» Articles » PMID: 35061713

Use of Glucocorticoids Megadoses in SARS-CoV-2 Infection in a Spanish Registry: SEMI-COVID-19

Abstract

Objective: To describe the impact of different doses of corticosteroids on the evolution of patients with COVID-19 pneumonia, based on the potential benefit of the non-genomic mechanism of these drugs at higher doses.

Methods: Observational study using data collected from the SEMI-COVID-19 Registry. We evaluated the epidemiological, radiological and analytical scenario between patients treated with megadoses therapy of corticosteroids vs low-dose of corticosteroids and the development of complications. The primary endpoint was all-cause in-hospital mortality according to use of corticosteroids megadoses.

Results: Of a total of 14,921 patients, corticosteroids were used in 5,262 (35.3%). Of them, 2,216 (46%) specifically received megadoses. Age was a factor that differed between those who received megadoses therapy versus those who did not in a significant manner (69 years [IQR 59-79] vs 73 years [IQR 61-83]; p < .001). Radiological and analytical findings showed a higher use of megadoses therapy among patients with an interstitial infiltrate and elevated inflammatory markers associated with COVID-19. In the univariate study it appears that steroid use is associated with increased mortality (OR 2.07 95% CI 1.91-2.24 p < .001) and megadose use with increased survival (OR 0.84 95% CI 0.75-0.96, p 0.011), but when adjusting for possible confounding factors, it is observed that the use of megadoses is also associated with higher mortality (OR 1.54, 95% CI 1.32-1.80; p < .001). There is no difference between megadoses and low-dose (p .298). Although, there are differences in the use of megadoses versus low-dose in terms of complications, mainly infectious, with fewer pneumonias and sepsis in the megadoses group (OR 0.82 95% CI 0.71-0.95; p < .001 and OR 0.80 95% CI 0.65-0.97; p < .001) respectively.

Conclusion: There is no difference in mortality with megadoses versus low-dose, but there is a lower incidence of infectious complications with glucocorticoid megadoses.

Citing Articles

Outcome of COVID-19 infections in patients with adrenal insufficiency and excess.

Nowotny H, Bryce J, Ali S, Giordano R, Baronio F, Chifu I Endocr Connect. 2023; 12(4).

PMID: 36715679 PMC: 10083676. DOI: 10.1530/EC-22-0416.

References
1.
Zhu N, Zhang D, Wang W, Li X, Yang B, Song J . A Novel Coronavirus from Patients with Pneumonia in China, 2019. N Engl J Med. 2020; 382(8):727-733. PMC: 7092803. DOI: 10.1056/NEJMoa2001017. View

2.
Lopez Zuniga M, Moreno-Moral A, Ocana-Granados A, Padilla-Moreno F, Castillo-Fernandez A, Guillamon-Fernandez D . High-dose corticosteroid pulse therapy increases the survival rate in COVID-19 patients at risk of hyper-inflammatory response. PLoS One. 2021; 16(1):e0243964. PMC: 7842890. DOI: 10.1371/journal.pone.0243964. View

3.
Casas-Rojo J, Anton-Santos J, Millan-Nunez-Cortes J, Lumbreras-Bermejo C, Ramos-Rincon J, Roy-Vallejo E . [Clinical characteristics of patients hospitalized with COVID-19 in Spain: Results from the SEMI-COVID-19 Registry]. Rev Clin Esp. 2021; 220(8):480-494. PMC: 7368900. DOI: 10.1016/j.rce.2020.07.003. View

4.
Jorgensen S, Tse C, Burry L, Dresser L . Baricitinib: A Review of Pharmacology, Safety, and Emerging Clinical Experience in COVID-19. Pharmacotherapy. 2020; 40(8):843-856. PMC: 7323235. DOI: 10.1002/phar.2438. View

5.
Fung M, Babik J . COVID-19 in Immunocompromised Hosts: What We Know So Far. Clin Infect Dis. 2021; 72(2):340-350. PMC: 7337668. DOI: 10.1093/cid/ciaa863. View