High versus standard doses of corticosteroids in severe COVID-19: a retrospective cohort study
Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanica...
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Published in | European journal of clinical microbiology & infectious diseases Vol. 40; no. 4; pp. 761 - 769 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.04.2021
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0934-9723 1435-4373 1435-4373 |
DOI | 10.1007/s10096-020-04078-1 |
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Abstract | Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54–73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59–3.81,
p
< 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35,
p
= 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1–1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients. |
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AbstractList | Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54–73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59–3.81, p < 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35, p = 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1–1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients. Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54–73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59–3.81, p < 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35, p = 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1–1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients. Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54-73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59-3.81, p < 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35, p = 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1-1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients.Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54-73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59-3.81, p < 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35, p = 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1-1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients. Despite the increasing evidence of the benefit of corticosteroids for the treatment of moderate-severe coronavirus disease 2019 (COVID-19) patients, no data are available about the potential role of high doses of steroids for these patients. We evaluated the mortality, the risk of need for mechanical ventilation (MV), or death and the risk of developing a severe acute respiratory distress syndrome (ARDS) between high (HD) and standard doses (SD) among patients with a severe COVID-19. All consecutive confirmed COVID-19 patients admitted to a single center were selected, including those treated with steroids and an ARDS. Patients were allocated to the HD (≥ 250 mg/day of methylprednisolone) of corticosteroids or the SD (≤ 1.5 mg/kg/day of methylprednisolone) at discretion of treating physician. Five hundred seventy-three patients were included: 428 (74.7%) men, with a median (IQR) age of 64 (54-73) years. In the HD group, a worse baseline respiratory situation was observed and male gender, older age, and comorbidities were significantly more common. After adjusting by baseline characteristics, HDs were associated with a higher mortality than SD (adjusted OR 2.46, 95% CI 1.59-3.81, p < 0.001) and with an increased risk of needing MV or death (adjusted OR 2.35, p = 0.001). Conversely, the risk of developing a severe ARDS was similar between groups. Interaction analysis showed that HD increased mortality exclusively in elderly patients. Our real-world experience advises against exceeding 1-1.5 mg/kg/day of corticosteroids for severe COVID-19 with an ARDS, especially in older subjects. This reinforces the rationale of modulating rather than suppressing immune responses in these patients. |
Author | Fortún, Jesús Monreal, Enric Walo-Delgado, Paulette Costa-Frossard, Lucienne Beltrán-Corbellini, Álvaro Rodríguez-Jorge, Fernando Montero-Errasquín, Beatriz Natera-Villalba, Elena Fernández-Velasco, Jose Ignacio Manzano, Luis Masjuan, Jaime Sainz de la Maza, Susana Muriel, Alfonso Zamora, Javier Alonso-Canovas, Araceli Villar, Luisa María |
Author_xml | – sequence: 1 givenname: Enric orcidid: 0000-0003-3293-0125 surname: Monreal fullname: Monreal, Enric email: enricmonreal@outlook.com organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 2 givenname: Susana surname: Sainz de la Maza fullname: Sainz de la Maza, Susana organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 3 givenname: Elena surname: Natera-Villalba fullname: Natera-Villalba, Elena organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 4 givenname: Álvaro surname: Beltrán-Corbellini fullname: Beltrán-Corbellini, Álvaro organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 5 givenname: Fernando surname: Rodríguez-Jorge fullname: Rodríguez-Jorge, Fernando organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 6 givenname: Jose Ignacio surname: Fernández-Velasco fullname: Fernández-Velasco, Jose Ignacio organization: Department of Immunology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 7 givenname: Paulette surname: Walo-Delgado fullname: Walo-Delgado, Paulette organization: Department of Immunology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 8 givenname: Alfonso surname: Muriel fullname: Muriel, Alfonso organization: Biostatistics Unit, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS, CIBERESP – sequence: 9 givenname: Javier surname: Zamora fullname: Zamora, Javier organization: Biostatistics Unit, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS, CIBERESP – sequence: 10 givenname: Araceli surname: Alonso-Canovas fullname: Alonso-Canovas, Araceli organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 11 givenname: Jesús surname: Fortún fullname: Fortún, Jesús organization: Department of Infectious Diseases, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 12 givenname: Luis surname: Manzano fullname: Manzano, Luis organization: Department of Internal Medicine, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 13 givenname: Beatriz surname: Montero-Errasquín fullname: Montero-Errasquín, Beatriz organization: Department of Geriatrics, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 14 givenname: Lucienne surname: Costa-Frossard fullname: Costa-Frossard, Lucienne organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 15 givenname: Jaime surname: Masjuan fullname: Masjuan, Jaime organization: Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS – sequence: 16 givenname: Luisa María surname: Villar fullname: Villar, Luisa María organization: Department of Immunology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, IRYCIS |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33083917$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Contributor | Fernández-Golfín, C Toledano, R Navas, E Buisán, J Serrano, S Domínguez, A R Villar, L M Quereda Rodríguez-Navarro, C Lucas, M Fernández Casado, J L Moreno-Cobo, M A Rodríguez de Santiago, E Almonacid, C Cobo, J Comeche, B Nieto, R Norman, J Corral, Í Máiz-Carro, L Pérez-Molina, J A Barbero, E Herrera, S Rita, C G Beltrán-Corbellini, Á Rayo, I Ron, R Conde, M López, M González, E Concejo-Badorrey, M C Chamorro, S García-Ribas, G Diz, S Moreno, E Hidalgo, F Barbolla-Díaz, I Mateos-Muñoz, B Sánchez-García, E M Aranzábal Orgaz, L Iturrieta-Zuazo, I Moreno, A De Andrés, A Pérez-Torre, P Sánchez-Sánchez, O Vázquez, M Hermida, J M Matute-Lozano, M C Espiño, M Martínez-Sanz, J Monge-Maillo, B García-Barragán, N Gioia, F Rincón-Díaz, L M Mateos Del Nozal, J López-Sendón, J L Moreno, J Vallés, A Chico-García, J L Ortiz Barraza, E Y |
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Copyright | Springer-Verlag GmbH Germany, part of Springer Nature 2020 Springer-Verlag GmbH Germany, part of Springer Nature 2020. |
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DOI | 10.1007/s10096-020-04078-1 |
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Keywords | COVID-19 Severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 Corticosteroids |
Language | English |
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Available at: https://www.recoverytrial.net/news/low-cost-dexamethasone-reduces-death-by-up-to-one-third-in-hospitalised-patients-with-severe-respiratory-complications-of-covid-19. Accessed Jul 12, 2020 – reference: ARDS Definition Task ForceRanieriVMRubenfeldGDAcute respiratory distress syndrome: the Berlin DefinitionJAMA2012307252625331:CAS:528:DC%2BC38XhtVCku7jI10.1001/jama.2012.5669 – reference: World Health Organization. Novel coronavirus – China. Available at: www.who.int/csr/don/12-january-2020-novel-coronavirus-china/en/. 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Title | High versus standard doses of corticosteroids in severe COVID-19: a retrospective cohort study |
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