Immunosuppressants drugs - versus potential COVID-19 treatments - for COVID-19 severe or critically pdf   xlsx method abbreviations

Outcome Relative effect 95%CI LoD Trt. better when I2 k (RCT/OBS) Bayesian probability Overall ROB Publication bias Degree of certainty Endpoint importance Published MA

efficacy endpoints 00

death D28 0.98 [0.68, 1.42]< 148%12 studies (12/-)53.4 %some concernlow moderatecrucial-
deaths 0.85 [0.66, 1.09]< 142%19 studies (19/-)89.7 %some concernlow moderatecrucial-
deaths (time to event analysis only) 1.23 [0.86, 1.77]< 137%4 studies (4/-)12.5 %some concernnot evaluable moderatecrucial-
clinical deterioration 0.48 [0.20, 1.20]< 16%2 studies (2/-)94.1 %some concernnot evaluable moderateimportant-
clinical improvement 1.44 [1.17, 1.78]> 127%8 studies (8/-)100.0 %some concernnot evaluable moderateimportant-
clinical improvement (14-day) 1.90 [1.33, 2.71]> 10%3 studies (3/-)100.0 %some concernnot evaluable moderateimportant-
clinical improvement (21-day) 1.50 [0.22, 10.08]> 10%1 study (1/-)66.1 %NAnot evaluable important-
clinical improvement (28-day) 1.33 [0.95, 1.87]> 10%4 studies (4/-)95.3 %some concernnot evaluable moderateimportant-
clinical improvement (7-day) 2.38 [0.38, 14.70]> 10%1 study (1/-)82.3 %NAnot evaluable important-
clinical improvement (time to event analysis only) 1.13 [0.92, 1.39]> 10%3 studies (3/-)87.3 %some concernnot evaluable moderateimportant-
death or ventilation 0.96 [0.65, 1.43]< 126%3 studies (3/-)57.8 %some concernnot evaluable moderateimportant-
hospital discharge 0.95 [0.79, 1.16]> 10%2 studies (2/-)31.3 %some concernnot evaluable moderateimportant-
mechanical ventilation 0.75 [0.36, 1.55]< 137%5 studies (5/-)78.0 %some concernnot evaluable moderateimportant-
radiologic improvement (14-day) 5.54 [1.01, 30.50]> 10%1 study (1/-)97.5 %NAnot evaluable important-
ICU admission 1.04 [0.17, 6.33]< 175%2 studies (2/-)48.5 %some concernnot evaluable moderatenon important-
recovery 1.30 [0.64, 2.66]> 19%2 studies (2/-)76.5 %lownot evaluable highnon important-

safety endpoints 00

related AE (TRAE) 1.26 [0.14, 11.07]< 10%2 studies (2/-)41.9 %some concernnot evaluable moderateimportant-
serious adverse events 0.99 [0.75, 1.32]< 125%7 studies (7/-)52.0 %some concernnot evaluable moderateimportant-
adverse events 1.16 [0.91, 1.49]< 111%8 studies (8/-)11.6 %some concernnot evaluable moderatenon important-

LoD: level of statistical demonstration: Statistically conclusive: statistically significant with a strict control of overall risk of type 1 error (statistically demonstrated), does not take into account the risk of bias; suggested: nominally statistically significant but without a strict control of overall risk of type 1 error; inconclusive: not nominally statistically significant; safety concerns;
Bayesian probability: Bayesian posterior probability of treatment effect (computed with a noninformative prior); ROB: risk of bias; k: number of studies; published MA: number of published meta-analysis on the same topic; degree of certainty adapted from GRADE. Trt. better when: indicates when the relative treatment effect shows that the studied treatment is better than control.