Published: 18 March, 2020 | Updated: 24 March, 2020
What's changed?
24 March, 2020 IMAC statement on 20 minute observation period added
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The influenza immunisation programme commenced on 18th March, 2020, for people eligible for funded vaccines and healthcare
workers (subject to vaccine availability). People who are not eligible for funded influenza vaccinations
should be asked to defer vaccination until on or after 13th April, 2020.
This change was made in response to the current situation with the COVID-19 (novel coronavirus) pandemic. Increasing
influenza vaccination rates in vulnerable patient groups and healthcare workers is a priority. An additional 400,000 doses
of influenza vaccine have been ordered in 2020 in anticipation of demand based on the experience of last year. Over 1.35
million doses of influenza vaccine were distributed in New Zealand during the 2019 season, more than any previous year,1
and an additional 55,000 doses were obtained mid-season.2
Four strains of influenza are included in the 2020 vaccine
The 2020 influenza vaccine includes four strains of inactivated influenza virus, of which three are new:3
- B/Phuket/3073/2013-like virus
- A/Brisbane/02/2018 (H1N1)pdm09-like virus*
- A/South Australia/34/2019 (H3N2)-like virus*
- B/Washington/02/2019-like virus*
*Not included in the 2019 influenza vaccine
Vaccine selection is determined by age
Two influenza vaccines are subsidised for the 2020 season:4
- Afluria Quad is approved for use in adults and children aged three years and over and is funded for
eligible people in this age group (see below)
- Afluria Quad Junior is approved for use in children aged six months to 35 months and is funded for
eligible children in this age group
The Afluria Quad vaccine began being distributed on 16th March, 2020. The Afluria Quad Junior vaccine is expected to be
available from 1st April, 2020.
Afluria Quad is given as a single, 0.5 mL dose and Afluria Quad Junior is given as a single, 0.25 mL dose.4 Children
aged six months to nine years, however, who are receiving an influenza vaccine for the first time should receive two doses,
at least four weeks apart.4 Both vaccines are contraindicated in children aged less than six months due to a lack of safety
and efficacy data in this age group.4
People who are eligible for free influenza vaccinations
People who are eligible for funded influenza vaccinations are at the greatest risk of serious illness this season and vaccinating
this group as soon as vaccines are available should be regarded as the highest priority for practices. This group
of people includes:*
- Women who are pregnant
- People aged 65 years and over
- People aged under 65 years with:
- Cardiovascular morbidity – excluding hypertension or dyslipidaemia without end-organ disease
- Diabetes
- Asthma who are taking preventative treatment
- Other long-term respiratory disease such chronic obstructive pulmonary disease
- Chronic kidney disease
- Any cancer†
- Autoimmune disease or immunosuppression
- Children aged under four years or under with a history of significant respiratory illness or hospitalisation for respiratory illness
*A full list of conditions and criteria that qualify a person for a funded vaccination is available from: https://schedule.pharmac.govt.nz/ScheduleOnline.php?osq=influenza+vaccine
†Influenza vaccination may be contraindicated in patients taking immune checkpoint inhibitors. If a patient is taking
atezolizumab, ipilimumab, nivolumab or pembrolizumab, contact the prescribing oncologist or 0800 IMMUNE for advice before
administering the vaccine.
It is important that all people aged 65 years and over are offered the annual influenza vaccination, particularly older
patients of Māori and Asian ethnicity. Guidance from the Ministry of Health (MOH) is that immunisation rates for these groups
are notably lower than in other ethnic groups.
