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H1N1 - Panvax
Swine Flu Vaccination
Vince Rettura
Delivering a Healthy WA

Page 2
24 September
2009
Slide 2
Final changes…….next 9 slides
provides an overview of the main
changes

Page 3
24 September
2009
Slide 3
What are the Changes………
Vaccination of Children
At present, Panvax H1N1 vaccine is not approved for
use in children under the age of 10 years.
Clinical trials in children have not yet been
completed but information from these trials should
be available towards the end of 2009
Health professionals will be notified when the
vaccine has been approved by the TGA for use in
children under the age of 10

Page 4
24 September
2009
Slide 4
Multi Dose Vial
Panvax H1N1 vaccine packed in blue boxes with blue
labels contains 18 doses per 10ml vial
Panvax H1N1 vaccine packed in red boxes with red
labels contains 10 doses per 5 ml vial
Each box of vaccine will contain stickers detailing
batch number and expiry. These stickers can be
affixed to consent forms an in paper patient records
– these are not compulsory to use
DOSAGE
The dosage for adults and children aged 10 years and over is
15ug in 0.5mls as a single dose.

Page 5
24 September
2009
Slide 5
Pre-filled syringes
Single-dose pre-filled glass syringes, complete with
needle for injection, are anticipated to become
available for use in young children once the TGA has
approved Panvax H1N1 for use in this age group.
Use with other vaccines
There are no data available to assess the
concomitant administration of Panvax H1N1 vaccine
with other vaccines
If Panvax H1N1 vaccine is to be given at the same
time as another injectable vaccine, the vaccines
should be given at different injection sites.

Page 6
24 September
2009
Slide 6
Administration
The vaccine should be administered by
intramuscular or deep subcutaneous injection
Clinical trials
Clinical data specific to Panvax® H1N1 Vaccine show that the
vaccine is safe and well tolerated in adults ≥ 18 to < 65 years of
age.
A total of 240 participants were administered a single dose of
vaccine containing 15 μg or 30 μg HA.
The most common solicited local (injection-site) adverse events
observed within 7 days of administration of the vaccine were
injection-site tenderness, pain and induration, with the majority
of reactions of mild intensity and self-limiting.

Page 7
24 September
2009
Slide 7
The most common solicited systemic adverse
reactions were headache, myalgia and malaise, with
the majority of these events mild to moderate in
intensity and similarly self-limiting
In addition, headache was identified as the most
common unsolicited adverse event, reported in 11.7
% of participants.
Other unsolicited adverse events, reported by more
than 2 % of participants, were back pain, arthralgia,
seasonal allergy, cough, oropharyngeal pain, nasal
congestion, diarrhoea and toothache.
There were no reports of serious adverse events.

Page 8
24 September
2009
Slide 8
GUILLAIN-BARRÉ SYNDROME
There have been reports of a possible association
with swine influenza vaccination and the
development of Guillain-Barré syndrome (GBS).
Whether this is causal or only a temporal association
is unclear.
Viral and bacterial infections, especially
Campylobacter jejuni and acute respiratory tract
infections are the commonest antecedents of GBS.
The estimated frequency of influenza-related GBS is
four to seven times higher than the estimated
frequency of influenza vaccine-associated GBS.
If there is a causal association with influenza
vaccine it is of the order of 1-2 per million people
vaccinated.

Page 9
24 September
2009
Slide 9
THIOMERSAL
Panvax® H1N1 vaccine has been formulated in multi-
dose vials containing the preservative, thiomersal.
Thiomersal, which contains a small amount of
mercury, has been used in medical products and
vaccines for more than 60 years and is the most
commonly used preservative in multi-dose vials. It
has a very long safety record.
Thiomersal was removed from vaccines given to
young children in Australia as a precaution to reduce
the theoretical risk of exposure to mercury in babies,
particularly those of very low birth weight.

Page 10
24 September
2009
Slide 10
However, there is no evidence that thiomersal
in vaccines has caused any developmental or
neurological abnormalities, such as Attention
Deficit Hyperactivity Disorder (ADHD), autism
or any other health problem.
Following a recent review of the evidence,
ATAGI has advised that influenza vaccines
containing thiomersal are considered safe.
Full details of ATAGI’s advice will be made
available on the
www.healthemergency.com.au website in the
near future.

