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. 2024 Apr 10;29(4):239–254. doi: 10.1136/bmjebm-2023-112767

Table 5.

Summary of results in outcomes with pairwise meta-analysis

Outcome Comparison Number of studies (number of participants) OR/IRR (95% CI) (95% PI) VE (95% CI) tau2 (95% CI) Q; Q df; Q P value I2 Certainty of evidence
Primary outcomes
LCI IIV3-HD : IIV3-SD 3(41,753) OR: 0.75 (0.63 to 0.88) (0.25,2.19) . 0.00 (0.00 to 2.72) 1.00;2;0.61 0%
IIV3-SD : Placebo 2(330) OR: 0.31 (0.13 to 0.75) . 0.33 1.40;1;0.25 26%
LC—matched strains (DiazGranados 2014 defined as Match) IIV3-HD : IIV3-SD 2(330) OR: 0.74 (0.63 to 0.88) . 0.00 0.86;1;0.35 0%
LCI—mismatched strains (DiazGranados 2014 defined as Match) IIV3-HD : IIV3-SD 1(9,158) OR: 0.87 (0.56 to 1.36) . . . .
LCI—matched strains (DiazGranados 2014 defined as Mismatch) IIV3-HD : IIV3-SD 1(612) OR: 0.52 (0.35 to 0.77) . . . .
LCI—mismatched strains (DiazGranados 2014 defined as Mismatch) IIV3-HD : IIV3-SD 2(31,141) OR: 0.76 (0.64 to 0.90) . 0.00 0.11;1;0.75 0%
ILI IIV3-HD : IIV3-SD 2(41141) OR: 0.98 (0.93 to 1.02) VE: 1.76 (−1.75 to 7.18) 0.00 0.14;1;0.71 0% High
IIV3-SD : Placebo 2(854) OR: 0.39 (0.15 to 1.02) VE: 57.79 (−1.75 to 83.22) 0.21 1.08;1;0.30 8% Low
Secondary outcomes
ER Visit for ILI IIV3-HD : IIV3-SD 2(41,141) OR: 0.94 (0.74 to 1.19) . 0.00 0.20;1;0.66 0% Moderate
Hospitalisation for ILI IIV3-HD : IIV3-SD 2(41,141) OR: 0.72 (0.57 to 0.92) . 0.00 0.40;1;0.52 0% High
Hospitalisation for ARI IIV3-HD : IIV3-SD 2(84,991) OR: 0.87 (0.79 to 0.95) . 0.00 0.00;1;0.98 0% Moderate
Number of vascular events IIV3-Adj : IIV3-SD 2(7,577) IRR: 0.83* (0.54 to 1.27) . 0.00 0.00;1;0.89 0%
IIV3-HD : IIV3-SD 4(45,656) IRR: 0.74* (0.43 to 1.29)
(0.21,2.58)
. 0.23 (0.00 to 0.20) 4.90;3;0.18 39%
Inpatient hospitalisation (any cause) IIV3-HD : IIV3-SD 3(38,816) OR: 0.76 (0.40 to 1.42) (0.01,50.27) . 0.27 (0.01 to 3.22) 14.00;2;0.00 86% Low
Inpatient hospitalisation (any cause)—low RoB subgroup IIV3-HD : IIV3-SD 2(34,940) OR: 0.76 (0.52 to 1.13) . 0.27 14.00;1;0.00 93% Moderate
Inpatient hospitalisation (any cause)—over 80 years subgroup IIV3-HD : IIV3-SD 2(35,859) OR: 0.92 (0.86 to 0.99) . 0.00 0.20;1;0.66 0% Moderate
Outpatient visit IIV3-HD : IIV3-SD 2(41,141) OR: 1.04 (0.99 to 1.09) . 0.00 0.80;1;0.38 0%
IIV3-SD : Placebo 2(814) OR: 0.40 (0.07 to 2.14) . 1.09 4.30;1;0.04 77%
All-cause mortality IIV3-Adj : IIV3-SD 2(7,577) OR: 1.09 (0.73 to 1.62) . 0.00 0.50;1;0.47 0%
IIV3-HD : IIV3-SD 6(101,187) OR: 0.97 (0.92 to 1.02) (0.90,1.04) . 0.00 (0.00 to 0.02) 1.20;5;0.95 0%
IIV4-SD : IIV3-SD 3(3864) OR: 1.08 (0.38 to 3.09) (0.00,970.40) . 0.00 (0.00 to 15.12) 0.70;2;0.70 0%
IIV3-SD : Placebo 2(854) OR: 1.47 (0.43 to 5.06) . 0.00 0.20;1;0.66 0%
Influenza-related mortality IIV3-Adj:IIV3-SD 1(6,961) OR: 0.75 (0.17 to 3.36) .
IIV4-SD:IIV3-SD 1(1,741) OR: 3.01 (0.12 to 73.19) .

*Incidence rate ratios were reported for number of vascular events. Other outcomes included ORs.

Adj, adjuvanted; ARI, acute respiratory infection; HD, high dosage; IIV3, inactivated influenza vaccine trivalent; IIV4, IIV quadrivalent; ILI, influenza-like illness; IRR, incidence rate ratio; LCI, laboratory-confirmed influenza; PI, prediction interval; RR, relative risk; SD, standard dosage; VE, vaccine efficacy.