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Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis
OBJECTIVE: Studies in the literature regarding the use of remdesivir to treat COVID-19 patients have shown conflicting results. This study sought to answer questions related to the use of remdesivir for the treatment of patients hospitalized with moderate to severe COVID-19. METHODS: This was a syst...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Pneumologia e Tisiologia
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836613/ https://www.ncbi.nlm.nih.gov/pubmed/35137874 http://dx.doi.org/10.36416/1806-3756/e20210393 |
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author | Tanni, Suzana E Silvinato, Antonio Floriano, Idevaldo Bacha, Hélio A Barbosa, Alexandre Naime Bernardo, Wanderley M |
author_facet | Tanni, Suzana E Silvinato, Antonio Floriano, Idevaldo Bacha, Hélio A Barbosa, Alexandre Naime Bernardo, Wanderley M |
author_sort | Tanni, Suzana E |
collection | PubMed |
description | OBJECTIVE: Studies in the literature regarding the use of remdesivir to treat COVID-19 patients have shown conflicting results. This study sought to answer questions related to the use of remdesivir for the treatment of patients hospitalized with moderate to severe COVID-19. METHODS: This was a systematic review and meta-analysis including phase 3 randomized clinical trials (RCTs) and observational cohort studies selected from various databases, comparing patients hospitalized with moderate to severe COVID-19 receiving remdesivir and controls. RESULTS: A total of 207 studies were retrieved, 9 of which met the eligibility criteria and were included in the study. The meta-analysis using RCTs alone showed no statistically significant differences regarding mortality or use of mechanical ventilation/extracorporeal membrane oxygenation between remdesivir and control groups, and the quality of evidence was moderate and low, respectively. The use of remdesivir increased the recovery rate by 6% (95% CI, 3-9); p = 0.004) and the clinical improvement rate by 7% (95% CI, 1-14); p = 0.02). Additionally, no significant differences in mortality were found between remdesivir and control groups when the meta-analysis used observational cohort studies alone (risk difference = −0.01 (95% CI, −0.02 to 0.01; p = 0.32), the quality of evidence being moderate, and the risk of adverse events was 4% ([95% CI, −0.08 to 0.01]; p = 0.09). CONCLUSIONS: The use of remdesivir for the treatment of patients with moderate to severe COVID-19 had no significant impact on clinically important outcomes. |
format | Online Article Text |
id | pubmed-8836613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Sociedade Brasileira de Pneumologia e Tisiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-88366132022-03-14 Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis Tanni, Suzana E Silvinato, Antonio Floriano, Idevaldo Bacha, Hélio A Barbosa, Alexandre Naime Bernardo, Wanderley M J Bras Pneumol Systematic Review and Meta-Analysis OBJECTIVE: Studies in the literature regarding the use of remdesivir to treat COVID-19 patients have shown conflicting results. This study sought to answer questions related to the use of remdesivir for the treatment of patients hospitalized with moderate to severe COVID-19. METHODS: This was a systematic review and meta-analysis including phase 3 randomized clinical trials (RCTs) and observational cohort studies selected from various databases, comparing patients hospitalized with moderate to severe COVID-19 receiving remdesivir and controls. RESULTS: A total of 207 studies were retrieved, 9 of which met the eligibility criteria and were included in the study. The meta-analysis using RCTs alone showed no statistically significant differences regarding mortality or use of mechanical ventilation/extracorporeal membrane oxygenation between remdesivir and control groups, and the quality of evidence was moderate and low, respectively. The use of remdesivir increased the recovery rate by 6% (95% CI, 3-9); p = 0.004) and the clinical improvement rate by 7% (95% CI, 1-14); p = 0.02). Additionally, no significant differences in mortality were found between remdesivir and control groups when the meta-analysis used observational cohort studies alone (risk difference = −0.01 (95% CI, −0.02 to 0.01; p = 0.32), the quality of evidence being moderate, and the risk of adverse events was 4% ([95% CI, −0.08 to 0.01]; p = 0.09). CONCLUSIONS: The use of remdesivir for the treatment of patients with moderate to severe COVID-19 had no significant impact on clinically important outcomes. Sociedade Brasileira de Pneumologia e Tisiologia 2022-01-24 /pmc/articles/PMC8836613/ /pubmed/35137874 http://dx.doi.org/10.36416/1806-3756/e20210393 Text en © 2022 Sociedade Brasileira de Pneumologia e Tisiologia https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Systematic Review and Meta-Analysis Tanni, Suzana E Silvinato, Antonio Floriano, Idevaldo Bacha, Hélio A Barbosa, Alexandre Naime Bernardo, Wanderley M Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title_full | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title_fullStr | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title_full_unstemmed | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title_short | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis |
title_sort | use of remdesivir in patients with covid-19: a systematic review and meta-analysis |
topic | Systematic Review and Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836613/ https://www.ncbi.nlm.nih.gov/pubmed/35137874 http://dx.doi.org/10.36416/1806-3756/e20210393 |
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