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Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol
Cefiderocol is a new broad-spectrum cephalosporin antibiotic with promising activity against various Gram-negative bacteria including carbapenem-resistant strains. A chlorocatechol group in the C-3 side chain provides cefiderocol with a siderophore activity, improving its stability against β-lactama...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613110/ https://www.ncbi.nlm.nih.gov/pubmed/34420182 http://dx.doi.org/10.1007/s40262-021-01063-5 |
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author | Bilal, Muhammad El Tabei, Lobna Büsker, Sören Krauss, Christian Fuhr, Uwe Taubert, Max |
author_facet | Bilal, Muhammad El Tabei, Lobna Büsker, Sören Krauss, Christian Fuhr, Uwe Taubert, Max |
author_sort | Bilal, Muhammad |
collection | PubMed |
description | Cefiderocol is a new broad-spectrum cephalosporin antibiotic with promising activity against various Gram-negative bacteria including carbapenem-resistant strains. A chlorocatechol group in the C-3 side chain provides cefiderocol with a siderophore activity, improving its stability against β-lactamases and facilitating the transportation of cefiderocol across outer bacterial membranes. Cefiderocol shows linear pharmacokinetics over a broad range of clinically relevant doses, with unchanged renal excretion constituting the main route of elimination. Geometric means (coefficient of variation) of the volume of distribution and clearance in individuals with normal kidney function were 15.8 (15%) L and 4.70 (27%) L/h, respectively. In patients with end-stage renal disease, clearance was 1.10 (24%) L/h. Time above the minimum inhibitory concentration is the main predictor of efficacy. There is no evidence for clinically relevant interactions of cefiderocol with other drugs mediated by metabolizing enzymes or drug transporters. Simulations based on population pharmacokinetic modeling suggest that dosing regimens should be adjusted based on kidney function to optimize therapeutic exposure to cefiderocol. Clinical efficacy trials indicated that cefiderocol is non-inferior to imipenem/cilastatin in the treatment of complicated urinary tract infections and acute uncomplicated pyelonephritis, and to meropenem in the treatment of nosocomial pneumonia. In the one study currently available, cefiderocol performed similarly to the best available therapy in the treatment of severe carbapenem-resistant Gram-negative infections regarding clinical and microbiological efficacy. In summary, cefiderocol shows favorable pharmacokinetic/pharmacodynamic properties and an acceptable safety profile, suggesting that cefiderocol might be a viable option to treat infections with bacteria resistant to other antibiotics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40262-021-01063-5. |
format | Online Article Text |
id | pubmed-8613110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-86131102021-12-10 Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol Bilal, Muhammad El Tabei, Lobna Büsker, Sören Krauss, Christian Fuhr, Uwe Taubert, Max Clin Pharmacokinet Review Article Cefiderocol is a new broad-spectrum cephalosporin antibiotic with promising activity against various Gram-negative bacteria including carbapenem-resistant strains. A chlorocatechol group in the C-3 side chain provides cefiderocol with a siderophore activity, improving its stability against β-lactamases and facilitating the transportation of cefiderocol across outer bacterial membranes. Cefiderocol shows linear pharmacokinetics over a broad range of clinically relevant doses, with unchanged renal excretion constituting the main route of elimination. Geometric means (coefficient of variation) of the volume of distribution and clearance in individuals with normal kidney function were 15.8 (15%) L and 4.70 (27%) L/h, respectively. In patients with end-stage renal disease, clearance was 1.10 (24%) L/h. Time above the minimum inhibitory concentration is the main predictor of efficacy. There is no evidence for clinically relevant interactions of cefiderocol with other drugs mediated by metabolizing enzymes or drug transporters. Simulations based on population pharmacokinetic modeling suggest that dosing regimens should be adjusted based on kidney function to optimize therapeutic exposure to cefiderocol. Clinical efficacy trials indicated that cefiderocol is non-inferior to imipenem/cilastatin in the treatment of complicated urinary tract infections and acute uncomplicated pyelonephritis, and to meropenem in the treatment of nosocomial pneumonia. In the one study currently available, cefiderocol performed similarly to the best available therapy in the treatment of severe carbapenem-resistant Gram-negative infections regarding clinical and microbiological efficacy. In summary, cefiderocol shows favorable pharmacokinetic/pharmacodynamic properties and an acceptable safety profile, suggesting that cefiderocol might be a viable option to treat infections with bacteria resistant to other antibiotics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40262-021-01063-5. Springer International Publishing 2021-08-22 2021 /pmc/articles/PMC8613110/ /pubmed/34420182 http://dx.doi.org/10.1007/s40262-021-01063-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review Article Bilal, Muhammad El Tabei, Lobna Büsker, Sören Krauss, Christian Fuhr, Uwe Taubert, Max Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title | Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title_full | Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title_fullStr | Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title_full_unstemmed | Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title_short | Clinical Pharmacokinetics and Pharmacodynamics of Cefiderocol |
title_sort | clinical pharmacokinetics and pharmacodynamics of cefiderocol |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613110/ https://www.ncbi.nlm.nih.gov/pubmed/34420182 http://dx.doi.org/10.1007/s40262-021-01063-5 |
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