Page 11
24 September
2009
Slide 11
It is now recommended to draw up the
vaccine from MDV with a 23g x 38mm needle
instead of a 19g needle
Vaccine drawn up and stored in syringes
Once vaccine has been drawn up from MDV and into
syringes, it must be used within 4 hours. After 4
hours syringes must be disposed of.
Drawing up needles

Page 12
24 September
2009
Slide 12
Goal
The goal of the pandemic vaccination
program is to provide protection to the
pandemic virus by vaccinating as many
people as quickly as possible, using an
approach which targets specific population
groups

Page 13
24 September
2009
Slide 13
Rationale
The underlying principles for targeting groups in Australia
include:
To prevent severe disease in those vulnerable to more
severe outcomes
To prevent spread of disease to the vulnerable by
vaccinating their contacts
To protect those at high risk of exposure because of their
work
To protect health care services and reduce healthcare
worker staff absenteeism
To mitigate potential economic impact on the Australian
pig industry
To provide herd immunity

Page 14
24 September
2009
Slide 14
Priority Tiers
First Tier
Pregnant women
Some women who have caught
H1N1 have miscarried or gone
into premature labour
Medically at risk- vulnerable
population
Health care workers
Indigenous
Second Tier (early 2010)
Children not covered by 1st tier
aged 6 months < 10years
School aged children

Page 15
24 September
2009
Slide 15
Age cut offs in Priority Tier One
Indigenous People - All people aged 10 years and
older will be included
Vulnerable (including medically at risk) - All people
aged 10 years and older will be included
There is no older age cut off proposed.

Page 16
24 September
2009
Slide 16
Defining of Health care workers
HCW: An employee, student or volunteer who has direct contact
with patients, either in the community or at a dedicated health
service sited, in both public and private sectors limited to the
following:
Aboriginal medical services
General practice
Ambulance services (includes RFDS)
Remote or community health clinics and nursing posts
Hospitals
Prisons
Satellite dialysis units
Post acute care services in the home (eg silver chain)

Page 17
24 September
2009
Slide 17
Community care workers: an employee,
student or volunteer who has direct contact
with patients, either in the community or at a
dedicated site, limited to the following:
Aged care
Disability services

Page 18
24 September
2009
Slide 18
Who gets the vaccine directly?
Metropolitan Public
Hospitals
Regional Hospitals
Private Hospitals and Day
Surgeries
St Johns Ambulance
Prisons
Community Health
Clinics
GP surgeries
Residential Aged Care
Facilities
Disability Service
Facilities
RFDS
Private satellite Dialysis
Units
Public Satellite Dialysis
Units
Aboriginal Medical
Services

Page 19
24 September
2009
Slide 19
Vaccine ordering and delivery is as per usual
ordering mechanisms for those recipients
listed under “who gets the vaccine directly”.

Page 20
24 September
2009
Slide 20
As this is a new strain of the influenza A virus,
most people do not have any natural immunity
so they are more likely to catch this new ‘flu
then they are to catch the seasonal flu.
This vaccine will prevent those with
underlying medical conditions from
developing severe illness
Why do people need to be
vaccinated

Page 21
Product Information
Information provided may change!
Refer to the first 9 slides for
Commonwealth changes

Page 22
24 September
2009
Slide 22
Which vaccine is to be used to treat
H1N1 Pandemic Influenza?

Page 23
24 September
2009
Slide 23
Panvax H1N1 monovalent
Vaccine - CSL
Panvax is a vaccine which
has been made to provide
immunity to the pandemic
2009 influenza strain of
the influenza A virus – a
new strain of the
influenza A virus

Page 24
24 September
2009
Slide 24
Product Description
Panvax is supplied as:
a clear liquid in
10ml Multi dose vials with a latex free rubber
stopper
Vaccine for children less than 10 years of age
will be provided in single dose pre-filled
syringes (thiomersal free) once approved by
the TGA
Boxes of 10 vials or may come to start with
boxes of 50 vials .

Page 25
24 September
2009
Slide 25

Page 26
24 September
2009
Slide 26
What’s in Panvax?
Vaccine
Specifications:

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24 September
2009
Slide 27
The basic vaccine formulation is as
follows:
Monovalent vaccine
15ug of antigen per 0.5mls
Unadjuvanted (Adjuvants are compounds used to
enhance the immune response to vaccination – The
use of adjuvanted vaccines on a large scale carries
the risk that previously unrecognised side effects will
occur. That the risk is increased if the adjuvant has
not been widely used in man or has not previously
been combined with influenza antigens)

Page 28
24 September
2009
Slide 28
10ml Multi Dose Vials (containing thiomersal
– compound partly composed of mercury and
ethylmercury.
- Used to prevent bacterial and fungal
contamination of vaccines

