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. 2019 Aug 1;24(31):1800461. doi: 10.2807/1560-7917.ES.2019.24.31.1800461

Table 2. Influenza vaccine effectiveness by vaccine type, regardless of vaccination history in patients ≥ 60 years old admitted to hospital, Valencia Hospital Network for the Study of Influenza (VAHNSI), Spain, 2017/18 influenza season (n = 1,477 patients).

Types, subtypes or lineage of influenza N Casesa Vaccinated cases Controlsb Vaccinated controls Overall IVE Overall IVE
(adjuvanted vaccine)
Overall IVE
(non-adjuvanted vaccine)
Adjuvanted
vaccine
Non-adjuvanted
vaccine
Total Adjuvanted
vaccine
Non-adjuvanted
vaccine
Total IVE 95% CI IVE 95% CI IVE 95% CI
All influenzac 1,477 483 100 140 240 994 239 271 510 9.86 −15.47 to 29.63 9.97 −24.43 to 34.86 7.82 −23.15 to 31.00
A(H1N1)pdm09d 684 77 12 16 28 607 137 189 326 48.33 13.51 to 69.13 34.38 −34.58 to 68.00 54.12 15.32 to 75.14
A(H3N2)e 1,226 232 54 77 131 994 239 271 510 −29.88 −79.09 to 5.81 −23.93 −87.94 to 18.28 −37.03 −98.15 to 5.24
B/Yamagataf 916 150 29 39 68 766 180 228 408 25.75 −8.83 to 49.35 30.09 −15.94 to 57.85 21.10 −24.43 to 49.97

CI: confidence interval; GP: general practitioner; IVE: influenza vaccine effectiveness; LCI: laboratory-confirmed influenza.

a Cases in this column were individuals included in the study with LCI who were admitted to hospital during the period when influenza viruses of the type or subtype in question circulated. For example, cases of all influenza comprised all LCI individuals admitted during the 2017/18 influenza season, while cases of influenza A(H1N1)pdm09, A(H3N2) and B/Yamagata lineage only included patients admitted during times when influenza A(H1N1)pdm09, A(H3N2) and B/Yamagata lineage viruses respectively circulated. For each virus type, the time of circulation was estimated as the period between the first of at least two consecutive weeks with two or more cases of this type and the previous week of the first of two consecutive weeks with no cases of this type.

b Controls in this column were individuals included in the study who tested negative for influenza in the laboratory and who were admitted to hospital during the time that viruses of the influenza type in question circulated. The time of circulation was estimated as described in the above footnote a.

c Adjusted by age, number of chronic conditions, sex, socioeconomic class (occupation), admission in the last 12 months, number of GP visits in the last 3 months, smoking habits, obesity status, days between symptoms onset and swab, hospital and epidemiological week at admission. Nine individuals vaccinated with a vaccine different from the ones under study were excluded from the IVE estimations by vaccine type (seven controls and two cases).

d Adjusted by age, sex and epidemiological week at admission. Four individuals vaccinated with a vaccine different from the ones under study were excluded from the IVE estimations by vaccine type; all four were controls.

e Adjusted by age, number of chronic conditions, sex, socioeconomic status (occupation), admission in the last 12 months, number of GP visits in the last 3 months, smoking habits, obesity status, days between symptoms onset and swab, hospital and epidemiological week at admission. Eight individuals vaccinated with a vaccine different from the ones under study were excluded from the IVE estimations by vaccine type (seven controls and one case).

f Adjusted by age, number of chronic conditions, sex, smoking habits and epidemiological week at admission. Seven individuals vaccinated with a vaccine different from the ones under study were excluded from the IVE estimations by vaccine type (six controls and one case).