Immunostimulants drugs - versus standard of care - 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 0.82 [0.58, 1.16]< 13%9 studies (9/-)86.8 %some concernnot evaluable moderatecrucial-
deaths 0.80 [0.61, 1.04]< 120%16 studies (16/-)95.4 %some concerncritical moderatecrucial-
deaths (time to event analysis only) 0.97 [0.12, 7.85]< 181%2 studies (2/-)51.0 %highnot evaluable lowcrucial-
clinical deterioration 0.63 [0.29, 1.40]< 10%1 study (1/-)87.0 %NAnot evaluable important-
clinical improvement 1.44 [0.97, 2.13]> 161%6 studies (6/-)96.3 %some concernserious moderateimportant-
clinical improvement (14-day) 2.27 [0.90, 5.72]> 10%1 study (1/-)95.9 %NAnot evaluable important-
clinical improvement (28-day) 1.61 [0.69, 3.76]> 174%3 studies (3/-)86.2 %some concernnot evaluable moderateimportant-
clinical improvement (7-day) 0.98 [0.27, 3.58]> 10%1 study (1/-)48.8 %NAnot evaluable important-
clinical improvement (time to event analysis only) 1.60 [1.11, 2.31]> 128%5 studies (5/-)99.4 %some concernserious moderateimportant-
hospital discharge 2.24 [0.99, 5.10]> 10%2 studies (2/-)97.3 %highnot evaluable lowimportant-
mechanical ventilation 0.86 [0.54, 1.36]< 10%6 studies (6/-)74.0 %some concernnot evaluable moderateimportant-
mechanical ventilation (time to event analysis only) 0.66 [0.25, 1.72]< 10%1 study (1/-)80.2 %NAnot evaluable important-
radiologic improvement (14-day) 2.33 [0.45, 12.00]> 10%1 study (1/-)84.4 %NAnot evaluable important-
viral clearance 6.97 [0.23, 210.35]> 189%2 studies (2/-)86.4 %some concernnot evaluable moderateimportant-
viral clearance by day 14 7.68 [0.34, 173.70]> 190%2 studies (2/-)89.7 %some concernnot evaluable moderateimportant-
ICU admission 0.60 [0.36, 0.98]< 10%5 studies (5/-)97.9 %some concernnot evaluable moderatenon important-
off oxygenation 8.57 [1.43, 51.36]> 10%1 study (1/-)99.0 %NAnot evaluable non important-

safety endpoints 00

serious adverse events 1.43 [0.81, 2.53]< 148%3 studies (3/-)11.0 %some concernnot evaluable moderateimportant-
superinfection 0.77 [0.06, 9.89]< 176%2 studies (2/-)57.8 %highnot evaluable lowimportant-
adverse events 1.10 [0.87, 1.39]< 10%2 studies (2/-)21.8 %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.