The researchers found that mechanical ventilation-free survival by day 29 was similar between the groups (87.0 percent in the baricitinib group and 87.6 percent in the dexamethasone group). The odds ratio for improved status in the dexamethasone group versus baricitinib group was 1.01 (95 percent confidence interval, 0.80 to 1.27). At least one adverse event occurred in 30 and 37 percent of patients in the baricitinib and dexamethasone groups, respectively. Overall, 4 and 10 percent of patients in the baricitinib and dexamethasone groups, respectively, had at least one treatment-related adverse event.
Cameron R. Wolfe, M.B.B.S., from Duke University in Durham, North Carolina, and colleagues conducted a randomized study enrolling 1,010 hospitalized adults with COVID-19 who required supplemental oxygen by low-flow, high-flow, or noninvasive mechanical ventilation modalities. Participants were randomly assigned to receive either baricitinib plus remdesivir plus placebo (516 patients) or dexamethasone plus remdesivir plus placebo (494 patients).