Study location | Study design | Sample size | Effectiveness of BNT162b2 | Effectiveness of ChAdOx1 | Study limitations |
---|---|---|---|---|---|
Israel Dangan et al. (2021) | Retrospective | 596,618 | Effectiveness increased with increase in time, and with receipt of second dose Effectiveness against symptomatic COVID-19 was 57% after 14–20 days and 66% after 21–27 days | – | Short follow-up after second dose, potential selection bias, risk of potential confounders, Potential exclusion of some eligible participants as a result of efforts to match |
Israel Chodlick et al. (2021) | Retrospective | 503,875 (≥ 16 years) | 51% effectiveness after within 24 days of first dose, effectiveness increased with increase in time | – | Potential unreported vaccination among potential eligible participants, not peer-reviewed as at the time of this review |
England Barnal et al. (2021a) | Retrospective | 174,731 (≥ 70 years old) | Single dose was 80% effective at preventing hospitalisation, 85% effective at preventing COVID-19 related death | Single dose was 80% effective at preventing hospitalisation | Inherent limitations of observational study, potential confounders, yet to be peer-reviewed as at the time of this review |
Denmark Moutsen-Helms et al. (2021) | Retrospective | 39,040 persons of 77–90 years and 33 039 persons of 36–57 years old | Protective effect was absent in older persons after first dose. Vaccine effectiveness was higher in the younger population (90%) than in older persons (64%) after 7 days of second vaccine dose | – | Study was not peer-reviewed as at the time of this study, observed variation in vaccine effectiveness may have been influenced by the large variation in sample size of the groups and potential confounders |
Scotland Vasileiou et al. (2021) | Retrospective | 1,331 993 (Mean age of 65 years old) | First dose was associated with 91% reduced COVID-19—related hospitalisation at 28–34 days after vaccination | First dose was associated with 88% reduced COVID-19—related hospitalisation at 28–34 days after vaccination | Risk of potential confounders |
England Bernal et al. (2021b) | Retrospective | 48,096 (≥ 70 years old) | Associated 44% and 69% reduced risk of death with one and two respective doses of BNT162b2 vaccination among COVID-19 cases | Associated 55% reduced risk of death from COVID-19 | Insufficient follow-up to ascertain effects of second dose of ChAdOx1 vaccine on risk of death. Yet to be peer-reviewed at the time of this study |
England Shroti et al. (2021) | Retrospective | 10,412 (older adults) | Reduction in SARS-CoV-2 infection after first and second dose | Reduction in SARS-CoV-2 infection after first and second dose | Study was yet to be peer-reviewed as at the time of this review. Risk of potential confounder bias may also be associated with the study |
England Hall et al. 2021 | Prospective | 23,324 (median age = 46.1) | Associated with 72% effectiveness after 21 days of first dose, and 86% effectiveness seven days after second dose | – | Risk of potential confounders |
United Kingdom Pritchard et al. (2021) | Retrospective | 383,812 (≥ 16 years old) | Reduced SARS-CoV-2 infections ≥ 21 days after the first dose at 66% and 80% after second dose | Reduced SARS-CoV-2 infections ≥ 21 days after the first dose at 61% and 79% after second dose | Risk of potential confounders |
Israel Haas et al. (2021) | Retrospective | (≥ 16 years old) | Associated with 95.3% preventing incidence of SARS-CoV-2 7 days after second dose, 97.2% and 96.7% against COVID-19 related hospitalisation and death respectively | – | Risk of potential confounders |
England Bernal et al. (2021) | Retrospective | 12,675 | Dose effectiveness of BNT162b2 reduced from 93.4% with B.1.1.7 to 87.9% with B.1.6172.2 | Associated effectiveness of two doses reduced 66.1% with B.1.1.7 to 59.8% with B.1.6172.2 | Potential misclassification of cases and control may have been influenced by sensitivity and specificity of the PCR, paper was yet to be validated by peer-review as at the time of this review |