anti-inflammatoty and immuno-therapy - versus placebo - for COVID 19 outpatients 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 0.83 [0.30, 2.29]< 10%7 studies (7/-)64.3 %lownot evaluable highcrucial-
deaths 0.49 [0.25, 0.94]< 10%12 studies (12/-)98.3 %lowlow highcrucial-
hospitalization or death 0.40 [0.28, 0.59]< 168%12 studies (12/-)100.0 %lowcritical highcrucial-
clinical deterioration 0.24 [0.10, 0.56]< 10%1 study (1/-)100.0 %NAnot evaluable important-
clinical improvement (14-day) 1.19 [0.78, 1.81]> 10%1 study (1/-)79.1 %NAnot evaluable important-
clinical improvement (28-day) 1.28 [0.84, 1.96]> 10%1 study (1/-)87.2 %NAnot evaluable important-
clinical improvement (7-day) 0.92 [0.51, 1.66]> 10%1 study (1/-)39.1 %NAnot evaluable important-
clinical improvement (time to event analysis only) 1.50 [1.30, 1.74]> 10%1 study (1/-)100.0 %NAnot evaluable important-
hospitalization 0.71 [0.51, 0.98]< 163%8 studies (8/-)98.1 %lownot evaluable highimportant-
mechanical ventilation 0.63 [0.29, 1.37]< 19%2 studies (2/-)87.6 %lownot evaluable highimportant-
Recovery (time to event analysis only) 1.50 [1.30, 1.74]> 10%1 study (1/-)100.0 %NAnot evaluable important-
symptomatic Covid-19 0.56 [0.31, 1.00]< 10%1 study (1/-)97.6 %NAnot evaluable important-
viral clearance 1.08 [0.45, 2.60]> 172%2 studies (2/-)56.6 %some concernnot evaluable moderateimportant-
viral clearance by day 7 1.03 [0.42, 2.52]> 179%4 studies (4/-)52.5 %lownot evaluable highimportant-
recovery 1.25 [0.71, 2.22]> 10%1 study (1/-)78.2 %NAnot evaluable non important-

safety endpoints 00

emergent treatment-resistant variants 0.64 [0.08, 4.94]< 167%2 studies (2/-)66.3 %some concernnot evaluable moderateimportant-
related AE (TRAE) 1.74 [1.50, 2.03]< 10%1 study (1/-)0.0 %NAnot evaluable important-
serious adverse events 0.75 [0.54, 1.05]< 12%2 studies (2/-)95.1 %lownot evaluable highimportant-
adverse events 0.76 [0.54, 1.06]< 143%3 studies (3/-)94.6 %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.