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The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia

BACKGROUND: Despite the proven benefits of dexamethasone in hospitalized coronavirus disease 2019 (COVID-19) patients, the optimum time for the administration of dexamethasone is unknown. We investigated the progression of COVID-19 pneumonia based on the timing of dexamethasone administration. METHO...

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Autores principales: Lee, Hyun Woo, Park, Jimyung, Lee, Jung-Kyu, Park, Tae Yeon, Heo, Eun Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Tuberculosis and Respiratory Diseases 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273022/
https://www.ncbi.nlm.nih.gov/pubmed/34078038
http://dx.doi.org/10.4046/trd.2021.0009
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author Lee, Hyun Woo
Park, Jimyung
Lee, Jung-Kyu
Park, Tae Yeon
Heo, Eun Young
author_facet Lee, Hyun Woo
Park, Jimyung
Lee, Jung-Kyu
Park, Tae Yeon
Heo, Eun Young
author_sort Lee, Hyun Woo
collection PubMed
description BACKGROUND: Despite the proven benefits of dexamethasone in hospitalized coronavirus disease 2019 (COVID-19) patients, the optimum time for the administration of dexamethasone is unknown. We investigated the progression of COVID-19 pneumonia based on the timing of dexamethasone administration. METHODS: A single-center, retrospective cohort study based on medical record reviews was conducted between June 10 and September 21, 2020. We compared the risk of severe COVID-19, defined as the use of a high-flow nasal cannula or a mechanical ventilator, between groups that received dexamethasone either within 24 hours of hypoxemia (early dexamethasone group) or 24 hours after hypoxemia (late dexamethasone group). Hypoxemia was defined as room-air SpO(2) <90%. RESULTS: Among 59 patients treated with dexamethasone for COVID-19 pneumonia, 30 were in the early dexamethasone group and 29 were in the late dexamethasone group. There was no significant difference in baseline characteristics, the time interval from symptom onset to diagnosis or hospitalization, or the use of antiviral or antibacterial agents between the two groups. The early dexamethasone group showed a significantly lower rate of severe COVID-19 compared to the control group (75.9% vs. 40.0%, p=0.012). Further, the early dexamethasone group showed a significantly shorter total duration of oxygen supplementation (10.45 days vs. 21.61 days, p=0.003) and length of stay in the hospital (19.76 days vs. 27.21 days, p=0.013). However, extracorporeal membrane oxygenation and in-hospital mortality rates were not significantly different between the two groups. CONCLUSION: Early administration of dexamethasone may prevent the progression of COVID-19 to a severe disease, without increased mortality.
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spelling pubmed-82730222021-07-26 The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia Lee, Hyun Woo Park, Jimyung Lee, Jung-Kyu Park, Tae Yeon Heo, Eun Young Tuberc Respir Dis (Seoul) Original Article BACKGROUND: Despite the proven benefits of dexamethasone in hospitalized coronavirus disease 2019 (COVID-19) patients, the optimum time for the administration of dexamethasone is unknown. We investigated the progression of COVID-19 pneumonia based on the timing of dexamethasone administration. METHODS: A single-center, retrospective cohort study based on medical record reviews was conducted between June 10 and September 21, 2020. We compared the risk of severe COVID-19, defined as the use of a high-flow nasal cannula or a mechanical ventilator, between groups that received dexamethasone either within 24 hours of hypoxemia (early dexamethasone group) or 24 hours after hypoxemia (late dexamethasone group). Hypoxemia was defined as room-air SpO(2) <90%. RESULTS: Among 59 patients treated with dexamethasone for COVID-19 pneumonia, 30 were in the early dexamethasone group and 29 were in the late dexamethasone group. There was no significant difference in baseline characteristics, the time interval from symptom onset to diagnosis or hospitalization, or the use of antiviral or antibacterial agents between the two groups. The early dexamethasone group showed a significantly lower rate of severe COVID-19 compared to the control group (75.9% vs. 40.0%, p=0.012). Further, the early dexamethasone group showed a significantly shorter total duration of oxygen supplementation (10.45 days vs. 21.61 days, p=0.003) and length of stay in the hospital (19.76 days vs. 27.21 days, p=0.013). However, extracorporeal membrane oxygenation and in-hospital mortality rates were not significantly different between the two groups. CONCLUSION: Early administration of dexamethasone may prevent the progression of COVID-19 to a severe disease, without increased mortality. The Korean Academy of Tuberculosis and Respiratory Diseases 2021-07 2021-03-29 /pmc/articles/PMC8273022/ /pubmed/34078038 http://dx.doi.org/10.4046/trd.2021.0009 Text en Copyright © 2021 The Korean Academy of Tuberculosis and Respiratory Diseases https://creativecommons.org/licenses/by-nc/4.0/It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ).
spellingShingle Original Article
Lee, Hyun Woo
Park, Jimyung
Lee, Jung-Kyu
Park, Tae Yeon
Heo, Eun Young
The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title_full The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title_fullStr The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title_full_unstemmed The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title_short The Effect of the Timing of Dexamethasone Administration in Patients with COVID-19 Pneumonia
title_sort effect of the timing of dexamethasone administration in patients with covid-19 pneumonia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273022/
https://www.ncbi.nlm.nih.gov/pubmed/34078038
http://dx.doi.org/10.4046/trd.2021.0009
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