Page 29
24 September
2009
Slide 29
Causes a toxic effect after it reaches a
certain level in the body
Whether or not it reaches a toxic effect after it
reaches a certain level in the body depends on
- the amount of mercury consumed and
- the persons body weight.
Individuals with very low body weight are usually
more susceptible to toxic effects from a certain
intake of mercury. HENCE…….
Vaccine for children less than 10 years of age will be
provided in single dose pre-filled syringes
(thiomersal free) once approved by the TGA

Page 30
24 September
2009
Slide 30
According to the Commonwealth
There is no evidence that thiomersal has
caused any developmental or neurological
abnormalities, such as ADHD or Autism

Page 31
24 September
2009
Slide 31
Other components According to
Product Information– Each 0.5mls
contains
Sub units of A/California/7/2009 (H1N1) v-like
virus
15ug haemagglutinin
As stated – 0.01%w/v Thiomersal as a
preservative

Page 32
24 September
2009
Slide 32
Each 0.5mls also contains
Sodium Chloride 4.1mg
Sodium phosphate –dibasic anhydrous 0.3mg
Sodium phosphate- monobasic 80ug
Potassium chloride 20 ug
Potassium phosphate – monobasic 20 ug
Calcium chloride 1.5ug
Explanation of contents in Appendices in 9th ed
handbook under Vaccine Content

Page 33
24 September
2009
Slide 33
The following are present per dose:
Taurodeoxycholate ≤ 5ug (Bile salt-related, anionic
detergent) (can give red eyes, blurred vision etc)
Ovalbumin ≤ 1.0ug
Sucrose <10ug
Neomycin ≤ 0.7ug check for allergies to this antibiotic
Polymyxin B sulfate ≤0.11ngcheck for allergies to this antibiotic
Beta-propiolactone ≤1.4ng

Page 34
24 September
2009
Slide 34
Dosage and Administration

Page 35
24 September
2009
Slide 35
Take note……..
Previously -- The vaccination course
consists of 2 doses of 15ug of antigen
at least 21 days apart. … This now no
longer applies
The vaccination course consists of
1 dose of 15ug of antigen 0.5mls
for those aged 10 years of age and
older

Page 36
24 September
2009
Slide 36
Children aged 6 months to <9yearsof
age require 2 doses with a minimal
interval of 21 days. This will be
available once the TGA has approved
the vaccine for this age group

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24 September
2009
Slide 37
Name
Doses
Tier of
administration
1st dose
2nd dose
Minimum
interval
between
doses
Panvax 1 (One) IM
dose
(0.5ml/dose)
10 years and
older
Can now be given
by deep sub
cutaneous
injection
TIER 1
Pregnant
women
Medically at
risk (10 years
of age and
over)
Health care
workers
Indigenous
( 10 years of
age and over)
Pregnant
women in
their 2nd and
3rd trimester
Individuals
aged 10
years old and
over will be
able to
receive this
formulation
of 15ug of
antigen per
0.5ml
Nil for
those 10
years and
over
Can give in
1st
Trimester
That is for
eg. given
accidently
not
knowing if
client was
pregnant
Or if client
requests it.
Nil for
those 10
years and
over

Page 38
24 September
2009
Slide 38
Please Note -- CHANGES
All children under 10 years of age will have to
wait for the thiomersal free vaccine once
approved by the TGA

Page 39
24 September
2009
Slide 39
Use with other vaccines?
Panvax can be given with other vaccines
It is not a live vaccine so no special waiting
times when administering other vaccines
If Panvax H1N1 vaccine is to be given at the
same time as another injectable vaccine, the
vaccines should be given at different
injection sites.

Page 40
24 September
2009
Slide 40
How much is given?
1 (One) IM or deep
sub cut dose (0.5ml/dose)
10 years of age and over

Page 41
24 September
2009
Slide 41
Administration and instructions for
use and handling
Panvax is for IM or deep subcut injection
Vaccine that has been drawn into syringes in
preparation for administration must be used
within 4 hours
Punctured Multi Dose Vials can remain in the
fridge for up to 24hours since date of first
opening (may change)

Page 42
24 September
2009
Slide 42
Check and observe vial for clear fluid
The contents of the vial should be inspected visually
before and after shaking for any foreign particulate
matter and or abnormal physical appearance prior to
administration
Once drawn up into a syringe it is for single use only
ALSO - once drawn up into syringe – must be
discarded at the end of the day/clinic etc DO NOT
STORE DRAWN UP SYRINGES FOR NEXT CLINIC
DAYS AND DO NOT DRAW UP VACCINE FOR THE
WHOLE WEEK OR FOR NUMEROUS VACCINATION
CLINICS! It only has a life span of 4 hours in a
syringe

