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Decreasing the time to achieve therapeutic vancomycin concentrations in critically ill patients: developing and testing of a dosing nomogram

dc.contributor.authorBaptista, JP
dc.contributor.authorRoberts, JA
dc.contributor.authorSousa, E
dc.contributor.authorFreitas, R
dc.contributor.authorDeveza, N
dc.contributor.authorPimentel, J
dc.date.accessioned2016-12-12T16:03:18Z
dc.date.available2016-12-12T16:03:18Z
dc.date.issued2014-12-05
dc.description.abstractINTRODUCTION: Achievement of optimal vancomycin exposure is crucial to improve the management of patients with life-threatening infections caused by susceptible Gram-positive bacteria and is of particular concern in patients with augmented renal clearance (ARC). The aim of this study was to develop a dosing nomogram for the administration of vancomycin by continuous infusion for the first 24 hours of therapy based on the measured urinary creatinine clearance (8 h CLCR). METHODS: This single-center study included all critically ill patients treated with vancomycin over a 13-month period (group 1), in which we retrospectively assessed the correlation between vancomycin clearance and 8 h CLCR. This data was used to develop a formula for optimised drug dosing. The efficiency of this formula was prospectively evaluated in a second cohort of 25 consecutive critically ill patients (group 2). Vancomycin serum concentrations between 20 to 30 mg/L were considered adequate. ARC was defined as 8 h CLCR more than 130 ml/min/1.73 m(2). RESULTS: The incidence of ARC was 36% (n = 29/79) and 40% (10/25) in group 1 (n = 79) and 2 (n = 25), respectively. The mean serum vancomycin concentration on day 1 was 21.5 (6.4) and 24.5 (5.2) mg/L, for both groups respectively. On the treatment day, vancomycin plasma clearance was 5.12 (1.9) L/h in group 1 and correlated significantly with the 8 h CLCR (r(2) = 0.66; P < 0.001). The achievement of adequate vancomycin serum concentrations in group 2 was 84% (n = 21/25) versus 51% (n = 40/79) - P < 0.005. CONCLUSIONS: This new vancomycin nomogram enabled the achievement of adequate serum concentrations in 84% of the patients on the first day of treatment.pt_PT
dc.identifier.citationCrit Care. 2014 Dec 5;18(6):654.pt_PT
dc.identifier.doi10.1186/s13054-014-0654-2pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/1996
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectVancomicinapt_PT
dc.subjectAntibacterianospt_PT
dc.subjectCuidados Intensivospt_PT
dc.subjectNomogramspt_PT
dc.titleDecreasing the time to achieve therapeutic vancomycin concentrations in critically ill patients: developing and testing of a dosing nomogrampt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue6pt_PT
oaire.citation.startPage654pt_PT
oaire.citation.volume18pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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