibiotics. Detection of high rates of C. difficile in children and Salmonella spp., as well as relatively high rates of Campylobacter spp., which were hard to isolate by routine stool culture, were remarkable.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue5
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipN/A
dc.description.versionPublisher version
dc.description.volume56
dc.formatpdf
dc.identifier.doi10.1128/JCM.00148-18
dc.identifier.eissn1098-660X
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR01516
dc.identifier.issn0095-1137
dc.identifier.linkhttps://doi.org/10.1128/JCM.00148-18
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85046246913
dc.identifier.urihttps://hdl.handle.net/20.500.14288/3400
dc.identifier.wos430856400007
dc.keywordsGastroenteritis
dc.keywordsAntimicrobial stewardship
dc.keywordsMultiplex
dc.keywordsMolecular test
dc.keywordsDiarrhea
dc.languageEnglish
dc.publisherAmerican Society for Microbiology
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/8070
dc.sourceJournal of Clinical Microbiology
dc.subjectMicrobiology
dc.titleRapid molecular detection of gastrointestinal pathogens and its role in antimicrobial stewardship
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authoridN/A
local.contributor.authoridN/A
local.contributor.authoridN/A
local.contributor.authorid0000-0003-1935-9235
local.contributor.kuauthorZabun, Burak
local.contributor.kuauthorAksoy, Kahraman
local.contributor.kuauthorCan, Füsun
local.contributor.kuauthorErgönül, Mehmet Önder
relation.isOrgUnitOfPublicationd6d00f52-d22d-4653-99e7-863efcd47b4a
relation.isOrgUnitOfPublication.latestForDiscoveryd6d00f52-d22d-4653-99e7-863efcd47b4a

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