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Importance of vancomycin loading doses in intermittent infusion regimens.
Síma, Martin; Hartinger, Jan; Cikánková, Tereza; Slanar, Ondrej.
Afiliação
  • Síma M; Department of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic. Electronic address: martin.sima@lf1.cuni.cz.
  • Hartinger J; Department of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic. Electronic address: jan.hartinger@vfn.cz.
  • Cikánková T; Department of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic. Electronic address: terez.dan@seznam.cz.
  • Slanar O; Department of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic. Electronic address: ondrej.slanar@lf1.cuni.cz.
J Infect Chemother ; 24(4): 247-250, 2018 Apr.
Article em En | MEDLINE | ID: mdl-29195829
ABSTRACT

PURPOSE:

Delayed achievement of target vancomycin serum concentrations may adversely affect clinical outcomes. The objective of this retrospective study was to explore the real frequency of loading dose use and to evaluate the impact of loading dose for the achievement of vancomycin PK/PD target in adult patients treated with intermittent vancomycin. As a secondary aim we determined optimal vancomycin loading dose based on individual pharmacokinetic calculations.

METHODS:

Vancomycin pharmacokinetic models were computed using two-compartmental analysis. Based on these models AUC24 were calculated. Unpaired t-test was used to compare AUC24 achieved in patients treated with and without vancomycin loading dose.

RESULTS:

Vancomycin loading dose was administered only in 17.8% patients. Volume of distribution and clearance median values (interquartile range) for vancomycin in whole study population (n = 45) were 0.69 (0.55-0.87) L/kg and 0.0304 (0.0217-0.0501) L/h/kg, respectively. The AUC24 was significantly higher in patients taking loading dose compared with the group without loading dose mean (SD) AUC24 was 496 (101) vs. 341 (77) mg h/L. Proportion of patients reaching PK/PD goal was 87.5% and 24.3% with and without loading dose administration, respectively. Considering individual pharmacokinetic parameters optimal vancomycin loading dose was 27.5 mg/kg of body weight.

CONCLUSIONS:

Loading dose administration plays crucial part in rapid attainment of vancomycin PK/PD target in adult patient treated with intermittent vancomycin, although it is not frequently used in clinical practise. The optimal loading dose of 25-30 mg/kg of body weight should be routinely administered to adult patients treated with intermittent vancomycin.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vancomicina / Monitoramento de Medicamentos / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: J Infect Chemother Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vancomicina / Monitoramento de Medicamentos / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: J Infect Chemother Ano de publicação: 2018 Tipo de documento: Article