antiviral and associated therapy - versus placebo - 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 0.87 [0.67, 1.12]< 130%3 studies (3/-)86.1 %some concernnot evaluable moderatecrucial-
deaths 0.81 [0.63, 1.05]< 120%11 studies (11/-)94.6 %some concernlow moderatecrucial-
deaths (time to event analysis only) 0.66 [0.46, 0.95]< 132%2 studies (2/-)98.7 %some concernnot evaluable moderatecrucial-
clinical deterioration 1.10 [0.65, 1.88]< 19%2 studies (2/-)35.7 %lownot evaluable highimportant-
clinical improvement 1.24 [1.10, 1.40]> 10%3 studies (3/-)100.0 %some concernnot evaluable moderateimportant-
clinical improvement (14-day) 1.06 [0.79, 1.42]> 10%2 studies (2/-)64.6 %lownot evaluable highimportant-
clinical improvement (28-day) 1.21 [0.97, 1.51]> 117%3 studies (3/-)95.2 %some concernnot evaluable moderateimportant-
clinical improvement (7-day) 0.95 [0.82, 1.09]> 10%3 studies (3/-)22.1 %some concernnot evaluable moderateimportant-
clinical improvement (time to event analysis only) 1.22 [1.09, 1.37]> 10%5 studies (5/-)100.0 %some concernnot evaluable moderateimportant-
death or ventilation 1.01 [0.65, 1.57]< 10%4 studies (4/-)47.8 %some concernnot evaluable moderateimportant-
hospital discharge 1.07 [0.82, 1.40]> 10%4 studies (4/-)69.0 %some concernnot evaluable moderateimportant-
mechanical ventilation 1.33 [0.49, 3.59]< 17%2 studies (2/-)28.9 %some concernnot evaluable moderateimportant-
viral clearance 0.92 [0.77, 1.09]> 10%1 study (1/-)17.3 %NAnot evaluable important-
viral clearance by day 7 0.91 [0.77, 1.08]> 10%2 studies (2/-)13.7 %lownot evaluable highimportant-
ICU admission 1.00 [0.41, 2.45]< 10%2 studies (2/-)49.8 %some concernnot evaluable moderatenon important-
off oxygenation 0.98 [0.64, 1.51]> 10%1 study (1/-)46.4 %NAnot evaluable non important-
recovery 0.97 [0.89, 1.05]> 10%1 study (1/-)23.5 %NAnot evaluable non important-

safety endpoints 00

AE leading to drug discontinuation 2.43 [0.79, 7.45]< 10%1 study (1/-)6.0 %NAnot evaluable important-
serious adverse events 0.75 [0.59, 0.96]< 10%4 studies (4/-)98.8 %some concernnot evaluable moderateimportant-
adverse events 2.44 [0.69, 8.69]< 189%4 studies (4/-)8.4 %some concernnot evaluable moderatenon important-
deep vein thrombosis 0.62 [0.23, 1.64]< 10%2 studies (2/-)83.1 %some concernnot evaluable moderatenon important-
elevated liver enzymes 0.58 [0.34, 0.97]< 16%2 studies (2/-)98.1 %some concernnot evaluable moderatenon important-
hyperbilirubinemia 0.97 [0.48, 1.93]< 10%2 studies (2/-)53.8 %lownot evaluable highnon important-
pulmonary embolism 0.82 [0.20, 3.29]< 10%2 studies (2/-)61.1 %some concernnot evaluable moderatenon important-
renal impairment 1.02 [0.64, 1.61]< 10%2 studies (2/-)47.2 %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.