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tocilizumab in COVID-19 severe or critically - Summary of results

OutcomeTE95% CInkI2ROBPub. bias death D28detailed resultsCORIMUNO-TOCI-ICU (Group 2), 2020 0.64 [0.23; 1.80] COVACTA (Rosas), 2020 1.02 [0.62; 1.68] Rosas (REMDACTA), 2021 0.95 [0.65; 1.39] Talaschian, 2021 1.56 [0.34; 7.13] Veiga, 2021 2.70 [0.92; 7.92] 1.04[0.77; 1.41]CORIMUNO-TOCI-ICU (Group 2), 2020, COVACTA (Rosas), 2020, Rosas (REMDACTA), 2021, Talaschian, 2021, Veiga, 202158%1,335moderatenot evaluable deathsdetailed resultsCORIMUNO-TOCI-1 (Group 1), 2020 0.92 [0.31; 2.71] CORIMUNO-TOCI-ICU (Group 2), 2020 0.64 [0.23; 1.80] COVACTA (Rosas), 2020 1.16 [0.73; 1.84] REMAP-CAP (tocilizumab), 2021 0.70 [0.51; 0.95] Rosas (REMDACTA), 2021 0.95 [0.65; 1.39] Talaschian, 2021 1.25 [0.30; 5.14] Veiga, 2021 2.70 [0.92; 7.92] 0.94[0.72; 1.23]CORIMUNO-TOCI-1 (Group 1), 2020, CORIMUNO-TOCI-ICU (Group 2), 2020, COVACTA (Rosas), 2020, REMAP-CAP (tocilizumab), 2021, Rosas (REMDACTA), 2021, Talaschian, 2021, Veiga, 2021729%2,230moderatenot evaluable deaths (time to event analysis only)detailed resultsCOVACTA (Rosas), 2020 1.16 [0.73; 1.84] Rosas (REMDACTA), 2021 0.95 [0.65; 1.39] Talaschian, 2021 1.25 [0.30; 5.14] 1.04[0.78; 1.38]COVACTA (Rosas), 2020, Rosas (REMDACTA), 2021, Talaschian, 202130%1,132moderatenot evaluable clinical deteriorationdetailed resultsCORIMUNO-TOCI-1 (Group 1), 2020 0.56 [0.26; 1.20] 0.56[0.26; 1.20]CORIMUNO-TOCI-1 (Group 1), 202010%130NAnot evaluable clinical improvementdetailed resultsCOVACTA (Rosas), 2020 1.19 [0.81; 1.75] REMAP-CAP (tocilizumab), 2021 1.64 [1.25; 2.15] 1.44[1.06; 1.96]COVACTA (Rosas), 2020, REMAP-CAP (tocilizumab), 2021244%1,193moderatenot evaluable clinical improvement (28-day)detailed resultsCOVACTA (Rosas), 2020 1.19 [0.81; 1.75] 1.19[0.81; 1.75]COVACTA (Rosas), 202010%438NAnot evaluable death or ventilationdetailed resultsCORIMUNO-TOCI-1 (Group 1), 2020 0.56 [0.24; 1.31] Rosas (REMDACTA), 2021 0.98 [0.72; 1.34] Veiga, 2021 1.54 [0.65; 3.63] 0.96[0.65; 1.43]CORIMUNO-TOCI-1 (Group 1), 2020, Rosas (REMDACTA), 2021, Veiga, 2021326%909moderatenot evaluable hospital dischargedetailed resultsRosas (REMDACTA), 2021 0.97 [0.79; 1.20] 0.97[0.79; 1.20]Rosas (REMDACTA), 202110%649NAnot evaluable mechanical ventilationdetailed resultsCOVACTA (Rosas), 2020 0.67 [0.39; 1.14] 0.67[0.39; 1.14]COVACTA (Rosas), 202010%273NAnot evaluable ICU admissiondetailed resultsCOVACTA (Rosas), 2020 0.48 [0.25; 0.94] 0.48[0.25; 0.94]COVACTA (Rosas), 202010%191NAnot evaluable recoverydetailed resultsTalaschian, 2021 0.64 [0.14; 2.92] 0.64[0.14; 2.92]Talaschian, 202110%36NAnot evaluable serious adverse eventsdetailed resultsCOVACTA (Rosas), 2020 0.81 [0.54; 1.22] Rosas (REMDACTA), 2021 0.83 [0.59; 1.18] Talaschian, 2021 7.93 [0.37; 171.38] Veiga, 2021 1.66 [0.60; 4.59] 0.90[0.65; 1.23]COVACTA (Rosas), 2020, Rosas (REMDACTA), 2021, Talaschian, 2021, Veiga, 2021419%1,245moderatenot evaluable adverse eventsdetailed resultsCOVACTA (Rosas), 2020 0.87 [0.52; 1.45] Rosas (REMDACTA), 2021 1.32 [0.92; 1.89] Veiga, 2021 1.65 [0.81; 3.37] 1.21[0.87; 1.67]COVACTA (Rosas), 2020, Rosas (REMDACTA), 2021, Veiga, 2021321%1,209moderatenot evaluable0.22.01.0relative treatment effectwww.metaEvidence.org2024-04-20 01:07 +02:00

TE: relative treatment effect (measured by a risk ratio, an odds ratio or an hazard ratio depending on what is reported in the papers); k: number of studies; n: total number of patients; ROB: risk of bias (ROB 2.0); Pub. bias: publication bias; OBS: observational studies; RCT: randomized clinical trials
studied treatment is better when TE > 1; studied treatment is better when TE < 1;

pathologies: 91 - treatments: 395 - roots T: 290