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Emulating a target trial of early compared with late initiation of appropriate antibiotic therapy for hospital-acquired monobacterial Gram-negative bloodstream infections

dc.contributor.authorAslan, Abdullah T.
dc.contributor.authorEzure, Yukiko
dc.contributor.authorTanriverdi, Elif Seren
dc.contributor.authorDag, Osman
dc.contributor.authorCimen, Cansu
dc.contributor.authorKalem, Ayse Kaya
dc.contributor.authorKayaaslan, Bircan
dc.contributor.authorAlkan, Sevil
dc.contributor.authorKoylu, Bahadir
dc.contributor.authorAta, Emine Busra
dc.contributor.authorCaglar, Bilge
dc.contributor.authorSaltoglu, Nese
dc.contributor.authorOnal, Ugur
dc.contributor.authorDeniz, Secil
dc.contributor.authorUral, Onur
dc.contributor.authorOz, Murtaza
dc.contributor.authorBakir, Mehmet
dc.contributor.authorYilmaz, Mesut
dc.contributor.authorCakmak, Rumeysa
dc.contributor.authorBatirel, Ayse
dc.contributor.authorAkdogan, Ozlem
dc.contributor.authorBaykam, Nurcan
dc.contributor.authorErol, Cigdem
dc.contributor.authorYanik-Yalcin, Tugba
dc.contributor.authorEren-Kutsoylu, Oya Ozlem
dc.contributor.authorTure-Yuce, Zeynep
dc.contributor.authorKalin-Unuvar, Gamze
dc.contributor.authorOzer-Simsek, Zuhal
dc.contributor.authorGuzeldag, Seda
dc.contributor.authorKose, Adem
dc.contributor.authorCihangiroglu, Mustafa
dc.contributor.authorYagci-Caglayik, Dilek
dc.contributor.authorSevinc, Muhammed Burak
dc.contributor.authorAktas, Zerrin
dc.contributor.authorOncul, Oral
dc.contributor.authorErsoz, Gulden
dc.contributor.authorKocagoz, Ayse Sesin
dc.contributor.authorHazirolan, Gulsen
dc.contributor.authorUnalan-Altintop, Tugce
dc.contributor.authorDinc, Bedia
dc.contributor.authorTuzemen, Nazmiye Ulku
dc.contributor.authorAkcali, Alper
dc.contributor.authorMacin, Salih
dc.contributor.authorCaliskan, Ahmet
dc.contributor.authorHasbek, Mursit
dc.contributor.authorErgon, Cem
dc.contributor.authorAy-Altintop, Yasemin
dc.contributor.authorSimsek, Muge
dc.contributor.authorOtlu, Baris
dc.contributor.authorRamsay, Kay A.
dc.contributor.authorHarris, Patrick N. A.
dc.contributor.authorAkova, Murat
dc.contributor.authorPaterson, David L.
dc.date.accessioned2026-11-05T11:08:55Z
dc.date.issued2026
dc.description.abstractBackground Delays in appropriate antimicrobial therapy can increase the risk of all-cause mortality (ACM) in hospital-acquired bloodstream infections (HA-BSIs) caused by Gram-negative bacteria (GNB). We aimed to evaluate the effectiveness of early appropriate antimicrobial therapy (EAAT) compared with late appropriate antimicrobial therapy (LAAT) in this population.Methods This study used data from a multi-centre, prospective cohort including adult patients with HA-BSI caused by GNB across 22 Turkish hospitals. A hypothetical target trial allocating participants with HA-BSI caused by monobacterial GNB to either EAAT or LAAT was emulated using the weighting approach. The primary outcome was 14 day ACM; 28 day ACM was a secondary outcome. Cox proportional hazards models with inverse probability weighting were applied to account for confounding, with antibiotic treatment incorporated as a time-dependent variable.Results Among 680 patients, 14 day ACM occurred in 14.7% (40/272) of the EAAT group and 42.9% (175/408) of the LAAT group. EAAT was associated with a lower risk of 14 day ACM [adjusted hazard ratio (aHR) = 0.41; 95% CI: 0.28-0.61). Similarly, 26.1% (71/272) of the patients treated with EAAT and 49.5% (202/408) of those receiving LAAT died during 28 day follow-up (aHR = 0.66; 95% CI: 0.50-0.86). In the carbapenem-resistant GNB subset, EAAT reduced the hazard of 14 day ACM (aHR = 0.36; 95% CI: 0.21-0.60) and 28 day ACM (aHR = 0.60; 95% CI: 0.44-0.84). All prespecified and post hoc analyses consistently supported these findings.Conclusions EAAT was associated with a survival benefit in individuals with HA-BSI due to GNB. Although these findings support early initiation of appropriate therapy, residual confounding cannot be excluded.
dc.description.issue6
dc.description.pagesdkag161
dc.description.sponsorshipPfizer provided financial support for this study (Grant ID: 65207785 to A.T.A and M.A.). We would also like to acknowledge financial support for the study from the University of Queensland.
dc.description.volume81
dc.identifier.doi10.1093/jac/dkag161
dc.identifier.issn0305-7453
dc.identifier.issn1460-2091
dc.identifier.urihttps://doi.org/10.1093/jac/dkag161
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11584
dc.identifier.wosWOS:001763793100001
dc.language.isoen
dc.publisherOXFORD UNIV PRESS
dc.relation.fundingPfizer(Pfizer)
dc.relation.fundingUniversity of Queensland(University of Queensland)
dc.relation.fundingPfizer [65207785]
dc.relation.fundingUniversity of Queensland
dc.relation.hasversion10.1093/jac/dkag161
dc.relation.ispartofJOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
dc.subjectCARE
dc.subjectInfectious Diseases
dc.subjectMicrobiology
dc.subjectPharmacology & Pharmacy
dc.titleEmulating a target trial of early compared with late initiation of appropriate antibiotic therapy for hospital-acquired monobacterial Gram-negative bloodstream infections
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue6
oaire.citation.volume81
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