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Rationale for azithromycin in COVID-19: an overview of existing evidence
Azithromycin has rapidly been adopted as a repurposed drug for the treatment of COVID-19, despite the lack of high-quality evidence. In this review, we critically appraise the current pharmacological, preclinical and clinical data of azithromycin for treating COVID-19. Interest in azithromycin has b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811960/ https://www.ncbi.nlm.nih.gov/pubmed/33441373 http://dx.doi.org/10.1136/bmjresp-2020-000806 |
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author | Gyselinck, Iwein Janssens, Wim Verhamme, Peter Vos, Robin |
author_facet | Gyselinck, Iwein Janssens, Wim Verhamme, Peter Vos, Robin |
author_sort | Gyselinck, Iwein |
collection | PubMed |
description | Azithromycin has rapidly been adopted as a repurposed drug for the treatment of COVID-19, despite the lack of high-quality evidence. In this review, we critically appraise the current pharmacological, preclinical and clinical data of azithromycin for treating COVID-19. Interest in azithromycin has been fuelled by favourable treatment outcomes in other viral pneumonias, a documented antiviral effect on SARS-CoV-2 in vitro and uncontrolled case series early in the pandemic. Its antiviral effects presumably result from interfering with receptor mediated binding, viral lysosomal escape, intracellular cell-signalling pathways and enhancing type I and III interferon expression. Its immunomodulatory effects may mitigate excessive inflammation and benefit tissue repair. Currently, in vivo reports on azithromycin in COVID-19 are conflicting and do not endorse its widespread use outside of clinical trials. They are, however, mostly retrospective and therefore inherently biased. The effect size of azithromycin may depend on when it is started. Also, extended follow-up is needed to assess benefits in the recovery phase. Safety data warrant monitoring of drug–drug interactions and subsequent cardiac adverse events, especially with hydroxychloroquine. More prospective data of large randomised controlled studies are expected and much-needed. Uniform reporting of results should be strongly encouraged to facilitate data pooling with the many ongoing initiatives. |
format | Online Article Text |
id | pubmed-7811960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-78119602021-01-19 Rationale for azithromycin in COVID-19: an overview of existing evidence Gyselinck, Iwein Janssens, Wim Verhamme, Peter Vos, Robin BMJ Open Respir Res Respiratory Infection Azithromycin has rapidly been adopted as a repurposed drug for the treatment of COVID-19, despite the lack of high-quality evidence. In this review, we critically appraise the current pharmacological, preclinical and clinical data of azithromycin for treating COVID-19. Interest in azithromycin has been fuelled by favourable treatment outcomes in other viral pneumonias, a documented antiviral effect on SARS-CoV-2 in vitro and uncontrolled case series early in the pandemic. Its antiviral effects presumably result from interfering with receptor mediated binding, viral lysosomal escape, intracellular cell-signalling pathways and enhancing type I and III interferon expression. Its immunomodulatory effects may mitigate excessive inflammation and benefit tissue repair. Currently, in vivo reports on azithromycin in COVID-19 are conflicting and do not endorse its widespread use outside of clinical trials. They are, however, mostly retrospective and therefore inherently biased. The effect size of azithromycin may depend on when it is started. Also, extended follow-up is needed to assess benefits in the recovery phase. Safety data warrant monitoring of drug–drug interactions and subsequent cardiac adverse events, especially with hydroxychloroquine. More prospective data of large randomised controlled studies are expected and much-needed. Uniform reporting of results should be strongly encouraged to facilitate data pooling with the many ongoing initiatives. BMJ Publishing Group 2021-01-13 /pmc/articles/PMC7811960/ /pubmed/33441373 http://dx.doi.org/10.1136/bmjresp-2020-000806 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Respiratory Infection Gyselinck, Iwein Janssens, Wim Verhamme, Peter Vos, Robin Rationale for azithromycin in COVID-19: an overview of existing evidence |
title | Rationale for azithromycin in COVID-19: an overview of existing evidence |
title_full | Rationale for azithromycin in COVID-19: an overview of existing evidence |
title_fullStr | Rationale for azithromycin in COVID-19: an overview of existing evidence |
title_full_unstemmed | Rationale for azithromycin in COVID-19: an overview of existing evidence |
title_short | Rationale for azithromycin in COVID-19: an overview of existing evidence |
title_sort | rationale for azithromycin in covid-19: an overview of existing evidence |
topic | Respiratory Infection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811960/ https://www.ncbi.nlm.nih.gov/pubmed/33441373 http://dx.doi.org/10.1136/bmjresp-2020-000806 |
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