Publication:
Population Pharmacokinetic Study of Amoxicillin-Treated Burn Patients Hospitalized at a Swiss Tertiary-Care Center.

cris.virtual.author-orcid0000-0001-9443-6101
cris.virtualsource.author-orcidce583f80-c3a5-4e4c-9e2d-acc1184e2bc9
datacite.rightsopen.access
dc.contributor.authorFournier, Anne
dc.contributor.authorGoutelle, Sylvain
dc.contributor.authorQue, Yok-Ai
dc.contributor.authorEggimann, Philippe
dc.contributor.authorPantet, Olivier
dc.contributor.authorSadeghipour, Farshid
dc.contributor.authorVoirol, Pierre
dc.contributor.authorCsajka, Chantal
dc.date.accessioned2024-10-07T16:32:06Z
dc.date.available2024-10-07T16:32:06Z
dc.date.issued2018-09
dc.description.abstractThe objective of this study was to investigate the population pharmacokinetics (PK) of amoxicillin in ICU burn patients and the optimal dosage regimens. This was a prospective study involving 21 consecutive burn patients receiving amoxicillin. PK data were analyzed using nonlinear mixed-effects modeling. Monte-Carlo simulations assessed the influence of various amoxicillin dosage regimens with identified covariates on the probability to achieve a target (PTA) value of time during which free amoxicillin concentrations in plasma exceeded the MIC (T>MIC). A two-compartment model best described the data. Creatinine clearance (CL) and body weight (BW) influenced amoxicillin CL and central volume of distribution (), respectively. The median CL (Cockcroft-Gault formula) was high (128 ml/min), with 25% of patients having CLs of >150 ml/min. The CL, , and half-life () values at steady state for a patient with a CL of 110 ml/min and BW of 70 kg were 13.6 liters/h, 9.7 liters, and 0.8 h, respectively. Simulations showed that a target T>MIC of ≥50% was achieved (PTA > 90%) with standard amoxicillin dosage regimens (1 to 2 g every 6 to 8 h [q6-8h]) when the MIC was low (<1 mg/liter). However, increased dosages of up to 2 g/4 h were necessary in patients with augmented CLs or higher MICs. Prolonging amoxicillin infusion from 30 min to 2 h had a favorable effect on target attainment. In conclusion, this population analysis shows an increased amoxicillin CL and substantial CL PK variability in burn patients compared to literature data with nonburn patients. Situations of augmented CL and/or high bacterial MIC target values may require dosage increases and longer infusion durations. (This study has been registered at ClinicalTrials.gov under identifier NCT01965340.).
dc.description.numberOfPages12
dc.description.sponsorshipUniversitätsklinik für Intensivmedizin
dc.identifier.doi10.7892/boris.120911
dc.identifier.pmid29914948
dc.identifier.publisherDOI10.1128/AAC.00505-18
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/60400
dc.language.isoen
dc.publisherAmerican Society for Microbiology
dc.relation.ispartofAntimicrobial agents and chemotherapy
dc.relation.issn0066-4804
dc.relation.organizationDCD5A442BADDE17DE0405C82790C4DE2
dc.subjectamoxicillin burn patients pharmacokinetics population pharmacokinetics
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titlePopulation Pharmacokinetic Study of Amoxicillin-Treated Burn Patients Hospitalized at a Swiss Tertiary-Care Center.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
dspace.file.typetext
oaire.citation.issue9
oaire.citation.volume62
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
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unibe.date.embargoChanged2019-02-28 01:30:05
unibe.date.licenseChanged2019-12-04 22:17:41
unibe.description.ispublishedpub
unibe.eprints.legacyId120911
unibe.journal.abbrevTitleANTIMICROB AGENTS CH
unibe.refereedtrue
unibe.subtype.articlejournal

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