anti-inflammatoty and immuno-therapy - 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 0.84 [0.64, 1.10]< 118%19 studies (18/1)90.2 %moderatecritical moderatecrucial-
death or transfer to ICU 0.93 [0.87, 0.99]< 10%1 study (-/1)98.6 %NAnot evaluable crucial-
deaths 0.70 [0.49, 1.01]< 194%37 studies (33/4)97.0 %moderatecritical moderatecrucial-
deaths (time to event analysis only) 0.79 [0.35, 1.77]< 196%8 studies (7/1)71.8 %moderateserious moderatecrucial-
clinical deterioration 0.63 [0.45, 0.88]< 10%4 studies (4/-)99.6 %some concernnot evaluable moderateimportant-
clinical improvement 1.57 [1.21, 2.05]> 164%12 studies (12/-)100.0 %some concerncritical moderateimportant-
clinical improvement (14-day) 1.54 [1.05, 2.25]> 147%5 studies (5/-)98.6 %highnot evaluable lowimportant-
clinical improvement (28-day) 2.00 [0.93, 4.28]> 170%5 studies (4/1)96.2 %moderateserious moderateimportant-
clinical improvement (7-day) 2.47 [0.37, 16.27]> 172%2 studies (2/-)82.5 %some concernnot evaluable moderateimportant-
clinical improvement (time to event analysis only) 1.60 [1.11, 2.31]> 128%5 studies (5/-)99.4 %some concernserious moderateimportant-
death or ventilation 1.31 [0.69, 2.46]< 156%4 studies (4/-)20.4 %highnot evaluable lowimportant-
hospital discharge 2.76 [1.36, 5.60]> 10%3 studies (2/1)99.8 %moderatenot evaluable moderateimportant-
mechanical ventilation 0.98 [0.65, 1.47]< 10%9 studies (9/-)53.9 %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) 3.53 [1.19, 10.46]> 10%2 studies (2/-)98.9 %some concernnot evaluable moderateimportant-
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 0.55 [0.29, 1.04]< 157%7 studies (6/1)96.7 %moderateserious moderatenon important-
off oxygenation 8.57 [1.43, 51.36]> 10%1 study (1/-)99.0 %NAnot evaluable non important-
recovery 0.64 [0.14, 2.92]> 10%1 study (1/-)28.3 %NAnot evaluable non important-

safety endpoints 00

serious adverse events 1.36 [0.95, 1.94]< 116%9 studies (9/-)4.9 %some concernnot evaluable moderateimportant-
superinfection 0.77 [0.06, 9.89]< 176%2 studies (2/-)57.8 %highnot evaluable lowimportant-
acute kidney injury 0.43 [0.14, 1.34]< 10%1 study (-/1)92.7 %NAnot evaluable non important-
adverse events 1.14 [0.92, 1.43]< 10%4 studies (4/-)11.7 %some concernnot evaluable moderatenon important-
arrhythmia 0.16 [0.03, 0.90]< 10%1 study (-/1)98.1 %NAnot evaluable non important-
elevated liver enzymes 0.52 [0.18, 1.51]< 10%1 study (-/1)88.5 %NAnot evaluable non important-
Myocardial infarction 0.87 [0.19, 3.92]< 10%1 study (-/1)57.2 %NAnot evaluable non important-
venous thromboembolism 5.23 [0.42, 65.62]< 10%1 study (-/1)10.2 %NAnot evaluable non 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.