Your browser doesn't support javascript.
loading
Population pharmacokinetics and dose simulation of vancomycin in critically ill patients during high-volume haemofiltration.
Escobar, Leslie; Andresen, Max; Downey, Patricio; Gai, Maria Nella; Regueira, Tomás; Bórquez, Tamara; Lipman, Jeffrey; Roberts, Jason A.
Afiliação
  • Escobar L; Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Santos Dumont 964, Santiago, Chile.
  • Andresen M; Department of Intensive Care Medicine, Hospital Clínico Universidad Católica de Chile, Marcoleta 347, Santiago 8330024, Chile. Electronic address: andresen@med.puc.cl.
  • Downey P; Department of Nephrology, Hospital Clínico Universidad Católica de Chile, Marcoleta 347, Santiago, Chile.
  • Gai MN; Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Santos Dumont 964, Santiago, Chile.
  • Regueira T; Department of Intensive Care Medicine, Hospital Clínico Universidad Católica de Chile, Marcoleta 347, Santiago 8330024, Chile.
  • Bórquez T; Department of Nephrology, Hospital Clínico Universidad Católica de Chile, Marcoleta 347, Santiago, Chile.
  • Lipman J; Burns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, QLD, Australia.
  • Roberts JA; Burns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, QLD, Australia; Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Int J Antimicrob Agents ; 44(2): 163-7, 2014 Aug.
Article em En | MEDLINE | ID: mdl-24837847
This study aimed to describe the population pharmacokinetics of vancomycin in critically ill patients with refractory septic shock undergoing continuous venovenous high-volume haemofiltration (HVHF) and to define appropriate dosing for these patients. This was a prospective pharmacokinetic study in the ICU of a university hospital. Eight blood samples were taken over one vancomycin dosing interval. Samples were analysed by a validated liquid chromatography-tandem mass spectrometry assay. Non-linear mixed-effects modelling was used to describe the population pharmacokinetics. Dosing simulations were used to define therapeutic vancomycin doses for different HVHF settings. Nine patients were included (five male). The mean weight and SOFA score were 70 kg and 11, respectively. Mean HVHF settings were: blood flow rate, 240 mL/min; and haemofiltration exchange rate, 100 mL/kg/h. A linear two-compartment model with zero-order input adequately described the data. Mean parameter estimates were: clearance, 2.9 L/h; volume of distribution of central compartment (V(1)), 11.8L; volume of distribution of peripheral compartment (V(2)), 18.0 L; and intercompartmental clearance, 9.3 L/h. HVHF intensity was strongly associated with vancomycin clearance (P < 0.05) and was a covariate in the final model. Simulations indicate that after a loading dose, vancomycin doses required for different HVHF intensities would be 750 mg every 12h (q12h) for 69 mL/kg/h, 1000 mg q12h for 100 mL/kg/h and 1500 mg q12h for 123 mL/kg/h. Continuous infusion would also be a valuable administration strategy. In conclusion, variable and much higher than standard vancomycin doses are required to achieve therapeutic concentrations during different HVHF settings.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Vancomicina / Hemofiltração / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Antimicrob Agents Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Chile País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Vancomicina / Hemofiltração / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Antimicrob Agents Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Chile País de publicação: Holanda