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dc.creatorMilaković, Dragana
dc.creatorKovačević, Tijana
dc.creatorKovačević, Peđa
dc.creatorBarišić, Vedrana
dc.creatorAvram, Sanja
dc.creatorDragić, Saša
dc.creatorZlojutro, Biljana
dc.creatorMomčičević, Danica
dc.creatorMiljković, Branislava
dc.creatorVučićević, Katarina
dc.date.accessioned2024-03-12T13:43:42Z
dc.date.available2024-03-12T13:43:42Z
dc.date.issued2024
dc.identifier.issn1999-4923
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/5557
dc.description.abstractDuring veno-venous extracorporeal membrane oxygenation (vv ECMO) therapy, antimicrobial drugs are frequently used, and appropriate dosing is challenging due to there being limited data to support the dosage. Linezolid is effective against multidrug-resistant Gram-positive pathogens frequently isolated in ECMO patients. In total, 53 steady-state linezolid levels were obtained following 600 mg intravenous (IV) injections every 8 h, and these were used to develop a population pharmacokinetic (PopPK) model in patients with COVID-19-associated acute respiratory distress syndrome (CARDS) on vv ECMO. The data were analyzed using a nonlinear mixed-effects modelling approach. Monte Carlo simulation generated 5000 patients’ individual PK parameters and corresponding concentration–time profiles using the PopPK model, following the administration of 600 mg/8 h (a higher-than-standard dosing) and 600 mg/12 h (standard). The probabilities of pharmacokinetic/pharmacodynamic (PK/PD) target attainment (PTA) and the cumulative fraction of responses (CFR) for three pathogens were calculated and compared between the two dosing scenarios. Linezolid 600 mg/8 h was predicted to achieve greater than or equal to 85%Tf>MIC in at least 90% of the patients with CARDS on vv ECMO compared to only approximately two thirds of the patients after dosing every 12 h at a minimal inhibitory concentration (MIC) of 2 mg/L. In addition, for the same MIC, fAUC24/MIC ≥ 80 was achieved in almost three times the number of patients following an 8-h versus a 12-h interval. PopPK simulation predicted that a significantly higher proportion of the patients with CARDS on vv ECMO would achieve the PK/PD targets following the 8-h dosing interval compared to standard linezolid dosing. Nevertheless, the safety concern, in particular, for thrombocytopenia, with higher-than-standard linezolid dosage is reasonable, and consequently, monitoring is essential.
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS//
dc.relationIn 2022 research grant support was approved for this study by the Zoll foundation.
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourcePharmaceutics
dc.subjectCOVID-19
dc.subjectdosing
dc.subjectECMO
dc.subjectlinezolid
dc.subjectpopulation pharmacokinetics
dc.subjectPTA
dc.titlePopulation Pharmacokinetic Model of Linezolid and Probability of Target Attainment in Patients with COVID-19-Associated Acute Respiratory Distress Syndrome on Veno-Venous Extracorporeal Membrane Oxygenation—A Step toward Correct Dosing
dc.typearticle
dc.rights.licenseBY
dc.citation.volume16
dc.citation.issue2
dc.identifier.wos001177068900001
dc.identifier.doi10.3390/pharmaceutics16020253
dc.identifier.pmid38399307
dc.identifier.scopus2-s2.0-85186111657
dc.identifier.fulltexthttp://farfar.pharmacy.bg.ac.rs/bitstream/id/15668/Population_Pharmacokinetic_Model_pub_2024.pdf
dc.type.versionpublishedVersion


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