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.authorLaikitmongkhon J.
dc.contributor.authorTassaneyasin T.
dc.contributor.authorSutherasan Y.
dc.contributor.authorPhuphuakrat A.
dc.contributor.authorSrichatrapimuk S.
dc.contributor.authorPetnak T.
dc.contributor.authorEksombatchai D.
dc.contributor.authorThammavaranucupt K.
dc.contributor.authorSungkanuparph S.
dc.contributor.correspondenceLaikitmongkhon J.
dc.contributor.otherMahidol University
dc.date.accessioned2024-11-24T18:07:12Z
dc.date.available2024-11-24T18:07:12Z
dc.date.issued2024-11-11
dc.description.abstractBACKGROUND: 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.citationBMC pulmonary medicine Vol.24 No.1 (2024) , 562
dc.identifier.doi10.1186/s12890-024-03364-4
dc.identifier.eissn14712466
dc.identifier.pmid39529039
dc.identifier.scopus2-s2.0-85209473434
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/102142
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleA comparative study between methylprednisolone versus dexamethasone as an initial anti-inflammatory treatment of moderate COVID-19 pneumonia: an open-label randomized controlled trial
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85209473434&origin=inward
oaire.citation.issue1
oaire.citation.titleBMC pulmonary medicine
oaire.citation.volume24
oairecerif.author.affiliationFaculty of Medicine Ramathibodi Hospital, Mahidol University

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