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Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis
Robust population pharmacokinetic (PK) data for fluconazole are scarce. The variability of fluconazole penetration into the central nervous system (CNS) is not known. A fluconazole PK study was conducted in 43 patients receiving oral fluconazole (usually 800 mg every 24 h [q24h]) in combination with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125572/ https://www.ncbi.nlm.nih.gov/pubmed/29914943 http://dx.doi.org/10.1128/AAC.00885-18 |
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author | Stott, Katharine E. Beardsley, Justin Kolamunnage-Dona, Ruwanthi Castelazo, Anahi Santoyo Kibengo, Freddie Mukasa Mai, Nguyen Thi Hoang Tùng, Nguyễn Lê Nhu’ Cuc, Ngo Thi Kim Day, Jeremy Hope, William |
author_facet | Stott, Katharine E. Beardsley, Justin Kolamunnage-Dona, Ruwanthi Castelazo, Anahi Santoyo Kibengo, Freddie Mukasa Mai, Nguyen Thi Hoang Tùng, Nguyễn Lê Nhu’ Cuc, Ngo Thi Kim Day, Jeremy Hope, William |
author_sort | Stott, Katharine E. |
collection | PubMed |
description | Robust population pharmacokinetic (PK) data for fluconazole are scarce. The variability of fluconazole penetration into the central nervous system (CNS) is not known. A fluconazole PK study was conducted in 43 patients receiving oral fluconazole (usually 800 mg every 24 h [q24h]) in combination with amphotericin B deoxycholate (1 mg/kg q24h) for cryptococcal meningitis (CM). A four-compartment PK model was developed, and Monte Carlo simulations were performed for a range of fluconazole dosages. A meta-analysis of trials reporting outcomes of CM patients treated with fluconazole monotherapy was performed. Adjusted for bioavailability, the PK parameter means (standard deviation) were the following: clearance, 0.72 (0.24) liters/h; volume of the central compartment, 18.07 (6.31) liters; volume of the CNS compartment, 32.07 (17.60) liters; first-order rate constant from the central to peripheral compartment, 12.20 (11.17) h(−1), from the peripheral to central compartment, 18.10 (8.25) h(−1), from the central to CNS compartment, 35.43 (13.74) h(−1), and from the CNS to central the compartment, 28.63 (10.03) h(−1). Simulations of the area under concentration-time curve resulted in median (interquartile range) values of 1,143.2 (range, 988.4 to 1,378.0) mg · h/liter in plasma (AUC(plasma)) and 982.9 (range, 781.0 to 1,185.9) mg · h/liter in cerebrospinal fluid (AUC(CSF)) after a dosage of 1,200 mg q24h. The mean simulated ratio of AUC(CSF)/AUC(plasma) was 0.89 (standard deviation [SD], 0.44). The recommended dosage of fluconazole for CM induction therapy fails to attain the pharmacodynamic (PD) target in respect to the wild-type MIC distribution for C. neoformans. The meta-analysis suggested modest improvements in both CSF sterility and mortality outcomes with escalating dosage. This study provides the pharmacodynamic rationale for the long-recognized fact that fluconazole monotherapy is an inadequate induction regimen for CM. |
format | Online Article Text |
id | pubmed-6125572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61255722018-09-17 Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis Stott, Katharine E. Beardsley, Justin Kolamunnage-Dona, Ruwanthi Castelazo, Anahi Santoyo Kibengo, Freddie Mukasa Mai, Nguyen Thi Hoang Tùng, Nguyễn Lê Nhu’ Cuc, Ngo Thi Kim Day, Jeremy Hope, William Antimicrob Agents Chemother Pharmacology Robust population pharmacokinetic (PK) data for fluconazole are scarce. The variability of fluconazole penetration into the central nervous system (CNS) is not known. A fluconazole PK study was conducted in 43 patients receiving oral fluconazole (usually 800 mg every 24 h [q24h]) in combination with amphotericin B deoxycholate (1 mg/kg q24h) for cryptococcal meningitis (CM). A four-compartment PK model was developed, and Monte Carlo simulations were performed for a range of fluconazole dosages. A meta-analysis of trials reporting outcomes of CM patients treated with fluconazole monotherapy was performed. Adjusted for bioavailability, the PK parameter means (standard deviation) were the following: clearance, 0.72 (0.24) liters/h; volume of the central compartment, 18.07 (6.31) liters; volume of the CNS compartment, 32.07 (17.60) liters; first-order rate constant from the central to peripheral compartment, 12.20 (11.17) h(−1), from the peripheral to central compartment, 18.10 (8.25) h(−1), from the central to CNS compartment, 35.43 (13.74) h(−1), and from the CNS to central the compartment, 28.63 (10.03) h(−1). Simulations of the area under concentration-time curve resulted in median (interquartile range) values of 1,143.2 (range, 988.4 to 1,378.0) mg · h/liter in plasma (AUC(plasma)) and 982.9 (range, 781.0 to 1,185.9) mg · h/liter in cerebrospinal fluid (AUC(CSF)) after a dosage of 1,200 mg q24h. The mean simulated ratio of AUC(CSF)/AUC(plasma) was 0.89 (standard deviation [SD], 0.44). The recommended dosage of fluconazole for CM induction therapy fails to attain the pharmacodynamic (PD) target in respect to the wild-type MIC distribution for C. neoformans. The meta-analysis suggested modest improvements in both CSF sterility and mortality outcomes with escalating dosage. This study provides the pharmacodynamic rationale for the long-recognized fact that fluconazole monotherapy is an inadequate induction regimen for CM. American Society for Microbiology 2018-08-27 /pmc/articles/PMC6125572/ /pubmed/29914943 http://dx.doi.org/10.1128/AAC.00885-18 Text en Copyright © 2018 Stott et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Pharmacology Stott, Katharine E. Beardsley, Justin Kolamunnage-Dona, Ruwanthi Castelazo, Anahi Santoyo Kibengo, Freddie Mukasa Mai, Nguyen Thi Hoang Tùng, Nguyễn Lê Nhu’ Cuc, Ngo Thi Kim Day, Jeremy Hope, William Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title | Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title_full | Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title_fullStr | Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title_full_unstemmed | Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title_short | Population Pharmacokinetics and Cerebrospinal Fluid Penetration of Fluconazole in Adults with Cryptococcal Meningitis |
title_sort | population pharmacokinetics and cerebrospinal fluid penetration of fluconazole in adults with cryptococcal meningitis |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125572/ https://www.ncbi.nlm.nih.gov/pubmed/29914943 http://dx.doi.org/10.1128/AAC.00885-18 |
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