Skip header and navigation

2 records – page 1 of 1.

Document Type
Rapid Review
Review Code
INF031801v019 RR
Question Submitted
March 18, 2021
Date Completed
December 26, 2021
Status
5. Updated review
Research Team
Infectious Disease
, 2021 Version: 19 Review History: INF031801 RR - INF031801v018 RR: March 31, 2021 – December 13
Document Type
Rapid Review
Review Code
INF031801v019 RR
Question Submitted
March 18, 2021
Date Completed
December 26, 2021
Status
5. Updated review
Research Team
Infectious Disease
Updated Key Findings
December 14, 2021
Ontario Immunization Advisory Committee recommended that if an 11 and 12-year-old child is inadvertently given a second dose of the Pfizer-BioNTech vaccine that is not authorized for their age, the dose should be considered valid and the series complete.
National Advisory Committee on Immunization (NACI) recommends that a booster dose of an authorized mRNA COVID-19 vaccine should be offered to vulnerable population and > 50 years old, =6 months after completion of a primary COVID-19 vaccine series.
Australian Technical Advisory Group on Immunization (ATAGI) recommends COVID-19 booster vaccination with either Pfizer (Comirnaty) or Moderna (Spikevax), which are considered equally acceptable, for anyone aged 18 and older who completed their primary course of COVID-19 vaccination 5 or more months ago.
On December 8th, 2021 in a press release by Pfizer-BioNTech said that preliminary laboratory studies demonstrate that three doses of the Pfizer-BioNTech COVID-19 vaccine neutralize the Omicron variant while two doses show significantly reduced neutralization titers. Data indicate that a third dose of BNT162b2 increases the neutralizing antibody titers by 25-fold compared to two doses.
Key Findings
December 3, 2021
The Therapeutic Goods Administration (TGA) has granted provisional approval to Moderna for the use of its vaccine in children (two 10µg doses) and as booster shot for adults (one 30µg dose) in preparation for the recent emergence of the Omicron variant. This is in addition to Pfizer, which was also recently approved.
The National Advisory Committee on Immunization (NACI) recommends that a complete series with the Pfizer-BioNTech COVID-19 vaccine (10 mcg) may be offered to children 5-11 years of age who do not have contraindications to the vaccine, with a dosing interval of at least 8 weeks between the first and second dose.
NNACI also recommends that children aged 5-11 years with a history of previous SARS-CoV-2 infection should be considered no longer infectious and symptoms of an acute illness should be completely resolved prior to vaccination.
Health Canada has authorized Moderna's COVID-19 vaccine (also known as Spikevax) to be used as a booster shot, using a half-dose of the vaccine.
Category
Epidemiology
Infection Prevention and Control
Subject
Vaccines
Immunity
Infection Prevention and Control
Clinical Presentation
Population
All
Clinical Setting
Community
ICU
Medicine Unit
Primary care
Public Health
Priority Level
Level 3 Two weeks (14 days)
Cite As
Jagwani, M; Lee, S; Shumilak, G; Reeder, B; Groot, G; Hernandez, L; Howell-Spooner, B; Miller, L. How effective are COVID-19 vaccines? 2021 Dec 26. Document no.: INF031801v019 RR. In: COVID-19 Rapid Evidence Reviews [Internet]. SK: SK COVID Evidence Support Team, c2021. 93 p. (CEST rapid review report)
Review History
INF031801v17 RR: November 23, 2021
INF031801v16 RR: November 12, 2021
INF031801v15 RR: October 28, 2021
INF031801v014 RR: October 16, 2021
INF031801v013 RR: September 24, 2021
INF031801v012 RR: September 10, 2021
INF031801v010 RR: August 25, 2021
INF031801v9 RR: August 23, 2021
INF031801v8 RR: August 9, 2021
INF031801v7 RR: July 20, 2021
INF031801v6 RR: July 2, 2021
INF031801v5 RR: June 22, 2021
INF031801v4 RR: June 3, 2021
INF031801v3 RR: May 24, 2021
INF031801v2 RR: May 14, 2021
INF031801 RR: March 31, 2021
Related Documents
Documents
Less detail
Document Type
Rapid Review
