Related Experiment Video
Updated: Jun 25, 2025

An Educational Video Demonstration of How to Prone a Critically Ill Intubated Patient
Published on: November 30, 2022
In-hospital survival of critically ill COVID-19 patients treated with glucocorticoids: a multicenter real-world data
Stefan Angermair1, Jan-Hendrik Hardenberg2,3, Kerstin Rubarth3,4
1Department of Anesthesiology and Intensive Care Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Campus Benjamin Franklin, Berlin, Germany. stefan.angermair@charite.de.
Insights
Glucocorticoid treatment did not impact 35-day survival in critically ill COVID-19 patients. However, low-dose glucocorticoids were associated with an increased hazard of death beyond 35 days in intensive care unit patients.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Pharmacology
Background:
- The COVID-19 pandemic necessitated rapid evaluation of treatment strategies, including the role of glucocorticoids.
- Glucocorticoids have been investigated for their anti-inflammatory effects in severe COVID-19, but optimal dosing remains unclear.
- Critically ill COVID-19 patients in intensive care units (ICUs) represent a vulnerable population where treatment decisions have significant survival implications.
Purpose of the Study:
- To compare in-hospital survival rates among critically ill COVID-19 patients treated with low-dose glucocorticoids, high-dose glucocorticoids, or no glucocorticoids.
- To investigate the association between different glucocorticoid dosages and mortality risk in ICU patients with COVID-19 pneumonia.
- To determine if glucocorticoid therapy influences survival beyond 35 days post-symptom onset in this patient cohort.
Main Methods:
- A multicenter, real-world data study involving critically ill COVID-19 patients admitted to the ICU between February 2020 and December 2021.
- Retrospective assignment of patients into three groups: no corticosteroid (NoC), low-dose corticosteroid (LowC), and high-dose corticosteroid (HighC) based on dexamethasone dosage or equivalent.
- Multivariable-adjusted Cox proportional hazard regression analysis was used to compare survival outcomes and mortality risk between the treatment groups.
Main Results:
- No significant difference in 35-day survival was observed between the NoC, LowC, and HighC groups.
- Landmark analysis revealed differences in survival beyond 35 days, with the NoC group having the longest restricted mean survival time.
- Multivariable analysis indicated a trend towards increased hazard of death with low-dose glucocorticoid treatment (HR 2.09, p=0.05) and no significant increase with high-dose treatment (HR 1.07, p=0.85) compared to no glucocorticoids.
Conclusions:
- Corticosteroid treatment, at the dosages studied, did not significantly influence 35-day survival in critically ill COVID-19 patients.
- Low-dose glucocorticoid therapy may be associated with an increased risk of death in critically ill COVID-19 patients beyond the initial 35-day period.
- Treatment decisions for glucocorticoids in severe COVID-19 should consider individual patient severity and potentially avoid low-dose regimens.
Abstract:
The COVID-19 pandemic has posed a major challenge to healthcare systems globally. Millions of people have been infected, and millions of deaths have been reported worldwide. Glucocorticoids have attracted worldwide attention for their potential efficacy in the treatment of COVID-19. Various glucocorticoids with different dosages and treatment durations have been studied in patients with different severities, with a suitable dosage and treatment duration not yet defined. This study aimed to investigate whether in-hospital survival differs between critically ill patients treated with low-dose glucocorticoids, high-dose glucocorticoids or no glucocorticoids. All critically ill patients admitted to the intensive care unit of the Charité Hospital-Universitätsmedizin Berlin between February 2020 and December 2021 with COVID-19 pneumonia receiving supplemental oxygen were eligible to participate in this multicenter real-world data study. Patients were retrospectively assigned to one of three groups: the high corticosteroid dose (HighC) group (receiving 6 mg parenteral dexamethasone or an equivalent corticosteroid dosage for ten days), the low corticosteroid dose (LowC) group (receiving less than 6 mg parenteral dexamethasone or an equivalent corticosteroid dosage for ten days), or the no corticosteroid (NoC) group. Overall survival and risk effects were compared among groups within the total observation period, as well as at 35 days after the onset of COVID-19 symptoms. Adjusted multivariable Cox proportional hazard regression analysis was performed to compare the risk of death between the treatment groups. Out of 1561 critically ill COVID-19 patients, 1014 were included in the baseline analysis. In the survival study, 1009 patients were assigned to the NoC (n = 346), HighC (n = 552), or LowC group (n = 111). The baseline characteristics were balanced between groups, except for age, BMI, APACHE II score, SOFA and SAPS II. While the 35-day survival did not show any differences, a landmark analysis of the patients surviving beyond 35 days revealed differences between groups. The restricted mean survival time was 112 days in the LowC group [95% CI: 97 - 128], 133 days in the HighC group [95% CI: 124 - 141] and 144 days in the NoC group [95% CI: 121 - 167]. The multivariable-adjusted Cox proportional hazard analysis indicated that, regardless of age, sex, health status or invasive oxygenation, a low-dose treatment increased the hazard of death of critically ill COVID-19 patients by a factor of 2.09 ([95% CI: 0.99, 4.4], p = 0.05) and a high-dose corticosteroid treatment increased the risk by a factor of 1.07 ([95% CI: 0.53, 2.15], p = 0.85) compared to no treatment with glucocorticoids. The analysis reveals that corticosteroid treatment does not influence the survival of critically ill COVID-19 patients in the intensive care unit within 35 days. Our evaluations further suggest that regardless of ventilation status, the decision-making process for administering corticosteroid therapy should account for the individual severity of the illness.
Related Concept Videos
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
Acute Respiratory Failure-V
Ensure that patients are monitored continuously for their response to therapy, including changes in...
Hypoglycemia and Glucagon
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Antiasthma Drugs: Inhaled Corticosteroids and Glucocorticoids
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
COPD: Management Using Bronchodilators and Corticosteroids

