published meta-analysis   sensitivity analysis   studies

potential COVID-19 treatments in COVID-19 prophylaxis (excluding children) - Summary of results

OutcomeTE95% CInkI2ROBPub. bias 6 months symptomatic COVIDdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.09 [0.07; 0.11] 0.09[0.07; 0.11]BNT162b2 phase 3 (C4591001, Polack), 202010%46,077NAnot evaluable confirmed Covid-19, from 1st dosedetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.18 [0.13; 0.25] 0.18[0.13; 0.25]BNT162b2 phase 3 (C4591001, Polack), 202010%42,572NAnot evaluable deathsdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.50 [0.09; 2.73] 0.50[0.09; 2.73]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable vaccine efficacy from randomization (ITT)detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.18 [0.13; 0.25] 0.18[0.13; 0.25]BNT162b2 phase 3 (C4591001, Polack), 202010%42,572NAnot evaluable confirmed COVID (any severity)detailed resultsC4591031- first boost, 2021 0.05 [0.02; 0.13] 0.05[0.02; 0.13]C4591031- first boost, 202110%10,125NAnot evaluable symptomatic Covid-19detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.05 [0.02; 0.10] 0.05[0.02; 0.10]BNT162b2 phase 3 (C4591001, Polack), 202010%36,523NAnot evaluable 6 months severe COVID-19detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.03 [0.00; 0.46] 0.03[0.00; 0.46]BNT162b2 phase 3 (C4591001, Polack), 202010%NAnot evaluable severe COVID-19 (FDA definition)detailed resultsC4591031- first boost, 2021 0.25 [0.01; 5.50] 0.25[0.01; 5.50]C4591031- first boost, 202110%10,125NAnot evaluable severe COVID-19 occurrencedetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.25 [0.01; 5.62] C4591031- first boost, 2021 0.25 [0.01; 5.50] 0.25[0.03; 2.24]BNT162b2 phase 3 (C4591001, Polack), 2020, C4591031- first boost, 202120%52,698lownot evaluable vaccine efficacy after dose 1 (and before dose 2)detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.48 [0.32; 0.71] 0.48[0.32; 0.71]BNT162b2 phase 3 (C4591001, Polack), 202010%43,355NAnot evaluable related AE (TRAE)detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 4.91 [4.58; 5.26] 4.91[4.58; 5.26]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable related SAE (TRSAE)detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 8.00 [0.42; 151.43] 8.00[0.42; 151.43]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable serious adverse eventsdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 1.14 [0.88; 1.47] 1.14[0.88; 1.47]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable adverse eventsdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 2.62 [2.49; 2.76] 2.62[2.49; 2.76]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable arrhythmiadetailed resultsC4591031- first boost, 2021 1.99 [0.07; 59.22] 1.99[0.07; 59.22]C4591031- first boost, 202110%10,075NAnot evaluable hypertensiondetailed resultsC4591031- first boost, 2021 0.50 [0.02; 14.80] 0.50[0.02; 14.80]C4591031- first boost, 202110%10,075NAnot evaluable life-threatening SAEdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 0.91 [0.51; 1.65] 0.91[0.51; 1.65]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable Myocardial infarction detailed resultsC4591031- first boost, 2021 0.74 [0.17; 3.33] 0.74[0.17; 3.33]C4591031- first boost, 202110%10,075NAnot evaluable pulmonary embolismdetailed resultsC4591031- first boost, 2021 0.17 [0.01; 3.30] 0.17[0.01; 3.30]C4591031- first boost, 202110%10,075NAnot evaluable severe adverse eventsdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 1.74 [1.41; 2.14] 1.74[1.41; 2.14]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable stroke (non-specific, hemorrhagic, and ischemic)detailed resultsC4591031- first boost, 2021 0.99 [0.06; 15.88] 