chloroquine and derivatives - versus control - 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 1.12 [0.99, 1.27]< 133%5 studies (4/1)3.2 %seriousnot evaluable lowcrucial-
deaths 0.83 [0.69, 1.00]< 177%41 studies (27/14)97.5 %moderatelow moderatecrucial-
deaths (time to event analysis only) 0.85 [0.64, 1.13]< 192%10 studies (3/7)87.4 %seriouslow lowcrucial-
clinical deterioration 1.05 [0.86, 1.27]< 10%7 studies (4/3)32.0 %seriousnot evaluable lowimportant-
clinical improvement 1.02 [0.77, 1.35]> 10%2 studies (2/-)54.9 %some concernnot evaluable moderateimportant-
clinical improvement (14-day) 0.95 [0.71, 1.25]> 10%3 studies (3/-)35.1 %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) 0.96 [0.81, 1.14]> 10%5 studies (4/1)32.9 %moderatenot evaluable moderateimportant-
death or ventilation 1.12 [1.02, 1.22]< 10%6 studies (5/1)0.6 %moderatenot evaluable moderateimportant-
hospital discharge 1.01 [0.82, 1.25]> 10%4 studies (3/1)54.5 %moderatenot evaluable moderateimportant-
mechanical ventilation 0.98 [0.64, 1.49]< 10%1 study (-/1)54.5 %NAnot evaluable important-
mechanical ventilation (time to event analysis only) 1.43 [0.53, 3.82]< 10%1 study (-/1)23.8 %NAnot evaluable important-
radiologic improvement (7-day) 3.43 [1.10, 10.70]> 10%1 study (1/-)98.3 %NAnot evaluable important-
viral clearance 1.60 [0.63, 4.05]> 176%4 studies (3/1)83.8 %moderatenot evaluable moderateimportant-
viral clearance (time to event analysis only) 1.00 [0.73, 1.38]> 120%3 studies (1/2)51.1 %seriousnot evaluable lowimportant-
viral clearance by day 14 1.91 [0.42, 8.74]> 182%3 studies (1/2)79.6 %seriousnot evaluable lowimportant-
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 1.91 [1.01, 3.62]< 10%2 studies (1/1)2.3 %seriousnot evaluable lowimportant-
serious adverse events 1.26 [0.56, 2.84]< 10%1 study (1/-)28.7 %NAnot evaluable important-
abnormal ECG findings 1.50 [0.88, 2.57]< 10%1 study (-/1)7.0 %NAnot evaluable non important-
adverse events 1.60 [1.14, 2.25]< 130%8 studies (8/-)0.4 %some concernnot evaluable moderatenon important-
arrhythmia 1.05 [0.57, 1.94]< 10%1 study (-/1)43.4 %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.