The safety of the influenza vaccine
The influenza vaccine is typically well tolerated. Adverse reactions to the vaccine are more frequent in children who
have not previously been exposed to the vaccine or influenza virus.5 The most common adverse reactions associated with
the administration of inactivated influenza vaccines are:3
- Injection site pain, erythema or swelling
- Headache, muscle ache and fatigue in adults
- Fever, irritability and loss of appetite, more commonly in children
Local and systemic adverse effects are generally mild and resolve within a day or two.3
Paracetamol or any other antipyretic medicine is not recommended before or after the influenza vaccination,
in the absence of pain or discomfort, as it may lower the patient’s initial immune response.6 In children, paracetamol
may be considered if the child is in pain, has a fever, or is distressed following the vaccination.6
Febrile convulsions have been associated with influenza vaccination in children, but only when it is given
in combination with other vaccines, e.g. the pneumococcal vaccine.7 In combination with other vaccines, the influenza
vaccine may increase the risk of a febrile convulsion by 16-30 per 100 000 children vaccinated.7 The influenza vaccination
given in isolation does not increase the rate of febrile convulsions, which occur in approximately 5% of all children by
age seven years.7
Anaphylaxis is the most serious adverse event associated with influenza vaccination.3 This generally
occurs within minutes of administration, once in approximately one million vaccine doses.3 Patients who have received
the influenza vaccination should be observed for 20 minutes following administration*,3 although rarely severe allergic
reactions to the vaccine may begin after this time.8 People with latex allergies can be safely given
the influenza vaccine as the Afluria Quad and Afluria Quad Junior vaccines are both latex free.3
* In light of the COVID-19 pandemic, this requirement may be relaxed for adults and adolescents who meet certain criteria,
if the risk of infectious disease transmission is greater than the low risk of anaphylaxis. See the IMAC statement for
further information: no longer available online; this information has now changed, see Bulletin 72.”
People with egg allergy can be given the Afluria Quad vaccines
The 2020 influenza vaccine can be safely given to people with a history of egg allergy, contrary to what is stated on
the vaccine’s data sheet.3 The Afluria Quad and the Afluria Quad Junior vaccines are grown in hens’ eggs, however, the
residual dose of ovalbumin in the vaccines is less than the one microgram necessary to trigger anaphylaxis in sensitive
individuals.3
Annual influenza vaccination is recommended
There are two primary reasons for recommending annual influenza vaccination:3
- The strains of influenza virus in circulation change over time and the seasonal vaccine is adjusted in response
- The protection provided by an influenza vaccination reduces over time
Some level of protection from influenza is expected from four days post-vaccination, however, it may take up to two weeks
for maximal immune response.3
The effectiveness of an influenza vaccine is determined by the degree to which the circulating strains of the virus match
the vaccine, and by the health, immune status and age of the recipient.3 From 2012 to 2015, the effectiveness of the seasonal
vaccination at preventing presentations of influenza-like illness in primary care and preventing influenza-related hospitalisations
was estimated to be around 50%.3 Effectiveness is expected to be higher for healthy children and adults and lower for
frail elderly people and those with significant co-morbidities. An additional potential benefit of vaccination is that it
may provide some protection against some strains of influenza virus that are not included
in the vaccine. For example, a large study found that the 2009 trivalent inactivated seasonal influenza vaccine administered
in New Zealand provided a moderate level of protection against the H1N1 strain that caused the 2009 pandemic, even though
that strain was not included in the 2009 vaccine.9
Approximately 80% of people who become infected with influenza are asymptomatic and can unknowingly risk infecting other
people who might be particularly vulnerable to influenza-related complications.3
Immunisation rates need to improve in healthcare workers
One of the primary goals of the influenza immunisation programme is to annually vaccinate at least 80% of healthcare
workers.3 The percentage of health care workers in New Zealand who received the influenza vaccination increased from
68% in 2018, to 73% in 2019.10 Employers of healthcare workers should actively promote staff influenza vaccinations and
healthcare workers should be proactive in getting vaccinated.
Annual vaccination decreases the rate of influenza complications in older people
People aged over 65 years who receive the annual influenza vaccination are less likely to be hospitalised or require
admission to an intensive care unit due to complications of influenza. 11
Influenza vaccination is estimated to reduce the risk of pneumonia by 23% for older people living in the community and
by 53% for frail older people living in residential care.11 The risk of major cardiovascular events in older people who
develop influenza is also reduced by 36% through annual influenza vaccinations.11
Pregnancy increases the risk of influenza complications
The benefits of influenza immunisation should be reinforced to all women who are pregnant or considering becoming pregnant.
Pregnant women who receive the influenza vaccine at any stage of pregnancy, and their babies, are significantly less likely
to develop influenza or its complications, for up to six months post-vaccination.12
Pregnant women who develop influenza are five times more likely to be hospitalised as non-pregnant women who contract
influenza, with the risk of hospitalisation increasing as gestation progresses.12 The risk of hospitalisation increases
if the pregnant woman has co-morbidities such as asthma, diabetes or cardiovascular disease.12
Further information about the 2020 seasonal influenza vaccination programme is available from The Immunisation Advisory Centre: