Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29102
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dc.contributor.authorUdy A.A.en
dc.contributor.authorMartin E.-L.en
dc.contributor.authorSchneider H.G.F.en
dc.contributor.authorNgo-Thai L.L.en
dc.contributor.authorMcGloughlin S.A.en
dc.contributor.authorPeleg A.Y.en
dc.contributor.authorPai Mangalore R.en
dc.contributor.authorPadiglione A.A.en
dc.date.accessioned2021-05-14T09:49:16Zen
dc.date.available2021-05-14T09:49:16Zen
dc.date.copyright2020en
dc.date.created20201024en
dc.date.issued2020-10-24en
dc.identifier.citationJournal of Pharmacy Practice and Research. 50 (4) (pp 345-350), 2020. Date of Publication: 01 Aug 2020.en
dc.identifier.issn1445-937Xen
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/29102en
dc.description.abstractAim: To determine if empirical anti-pseudomonal beta-lactam antibiotic (BLA) dosing achieves adequate drug exposure in septic patients. Method(s): A single-centre, prospective pharmacokinetic study was conducted in Intensive Care Unit (ICU) patients with sepsis, receiving empirical therapy with piperacillin/tazobactam or meropenem. The pharmacokinetic/pharmacodynamic (PK/PD) targets were free BLA concentrations above the MIC at the mid-point (Concentration A, 50%f T > MIC) and end of the dosing interval (Concentration B, 100% fT > MIC). Sub-therapeutic concentrations were defined as concentration A < MIC, and sub-optimal as concentration B < MIC. The MIC breakpoint for Pseudomonas aeruginosa, as defined by The European Committee on Antimicrobial Susceptibility Testing (EUCAST) (available from <http://www.eucast.org/clinical_breakpoints>) was used. Result(s): Of the 37 eligible patients, 20 were receiving piperacillin/tazobactam (TZP), and 17 meropenem (MEM). PK data were available for 36 patients (concentration A) and 34 patients (concentration B). The median measured plasma concentrations (mg/L) were: piperacillin for doses 4 g 8-hourly and 4 g 6-hourly - concentration A 53.9 [14.38-123.71] and 36.44 [13.38-107.45], concentration B 8.01 [2.57-71.08] and 27.31 [3.32-59.76], MEM for doses 1 g 8-hourly and 2 g 8-hourly - concentration A 12.49 [7.35-23.63] and 30.5, concentration B 7.47 [2.97-11.33] and 9.31. 27.8% (10 of 36) of patients had sub-therapeutic concentrations (concentration A) and 50% (17 of 34) had sub-optimal concentrations (concentration B). Conclusion(s): Our study confirms that sub-therapeutic unbound plasma anti-pseudomonal BLA concentrations are common in critically ill septic patients and underscores the urgent need for future trials exploring the efficacy of BLA therapeutic drug monitoring in these patients.Copyright © 2020 The Society of Hospital Pharmacists of Australiaen
dc.languageEnglishen
dc.languageenen
dc.publisherWiley-Blackwell (E-mail: info@wiley.com)en
dc.relation.ispartofJournal of Pharmacy Practice and Researchen
dc.titleInsufficient plasma concentrations of empiric anti-pseudomonal beta-lactam antibiotics in critically ill patients with suspected sepsis.en
dc.typeArticleen
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1002/jppr.1639-
dc.publisher.placeAustraliaen
dc.identifier.source2005426218en
dc.identifier.institution(Pai Mangalore, Padiglione, McGloughlin, Peleg) Department of Infectious Diseases, The Alfred Hospital and Central Clinical School, Monash University, Melbourne, Australia (Padiglione, Martin, Ngo-Thai, McGloughlin, Udy) Department of Hyperbaric and Intensive Care Medicine, The Alfred Hospital, Melbourne, Australia (Peleg) Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, Australia (Padiglione) Department of Infectious Diseases, Monash Medical Centre, Clayton, Australia (Schneider) Department of Pathology, The Alfred Hospital, Melbourne, Australia (Martin, Ngo-Thai) Pharmacy, The Alfred Hospital, Melbourne, Australia (McGloughlin, Udy) School of Public Health and Preventive Medicine, Monash University, Melbourne, Australiaen
dc.description.addressR. Pai Mangalore, Department of Infectious Diseases, The Alfred Hospital and Central Clinical School, Monash University, Melbourne, Australia. E-mail: R.Paimangalore@alfred.org.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.subect.keywordsbeta-lactam antibiotics critically ill ICU pharmacodynamics pharmacokinetics sepsis TDMen
dc.identifier.authoremailPai Mangalore R.; R.Paimangalore@alfred.org.auen
dc.description.grantNo: Small Project Grant Organization: *Alfred Research Trusts, Alfred Health* Organization No: 501100002716 Country: Australiaen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
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