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Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study
BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic has spread all over the world resulting in high mortality, yet no specific antiviral treatment has been recommended. METHODS: A retrospective descriptive study was conducted involving 19 consecutive critically ill patients during January 2...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672023/ https://www.ncbi.nlm.nih.gov/pubmed/34916812 http://dx.doi.org/10.2147/IDR.S330743 |
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author | Xu, Yonghao Li, Manshu Zhou, Liang Liu, Dongdong He, Weiqun Liang, Weibo Sun, Qingwen Sun, Huadong Li, Yimin Liu, Xiaoqing |
author_facet | Xu, Yonghao Li, Manshu Zhou, Liang Liu, Dongdong He, Weiqun Liang, Weibo Sun, Qingwen Sun, Huadong Li, Yimin Liu, Xiaoqing |
author_sort | Xu, Yonghao |
collection | PubMed |
description | BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic has spread all over the world resulting in high mortality, yet no specific antiviral treatment has been recommended. METHODS: A retrospective descriptive study was conducted involving 19 consecutive critically ill patients during January 27, 2020 to April 18, 2020. Ribavirin was given at 0.15g q8h orally upon ICU admission for 7 to 21 days. Here, 28-day mortality, lower respiratory tract specimens (ETA), and ribavirin side effect on the day of ICU admission (Day 1), Day 7, Day 14 and Day 21 were analyzed. RESULTS: All the nineteen critically ill COVID-19 patients (14 males and 5 females, median age 56yr) survived through to the 28th day of observations with 6 patients (31.58%) being discharged from the ICU. The SARS-CoV-2 viral positivity in sputum/ETA was 100% (19/19) on Day 1, 73.68% (14/19) on Day 7, 57.89% (11/19) on Day 14 and 36.84% (7/19) on Day 21. Ribavirin side effect was not observed in these patients. CONCLUSION: Ribavirin is well tolerated in critically ill patients with COVID-19 and may benefit COVID-19 patients through increasing the virus clearance. |
format | Online Article Text |
id | pubmed-8672023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-86720232021-12-15 Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study Xu, Yonghao Li, Manshu Zhou, Liang Liu, Dongdong He, Weiqun Liang, Weibo Sun, Qingwen Sun, Huadong Li, Yimin Liu, Xiaoqing Infect Drug Resist Rapid Communication BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic has spread all over the world resulting in high mortality, yet no specific antiviral treatment has been recommended. METHODS: A retrospective descriptive study was conducted involving 19 consecutive critically ill patients during January 27, 2020 to April 18, 2020. Ribavirin was given at 0.15g q8h orally upon ICU admission for 7 to 21 days. Here, 28-day mortality, lower respiratory tract specimens (ETA), and ribavirin side effect on the day of ICU admission (Day 1), Day 7, Day 14 and Day 21 were analyzed. RESULTS: All the nineteen critically ill COVID-19 patients (14 males and 5 females, median age 56yr) survived through to the 28th day of observations with 6 patients (31.58%) being discharged from the ICU. The SARS-CoV-2 viral positivity in sputum/ETA was 100% (19/19) on Day 1, 73.68% (14/19) on Day 7, 57.89% (11/19) on Day 14 and 36.84% (7/19) on Day 21. Ribavirin side effect was not observed in these patients. CONCLUSION: Ribavirin is well tolerated in critically ill patients with COVID-19 and may benefit COVID-19 patients through increasing the virus clearance. Dove 2021-12-10 /pmc/articles/PMC8672023/ /pubmed/34916812 http://dx.doi.org/10.2147/IDR.S330743 Text en © 2021 Xu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Rapid Communication Xu, Yonghao Li, Manshu Zhou, Liang Liu, Dongdong He, Weiqun Liang, Weibo Sun, Qingwen Sun, Huadong Li, Yimin Liu, Xiaoqing Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title | Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title_full | Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title_fullStr | Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title_full_unstemmed | Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title_short | Ribavirin Treatment for Critically Ill COVID-19 Patients: An Observational Study |
title_sort | ribavirin treatment for critically ill covid-19 patients: an observational study |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672023/ https://www.ncbi.nlm.nih.gov/pubmed/34916812 http://dx.doi.org/10.2147/IDR.S330743 |
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