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Published in: Critical Care 1/2019

Open Access 01-12-2019 | Pharmacokinetics | Letter

Adsorption and caspofungin dosing during continuous renal replacement therapy

Authors: Patrick M. Honore, David De Bels, Rachid Attou, Sebastien Redant, Andrea Gallerani, Kianoush Kashani

Published in: Critical Care | Issue 1/2019

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Excerpt

In a recent letter by Aguilar et al., the pharmacokinetics of caspofungin during continuous renal replacement therapy (CRRT) and the potential impact of adsorptive membrane capacity on its removal were described [1]. In this study, administered loading caspofungin dose was 50 or 70 mg based on patient weight. As the investigators demonstrated and considering that echinocandins are highly protein-bound and non-renally eliminated, caspofungin removal with CRRT was negligible [1]. Polysulphone membranes that were used by the investigators have minimal adsorptive capacity [2]. However, highly adsorptive membranes (HAMs; e.g., AN69 surface-treated and polymethylmethacrylate filters) could potentially adsorb echinocandins effectively. HAMs’ slow saturation rate would likely increase echinocandins elimination to a clinically relevant level. This, in turn, could lower maximal concentration (Cmax). By reducing Cmax/minimal inhibitory concentration (MIC) ratio for this class of antifungals, their effectiveness could be compromised [3]. This may lead to the need for dose adjustment while on CRRT [4]. In a recent study, Roger et al. showed a higher loading dose (100 mg) is necessary for critically ill patients on CRRT, which is higher than the dosing scheme used by Aguilar et al. [5]. It is essential to highlight that despite the fact that Aguilar and colleagues found minimal caspofungin elimination by CRRT, a third of their patients had subtherapeutic blood levels. Therefore, the standard dosing scheme (50 or 70 mg based on patient weight) when HAMs are used may result in significantly low caspofungin blood levels. We believe, further studies should be conducted focusing on caspofungin dosing on CRRT with HAM filters in order to evaluate the pharmacokinetics of caspofungin and determine its correct dosing strategy. …
Literature
1.
go back to reference Aguilar G, Ferriols R, Lozano A, Ezquer C, Carbonell JA, Jurado A, et al. Optimal doses of caspofungin during continuous venovenous hemodiafiltration in critically ill patients. Crit Care. 2017;21:17.CrossRef Aguilar G, Ferriols R, Lozano A, Ezquer C, Carbonell JA, Jurado A, et al. Optimal doses of caspofungin during continuous venovenous hemodiafiltration in critically ill patients. Crit Care. 2017;21:17.CrossRef
2.
go back to reference Honore PM, Jacobs R, Joannes-Boyau O, De Regt J, De Waele E, et al. Newly designed CRRT membranes for sepsis and SIRS--a pragmatic approach for bedside intensivists summarizing the more recent advances: a systematic structured review. ASAIO J. 2013;59:99–106.CrossRef Honore PM, Jacobs R, Joannes-Boyau O, De Regt J, De Waele E, et al. Newly designed CRRT membranes for sepsis and SIRS--a pragmatic approach for bedside intensivists summarizing the more recent advances: a systematic structured review. ASAIO J. 2013;59:99–106.CrossRef
4.
go back to reference Tomasa TM. Echinocandins and continuous renal replacement therapies: the role of adsorption. J Nephrol Kidney Dis. 2018;2(1):118. Tomasa TM. Echinocandins and continuous renal replacement therapies: the role of adsorption. J Nephrol Kidney Dis. 2018;2(1):118.
Metadata
Title
Adsorption and caspofungin dosing during continuous renal replacement therapy
Authors
Patrick M. Honore
David De Bels
Rachid Attou
Sebastien Redant
Andrea Gallerani
Kianoush Kashani
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Critical Care / Issue 1/2019
Electronic ISSN: 1364-8535
DOI
https://doi.org/10.1186/s13054-019-2526-2

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