Table 5

Summary of results in outcomes with pairwise meta-analysis

OutcomeComparisonNumber of studies (number of participants)OR/IRR (95% CI) (95% PI)VE (95% CI)tau2 (95% CI)Q; Q df; Q P valueI2 Certainty of evidence
Primary outcomes
LCIIIV3-HD : IIV3-SD3(41,753)OR: 0.75 (0.63 to 0.88) (0.25,2.19).0.00 (0.00 to 2.72)1.00;2;0.610%
IIV3-SD : Placebo2(330)OR: 0.31 (0.13 to 0.75).0.331.40;1;0.2526%
LC—matched strains (DiazGranados 2014 defined as Match)IIV3-HD : IIV3-SD2(330)OR: 0.74 (0.63 to 0.88).0.000.86;1;0.350%
LCI—mismatched strains (DiazGranados 2014 defined as Match)IIV3-HD : IIV3-SD1(9,158)OR: 0.87 (0.56 to 1.36)....
LCI—matched strains (DiazGranados 2014 defined as Mismatch)IIV3-HD : IIV3-SD1(612)OR: 0.52 (0.35 to 0.77)....
LCI—mismatched strains (DiazGranados 2014 defined as Mismatch)IIV3-HD : IIV3-SD2(31,141)OR: 0.76 (0.64 to 0.90).0.000.11;1;0.750%
ILIIIV3-HD : IIV3-SD2(41141)OR: 0.98 (0.93 to 1.02)VE: 1.76 (−1.75 to 7.18)0.000.14;1;0.710%High
IIV3-SD : Placebo2(854)OR: 0.39 (0.15 to 1.02)VE: 57.79 (−1.75 to 83.22)0.211.08;1;0.308%Low
Secondary outcomes
ER Visit for ILIIIV3-HD : IIV3-SD2(41,141)OR: 0.94 (0.74 to 1.19).0.000.20;1;0.660%Moderate
Hospitalisation for ILIIIV3-HD : IIV3-SD2(41,141)OR: 0.72 (0.57 to 0.92).0.000.40;1;0.520%High
Hospitalisation for ARIIIV3-HD : IIV3-SD2(84,991)OR: 0.87 (0.79 to 0.95).0.000.00;1;0.980%Moderate
Number of vascular eventsIIV3-Adj : IIV3-SD2(7,577)IRR: 0.83* (0.54 to 1.27).0.000.00;1;0.890%
IIV3-HD : IIV3-SD4(45,656)IRR: 0.74* (0.43 to 1.29)
(0.21,2.58)
.0.23 (0.00 to 0.20)4.90;3;0.1839%
Inpatient hospitalisation (any cause)IIV3-HD : IIV3-SD3(38,816)OR: 0.76 (0.40 to 1.42) (0.01,50.27).0.27 (0.01 to 3.22)14.00;2;0.0086%Low
Inpatient hospitalisation (any cause)—low RoB subgroupIIV3-HD : IIV3-SD2(34,940)OR: 0.76 (0.52 to 1.13).0.2714.00;1;0.0093%Moderate
Inpatient hospitalisation (any cause)—over 80 years subgroupIIV3-HD : IIV3-SD2(35,859)OR: 0.92 (0.86 to 0.99).0.000.20;1;0.660%Moderate
Outpatient visitIIV3-HD : IIV3-SD2(41,141)OR: 1.04 (0.99 to 1.09).0.000.80;1;0.380%
IIV3-SD : Placebo2(814)OR: 0.40 (0.07 to 2.14).1.094.30;1;0.0477%
All-cause mortalityIIV3-Adj : IIV3-SD2(7,577)OR: 1.09 (0.73 to 1.62).0.000.50;1;0.470%
IIV3-HD : IIV3-SD6(101,187)OR: 0.97 (0.92 to 1.02) (0.90,1.04).0.00 (0.00 to 0.02)1.20;5;0.950%
IIV4-SD : IIV3-SD3(3864)OR: 1.08 (0.38 to 3.09) (0.00,970.40).0.00 (0.00 to 15.12)0.70;2;0.700%
IIV3-SD : Placebo2(854)OR: 1.47 (0.43 to 5.06).0.000.20;1;0.660%
Influenza-related mortalityIIV3-Adj:IIV3-SD1(6,961)OR: 0.75 (0.17 to 3.36).
IIV4-SD:IIV3-SD1(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.