J 2022

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

MURÍNOVÁ, Irena, Martin SVIDRNOCH, Tomas GUCKY, David REZAC, Jan HLAVAC et. al.

Základní údaje

Originální název

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

Autoři

MURÍNOVÁ, Irena (203 Česká republika, domácí), Martin SVIDRNOCH, Tomas GUCKY, David REZAC, Jan HLAVAC, Ondrej SLANAR a Martin SIMA (garant)

Vydání

EUROPEAN JOURNAL OF HOSPITAL PHARMACY, London, BMJ Publishing Group, 2022, 2047-9956

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30104 Pharmacology and pharmacy

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 1.700

Kód RIV

RIV/00216224:14160/22:00127365

Organizační jednotka

Farmaceutická fakulta

UT WoS

000877092100001

Klíčová slova anglicky

critical care; administration; intravenous; drug monitoring; pharmacy service; hospital; practice guideline

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 8. 12. 2022 10:23, JUDr. Sabina Krejčiříková

Anotace

V originále

Objectives The objective of this study was to develop a population pharmacokinetic model of meropenem in a heterogeneous population of patients with a serious bacterial infection in order to propose dosing optimisation leading to improved achievement of the pharmacokinetic/pharmacodynamic (PK/PD) target. Methods A total of 174 meropenem serum levels obtained from 144 patients during therapeutic drug monitoring were analysed using a non-linear mixed-effects modelling approach and Monte Carlo simulation was then used to compare various dosing regimens in order to optimise PK/PD target attainment. Results The meropenem volume of distribution of the patient population was 54.95 L, while clearance started at 3.27 L/hour and increased by 0.91 L/hour with each 1 mL/s/1.73 m2 of estimated glomerular filtration rate. Meropenem clearance was also 0.31 L/hour higher in postoperative patients with central nervous system infection. Meropenem administration by continuous infusion showed a significantly higher probability of attaining the PK/PD target than a standard 30 min infusion (95.3% vs 49.5%). Conclusions A daily meropenem dose of 3 g, 6 g and 10.5 g administered by continuous infusion was shown to be accurate for patients with moderate to severe renal impairment, normal renal function to mild renal impairment and augmented renal clearance, respectively