Publication:
Combination therapy does not decrease 30-day mortality but increases antibiotic consumption in methicillin-sensitive S. aureus bacteraemia

dc.contributor.coauthorÖzgen-Top, Ö.
dc.contributor.coauthorAysert-Yildiz, P.
dc.contributor.coauthorHabibi, H.
dc.contributor.coauthorHatipoğlu, İ. O.
dc.contributor.coauthorŞahin, E. A.
dc.contributor.coauthorTekin Taş, Z.
dc.contributor.coauthorDizbay, M.
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.kuauthorÖzger, Hasan Selçuk
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.date.accessioned2026-07-07T08:48:45Z
dc.date.issued2026
dc.description.abstractThe study aimed to compare the impact of combination and monotherapy on mortality, antibiotic consumption using ‘Days of Therapy (DOT)’, and antibiotic-related adverse events in patients with methicillin-susceptible S. aureus (MSSA) bacteraemia.Methods This retrospective study included all adult patients (>18 years) with MSSA bacteraemia who received either monotherapy (beta-lactam alone) or combination therapy (beta-lactam plus teicoplanin or daptomycin or linezolid) between 2018 and 2023. Mortality, antibiotic consumption, and factors predicting mortality were analysed. Groups were compared for 30-d mortality with survival analysis. Logistic regression models were used to identify risk factors for mortality. Antibiotic consumption was calculated by DOT.Results Among 395 patients screened, 185 patients who had an MSSA bacteraemia received either monotherapy (n = 73, 39.5%) or combination therapy (n = 112, 60.5%). The 30-d mortality rate was similar between groups (%15.1 vs. 21.4, P = 0.280). Time to bacterial clearance was also similar (median (IQR): 4 (3–7) vs. 4 (3–7) d, P = 0.699). DOT per 1000 patient days was significantly higher in the combination therapy group than in the monotherapy group (median, IQR: 1420, 827–1836 vs. 933, 732–1000), P
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ3
dc.identifier.doi10.1080/1120009x.2025.2556578
dc.identifier.eissn1973-9478
dc.identifier.embargoN/A
dc.identifier.endpage144
dc.identifier.issn1120-009X
dc.identifier.issue2
dc.identifier.pubmed40928063
dc.identifier.scopus2-s2.0-105016619657
dc.identifier.startpage138
dc.identifier.urihttp://doi.org/10.1080/1120009x.2025.2556578
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33233
dc.identifier.volume38
dc.identifier.wos001570486900001
dc.keywordsAntibiotic consumption
dc.keywordsCombination therapy
dc.keywordsMonotherapy
dc.keywordsMortality
dc.keywordsStaphylococcus aureus
dc.keywordsStaphylococcus aureus bacteraemia
dc.languageeng
dc.publisherTaylor and Francis
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of Chemotherapy
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectOncology
dc.subjectInfectious diseases
dc.subjectPathology
dc.subjectPharmacology
dc.subjectPharmacy
dc.titleCombination therapy does not decrease 30-day mortality but increases antibiotic consumption in methicillin-sensitive S. aureus bacteraemia
dc.typeJournal Article
dspace.entity.typePublication
relation.isOrgUnitOfPublicationf91d21f0-6b13-46ce-939a-db68e4c8d2ab
relation.isOrgUnitOfPublication.latestForDiscoveryf91d21f0-6b13-46ce-939a-db68e4c8d2ab
relation.isParentOrgUnitOfPublication055775c9-9efe-43ec-814f-f6d771fa6dee
relation.isParentOrgUnitOfPublication.latestForDiscovery055775c9-9efe-43ec-814f-f6d771fa6dee

Files