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A Retrospective Controlled Cohort Study of the Impact of Glucocorticoid Treatment in SARS-CoV-2 Infection Mortality
- Source :
- Antimicrobial Agents and Chemotherapy
- Publication Year :
- 2020
- Publisher :
- American Society for Microbiology, 2020.
-
Abstract
- Evidence to support the use of steroids in coronavirus disease 2019 (COVID-19) pneumonia is lacking. We aim to determine the impact of steroid use for COVID-19 pneumonia on hospital mortality. We performed a single-center retrospective cohort study in a university hospital in Madrid, Spain, during March of 2020. To determine the role of steroids in in-hospital mortality, patients admitted with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia and treated with steroids were compared to patients not treated with steroids, and we adjusted with a propensity score for patients on steroid treatment.<br />Evidence to support the use of steroids in coronavirus disease 2019 (COVID-19) pneumonia is lacking. We aim to determine the impact of steroid use for COVID-19 pneumonia on hospital mortality. We performed a single-center retrospective cohort study in a university hospital in Madrid, Spain, during March of 2020. To determine the role of steroids in in-hospital mortality, patients admitted with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia and treated with steroids were compared to patients not treated with steroids, and we adjusted with a propensity score for patients on steroid treatment. Survival times were compared using the log rank test. Different steroid regimens were compared and adjusted with a second propensity score. During the study period, 463 out of 848 hospitalized patients with COVID-19 pneumonia fulfilled inclusion criteria. Among them, 396 (46.7%) patients were treated with steroids and 67 patients were not. Global mortality was 15.1%. The median time to steroid treatment from symptom onset was 10 days (interquartile range [IQR], 8 to 13 days). In-hospital mortality was lower in patients treated with steroids than in controls (13.9% [55/396] versus 23.9% [16/67]; hazard ratio [HR], 0.51 [95% confidence interval, 0.27 to 0.96]; P = 0.044). Steroid treatment reduced mortality by 41.8% relative to the mortality with no steroid treatment (relative risk reduction, 0.42 [95% confidence interval, 0.048 to 0.65]). Initial treatment with 1 mg/kg of body weight/day of methylprednisolone versus steroid pulses was not associated with in-hospital mortality (13.5% [42/310] versus 15.1% [13/86]; odds ratio [OR], 0.880 [95% confidence interval, 0.449 to 1.726]; P = 0.710). Our results show that the survival of patients with SARS-CoV-2 pneumonia is higher in patients treated with glucocorticoids than in those not treated. Rates of in-hospital mortality were not different between initial regimens of 1 mg/kg/day of methylprednisolone and glucocorticoid pulses.
- Subjects :
- Male
Comorbidity
Azithromycin
030204 cardiovascular system & hematology
Lopinavir
Hospitals, University
0302 clinical medicine
Interquartile range
Neoplasms
Medicine
Pharmacology (medical)
030212 general & internal medicine
Hazard ratio
Middle Aged
Drug Combinations
Intensive Care Units
Infectious Diseases
Methylprednisolone
Cardiovascular Diseases
Drug Therapy, Combination
Female
Coronavirus Infections
steroids
Hydroxychloroquine
medicine.drug
Cohort study
medicine.medical_specialty
Pneumonia, Viral
Antiviral Agents
Drug Administration Schedule
Betacoronavirus
03 medical and health sciences
Internal medicine
Diabetes Mellitus
Humans
Pandemics
Aged
Dyslipidemias
Retrospective Studies
Pharmacology
Ritonavir
SARS-CoV-2
business.industry
COVID-19
Retrospective cohort study
Odds ratio
Length of Stay
Editor's Pick
medicine.disease
mortality
Survival Analysis
Confidence interval
Pneumonia
Interferons
business
Subjects
Details
- Language :
- English
- ISSN :
- 10986596 and 00664804
- Database :
- OpenAIRE
- Journal :
- Antimicrobial Agents and Chemotherapy
- Accession number :
- edsair.doi.dedup.....63a3e7e533e58dcaaffdc21a4bdc9c43
- Full Text :
- https://doi.org/10.1128/aac.01168-20