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A simulation of loading doses for vancomycin continuous infusion regimens in intensive care

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F17%3A10364155" target="_blank" >RIV/00216208:11110/17:10364155 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1080/23744235.2017.1328741" target="_blank" >http://dx.doi.org/10.1080/23744235.2017.1328741</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/23744235.2017.1328741" target="_blank" >10.1080/23744235.2017.1328741</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A simulation of loading doses for vancomycin continuous infusion regimens in intensive care

  • Original language description

    Background: Delayed achievement of target vancomycin serum concentrations may adversely affect clinical outcomes. The objective of this retrospective study was to compare the prediction accuracy of different body weight descriptors for volume of distribution and to propose an optimal loading dose (LD) for continuous infusion regimens in adults.Methods: Pharmacokinetic variables were computed using one-compartmental analysis. Simulated LDs of vancomycin were evaluated for each patient.Results: Volume of distribution, clearance, and half-life median values (interquartile range) for vancomycin in the study population (n = 30) were 0.45 (0.39-0.61) L.kg(-1), 0.026 (0.015-0.040) L.h(-1).kg(-1), and 10.3 (7.7-21.3) h, respectively. The observed volume of distribution was better predicted by total body weight (TBW) than by the ideal body weight or the adjusted body weight.Conclusions: An LD of 10.7 mg per kg TBW was optimal in our study population. Using this LD, 17.9% of simulated vancomycin serum levels were just below the therapeutic range, only 10.7% concentrations exceeded the target range and no concentration was toxic. The use of a LD would lead to reduced median time to reach target concentrations from 17 to 1h.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Infectious Diseases

  • ISSN

    2374-4235

  • e-ISSN

  • Volume of the periodical

    49

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    6

  • Pages from-to

    674-679

  • UT code for WoS article

    000403158500005

  • EID of the result in the Scopus database

    2-s2.0-85019210992