0.99[0.06; 15.88]C4591031- first boost, 202110%10,075NAnot evaluable cerebral venous sinus thrombosis (CVST)detailed resultsC4591031- first boost, 2021 0.50 [0.02; 14.80] 0.50[0.02; 14.80]C4591031- first boost, 202110%10,075NAnot evaluable appendicitisdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 2.00 [0.60; 6.65] C4591031- first boost, 2021 3.97 [0.18; 88.14] 2.19[0.71; 6.70]BNT162b2 phase 3 (C4591001, Polack), 2020, C4591031- first boost, 202120%53,523moderatenot evaluable Bell's palsydetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 7.99 [0.42; 151.24] 7.99[0.42; 151.24]BNT162b2 phase 3 (C4591001, Polack), 202010%37,586NAnot evaluable hypersensitivity, all termsdetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 2.17 [0.82; 5.71] 2.17[0.82; 5.71]BNT162b2 phase 3 (C4591001, Polack), 202010%43,252NAnot evaluable immediate allergic reactiondetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 1.00 [0.02; 50.42] 1.00[0.02; 50.42]BNT162b2 phase 3 (C4591001, Polack), 202010%43,448NAnot evaluable lymphadenopathy, anydetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 10.69 [4.63; 24.69] 10.69[4.63; 24.69]BNT162b2 phase 3 (C4591001, Polack), 202010%37,586NAnot evaluable musculoskeletal and connective tissue disorders, anydetailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 3.65 [3.26; 4.09] 3.65[3.26; 4.09]BNT162b2 phase 3 (C4591001, Polack), 202010%37,586NAnot evaluable local adverse reaction, any, dose 1detailed resultsOut of scaleBNT162b2 phase 3 (C4591001, Polack), 2020 24.90 [22.13; 28.03] 24.90[22.13; 28.03]BNT162b2 phase 3 (C4591001, Polack), 202010%8,183NAnot evaluable local adverse reaction, any, dose 2detailed resultsOut of scaleBNT162b2 phase 3 (C4591001, Polack), 2020 23.04 [20.30; 26.15] 23.04[20.30; 26.15]BNT162b2 phase 3 (C4591001, Polack), 202010%7,507NAnot evaluable systemic adverse reaction, any, dose 1detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 1.63 [1.50; 1.78] 1.63[1.50; 1.78]BNT162b2 phase 3 (C4591001, Polack), 202010%8,183NAnot evaluable systemic adverse reaction, any, dose 2detailed resultsBNT162b2 phase 3 (C4591001, Polack), 2020 4.55 [4.13; 5.01] 4.55[4.13; 5.01]BNT162b2 phase 3 (C4591001, Polack), 202010%7,507NAnot evaluable0.020.01.0relative treatment effectwww.metaEvidence.org2024-05-04 14:26 +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: 89 - treatments: 290,547,608,830,831,829,901,680,595,828,681,1209,833,629,689,543,617,625,859,511,960,546,564,944,682,1266,943,894,560,1102,598,563,668,753,752,836,639,541,534,581,615,679,522,582,666,1149,1150,737,544,733,597,524,611,538,957,958,521,566,517,881,904,882,897,896,899,1235,898,687,740,883,947,536,591,729,887,742,878,975,570,771,888,1141,690,880,1255,567,596,1437,600,652,557,635,1236,553,628,646,645,607,395,920,1438,927,932,931,1263,599,614,942,1436,928,923,535,1046,727,818,606,954,964,962,963,1045,638,677,627,533,526,616,926,1246,726,580,568,527,588,539,585,691,1210,525,843,827,1047,1048,819,545,1253,519,619,537,514,688,529,508,656,657,832,530,512,515,754,1142,1419,513,884,632,559,889,956,684,886,631,574,509,542,1145,555,554,941,961,1250,633,676,518,532,510,528,520,955,815,893,623,622,630,593,569,516,814,649,650,589,651,968,1245,610,751,747,695,548,970,594,565,879,1257,571,626,697,572,1234,586,573,540,592,930,949,838,698,934,735,929,948,946,945,587,655,1146,531,933,613,919,725,678,921,621,959,748,1348,1256,924,1243,925,658,699,612,552,590,891,605,892,722,618,609,551,834,763,922,935,620,1317,1265,824,766,857,1291,1088,1331,1330,1329,1344,1328,1327,979,822,762,805,950,757,761,806,758,826,755,821,1288,1287,1286,760,1284,802,765,1285,759,823,804,1264,764,858,835,1262,1290,1316,1341,1342,1343,825,803,1244,523,885,734,1439 - roots T: 290