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Meropenem population pharmacokinetics and model-based dosing optimisation in patients with serious bacterial infection

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61383082%3A_____%2F22%3A00001204" target="_blank" >RIV/61383082:_____/22:00001204 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14160/22:00127365

  • Result on the web

    <a href="https://pubmed.ncbi.nlm.nih.gov/36307183/" target="_blank" >https://pubmed.ncbi.nlm.nih.gov/36307183/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1136/ejhpharm-2022-003535" target="_blank" >10.1136/ejhpharm-2022-003535</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Meropenem population pharmacokinetics and model-based dosing optimisation in patients with serious bacterial infection

  • Original language description

    Abstract: Considering its very short elimination half-life, the approved oxacillin dosage might not be sufficient to maintain the pharmacokinetic/pharmacodynamics (PK/PD) target of time-dependent antibiotics. This study aimed to describe the population pharmacokinetics of oxacillin and to explore the probability of PK/PD target attainment by using various dosing regimens with oxacillin in staphylococcal infections. Both total and unbound oxacillin plasma concentrations retrieved as a part of routine therapeutic drug-monitoring practice were analyzed using nonlinear mixed-effects modeling. Monte Carlo simulations were used to generate the theoretical distribution of unbound oxacillin plasma concentration–time profiles at various dosage regimens. Data from 24 patients treated with oxacillin for staphylococcal infection have been included into the analysis. The volume of distribution of oxacillin in the population was 11.2 L, while the elimination rate constant baseline of 0.73 h−1 increased by 0.3 h−1 with each 1 mL/s/1.73 m2 of the estimated glomerular filtration rate (eGFR). The median value of oxacillin binding to plasma proteins was 86%. The superiority of continuous infusion in achieving target PK/PD values was demonstrated and dosing according to eGFR was proposed. Daily oxacillin doses of 9.5 g, 11 g, or 12.5 g administered by continuous infusion have been shown to be optimal for achieving target PK/PD values in patients with moderate, mild, or normal renal function, respectively

  • 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

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EUROPEAN JOURNAL OF HOSPITAL PHARMACY

  • ISSN

    2047-9956

  • e-ISSN

  • Volume of the periodical

    2022

  • Issue of the periodical within the volume

    Oct

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    1-11

  • UT code for WoS article

    000877092100001

  • EID of the result in the Scopus database

    2-s2.0-85142782956