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dc.contributor.authorRoberts, Jason A.
dc.contributor.authorPaul, Sanjoy K.
dc.contributor.authorAkova, Murat
dc.contributor.authorBassetti, Matteo
dc.contributor.authorDe Waele, Jan J.
dc.contributor.authorDimopoulos, George
dc.contributor.authorKaukonen, Kirsi-Maija
dc.contributor.authorKoulenti, Despoina
dc.contributor.authorMartin, Claude
dc.contributor.authorMontravers, Philippe
dc.contributor.authorRello, Jordi
dc.contributor.authorRhodes, Andrew
dc.contributor.authorStarr, Therese
dc.contributor.authorWallis, Steven C.
dc.contributor.authorLipman, Jeffrey
dc.date.accessioned2019-12-10T11:11:29Z
dc.date.available2019-12-10T11:11:29Z
dc.date.issued2014
dc.identifier.issn1058-4838
dc.identifier.urihttps://doi.org/10.1093/cid/ciu027
dc.identifier.urihttp://hdl.handle.net/11655/14969
dc.description.abstractBackground. Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether beta-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affect patient outcome. Methods. This was a prospective, multinational pharmacokinetic point-prevalence study including 8 beta-lactam antibiotics. Two blood samples were taken from each patient during a single dosing interval. The primary pharmacokinetic/pharmacodynamic targets were free antibiotic concentrations above the minimum inhibitory concentration (MIC) of the pathogen at both 50% (50% sic T-> MIC) and 100% (100% sic T > MIC) of the dosing interval. We used skewed logistic regression to describe the effect of antibiotic exposure on patient outcome. Results. We included 384 patients (361 evaluable patients) across 68 hospitals. The median age was 61 (interquartile range [IQR], 48-73) years, the median Acute Physiology and Chronic Health Evaluation II score was 18 (IQR, 14-24), and 65% of patients were male. Of the 248 patients treated for infection, 16% did not achieve 50% sic T-> MIC and these patients were 32% less likely to have a positive clinical outcome (odds ratio [OR], 0.68; P =.009). Positive clinical outcome was associated with increasing 50% sic T-> MIC and 100% sic T-> MIC ratios (OR, 1.02 and 1.56, respectively; P <.03), with significant interaction with sickness severity status. Conclusions. Infected critically ill patients may have adverse outcomes as a result of inadeqaute antibiotic exposure; a paradigm change to more personalized antibiotic dosing may be necessary to improve outcomes for these most seriously ill patients.
dc.language.isoen
dc.publisherOxford Univ Press
dc.relation.isversionof10.1093/cid/ciu027
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectImmunology
dc.subjectInfectious Diseases
dc.subjectMicrobiology
dc.titleDali: Defining Antibiotic Levels In Intensive Care Unit Patients: Are Current Beta-Lactam Antibiotic Doses Sufficient For Critically Ill Patients?
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalClinical Infectious Diseases
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume58
dc.identifier.issue8
dc.identifier.startpage1072
dc.identifier.endpage1083
dc.description.indexWoS
dc.description.indexScopus


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