Second week methyl-prednisolone pulses improve prognosis in patients with severe coronavirus disease 2019 pneumonia: An observational comparative study using routine care data.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 30 07 2020
accepted: 06 09 2020
entrez: 22 9 2020
pubmed: 23 9 2020
medline: 21 10 2020
Statut: epublish

Résumé

To analyze the effects of a short course of methyl-prednisolone pulses (MP) during the second week of disease (week-2) in patients with severe coronavirus disease 2019 (COVID-19) pneumonia. Comparative observational study using data collected from routine care at Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain in patients with COVID-19 pneumonia. We compared patients who received week-2-MP (125-250 mg/d x3) with those who did not, with the end-points time to death and time to death or endotracheal intubation. We included 242 patients with COVID-19 pneumonia and elevated inflammatory markers at admission. Sixty-one patients (25%) received week-2-MP. Twenty-two patients (9%) died and 31 (12.8%) suffered death or intubation. The adjusted HRs for death and death or intubation for patients in the week-2-MP group were 0.35 (95%CI 0.11 to 1.06, p = 0.064) and 0.33 (95%CI 0.13 to 0.84, p = 0.020), respectively. These differences were specifically seen in the subcohort of patients with a SpO2/FiO2 at day 7 lower than 353 (adjusted HR 0.31, 95% CI 0.08 to 1.12, p = 0.073 and HR 0.34, 95%CI 0.12 to 0.94, p = 0.038, respectively) but not in patients with higher SpO2/FiO2. Patients receiving out-of-week-2-MP, non-pulse glucocorticoids or no glucocorticoids had an increased adjusted risk for both outcomes compared with week-2-MP group: HR 5.04 (95% CI 0.91-27.86), HR 10.09 (95% CI 2.14-47.50), HR 4.14 (95% CI 0.81-21.23), respectively, for death; HR 7.38 (95% CI 1.86-29.29), HR 13.71 (95% CI 3.76-50.07), HR 3.58 (95% CI 0.89-14.32), respectively, for death or intubation. These differences were significant only in the subgroup with low SpO2/FiO2. Week-2-MP are effective in improving the prognosis of patients with COVID-19 pneumonia with features of inflammatory activity and respiratory deterioration entering the second week of disease. The recognition of this high-risk population should prompt early use of MP at this point.

Identifiants

pubmed: 32960899
doi: 10.1371/journal.pone.0239401
pii: PONE-D-20-23728
pmc: PMC7508405
doi:

Substances chimiques

Glucocorticoids 0
Oxygen S88TT14065
Methylprednisolone X4W7ZR7023

Types de publication

Comparative Study Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0239401

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Guillermo Ruiz-Irastorza (G)

Autoimmune Diseases Research Unit, Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Jose-Ignacio Pijoan (JI)

Biocruces Bizkaia Health Research Institute, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Service of Rheumatology, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Elena Bereciartua (E)

University of the Basque Country (UPV/EHU), Leioa, BI, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Susanna Dunder (S)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Jokin Dominguez (J)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Paula Garcia-Escudero (P)

CIBER of Epidemiology and Public Health (CIBERESP), Madrid, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Alejandro Rodrigo (A)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Carlota Gomez-Carballo (C)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Jimena Varona (J)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Laura Guio (L)

University of the Basque Country (UPV/EHU), Leioa, BI, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Marta Ibarrola (M)

University of the Basque Country (UPV/EHU), Leioa, BI, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Amaia Ugarte (A)

Autoimmune Diseases Research Unit, Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

Agustin Martinez-Berriotxoa (A)

Clinical Epidemiology Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Infectious Diseases Unit, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.
Service of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain.

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