Page 43
24 September
2009
Slide 43
Preparing Panvax

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24 September
2009
Slide 44
Record the date and time of opening on
the MDV
DO NOT USE MDV if:
-sterility is breached
-cold chain is breached (outside 2-8°C)
-expiry date reached
-More than 24 hours since date of first
opening (may change again) and
contact_________________________
for advice on how to discard (see cold
chain section)
Wipe the diaphragm of the MDV
with an alcohol swap
If taking doses from an already
opened MDV, check opening date
and then wipe the diaphragm with
alcohol prior to use
ONE
TWO

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24 September
2009
Slide 45
Using an aseptic ‘no-touch’
technique, insert into the diaphragm a
new single use sterile drawing up
needle for the extraction of doses
Draw up each single dose required
into separate new sterile syringes
and attached a new sterile
administration needle
Each single dose vaccine must be
used (within 4 hours of drawing up
vaccine) and/discarded after 4
hours
THREE
FOUR

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24 September
2009
Slide 46
When the required number
of doses have been
extracted, remove the
drawing up needle and
dispose in appropriate
sharps container
If contents of the MDV are
not all used, refrigerate the
MDV (+2-8°C)
NB: Unused vaccine
should be discarded
through normal medical
waste mechanisms
FIVE
SIX

Page 47
24 September
2009
Slide 47
Gloves are not recommended for routine
immunisation service providers. However, in
a pandemic influenza environment, PPE -
mask, eyewear, gloves and gown may be
indicated for protection of the vaccine
administrator if need be.

Page 48
24 September
2009
Slide 48
Vaccine distribution
First delivery of vaccines – Contact the 9388
number on the order form if you require more
vaccines on your first order
50 pack of 10ml vials = 18-20 doses per vial
10 pack of 10ml vials = 18-20 doses per vial
End of September delivery changes
10 pack of 5ml vials = 10 doses per vial

Page 49
24 September
2009
Slide 49
Cold Chain
As per Strive for 5 Guidelines
Store at +2-+8oC
Refrigerate do not Freeze and protect from light
If the vaccine has been exposed to a cold chain breach, do not
discard but isolate vaccines, inform other staff and label them
“Do not use”. Keep the vaccines stored at +2-+8°C and contact
________________________ for advice
Cold chain breaches are to be reported through normal
channels of reporting. For eg. contacting the divisions of
general practice, Regional Immunisation Coordinators, the
Central Immunisation clinic etc in order to obtain advice.

Page 50
24 September
2009
Slide 50
If MDV is to be used throughout an immunisation clinic and left
on a work bench for easy access so you do not have to go into
the fridge repeatedly -
- ensure that the MDV is placed within a kidney dish, protected
from light and the kidney dish is placed on top of an ice block to
maintain the cold chain.
- drawn up vaccines can remain within the kidney dish whilst
vaccinating
NB: always check the coldness of the cold pack an the cold
pack must be ‘sweated’ first upon removal from the freezer.

Page 51
24 September
2009
Slide 51
Common Questions

Page 52
24 September
2009
Slide 52
If I had Human Swine flu do I need to
be vaccinated?

Page 53
24 September
2009
Slide 53
If you have been diagnosed with swine flu
confirmed by testing, then No vaccination is
required
If you have been told you had swine flu but
not confirmed testing then you can get
vaccinated

Page 54
24 September
2009
Slide 54
If someone was on Tamiflu can they
be vaccinated?

Page 55
24 September
2009
Slide 55
Yes
Tamiflu is an antiviral working on infections

Page 56
24 September
2009
Slide 56
How long after the vaccination am I
protected

Page 57
24 September
2009
Slide 57
On average it takes about 2-4 weeks to fully
develop protection against Human Swine Flu

Page 58
24 September
2009
Slide 58
How long am I protected??

Page 59
24 September
2009
Slide 59
1 year protection

Page 60
24 September
2009
Slide 60
Is the vaccine safe???

Page 61
24 September
2009
Slide 61
Clinical data specific to Panvax® H1N1 Vaccine show that the
vaccine is safe and well tolerated in adults ≥ 18 to < 65 years of
age.
A total of 240 participants were administered a single dose of
vaccine containing 15 μg or 30 μg HA.
The most common solicited local (injection-site) adverse events
observed within 7 days of administration of the vaccine were
injection-site tenderness, pain and induration, with the majority
of reactions of mild intensity and self-limiting.
The most common solicited systemic adverse reactions were
headache, myalgia and malaise, with the majority of these
events mild to moderate in intensity and similarly self-limiting

Page 62
24 September
2009
Slide 62
Can Thiomersal be given to pregnant
women?

