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Dexamethasone for Inpatients With COVID-19 in a National Cohort
IMPORTANCE: Limited effective therapeutics are available to hospitalized patients with COVID-19. Clinical trials and observational studies have shown varying effects of systemic corticosteroids, including dexamethasone, in hospitalized patients with COVID-19, with limited descriptions of important p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111178/ https://www.ncbi.nlm.nih.gov/pubmed/37067800 http://dx.doi.org/10.1001/jamanetworkopen.2023.8516 |
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author | Mourad, Ahmad Thibault, Dylan Holland, Thomas L. Yang, Siyun Young, Allison R. Arnold Egloff, Shanna A. Thomas, Laine E. |
author_facet | Mourad, Ahmad Thibault, Dylan Holland, Thomas L. Yang, Siyun Young, Allison R. Arnold Egloff, Shanna A. Thomas, Laine E. |
author_sort | Mourad, Ahmad |
collection | PubMed |
description | IMPORTANCE: Limited effective therapeutics are available to hospitalized patients with COVID-19. Clinical trials and observational studies have shown varying effects of systemic corticosteroids, including dexamethasone, in hospitalized patients with COVID-19, with limited descriptions of important patient subgroups. OBJECTIVE: To examine the clinical use of dexamethasone for hospitalized patients with COVID-19 respiratory illness and to explore the heterogeneity of treatment outcomes across different subgroups. DESIGN, SETTING, AND PARTICIPANTS: This is a retrospective, propensity score–weighted cohort study of adult patients hospitalized for at least 48 hours for COVID-19 respiratory illness between July 1, 2020, and October 31, 2021, at a large health care network of 156 hospitals across the US. Data analysis was performed from March 2022 to February 2023. EXPOSURES: Systemic dexamethasone administered within 48 hours of either admission or escalation in oxygen support. MAIN OUTCOMES AND MEASURES: All-cause in-hospital mortality or discharge to hospice. RESULTS: A total of 80 699 patients who met the eligibility criteria were identified (median [IQR] age, 64 [52-76] years; 37 606 women [46.6%]); 13 230 patients (16.4%) identified as Black, 49 222 (60.9%) as White, 18 247 (22.6%) as other race, and 20 340 (25.2%) as Hispanic ethnicity. Of these patients, 13 040 (16.2%) did not require supplemental oxygen within 48 hours of admission, 56 368 (69.8%) required supplemental oxygen, 7618 (9.4%) required noninvasive positive pressure ventilation (NIPPV), and 3673 (4.6%) required mechanical ventilation (MV) and/or extracorporeal membrane oxygenation (ECMO). After adjustment by propensity score overlap weighting, early use of dexamethasone was associated with reduction in a composite outcome of in-hospital mortality or discharge to hospice for patients receiving supplemental oxygen (aOR, 0.92; 95% CI, 0.86-0.98) and MV and/or ECMO (aOR, 0.82; 95% CI, 0.68-0.99). In contrast, all-cause inpatient mortality or discharge to hospice was not lower for patients who received dexamethasone in the no supplemental oxygen group (aOR, 0.90; 95% CI, 0.78-1.03) and in the NIPPV group (aOR, 0.87; 95% CI, 0.73-1.04). Importantly, patients with more comorbidities had greater benefit from dexamethasone use. CONCLUSIONS AND RELEVANCE: In this national multicenter cohort study of inpatients with COVID-19, early administration of dexamethasone was associated with significantly reduced odds of mortality or discharge to hospice in those requiring supplemental oxygen or MV and/or ECMO but not in those requiring no supplemental oxygen or NIPPV. These results support the continued use of systemic dexamethasone in patients hospitalized with COVID-19. |
format | Online Article Text |
id | pubmed-10111178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-101111782023-04-19 Dexamethasone for Inpatients With COVID-19 in a National Cohort Mourad, Ahmad Thibault, Dylan Holland, Thomas L. Yang, Siyun Young, Allison R. Arnold Egloff, Shanna A. Thomas, Laine E. JAMA Netw Open Original Investigation IMPORTANCE: Limited effective therapeutics are available to hospitalized patients with COVID-19. Clinical trials and observational studies have shown varying effects of systemic corticosteroids, including dexamethasone, in hospitalized patients with COVID-19, with limited descriptions of important patient subgroups. OBJECTIVE: To examine the clinical use of dexamethasone for hospitalized patients with COVID-19 respiratory illness and to explore the heterogeneity of treatment outcomes across different subgroups. DESIGN, SETTING, AND PARTICIPANTS: This is a retrospective, propensity score–weighted cohort study of adult patients hospitalized for at least 48 hours for COVID-19 respiratory illness between July 1, 2020, and October 31, 2021, at a large health care network of 156 hospitals across the US. Data analysis was performed from March 2022 to February 2023. EXPOSURES: Systemic dexamethasone administered within 48 hours of either admission or escalation in oxygen support. MAIN OUTCOMES AND MEASURES: All-cause in-hospital mortality or discharge to hospice. RESULTS: A total of 80 699 patients who met the eligibility criteria were identified (median [IQR] age, 64 [52-76] years; 37 606 women [46.6%]); 13 230 patients (16.4%) identified as Black, 49 222 (60.9%) as White, 18 247 (22.6%) as other race, and 20 340 (25.2%) as Hispanic ethnicity. Of these patients, 13 040 (16.2%) did not require supplemental oxygen within 48 hours of admission, 56 368 (69.8%) required supplemental oxygen, 7618 (9.4%) required noninvasive positive pressure ventilation (NIPPV), and 3673 (4.6%) required mechanical ventilation (MV) and/or extracorporeal membrane oxygenation (ECMO). After adjustment by propensity score overlap weighting, early use of dexamethasone was associated with reduction in a composite outcome of in-hospital mortality or discharge to hospice for patients receiving supplemental oxygen (aOR, 0.92; 95% CI, 0.86-0.98) and MV and/or ECMO (aOR, 0.82; 95% CI, 0.68-0.99). In contrast, all-cause inpatient mortality or discharge to hospice was not lower for patients who received dexamethasone in the no supplemental oxygen group (aOR, 0.90; 95% CI, 0.78-1.03) and in the NIPPV group (aOR, 0.87; 95% CI, 0.73-1.04). Importantly, patients with more comorbidities had greater benefit from dexamethasone use. CONCLUSIONS AND RELEVANCE: In this national multicenter cohort study of inpatients with COVID-19, early administration of dexamethasone was associated with significantly reduced odds of mortality or discharge to hospice in those requiring supplemental oxygen or MV and/or ECMO but not in those requiring no supplemental oxygen or NIPPV. These results support the continued use of systemic dexamethasone in patients hospitalized with COVID-19. American Medical Association 2023-04-17 /pmc/articles/PMC10111178/ /pubmed/37067800 http://dx.doi.org/10.1001/jamanetworkopen.2023.8516 Text en Copyright 2023 Mourad A et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Mourad, Ahmad Thibault, Dylan Holland, Thomas L. Yang, Siyun Young, Allison R. Arnold Egloff, Shanna A. Thomas, Laine E. Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title | Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title_full | Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title_fullStr | Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title_full_unstemmed | Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title_short | Dexamethasone for Inpatients With COVID-19 in a National Cohort |
title_sort | dexamethasone for inpatients with covid-19 in a national cohort |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111178/ https://www.ncbi.nlm.nih.gov/pubmed/37067800 http://dx.doi.org/10.1001/jamanetworkopen.2023.8516 |
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