patient subgroup... 
                     age >= 55 yr  age >= 65 yr  critical disease  
                  
            
             
            
                Top evidence (RCT only, high risk of bias excluded) 
                Best available evidence (possibly low or very low) 
                All RCTs 
                All studies (RCT+OBS) 
             
            
         
        
        
        
        
        
            convalescent plasma treatment  - versus control  - for COVID 19 hospitalized 
            
                
                     
                 
                
                     
            
                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 
             
            
            00 death D28  0.99  [0.93, 1.05]< 1 0% 24 studies (24/-) 63.9 % some concern critical   moderate crucial -  deaths  0.98  [0.92, 1.04]< 1 0% 37 studies (37/-) 77.4 % some concern critical   moderate crucial 1  deaths (time to event analysis only)  0.99  [0.79, 1.24]< 1 0% 7 studies (7/-) 54.7 % some concern not evaluable   moderate crucial -  clinical deterioration  0.87  [0.71, 1.06]< 1 9% 5 studies (5/-) 91.7 % some concern not evaluable   moderate important -  clinical improvement  1.09  [0.87, 1.38]> 1 39% 8 studies (8/-) 77.9 % some concern not evaluable   moderate important -  clinical improvement (14-day)  2.27  [0.90, 5.72]> 1 0% 1 study (1/-) 95.9 % NA not evaluable  important -  clinical improvement (28-day)  1.33  [0.83, 2.14]> 1 53% 5 studies (5/-) 88.1 % some concern not evaluable   moderate important -  clinical improvement (7-day)  0.98  [0.27, 3.58]> 1 0% 1 study (1/-) 48.8 % NA not evaluable  important -  clinical improvement (time to event analysis only)  1.08  [0.90, 1.29]> 1 0% 5 studies (5/-) 80.5 % low not evaluable   high important -  death or ventilation  0.98  [0.94, 1.03]< 1 0% 5 studies (5/-) 79.2 % some concern not evaluable   moderate important -  hospital discharge  1.00  [0.94, 1.07]> 1 0% 3 studies (3/-) 52.3 % some concern not evaluable   moderate important -  mechanical ventilation  0.83  [0.64, 1.08]< 1 24% 7 studies (7/-) 91.7 % some concern not evaluable   moderate important 1  mechanical ventilation (time to event analysis only)  0.97  [0.62, 1.52]< 1 0% 2 studies (2/-) 55.5 % some concern not evaluable   moderate important -  viral clearance   1.10  [0.19, 6.30]> 1 0% 2 studies (2/-) 54.1 % some concern not evaluable   moderate important -  viral clearance by day 14  0.96  [0.77, 1.20]> 1 0% 2 studies (2/-) 35.7 % some concern not evaluable   moderate important -  viral clearance by day 7  0.87  [0.65, 1.16]> 1 0% 2 studies (2/-) 17.4 % some concern not evaluable   moderate important -  ICU admission  0.67  [0.32, 1.41]< 1 1% 2 studies (2/-) 85.6 % some concern not evaluable   moderate non important -  00 serious adverse events  1.19  [0.94, 1.50]< 1 45% 6 studies (6/-) 7.8 % some concern not evaluable   moderate important -  adverse events  1.08  [0.86, 1.37]< 1 0% 2 studies (2/-) 24.8 % some concern not evaluable   moderate non important -  
        
        
            LoD: level of statistical demonstration: