ATAGI clinical guidance on COVID-19 vaccine administration errors
ATAGI has provided the below guidance for clinicians outlining the appropriate management of common COVID-19 vaccine administration errors. It includes scenarios where the vaccine is administered in the following circumstances:
- Via the incorrect site/route
- At a higher/lower dose
- Following incorrect storage and handling
- In an unapproved age group
- Mixed vaccine schedules
- With incorrect intervals
It is important to note that in Victoria, any vaccine administration error should be reported to SAEFVIC. Following the identification of a vaccine error, open disclosure with the vaccine recipient is important and addressing the cause of the error will prevent errors from occurring again in the future.
To read the full guideline, follow the link below:
ATAGI clinical guidance on COVID-19 vaccine administration errors
New resource: NCIRS Decision aid (5–15 years): Should I get the COVID-19 vaccine for my child?
NCIRS have designed a new decision aid resource to help families make an informed decision about whether COVID-19 vaccination is right for their children.
The tool provides evidence-based information about the disease and the vaccine and takes the user through five simple steps to help weigh up the risks and benefits of vaccination.
To access the decision guide, please click on the link below.
New resource: NCIRS Decision aid (5–15 years): Should I get the COVID-19 vaccine for my child?
Clinical recommendations for COVID-19 vaccines- updated booster advice
The Australian Technical Advisory Group on Immunisation (ATAGI) have provided updated recommendations on the use of booster doses of COVID-19 vaccines:
- Individuals aged 18 years and above are recommended to receive a single booster dose of either mRNA vaccine (Pfizer or Moderna), 3 months after the completion of a primary course of vaccination.
- Individuals aged 16-17 years are recommended to receive a single dose of Comirnaty (Pfizer) as their booster, 3 months following the completion of their primary course. Alternate COVID-19 vaccine brands are not registered for use as a booster dose in this age group.
- Whilst Nuvaxovid (Novavax) is not TGA-registered for use as a booster dose, ATAGI recommends that it may be used as a booster in individuals aged 18 years or older in circumstances where there is a contraindication to mRNA vaccines. There is limited safety and efficacy data to support the use of Nuvaxovid as a booster dose, however there are no theoretical concerns.
- Vaxzevria (AstraZeneca) is no longer recommended for use as a booster dose. Individuals who have already received Vaxzevria (AstraZeneca) as their booster dose do not need a repeat booster dose of an alternate brand.
For further information regarding the ATAGI recommendations on the use of a booster dose of COVID-19 vaccine, please refer to the links below:
ATAGI recommendations on the use of a booster dose of COVID-19 vaccine
ATAGI recommendations on the use of Spikevax (Moderna) COVID-19 vaccine in children aged 6 to 11 years
Following the TGA’s provisional approval, ATAGI has put forth a guideline that recommends the use of Moderna’s COVID-19 vaccine (Spikevax) in children aged 6 to 11 years.
Clinical data supports that Spikevax produces a strong immune response and reduces the likelihood of children in this cohort developing COVID-19.
This statement addresses the recommendations, considerations and rationale for the use of Moderna’s COVID-19 vaccine in children aged 6 to 11.
To read the full statement, follow the link below.
The Conversation: The Moderna vaccine is now available for 6 to 11 year olds. Here’s what parents need to know
The Moderna COVID-19 vaccine is now approved for use in children aged 6 to 11 years. With just under half of Australian primary-school-age children having received their first COVID vaccine dose, the approval of Moderna’s COVID vaccine provides parents with an additional opportunity to protect their children against severe disease.
Following the KidCOVE clinical trial, this article explores the ongoing safety and efficacy as well as the considerations and administrative recommendations for the use of Moderna’s COVID-19 vaccine in the 6 to 11 years cohort.
To read the full article, follow the link below.
ATAGI update following weekly COVID-19 meeting – 16 February 2022
ATAGI held their weekly meeting on Wednesday 16 February to discuss the latest developments and recommendations relating to COVID-19 immunisations.
The meeting addressed the use of Moderna’s COVID-19 vaccine in children aged 6 to 11 years, as well as, the use of Novavax’s COVID-19 vaccine as a booster and recommendations regarding the vaccine dose interval for children.
To read the full update, follow the link below:
ATAGI update following weekly COVID-19 meeting – 16 February 2022
NCIRS Webinar - Living with COVID-19: Getting back to immunisation business as usual
NCIRS will be hosting a webinar on Thursday 3 March featuring a panel of expert speakers including MVEC’s A/Prof Nigel Crawford. The topic for the webinar is Living with COVID-19: Getting back to immunisation business as usual and will cover:
- an update on Australian COVID‑19 vaccine recommendations
- COVID-19 and routine immunisation programs regionally and globally – what’s needed
- new COVID-19 vaccines – do we need to change our strategy in response to new variants?
Further information and details on registration can be found via the link below:
NCIRS Webinar - Living with COVID-19: Getting back to immunisation business as usual
ABC News: Chickenpox defies COVID-19 restrictions, prompting vaccination warning
Throughout the pandemic, the highly transmissible varicella zoster virus, which causes chickenpox has continued to spread with more than 10,000 cases recorded in Queensland last year and similar levels observed in 2020.
While the pandemic has shown social and physical distancing to be very effective in limiting the spread of diseases, this article reveals that we can expect to see a number of infectious diseases increase as measures are relaxed.
Immunising against the varicella zoster virus is the best way to protect against infection. Data shows that the vaccine is 95 to 99 per cent effective at preventing severe chickenpox so there is a need to encourage individuals – especially pregnant women – to ensure they are up to date with their vaccinations.
To read the article in full, please click on the link below.
ABC News: Chickenpox defies COVID-19 restrictions, prompting vaccination warning
The Conversation: Do COVID boosters cause more or fewer side effects? How quickly does protection wane? Your questions answered
With more than 2,400 people currently in hospital, the Australian Technical Advisory Group on Immunisation (ATAGI) recommends Australians aged 16 years and older have a COVID-19 booster vaccine to ensure high levels of protection against severe disease and hospitalisation. A booster dose of the COVID vaccine, three months following the completion of the primary course can provide a similar level of protection against Omicron as two primary doses against Delta.
Additionally, data shows that the booster dose renders milder side effects compared to the first 2 doses with less than 1% of people reporting the need for a medical consultation.
This article explores the benefits of a booster vaccine compared to the primary 2 doses, the time frame recommendation for receiving a booster following COVID infection, and whether additional vaccine doses will be required in the future.
Follow the link below to read the full article:
Moderna's COVID-19 vaccine (SPIKEVAX) provisionally approved for use in individuals 6 years and older
The Therapeutic Goods Administration (TGA) has provisionally approved the Moderna COVID-19 vaccine, SPIKEVAX, for use in individuals aged 6 years and older. This follows provisional approvals granted by the TGA to Moderna for the use of SPIKEVAX in individuals aged 12 years and older on 3 September 2021, and on 7 December 2021 the SPIKEVAX booster dose for use in adults 18 years and older.
The TGA carefully assessed the data following the KidCOVE clinical trial which included up to 4,000 participants aged 6 to 11 years across the US and Canada, demonstrating that the immune response to the vaccine in children was similar to that seen in older age groups.
In addition to this, clinical data showed that the safety profile in children is similar to that seen in adults. The most frequent side effects in this age cohort were short term and non-severe. These included injection site pain, redness and/or swelling, axillary (groin) swelling or tenderness, fatigue, headache, fever and muscle pain.
Further advice on the rollout of SPIKEVAX to this age group will be provided to the Government by the Australian Technical Advisory Group on Immunisation (ATAGI).
To read the statement in full, please click on the link below: