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Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients

INTRODUCTION: Corticosteroids are one of the most promising therapeutic agents for critically ill patients with coronavirus disease 2019 (COVID-19). Despite emerging data, assessed populations and regimens vary, and there are patient subgroups whose response to steroids remains unclear. We aimed to...

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Autores principales: Oganesyan, Armen, Menzulin, Ruslan, Surovoy, Yury, Nikiforchin, Andrei, Zykov, Kirill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645403/
https://www.ncbi.nlm.nih.gov/pubmed/34877019
http://dx.doi.org/10.1155/2021/5557302
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author Oganesyan, Armen
Menzulin, Ruslan
Surovoy, Yury
Nikiforchin, Andrei
Zykov, Kirill
author_facet Oganesyan, Armen
Menzulin, Ruslan
Surovoy, Yury
Nikiforchin, Andrei
Zykov, Kirill
author_sort Oganesyan, Armen
collection PubMed
description INTRODUCTION: Corticosteroids are one of the most promising therapeutic agents for critically ill patients with coronavirus disease 2019 (COVID-19). Despite emerging data, assessed populations and regimens vary, and there are patient subgroups whose response to steroids remains unclear. We aimed to evaluate the outcomes of COVID-19 patients admitted to the intensive care unit (ICU) and treated with a short dexamethasone course to determine which patient categories derive the highest benefit. METHODS: A retrospective cohort study was conducted using a prospectively collected single-center ICU database (April 1–October 1, 2020). Adult COVID-19 patients were assigned to dexamethasone (12 mg × 3 days) and usual care groups. Patient, management, and outcome data were extracted. The primary outcome was the 28-day ICU mortality. Subgroup analysis was performed to assess the impact of dexamethasone on mortality in patients with invasive mechanical ventilation (IMV). RESULTS: Of 233 patients, 220 (median age: 65 years, 38% female) were included: 83 patients received dexamethasone and 137 received usual care. Overall, 28 (33.7%) and 54 (39.4%) patients in the dexamethasone and usual care groups, respectively, died within 28 days since ICU admission (rate ratio (RR) 0.86; 95% confidence interval (95% CI): 0.59–1.23; p=0.405). In the IMV cohort, dexamethasone did not decrease the 28-day mortality compared with usual care (47.5% vs. 62.0%; RR 0.78; 95% CI: 0.57–1.09; p=0.107). A subgroup analysis revealed significantly lower 28-day mortality in IMV patients <65 years receiving dexamethasone vs. usual care (22.6% vs. 48.5%; RR 0.47; 95% CI: 0.22–0.98; p=0.043), which was not seen in IMV patients ≥65 years (75.0% vs. 71.1%; RR 1.06; 95% CI: 0.79–1.42; p=0.719). Patients ≥65 years experienced hyperglycemia, bacterial infection, and septic shock significantly more often than younger patients who received dexamethasone (p=0.002, p=0.025, and p < 0.001, respectively). CONCLUSIONS: A 3-day dexamethasone course is not associated with lower 28-day mortality in critically ill COVID-19 patients, either in the entire ICU cohort or in the IMV. Dexamethasone may significantly reduce the 28-day mortality in IMV patients <65 years, but not in the older IMV subgroup. Dexamethasone administration in patients ≥65 years is associated with a significantly higher rate of adverse events than that in younger patients.
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spelling pubmed-86454032021-12-06 Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients Oganesyan, Armen Menzulin, Ruslan Surovoy, Yury Nikiforchin, Andrei Zykov, Kirill Crit Care Res Pract Research Article INTRODUCTION: Corticosteroids are one of the most promising therapeutic agents for critically ill patients with coronavirus disease 2019 (COVID-19). Despite emerging data, assessed populations and regimens vary, and there are patient subgroups whose response to steroids remains unclear. We aimed to evaluate the outcomes of COVID-19 patients admitted to the intensive care unit (ICU) and treated with a short dexamethasone course to determine which patient categories derive the highest benefit. METHODS: A retrospective cohort study was conducted using a prospectively collected single-center ICU database (April 1–October 1, 2020). Adult COVID-19 patients were assigned to dexamethasone (12 mg × 3 days) and usual care groups. Patient, management, and outcome data were extracted. The primary outcome was the 28-day ICU mortality. Subgroup analysis was performed to assess the impact of dexamethasone on mortality in patients with invasive mechanical ventilation (IMV). RESULTS: Of 233 patients, 220 (median age: 65 years, 38% female) were included: 83 patients received dexamethasone and 137 received usual care. Overall, 28 (33.7%) and 54 (39.4%) patients in the dexamethasone and usual care groups, respectively, died within 28 days since ICU admission (rate ratio (RR) 0.86; 95% confidence interval (95% CI): 0.59–1.23; p=0.405). In the IMV cohort, dexamethasone did not decrease the 28-day mortality compared with usual care (47.5% vs. 62.0%; RR 0.78; 95% CI: 0.57–1.09; p=0.107). A subgroup analysis revealed significantly lower 28-day mortality in IMV patients <65 years receiving dexamethasone vs. usual care (22.6% vs. 48.5%; RR 0.47; 95% CI: 0.22–0.98; p=0.043), which was not seen in IMV patients ≥65 years (75.0% vs. 71.1%; RR 1.06; 95% CI: 0.79–1.42; p=0.719). Patients ≥65 years experienced hyperglycemia, bacterial infection, and septic shock significantly more often than younger patients who received dexamethasone (p=0.002, p=0.025, and p < 0.001, respectively). CONCLUSIONS: A 3-day dexamethasone course is not associated with lower 28-day mortality in critically ill COVID-19 patients, either in the entire ICU cohort or in the IMV. Dexamethasone may significantly reduce the 28-day mortality in IMV patients <65 years, but not in the older IMV subgroup. Dexamethasone administration in patients ≥65 years is associated with a significantly higher rate of adverse events than that in younger patients. Hindawi 2021-07-16 /pmc/articles/PMC8645403/ /pubmed/34877019 http://dx.doi.org/10.1155/2021/5557302 Text en Copyright © 2021 Armen Oganesyan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oganesyan, Armen
Menzulin, Ruslan
Surovoy, Yury
Nikiforchin, Andrei
Zykov, Kirill
Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title_full Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title_fullStr Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title_full_unstemmed Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title_short Target Groups for a Short Dexamethasone Course among Critically Ill COVID-19 Patients
title_sort target groups for a short dexamethasone course among critically ill covid-19 patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645403/
https://www.ncbi.nlm.nih.gov/pubmed/34877019
http://dx.doi.org/10.1155/2021/5557302
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