Review Code
EOC031801v019 RR
Question Submitted
March 18, 2021
Date Completed
December 20, 2021
Status
5. Updated review
Research Team
EOC
Review History: EOC031801 RR – EOC031801v018 RR: March 25 – December 6, 2021 Cite As: Asamoah
Document Type
Rapid Review
Review Code
EOC031801v019 RR
Question Submitted
March 18, 2021
Date Completed
December 20, 2021
Status
5. Updated review
Research Team
EOC
Updated Key Findings
December 20, 2021 - Delta dominance - Delta remains the predominant variant accounting for most of variants sequenced from surveillance data from Public Health Ontario, Public Health England and ECDC as of the 6th of December; this is rapidly changing. - Expect opinions from PHAC indicate that Omicron will likely outpace Delta and drive infections up to 26,600 a day by mid-January in Canada. - ECDC projects Omicron could cause over half of all SARS-CoV-2 infections in the EU/EEA within the next few months, with probability of further introduction and community spread and impact of the spread assessed HIGH and VERY HIGH respectively. - Preliminary evidence suggests that the various mutations in Omicron may increase transmissibility and replication; increase evasion of antibody neutralization by COVID-19 infection, vaccine-based, or monoclonal-based antibodies; increase the binding affinity of the virus to the ACE2 receptors on host cells; and may be associated with increased infectivity. - Evidence is still emerging on the disease severity with omicron compared to Delta, however the first Omicron death has been reported in the UK during the week of December 13, 2021. - The Delta sub-lineage AY.4.2 (Delta plus) continues account for an increasing proportion of Delta cases in the UK, with cases detected in Canada.
Key Findings
December 6, 2021 - A new SARS-CoV-2 variant designated Omicron has emerged and classified as a VOC by WHO. The heavily mutated variant (50 mutations -- 32 of them on the spike protein) was first identified in South Africa and has already spread to many parts of the world. - Preliminary evidence suggests there may be an increased risk of reinfection with Omicron, however, there is still emerging evidence of the transmissibility, severity of disease, effectiveness of vaccines, and the effectiveness of current tests and treatment. - Delta dominance - Delta remains the predominant variant accounting for most of variants sequenced from surveillance data from Public Health Ontario, Public Health England and ECDC. - The Delta sub-lineage AY.4.2 (Delta plus) continues account for an increasing proportion of Delta cases in the UK. - Delta variant sub-lineage AY.25 and AY.27 have been detected in Canada, with majority of the cases identified in Saskatchewan, followed by Alberta and B.C. However, experts say there’s no data to determine if these sub-lineages will be more transmissible than its parent strain.
Category
Epidemiology
Healthcare Services
Subject
Health Planning
Variants
Population
All
Clinical Setting
Community
Public Health
Priority Level
Level 3 Two weeks (14 days)
Cite As
Asamoah, G; Badea, A; Lee, S; Shumilak, G; Reeder, B; Groot, G; Muhajarine, N; Hernandez-Ronquillo L; Miller, L; Howell-Spooner, B. What is the epidemiology of variants and what are the implications for healthcare? 2021 Dec 20. Document no.: EOC031801v019 RR. In: COVID-19 Rapid Evidence Reviews [Internet]. SK: SK COVID Evidence Support Team, c2021. 50 p. (CEST rapid review report).
Review History
EOC031801v18 RR
EOC031801v17 RR
EOC031801v16 RR
EOC031801v15 RR
EOC031801v14 RR
v012 and v013 RR were combined into v013
EOC031801v011 RR: August 27, 2021
v010 and v011 RR were combined into v011
EOC031801v9 RR: August 19, 2021
EOC031801v8 RR: July 12, 2021
EOC031801v7 RR; June 24, 2021
EOC031801v6 RR; June 17, 2021
EOC031801v5 RR; June 2, 2021
EOC031801v4 RR; May 17, 2021
EOC031801v3 RR: May 3, 2021
EOC031801v2 RR: April 20, 2021
EOC031801 RR: March 25, 2021
Related Documents
Documents
Less detail