dc.contributor | Universidade Estadual Paulista (UNESP) | |
dc.contributor | Associação Médica Brasileira | |
dc.contributor | Cooperativa Baixa Mogiana | |
dc.contributor | Hospital Israelita Albert Einstein | |
dc.contributor | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2022-04-29T08:39:27Z | |
dc.date.accessioned | 2022-12-20T03:02:43Z | |
dc.date.available | 2022-04-29T08:39:27Z | |
dc.date.available | 2022-12-20T03:02:43Z | |
dc.date.created | 2022-04-29T08:39:27Z | |
dc.date.issued | 2022-01-01 | |
dc.identifier | Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia, v. 48, n. 1, p. e20210393-, 2022. | |
dc.identifier | 1806-3756 | |
dc.identifier | http://hdl.handle.net/11449/230356 | |
dc.identifier | 10.36416/1806-3756/e20210393 | |
dc.identifier | 2-s2.0-85124254896 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/5410490 | |
dc.description.abstract | 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. | |
dc.language | eng | |
dc.language | por | |
dc.relation | Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia | |
dc.source | Scopus | |
dc.title | Use of remdesivir in patients with COVID-19: a systematic review and meta-analysis | |
dc.type | Artículos de revistas | |