Skip to main content
letter
. 2021 Dec 29:NEJMc2119270. doi: 10.1056/NEJMc2119270

Table 2. Effectiveness of Two Doses of BNT162b2 Vaccine before and during Proxy Omicron Period.*.

Variable Vaccine Effectiveness
(95% CI)
Comparator Period Proxy Omicron Period
%
Overall estimate 93 (90–94) 70 (62–76)
Sensitivity analyses of PCR results
Patients with S-gene target failure 69 (48–81)
Patients in Gauteng province 70 (59–78)
Patients with Covid-19 symptoms 50 (35–62)
*

The overall estimates of vaccine effectiveness were calculated according to a test-negative design after adjustment for confounders. The three sensitivity analyses included the results of polymerase-chain-reaction (PCR) tests showing S-gene target failure (as an indication of omicron infection), PCR results obtained only from patients in Gauteng province, and PCR results obtained only from patients who had been hospitalized (i.e., symptomatic population).