Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12743
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dc.contributor.authorRoberts, Darren Men
dc.contributor.authorLiu, Xinen
dc.contributor.authorRoberts, Jason Aen
dc.contributor.authorNair, Priyaen
dc.contributor.authorCole, Louiseen
dc.contributor.authorRoberts, Michael Sen
dc.contributor.authorLipman, Jeffreyen
dc.contributor.authorBellomo, Rinaldoen
dc.date.accessioned2015-05-16T02:28:34Z-
dc.date.available2015-05-16T02:28:34Z-
dc.date.issued2015-03-13en
dc.identifier.citationCritical Care 2015; 19(): 84en
dc.identifier.govdoc25881576en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12743en
dc.description.abstractContinuous renal replacement therapy (CRRT) may alter antibiotic pharmacokinetics and increase the risk of incorrect dosing. In a nested cohort within a large randomized controlled trial, we assessed the effect of higher (40 mL/kg per hour) and lower (25 mL/kg per hour) intensity CRRT on antibiotic pharmacokinetics.We collected serial blood samples to measure ciprofloxacin, meropenem, piperacillin-tazobactam, and vancomycin levels. We calculated extracorporeal clearance (CL), systemic CL, and volume of distribution (Vd) by non-linear mixed-effects modelling. We assessed the influence of CRRT intensity and other patient factors on antibiotic pharmacokinetics.We studied 24 patients who provided 179 pairs of samples. Extracorporeal CL increased with higher-intensity CRRT but the increase was significant for vancomycin only (mean 28 versus 22 mL/minute; P = 0.0003). At any given prescribed CRRT effluent rate, extracorporeal CL of individual antibiotics varied widely, and the effluent-to-plasma concentration ratio decreased with increasing effluent flow. Overall, systemic CL varied to a greater extent than Vd, particularly for meropenem, piperacillin, and tazobactam, and large intra-individual differences were also observed. CRRT dose did not influence overall (systemic) CL, Vd, or half-life. The proportion of systemic CL due to CRRT varied widely and was high in some cases.In patients receiving CRRT, there is great variability in antibiotic pharmacokinetics, which complicates an empiric approach to dosing and suggests the need for therapeutic drug monitoring. More research is required to investigate the apparent relative decrease in clearance at higher CRRT effluent rates.ClinicalTrials.gov NCT00221013 . Registered 14 September 2005.en
dc.language.isoenen
dc.titleA multicenter study on the effect of continuous hemodiafiltration intensity on antibiotic pharmacokinetics.en
dc.typeJournal Articleen
dc.identifier.journaltitleCritical Careen
dc.identifier.affiliationIntensive Care Unit, St Vincent's Hospital, Victoria Street, Darlinghurst, NSW, 2010, Australiaen
dc.identifier.affiliationBurns Trauma and Critical Care Research Centre, The University of Queensland, Level 3 Ned Hanlon Building, Royal Brisbane and Women's Hospital, Butterfield Street, Brisbane, Queensland, 4029, Australiaen
dc.identifier.affiliationIntensive Care Unit, Nepean Hospital, Derby Street, Kingswood, NSW, 2747, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationTherapeutics Research Centre, School of Medicine, University of Queensland, Princess Alexandra Hospital, Ipswich Road, Brisbane, Queensland, 4102, Australiaen
dc.identifier.doi10.1186/s13054-015-0818-8en
dc.description.pages84en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25881576en
dc.contributor.corpauthorRENAL Replacement Therapy Study Investigatorsen
dc.type.austinJournal Articleen
local.name.researcherBellomo, Rinaldo
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeJournal Article-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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