Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium

Detalhes bibliográficos
Autor(a) principal: Menezes, Bruna Kochhann
Data de Publicação: 2020
Outros Autores: Alves, Izabel Almeida, Staudt, Keli Jaqueline, Beltrame, Betina Montanari, Venz, Letícia, Michelin, Lessandra, Araújo, Bibiana Verlindo de, Tasso, Leandro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/249606
Resumo: Objectives The aim of this study was to investigate the effect of daptomycin against vancomycin-resistant Enterococcus faecium bacteraemia using computer modelling. Methods Data obtained in vitro from time-kill curves were evaluated by PK/PD modelling and Monte Carlo simulations to determine the logarithmic reduction in the number of colony-forming units (CFU)/mL over 18 days of daptomycin treatment at 6, 8, and 10 mg/kg doses every 24 or 48 h and with variations in creatinine clearance (CLCR) of 15–29, 30–49, and 50–100 mL/min/1.73 m2. Monte Carlo simulations were performed to evaluate the probability of target attainment (PTA) for an area under the unbound drug concentration-time curve/minimum inhibitory concentration (fAUC/MIC) > 36 at the same doses and CLCR. Results Static time-kill model was employed to investigate the antibacterial efficacy of constant daptomycin concentrations. The time-kill curve analysis was performed using mathematical modelling based on a Hill coefficient factor. There was an expressive reduction (> 2 Log CFU/mL) over 18 days of daptomycin treatment in 75th percentile of individuals with CLCR of 15–100 mL/min/1.73 m2) with daptomycin 6–10 mg/kg/day, except for daptomycin every 48 h. Using fAUC/MIC > 36, PTA was > 90% at MICs ≤ 2 μg/mL. Conclusions Higher daptomycin doses were associated with higher mortality in time-kill curves. The simulations indicated that independent of the CLCR the therapeutic responses of VRE occur with doses of daptomycin ≥ 6 mg/kg/day and daptomycin every 48 h is insufficient to treat enterococcal bacteraemia.
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spelling Menezes, Bruna KochhannAlves, Izabel AlmeidaStaudt, Keli JaquelineBeltrame, Betina MontanariVenz, LetíciaMichelin, LessandraAraújo, Bibiana Verlindo deTasso, Leandro2022-10-03T04:48:57Z20201517-8382http://hdl.handle.net/10183/249606001149158Objectives The aim of this study was to investigate the effect of daptomycin against vancomycin-resistant Enterococcus faecium bacteraemia using computer modelling. Methods Data obtained in vitro from time-kill curves were evaluated by PK/PD modelling and Monte Carlo simulations to determine the logarithmic reduction in the number of colony-forming units (CFU)/mL over 18 days of daptomycin treatment at 6, 8, and 10 mg/kg doses every 24 or 48 h and with variations in creatinine clearance (CLCR) of 15–29, 30–49, and 50–100 mL/min/1.73 m2. Monte Carlo simulations were performed to evaluate the probability of target attainment (PTA) for an area under the unbound drug concentration-time curve/minimum inhibitory concentration (fAUC/MIC) > 36 at the same doses and CLCR. Results Static time-kill model was employed to investigate the antibacterial efficacy of constant daptomycin concentrations. The time-kill curve analysis was performed using mathematical modelling based on a Hill coefficient factor. There was an expressive reduction (> 2 Log CFU/mL) over 18 days of daptomycin treatment in 75th percentile of individuals with CLCR of 15–100 mL/min/1.73 m2) with daptomycin 6–10 mg/kg/day, except for daptomycin every 48 h. Using fAUC/MIC > 36, PTA was > 90% at MICs ≤ 2 μg/mL. Conclusions Higher daptomycin doses were associated with higher mortality in time-kill curves. The simulations indicated that independent of the CLCR the therapeutic responses of VRE occur with doses of daptomycin ≥ 6 mg/kg/day and daptomycin every 48 h is insufficient to treat enterococcal bacteraemia.application/pdfengBrazilian journal of microbiology. São Paulo. Vol. 51 (2020), p. 169-176DaptomicinaEnterococcus faeciumAntibacterianosDaptomycinBacteraemiaEnterococcus faeciumPK/PD modellingTime-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faeciuminfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001149158.pdf.txt001149158.pdf.txtExtracted Texttext/plain30446http://www.lume.ufrgs.br/bitstream/10183/249606/2/001149158.pdf.txt09dae4845a0a03473d9c0f51445e36dbMD52ORIGINAL001149158.pdfTexto completo (inglês)application/pdf917319http://www.lume.ufrgs.br/bitstream/10183/249606/1/001149158.pdfc95accda9c5ab238f655bc64d9ea1ddbMD5110183/2496062022-10-04 05:01:30.55643oai:www.lume.ufrgs.br:10183/249606Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2022-10-04T08:01:30Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
title Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
spellingShingle Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
Menezes, Bruna Kochhann
Daptomicina
Enterococcus faecium
Antibacterianos
Daptomycin
Bacteraemia
Enterococcus faecium
PK/PD modelling
title_short Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
title_full Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
title_fullStr Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
title_full_unstemmed Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
title_sort Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
author Menezes, Bruna Kochhann
author_facet Menezes, Bruna Kochhann
Alves, Izabel Almeida
Staudt, Keli Jaqueline
Beltrame, Betina Montanari
Venz, Letícia
Michelin, Lessandra
Araújo, Bibiana Verlindo de
Tasso, Leandro
author_role author
author2 Alves, Izabel Almeida
Staudt, Keli Jaqueline
Beltrame, Betina Montanari
Venz, Letícia
Michelin, Lessandra
Araújo, Bibiana Verlindo de
Tasso, Leandro
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Menezes, Bruna Kochhann
Alves, Izabel Almeida
Staudt, Keli Jaqueline
Beltrame, Betina Montanari
Venz, Letícia
Michelin, Lessandra
Araújo, Bibiana Verlindo de
Tasso, Leandro
dc.subject.por.fl_str_mv Daptomicina
Enterococcus faecium
Antibacterianos
topic Daptomicina
Enterococcus faecium
Antibacterianos
Daptomycin
Bacteraemia
Enterococcus faecium
PK/PD modelling
dc.subject.eng.fl_str_mv Daptomycin
Bacteraemia
Enterococcus faecium
PK/PD modelling
description Objectives The aim of this study was to investigate the effect of daptomycin against vancomycin-resistant Enterococcus faecium bacteraemia using computer modelling. Methods Data obtained in vitro from time-kill curves were evaluated by PK/PD modelling and Monte Carlo simulations to determine the logarithmic reduction in the number of colony-forming units (CFU)/mL over 18 days of daptomycin treatment at 6, 8, and 10 mg/kg doses every 24 or 48 h and with variations in creatinine clearance (CLCR) of 15–29, 30–49, and 50–100 mL/min/1.73 m2. Monte Carlo simulations were performed to evaluate the probability of target attainment (PTA) for an area under the unbound drug concentration-time curve/minimum inhibitory concentration (fAUC/MIC) > 36 at the same doses and CLCR. Results Static time-kill model was employed to investigate the antibacterial efficacy of constant daptomycin concentrations. The time-kill curve analysis was performed using mathematical modelling based on a Hill coefficient factor. There was an expressive reduction (> 2 Log CFU/mL) over 18 days of daptomycin treatment in 75th percentile of individuals with CLCR of 15–100 mL/min/1.73 m2) with daptomycin 6–10 mg/kg/day, except for daptomycin every 48 h. Using fAUC/MIC > 36, PTA was > 90% at MICs ≤ 2 μg/mL. Conclusions Higher daptomycin doses were associated with higher mortality in time-kill curves. The simulations indicated that independent of the CLCR the therapeutic responses of VRE occur with doses of daptomycin ≥ 6 mg/kg/day and daptomycin every 48 h is insufficient to treat enterococcal bacteraemia.
publishDate 2020
dc.date.issued.fl_str_mv 2020
dc.date.accessioned.fl_str_mv 2022-10-03T04:48:57Z
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dc.identifier.issn.pt_BR.fl_str_mv 1517-8382
dc.identifier.nrb.pt_BR.fl_str_mv 001149158
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Brazilian journal of microbiology. São Paulo. Vol. 51 (2020), p. 169-176
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