chloroquine and derivatives - versus potential COVID-19 treatments - 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 1.07 [0.95, 1.21]< 16%4 studies (4/-)13.6 %some concernnot evaluable moderatecrucial-
deaths 1.07 [0.97, 1.19]< 10%28 studies (28/-)8.7 %some concernlow moderatecrucial-
deaths (time to event analysis only) 1.08 [0.95, 1.23]< 111%3 studies (3/-)12.1 %some concernnot evaluable moderatecrucial-
clinical deterioration 1.13 [0.81, 1.60]< 10%5 studies (5/-)23.5 %some concernnot evaluable moderateimportant-
clinical improvement 1.07 [0.83, 1.39]> 10%3 studies (3/-)69.8 %some concernnot evaluable moderateimportant-
clinical improvement (14-day) 1.01 [0.78, 1.30]> 10%4 studies (4/-)52.1 %lownot evaluable highimportant-
clinical improvement (28-day) 0.97 [0.69, 1.37]> 10%1 study (1/-)43.2 %NAnot evaluable important-
clinical improvement (7-day) 1.16 [0.84, 1.61]> 10%1 study (1/-)81.4 %NAnot evaluable important-
clinical improvement (time to event analysis only) 0.95 [0.80, 1.14]> 10%4 studies (4/-)29.6 %some concernnot evaluable moderateimportant-
death or ventilation 1.13 [1.03, 1.24]< 10%5 studies (5/-)0.5 %some concernnot evaluable moderateimportant-
hospital discharge 1.09 [0.82, 1.44]> 143%5 studies (5/-)71.8 %some concernnot evaluable moderateimportant-
radiologic improvement (14-day) 1.33 [0.94, 1.88]> 10%1 study (1/-)94.7 %NAnot evaluable important-
radiologic improvement (7-day) 3.19 [1.16, 8.79]> 10%2 studies (2/-)98.7 %highnot evaluable lowimportant-
viral clearance 0.97 [0.73, 1.29]> 10%3 studies (3/-)42.8 %highnot evaluable lowimportant-
viral clearance (time to event analysis only) 0.85 [0.58, 1.23]> 10%1 study (1/-)19.3 %NAnot evaluable important-
viral clearance by day 14 1.09 [0.95, 1.26]> 10%2 studies (2/-)88.8 %some concernnot evaluable moderateimportant-
viral clearance by day 7 1.20 [0.60, 2.40]> 10%1 study (1/-)69.7 %NAnot evaluable important-
ICU admission 1.19 [0.72, 1.96]< 14%2 studies (2/-)24.6 %some concernnot evaluable moderatenon important-
off oxygenation 0.98 [0.64, 1.51]> 10%1 study (1/-)46.4 %NAnot evaluable non important-

safety endpoints 00

cardiac arrest 1.92 [0.35, 10.49]< 10%1 study (1/-)22.7 %NAnot evaluable important-
serious adverse events 1.26 [0.56, 2.84]< 10%1 study (1/-)28.7 %NAnot evaluable important-
adverse events 1.57 [1.15, 2.15]< 120%9 studies (9/-)0.2 %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.