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Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment

INTRODUCTION: In December 2019, an outbreak of a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began, resulting in a number of antivirals and immune modulators being repurposed to treat the associated coronavirus disease 2019 (COVID-19). Many patients requiring treatment for COV...

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Autores principales: Marra, Fiona, Smolders, Elise J., El-Sherif, Omar, Boyle, Alison, Davidson, Katherine, Sommerville, Andrew J., Marzolini, Catia, Siccardi, Marco, Burger, David, Gibbons, Sara, Khoo, Saye, Back, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745756/
https://www.ncbi.nlm.nih.gov/pubmed/33336316
http://dx.doi.org/10.1007/s40268-020-00333-0
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author Marra, Fiona
Smolders, Elise J.
El-Sherif, Omar
Boyle, Alison
Davidson, Katherine
Sommerville, Andrew J.
Marzolini, Catia
Siccardi, Marco
Burger, David
Gibbons, Sara
Khoo, Saye
Back, David
author_facet Marra, Fiona
Smolders, Elise J.
El-Sherif, Omar
Boyle, Alison
Davidson, Katherine
Sommerville, Andrew J.
Marzolini, Catia
Siccardi, Marco
Burger, David
Gibbons, Sara
Khoo, Saye
Back, David
author_sort Marra, Fiona
collection PubMed
description INTRODUCTION: In December 2019, an outbreak of a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began, resulting in a number of antivirals and immune modulators being repurposed to treat the associated coronavirus disease 2019 (COVID-19). Many patients requiring treatment for COVID-19 may have either pre-existing renal or hepatic disease or experience acute renal/hepatic injury as a result of the acute infection. Altered renal or hepatic function can significantly affect drug concentrations of medications due to impaired drug metabolism and excretion, resulting in toxicity or reduced efficacy. The aim of this paper is to review the pharmacokinetics and available study data for the experimental COVID-19 therapies in patients with any degree of renal or hepatic impairment to make recommendations for dosing. METHODS: COVID-19 agents included in these recommendations were listed as primaries on the University of Liverpool COVID-19 drug interaction website (www.covid19-druginteractions.org), initially identified from Clinicialtrials.gov and ChicCTR.org.cn. A literature search was performed using PubMed and EMBASE as well as product licences and pharmacokinetic databases. FINDINGS: Remdesivir, dexamethasone, azithromycin, favipiravir, lopinavir/ritonavir, atazanavir, hydroxychloroquine, interferon beta, ribavirin, tocilizumab, anakinra and sarilumab were identified as experimental drugs being used in COVID-19 trials as of November 2020. Limited study data was found for these drugs in patients with renal or hepatic impairment for COVID-19 or other indications. Recommendations were made based on available data, consideration of pharmacokinetic properties (including variability), the dosing and anticipated treatment duration of each regimen in COVID-19 and known toxicities. CONCLUSION: Dosing of drugs used to treat COVID-19 in patients with renal or hepatic impairment is complex. These recommendations were produced to provide guidance to clinicians worldwide who are treating patients with COVID-19, many of whom will have some degree of acute or chronic renal or hepatic impairment.
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spelling pubmed-77457562020-12-18 Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment Marra, Fiona Smolders, Elise J. El-Sherif, Omar Boyle, Alison Davidson, Katherine Sommerville, Andrew J. Marzolini, Catia Siccardi, Marco Burger, David Gibbons, Sara Khoo, Saye Back, David Drugs R D Review Article INTRODUCTION: In December 2019, an outbreak of a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began, resulting in a number of antivirals and immune modulators being repurposed to treat the associated coronavirus disease 2019 (COVID-19). Many patients requiring treatment for COVID-19 may have either pre-existing renal or hepatic disease or experience acute renal/hepatic injury as a result of the acute infection. Altered renal or hepatic function can significantly affect drug concentrations of medications due to impaired drug metabolism and excretion, resulting in toxicity or reduced efficacy. The aim of this paper is to review the pharmacokinetics and available study data for the experimental COVID-19 therapies in patients with any degree of renal or hepatic impairment to make recommendations for dosing. METHODS: COVID-19 agents included in these recommendations were listed as primaries on the University of Liverpool COVID-19 drug interaction website (www.covid19-druginteractions.org), initially identified from Clinicialtrials.gov and ChicCTR.org.cn. A literature search was performed using PubMed and EMBASE as well as product licences and pharmacokinetic databases. FINDINGS: Remdesivir, dexamethasone, azithromycin, favipiravir, lopinavir/ritonavir, atazanavir, hydroxychloroquine, interferon beta, ribavirin, tocilizumab, anakinra and sarilumab were identified as experimental drugs being used in COVID-19 trials as of November 2020. Limited study data was found for these drugs in patients with renal or hepatic impairment for COVID-19 or other indications. Recommendations were made based on available data, consideration of pharmacokinetic properties (including variability), the dosing and anticipated treatment duration of each regimen in COVID-19 and known toxicities. CONCLUSION: Dosing of drugs used to treat COVID-19 in patients with renal or hepatic impairment is complex. These recommendations were produced to provide guidance to clinicians worldwide who are treating patients with COVID-19, many of whom will have some degree of acute or chronic renal or hepatic impairment. Springer International Publishing 2020-12-17 2021-03 /pmc/articles/PMC7745756/ /pubmed/33336316 http://dx.doi.org/10.1007/s40268-020-00333-0 Text en © The Author(s) 2020 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/.
spellingShingle Review Article
Marra, Fiona
Smolders, Elise J.
El-Sherif, Omar
Boyle, Alison
Davidson, Katherine
Sommerville, Andrew J.
Marzolini, Catia
Siccardi, Marco
Burger, David
Gibbons, Sara
Khoo, Saye
Back, David
Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title_full Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title_fullStr Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title_full_unstemmed Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title_short Recommendations for Dosing of Repurposed COVID-19 Medications in Patients with Renal and Hepatic Impairment
title_sort recommendations for dosing of repurposed covid-19 medications in patients with renal and hepatic impairment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745756/
https://www.ncbi.nlm.nih.gov/pubmed/33336316
http://dx.doi.org/10.1007/s40268-020-00333-0
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