A comparative study between methylprednisolone versus dexamethasone as an initial anti-inflammatory treatment of moderate COVID-19 pneumonia: an open-label randomized controlled trial
| dc.contributor.author | Laikitmongkhon J. | |
| dc.contributor.author | Tassaneyasin T. | |
| dc.contributor.author | Sutherasan Y. | |
| dc.contributor.author | Phuphuakrat A. | |
| dc.contributor.author | Srichatrapimuk S. | |
| dc.contributor.author | Petnak T. | |
| dc.contributor.author | Eksombatchai D. | |
| dc.contributor.author | Thammavaranucupt K. | |
| dc.contributor.author | Sungkanuparph S. | |
| dc.contributor.correspondence | Laikitmongkhon J. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2024-11-24T18:07:12Z | |
| dc.date.available | 2024-11-24T18:07:12Z | |
| dc.date.issued | 2024-11-11 | |
| dc.description.abstract | BACKGROUND: The most appropriate anti-inflammatory treatment for moderate COVID-19 pneumonia remains uncertain. We aimed to compare the effectiveness of a high-dose methylprednisolone versus a high-dose dexamethasone in hospitalized moderate COVID-19 pneumonia, regarding the WHO clinical progression scales, mortality, and the length of hospitalization. METHODS: In this open-labeled randomized controlled trial, we enrolled patients with age > 18 years old who were diagnosed moderate COVID-19 pneumonia confirmed by real-time PCR, evidence of pneumonia by chest imaging and resting oxygen saturation between 90 and 94%. Patients were randomized at a 1:1 ratio to receive methylprednisolone 250 mg/day or dexamethasone 20 mg/day over the first three days. Then the patients in both groups received dexamethasone 20 mg/day on days 4-5, and 10 mg/day on days 6-10. Primary outcome was assessed by a 10-point WHO clinical progression scales ranging from uninfected (point 0) to death (point 10) on the fifth day of treatment. Secondary outcomes including 90-day mortality, length of hospitalization, rate of intensive care unit (ICU) transfer and complications were determined. RESULTS: Of 98 eligible patients, the mean age was 76.0 ± 13.3 years. The median date of illness at the time of randomization was 3 days (interquartile range 2, 5). Baseline clinical characteristics and severity did not differ between groups. The WHO clinical progression scales were similar between methylprednisolone and dexamethasone group at 5 and 10 days of treatment [4.84, (95% confidence interval(CI), 4.35-5.33) vs. 4.76 (95% CI, 4.27-5.25), p = 0.821 and 4.32 (95% CI, 3.83-4.81) vs. 3.80 (95% CI, 3.31-4.29), p = 0.140, respectively)]. Both groups did not differ in-hospital mortality, length of hospitalization, and rate of ICU transfer. There were also no differences in steroid-related complications between groups until 90 days of follow-up. CONCLUSIONS: In patients with moderate COVID-19 pneumonia, initial anti-inflammatory treatment with 250 mg/day of methylprednisolone for three days does not yield better outcomes over high-dose dexamethasone. TRIAL REGISTRATION: This study was registered at Thai Clinical Trials Registry on October 17, 2021, with the identifier TCTR20211017001. | |
| dc.identifier.citation | BMC pulmonary medicine Vol.24 No.1 (2024) , 562 | |
| dc.identifier.doi | 10.1186/s12890-024-03364-4 | |
| dc.identifier.eissn | 14712466 | |
| dc.identifier.pmid | 39529039 | |
| dc.identifier.scopus | 2-s2.0-85209473434 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/102142 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Medicine | |
| dc.title | A comparative study between methylprednisolone versus dexamethasone as an initial anti-inflammatory treatment of moderate COVID-19 pneumonia: an open-label randomized controlled trial | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85209473434&origin=inward | |
| oaire.citation.issue | 1 | |
| oaire.citation.title | BMC pulmonary medicine | |
| oaire.citation.volume | 24 | |
| oairecerif.author.affiliation | Faculty of Medicine Ramathibodi Hospital, Mahidol University |
