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Published in: International Journal of Clinical Pharmacy 1/2017

01-02-2017 | Short Research Report

Evaluation of nucleoside reverse transcriptase inhibitor dosing during continuous veno-venous hemofiltration

Authors: Milena M. McLaughlin, Inela Masic, Lana Gerzenshtein

Published in: International Journal of Clinical Pharmacy | Issue 1/2017

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Abstract

Background Unpredictable drug concentrations may lead to suboptimal exposure to nucleoside reverse transcriptase inhibitors (NRTIs) due to inadequate doses administered during continuous veno-venous hemofiltration (CVVH), which in turn may lead to decreased antiretroviral efficacy and possibly further HIV disease progression. Objective To compare administered doses of NRTIs to calculated doses of NRTIs to evaluate if patients were expected to have a favorable pharmacokinetic exposure profile while receiving CVVH. Methods The NRTI dose was compared to a table of recommendations based on a mathematical formula that estimates the amount of drug expected to be removed during CVVH. Results Twelve patients were on 27 NRTIs. Eleven (41%) NRTI doses were expected to provide a favorable pharmacokinetic profile based on pharmacokinetic mathematical calculations. Conclusion The majority of NRTIs were potentially not optimally dosed based on proposed pharmacokinetic calculations.
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Metadata
Title
Evaluation of nucleoside reverse transcriptase inhibitor dosing during continuous veno-venous hemofiltration
Authors
Milena M. McLaughlin
Inela Masic
Lana Gerzenshtein
Publication date
01-02-2017
Publisher
Springer International Publishing
Published in
International Journal of Clinical Pharmacy / Issue 1/2017
Print ISSN: 2210-7703
Electronic ISSN: 2210-7711
DOI
https://doi.org/10.1007/s11096-016-0401-7

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