published meta-analysis   sensitivity analysis   studies

antiviral and associated therapy in COVID 19 all comers - Summary of results

OutcomeTE95% CInkI2ROBPub. bias death D28detailed resultsNIH NIAID ACTT-1, 2020 0.73 [0.52; 1.03] 0.73[0.52; 1.03]NIH NIAID ACTT-1, 202010%1,062NAnot evaluable deathsdetailed resultsLou (FAVIPIRAVIR), 2020 1.12 [0.02; 62.74] NIH NIAID ACTT-1, 2020 0.55 [0.36; 0.84] NOR-Solidarity (hydroxychloroquine), 2021 3.10 [0.29; 33.20] 0.61[0.35; 1.09]Lou (FAVIPIRAVIR), 2020, NIH NIAID ACTT-1, 2020, NOR-Solidarity (hydroxychloroquine), 202134%1,193moderatenot evaluable deaths (time to event analysis only)detailed resultsNIH NIAID ACTT-1, 2020 0.55 [0.36; 0.84] NOR-Solidarity (hydroxychloroquine), 2021 3.10 [0.29; 33.20] 0.87[0.19; 3.85]NIH NIAID ACTT-1, 2020, NOR-Solidarity (hydroxychloroquine), 2021250%1,174moderatenot evaluable clinical improvementdetailed resultsLou (FAVIPIRAVIR), 2020 1.25 [0.21; 7.62] NIH NIAID ACTT-1, 2020 1.29 [1.12; 1.49] 1.29[1.12; 1.49]Lou (FAVIPIRAVIR), 2020, NIH NIAID ACTT-1, 202020%1,081moderatenot evaluable clinical improvement (14-day)detailed resultsLou (FAVIPIRAVIR), 2020 1.25 [0.21; 7.62] 1.25[0.21; 7.62]Lou (FAVIPIRAVIR), 202010%19NAnot evaluable clinical improvement (28-day)detailed resultsNIH NIAID ACTT-1, 2020 1.35 [1.03; 1.76] 1.35[1.03; 1.76]NIH NIAID ACTT-1, 202010%1,062NAnot evaluable clinical improvement (time to event analysis only)detailed resultsNIH NIAID ACTT-1, 2020 1.29 [1.12; 1.49] 1.29[1.12; 1.49]NIH NIAID ACTT-1, 202010%1,062NAnot evaluable viral clearance detailed resultsLou (FAVIPIRAVIR), 2020 0.18 [0.01; 4.75] 0.18[0.01; 4.75]Lou (FAVIPIRAVIR), 202010%19NAnot evaluable viral clearance by day 14detailed resultsLou (FAVIPIRAVIR), 2020 0.18 [0.01; 4.75] 0.18[0.01; 4.75]Lou (FAVIPIRAVIR), 202010%19NAnot evaluable ICU admissiondetailed resultsLou (FAVIPIRAVIR), 2020 5.43 [0.21; 139.89] 5.43[0.21; 139.89]Lou (FAVIPIRAVIR), 202010%19NAnot evaluable serious adverse eventsdetailed resultsNIH NIAID ACTT-1, 2020 0.72 [0.54; 0.96] 0.72[0.54; 0.96]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable deep vein thrombosisdetailed resultsNIH NIAID ACTT-1, 2020 0.64 [0.23; 1.81] 0.64[0.23; 1.81]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable elevated liver enzymesdetailed resultsNIH NIAID ACTT-1, 2020 0.67 [0.38; 1.18] 0.67[0.38; 1.18]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable hyperbilirubinemiadetailed resultsNIH NIAID ACTT-1, 2020 0.84 [0.30; 2.34] 0.84[0.30; 2.34]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable pulmonary embolismdetailed resultsNIH NIAID ACTT-1, 2020 0.96 [0.19; 4.80] 0.96[0.19; 4.80]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable renal impairmentdetailed resultsNIH NIAID ACTT-1, 2020 1.02 [0.64; 1.61] 1.02[0.64; 1.61]NIH NIAID ACTT-1, 202010%1,063NAnot evaluable0.010.01.0relative treatment effectwww.metaEvidence.org2024-04-20 14:58 +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: 94 - treatments: 545,1253,519,619,537,514,688,529,508,656,657,832,530,512,515,754,1142,1419,513,884,632,559,889,956,684,886,631,574,509,542,1145,555,554,941,961,1250,633,676,518,532,510,528,520,955,815,893,623,622,630,593,569,516,814 - roots T: 290