demonstrated 16 % increase in clinical improvement,clinical improvement (time to event analysis only) (PE) with a high degree of certainty due to low risk of bias
suggested 31 % decrease in death or ventilation with a high degree of certainty due to low risk of bias
suggested 36 % decrease in mechanical ventilation with a high degree of certainty due to low risk of bias
suggested 7 % decrease in death or transfer to ICU (PE)
suggested 53 % decrease in deaths
When we analyzed mortality separately, older age, lower PaO2/FiO2 ratio, and the use of HFNC but not remdesivir orbaricitinib were associated with reduced mortality. Baricitinib was not associated with shorter time to improvement
PE: primary endpoint; (a): to be demonstrated a result must be statistically significant on a primary endpoint (with multiplicity adjustment if necessary);
Study risk of bias assessed for the study primary endpoint(s) or the main endpoints in case of no formally defined primary endpoint(s).
delta: difference in rate or median (if available)