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. 2017 Feb 9;22(6):30460. doi: 10.2807/1560-7917.ES.2017.22.6.30460

Table 2. Interim vaccine effectiveness estimates for influenza A(H3N2), Canadian Sentinel Practitioner Surveillance Network, 1 November 2016–21 January 2017 (n = 906).

Model n total Cases Controls VE %
(95% CI)
n % vaccinated n % vaccinated
Primary analysisa
Unadjusted 906 370 24 536 30 27 (1 to 46)
Individual covariate adjustment
Age group (1–8, 9–19, 20–49, 50–64, ≥ 65 years) 30 (4 to 50)
Provinceb 32 (7 to 50)
Specimen collection interval from ILI onset (≤ 4, 5–7 days) 23 (−5 to 44)
Specimen collection date (2-week interval) 38 (15 to 55)
Full covariate adjustment
Adjusted 42 (18 to 59)
Restricted by provincec
Alberta
Unadjusted 278 110 18 168 30 49 (8 to 72)
Adjusted 62 (26 to 80)
British Columbia
Unadjusted 327 134 28 193 29 4 (−56 to 41)
Adjusted 28 (−30 to 60)
Ontariod
Unadjusted 179 87 29 92 42 45 (−2 to 71)
Adjusted 27 (−60 to 66)
Quebec
Unadjusted 122 39 13 83 17 28 (−118 to 76)
Adjusted NE
All provinces excluding Alberta
Unadjusted 628 260 26 368 29 16 (−19 to 42)
Adjustede 34 (−1 to 57)

CI: confidence interval; ILI: influenza-like illness; NE: not estimated (insufficient sample size); VE: vaccine effectiveness.

a Analysis adjusted for age group, province, specimen collection interval from ILI onset and specimen collection date (2-week interval).

b Alberta, British Columbia, Ontario, Quebec.

c Analysis adjusted for age group, specimen collection interval and specimen collection date (2-week interval).

d Due to logistical issues, specimen collection for the 2016/17 season began late in Ontario. The study period for Ontario-specific VE analysis was defined as 12 December 2016 (week 50) to 21 January 2017 (week 3).

e Analysis adjusted for age group, province (British Columbia, Ontario, Quebec), specimen collection interval and specimen collection date (2-week interval).