Comparison of the efficacy of equivalent doses of dexamethasone, methylprednisolone, and hydrocortisone for treatment of COVID-19-related acute respiratory distress syndrome: a prospective three-arm randomized clinical trial
- 09.01.2023
- original article
- Verfasst von
- Abbas Taher
- Marjan Lashkari
- Fariba Keramat
- Seyyed Hamid Hashemi
- Ladan Sedighi
- Jalal Poorolajal
- Associate Professor Maryam Mehrpooya
- Erschienen in
- Wiener Medizinische Wochenschrift | Ausgabe 5-6/2023
Summary
Background
This prospective controlled clinical trial aimed to compare the efficacy of methylprednisolone, dexamethasone, and hydrocortisone at equivalent doses in patients with severe COVID-19.
Methods
In total, 106 patients with mild to moderate COVID-19-related acute respiratory distress syndrome (ARDS) were randomized to receive either dexamethasone (6 mg once a day), methylprednisolone (16 mg twice a day), or hydrocortisone (50 mg thrice a day) for up to 10 days. All participants received a standard of care for COVID-19. The primary and secondary efficacy outcomes included all-cause 28-day mortality, clinical status on day 28 assessed using the World Health Organization (WHO) eight-category ordinal clinical scale, number of patients requiring mechanical ventilation and intensive care unit (ICU) care, number of ventilator-free days, length of hospital and ICU stay, change in PaO2:FiO2 ratios during the first 5 days after treatment, and incidence of serious adverse events. P-values below 0.008 based on Bonferroni’s multiple-testing correction method were considered statistically significant.
Results
According to the obtained results, there was a trend toward more favorable clinical outcomes in terms of needing mechanical ventilation and ICU care, number of ventilator-free days, change in PaO2:FiO2 ratios during the first 5 days after treatment, clinical status score at day 28, length of ICU and hospital stay, and overall 28-day mortality in patients receiving dexamethasone compared to those receiving methylprednisolone or hydrocortisone; however, likely due to the study’s small sample size, the difference between groups reached a significant level only in the case of clinical status score on day 28 (p-value = 0.003). There was no significant difference in the incidence of serious adverse events between the study groups.
Conclusion
Based on the results, severe cases of COVID-19 treated with dexamethasone might have a better clinical status at 28-day follow-up compared to methylprednisolone and hydrocortisone at an equivalent dose. Larger multicenter trials are required to confirm our findings.
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- Titel
- Comparison of the efficacy of equivalent doses of dexamethasone, methylprednisolone, and hydrocortisone for treatment of COVID-19-related acute respiratory distress syndrome: a prospective three-arm randomized clinical trial
- Verfasst von
-
Abbas Taher
Marjan Lashkari
Fariba Keramat
Seyyed Hamid Hashemi
Ladan Sedighi
Jalal Poorolajal
Associate Professor Maryam Mehrpooya
- Publikationsdatum
- 09.01.2023
- Verlag
- Springer Vienna
- Erschienen in
-
Wiener Medizinische Wochenschrift / Ausgabe 5-6/2023
Print ISSN: 0043-5341
Elektronische ISSN: 1563-258X - DOI
- https://doi.org/10.1007/s10354-022-00993-4
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