potential COVID-19 treatments - versus anti-inflammatoty and immuno-therapy - for COVID 19 hospitalized 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 1.76 [0.58, 5.29]< 10%2 studies (2/-)15.9 %some concernnot evaluable moderatecrucial-
deaths 0.99 [0.48, 2.05]< 128%5 studies (5/-)51.3 %some concernnot evaluable moderatecrucial1
deaths (time to event analysis only) 3.26 [0.62, 17.12]< 10%1 study (1/-)8.2 %NAnot evaluable crucial-
clinical deterioration 1.28 [0.43, 3.77]< 10%3 studies (3/-)32.8 %lownot evaluable highimportant-
clinical improvement 1.34 [0.94, 1.90]> 136%3 studies (3/-)94.8 %some concernnot evaluable moderateimportant-
clinical improvement (14-day) 2.86 [1.24, 6.62]> 10%1 study (1/-)99.3 %NAnot evaluable important-
clinical improvement (28-day) 4.26 [1.10, 16.44]> 10%1 study (1/-)98.2 %NAnot evaluable important-
clinical improvement (7-day) 1.83 [0.41, 8.14]> 10%1 study (1/-)78.5 %NAnot evaluable important-
clinical improvement (time to event analysis only) 1.34 [0.94, 1.90]> 136%3 studies (3/-)94.8 %some concernnot evaluable moderateimportant-
death or ventilation 0.91 [0.22, 3.80]< 10%2 studies (2/-)55.1 %lownot evaluable highimportant-
hospital discharge 0.88 [0.55, 1.40]> 10%1 study (1/-)28.9 %NAnot evaluable important-
mechanical ventilation 0.72 [0.33, 1.58]< 126%4 studies (4/-)79.2 %some concernnot evaluable moderateimportant1
radiologic improvement (14-day) 0.32 [0.06, 1.63]> 10%1 study (1/-)8.6 %NAnot evaluable important-
viral clearance 3.59 [1.15, 11.21]> 10%2 studies (2/-)98.6 %lownot evaluable highimportant-
viral clearance (time to event analysis only) 1.74 [1.10, 2.75]> 10%1 study (1/-)99.1 %NAnot evaluable important-
viral clearance by day 14 1.74 [0.71, 4.29]> 10%1 study (1/-)88.7 %NAnot evaluable important-
viral clearance by day 7 2.32 [1.14, 4.73]> 10%2 studies (2/-)99.0 %some concernnot evaluable moderateimportant-

safety endpoints 00

related SAE (TRSAE) 2.04 [0.07, 63.93]< 10%1 study (1/-)34.4 %NAnot evaluable important-
serious adverse events 4.54 [0.20, 105.23]< 10%1 study (1/-)17.6 %NAnot evaluable important-
adverse events 1.97 [0.38, 10.24]< 137%2 studies (2/-)21.1 %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.