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

. 2024 Apr 23 ; 31 (3) : 253-258. [epub] 20240423

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid36307183

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.

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Papp-Wallace KM, Endimiani A, Taracila MA, et al. . Carbapenems: past, present, and future. Antimicrob Agents Chemother 2011;55:4943–60. 10.1128/AAC.00296-11 PubMed DOI PMC

Craig WA. The pharmacology of meropenem, a new carbapenem antibiotic. Clin Infect Dis 1997;24 Suppl 2:S266–75. 10.1093/clinids/24.Supplement_2.S266 PubMed DOI

Boucher BA, Wood GC, Swanson JM. Pharmacokinetic changes in critical illness. Crit Care Clin 2006;22:255–71. 10.1016/j.ccc.2006.02.011 PubMed DOI

Wong G, Briscoe S, McWhinney B, et al. . Therapeutic drug monitoring of β-lactam antibiotics in the critically ill: direct measurement of unbound drug concentrations to achieve appropriate drug exposures. J Antimicrob Chemother 2018;73:3087–94. 10.1093/jac/dky314 PubMed DOI

Scharf C, Liebchen U, Paal M, et al. . The higher the better? Defining the optimal beta-lactam target for critically ill patients to reach infection resolution and improve outcome. J Intensive Care 2020;8:86. 10.1186/s40560-020-00504-w PubMed DOI PMC

European Committee on Antimicrobial Susceptibility Testing . Clinical breakpoints - breakpoints and guidance. Available: https://www.eucast.org/fileadmin/src/media/PDFs/EUCAST_files/Breakpoint_tables/v_12.0_Breakpoint_Tables.pdf [Accessed 11 Oct 2022].

Bradley JS, Garau J, Lode H, et al. . Carbapenems in clinical practice: a guide to their use in serious infection. Int J Antimicrob Agents 1999;11:93–100. 10.1016/S0924-8579(98)00094-6 PubMed DOI

Lansbury L, Lim B, Baskaran V, et al. . Co-Infections in people with COVID-19: a systematic review and meta-analysis. J Infect 2020;81:266–75. 10.1016/j.jinf.2020.05.046 PubMed DOI PMC

Rawson TM, Moore LSP, Zhu N, et al. . Bacterial and fungal coinfection in individuals with coronavirus: a rapid review to support COVID-19 antimicrobial prescribing. Clin Infect Dis 2020;71:2459–68. 10.1093/cid/ciaa530 PubMed DOI PMC

Goncalves-Pereira J, Silva NE, Mateus A, et al. . Assessment of pharmacokinetic changes of meropenem during therapy in septic critically ill patients. BMC Pharmacol Toxicol 2014;15:21. 10.1186/2050-6511-15-21 PubMed DOI PMC

McClelland S, Hall WA. Postoperative central nervous system infection: incidence and associated factors in 2111 neurosurgical procedures. Clin Infect Dis 2007;45:55–9. 10.1086/518580 PubMed DOI

Schneider F, Gessner A, El-Najjar N. Efficacy of vancomycin and meropenem in central nervous system infections in children and adults: current update. Antibiotics 2022;11:173. 10.3390/antibiotics11020173 PubMed DOI PMC

Almalki MH, Ahmad MM, Brema I, et al. . Management of diabetes insipidus following surgery for pituitary and suprasellar tumours. Sultan Qaboos Univ Med J 2021;21:354–64. 10.18295/squmj.4.2021.010 PubMed DOI PMC

Yu Z, Pang X, Wu X, et al. . Clinical outcomes of prolonged infusion (extended infusion or continuous infusion) versus intermittent bolus of meropenem in severe infection: a meta-analysis. PLoS One 2018;13:e0201667. 10.1371/journal.pone.0201667 PubMed DOI PMC

Truong AQ, Dao XC, Vu DH, et al. . Optimizing meropenem in highly resistant Klebsiella pneumoniae environments: population pharmacokinetics and dosing simulations in critically ill patients. Antimicrob Agents Chemother 2022:e0032122. 10.1128/aac.00321-22 PubMed DOI PMC

Thémans P, Marquet P, Winkin JJ, et al. . Towards a generic tool for prediction of meropenem systemic and infection-site exposure: a physiologically based pharmacokinetic model for adult patients with pneumonia. Drugs R D 2019;19:177–89. 10.1007/s40268-019-0268-x PubMed DOI PMC

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