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Intravenous Methylprednisolone Pulse As a Treatment for Hospitalised Severe Covid-19 Patients: Results From a Randomised Controlled Clinical Trial Publisher Pubmed



Edalatifard M1 ; Akhtari M2, 3 ; Salehi M4 ; Naderi Z5 ; Jamshidi A2 ; Mostafaei S6 ; Najafizadeh SR7 ; Farhadi E2, 3 ; Jalili N8 ; Esfahani M9 ; Rahimi B1 ; Kazemzadeh H1 ; Aliabadi MM10 ; Ghazanfari T11 Show All Authors
Authors
  1. Edalatifard M1
  2. Akhtari M2, 3
  3. Salehi M4
  4. Naderi Z5
  5. Jamshidi A2
  6. Mostafaei S6
  7. Najafizadeh SR7
  8. Farhadi E2, 3
  9. Jalili N8
  10. Esfahani M9
  11. Rahimi B1
  12. Kazemzadeh H1
  13. Aliabadi MM10
  14. Ghazanfari T11
  15. Sattarian M12
  16. Louyeh HE13
  17. Raeeskarami SR14
  18. Jamalimoghadamsiahkali S15
  19. Khajavirad N16
  20. Mahmoudi M2, 3
  21. Rostamian A7

Source: European Respiratory Journal Published:2020


Abstract

Introduction: There are no determined treatment agents for severe COVID-19. It is suggested that methylprednisolone, as an immunosuppressive treatment, can reduce the inflammation of the respiratory system in COVID-19 patients. Methods: We conducted a single-blind, randomised controlled clinical trial involving severe hospitalised patients with confirmed COVID-19 at the early pulmonary phase of the illness in Iran. The patients were randomly allocated in a 1:1 ratio by the block randomisation method to receive standard care with methylprednisolone pulse (intravenous injection, 250 mg·day−1 for 3 days) or standard care alone. The study end-point was the time of clinical improvement or death, whichever came first. Primary and safety analysis was done in the intention-to-treat (ITT) population. Results: 68 eligible patients underwent randomisation (34 patients in each group) from April 20, 2020 to June 20, 2020. In the standard care group, six patients received corticosteroids by the attending physician before the treatment and were excluded from the overall analysis. The percentage of improved patients was higher in the methylprednisolone group than in the standard care group (94.1% versus 57.1%) and the mortality rate was significantly lower in the methylprednisolone group (5.9% versus 42.9%; p<0.001). We demonstrated that patients in the methylprednisolone group had a significantly increased survival time compared with patients in the standard care group (log-rank test: p<0.001; hazard ratio 0.293, 95% CI 0.154-0.556). Two patients (5.8%) in the methylprednisolone group and two patients (7.1%) in the standard care group showed severe adverse events between initiation of treatment and the end of the study. Conclusions: Our results suggest that methylprednisolone pulse could be an efficient therapeutic agent for hospitalised severe COVID-19 patients at the pulmonary phase. Copyright © ERS 2020. This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
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