Page 63
24 September
2009
Slide 63
YES
Thiomersal has a very long safety record and has not
been shown to have any long term problems
Influenza vaccines are safe during pregnancy and are
normally recommended for pregnant women. The
Panvax® H1N1 vaccine is not a ‘live’ vaccine and is
not a risk to unborn babies.
Expectant mothers may have some side effects from
vaccination but this is usually only a sore, red arm,
or slight headache.

Page 64
24 September
2009
Slide 64
Following a recent review of the evidence,
ATAGI has advised that influenza vaccines
containing thiomersal are considered safe.
Full details of ATAGI’s advice will be made
available on the
www.healthemergency.com.au website in the
near future.

Page 65
24 September
2009
Slide 65
If I had the seasonal flu do I need to
get this additional vaccine (even
during pregnancy?) ?

Page 66
24 September
2009
Slide 66
Yes
This new vaccine protects people against
pandemic influenza – Human Swine Flu.
The seasonal vaccine gives no protection
against this new strain

Page 67
Who should not get the
vaccine?
Children under the age of 10 cannot
be vaccinated with Panvax H1N1
vaccine as it is not approved for use
by the TGA

Page 68
24 September
2009
Slide 68
People with a known severe allergy to eggs
should not be given the vaccine ---
(anaphylactic hypersensitivity)
Characterised by
Generalised hives
Swelling of the mouth and throat
Difficulty in breathing, wheeze
Low BP and
Shock

Page 69
24 September
2009
Slide 69
And as usual:
- Anaphylaxis following a previous dose of the
relevant vaccine, and
- Anaphylaxis following any component of the relevant
vaccine
Also check allergies to:
- Neomycin
- Polymyxin B
- Especially if the client has had an anaphylactic
hypersensitivity to the above anti biotics

Page 70
24 September
2009
Slide 70
Be aware of false contraindications
to vaccinations
Conditions listed in Table 1.3.4 page 21 in the
Immunisation hand book outlines false
contraindications.
People with these conditions should be
vaccinated with all recommended vaccines

Page 71
24 September
2009
Slide 71
Corticosteroids – just take note...
Clients on daily doses of corticosteroids (Adults in excess of
60mgof prednisilone; Children in excess of either 2mg/kg per
day for more than a week or 1mg/kg daily for 4 weeks) will
greatly suppress the immune system
which means that not only is the vaccine unlikely to be
effective, but there is an increased chance of adverse events
occurring as a result of immunosuppression
just like any vaccine you can still vaccinate however the
protection offered will be greatly reduced…….
- Partial protection is better than no protection. If the client
was to catch swine flu and was vaccinated --- the
symptoms may not be as severe

Page 72
24 September
2009
Slide 72
What about other medication??

Page 73
24 September
2009
Slide 73
Some medications may interfere with
influenza vaccines as discussed.
Others include:
- Some treatments for cancer (including
radiation therapy)
- Cyclosporine- immunosuppressant drug

Page 74
24 September
2009
Slide 74
What are the side effects from the
vaccine?

Page 75
24 September
2009
Slide 75
- Pain and redness at the injection site
- Drowsiness or tiredness
- Muscle aches
- Low grade fever
- Malaise
- Headache
Common side effects include:

Page 76
24 September
2009
Slide 76
Very rare side effects
Severe allergic reaction (anaphylaxis)
Guillian-Barre Syndrome (nervous system
disorder featuring paralysis)

Page 77
24 September
2009
Slide 77
History of Guillian-Barre Syndrome
(GBS)
Risks and benefits of the influenza and H1N1
pandemic influenza vaccine should be
weighed against the potential risk of GBS
recurrence
Specialist advice advised
NB People with a history of GBS may be at
risk of recurrence of the condition following
influenza vaccine

Page 78
24 September
2009
Slide 78
Will I get GBS from this vaccine?
From the evidence collected by experts:
GBS is 4 to 7 times more likely after an attack
of the actual flu than after the influenza
vaccine
There have been reports overseas of a
possible association between influenza
vaccinations and GBS

Page 79
24 September
2009
Slide 79
Hasn’t the pandemic flu peaked –
isn’t it too late for me to benefit from
the vaccine??

Page 80
24 September
2009
Slide 80
We don’t know that the pandemic has peaked
Its never too late to gain immunity
Experience from countries in the northern
hemisphere this year has also shown that
pandemic influenza can continue to spread in
the summer months
Vaccination will protect you through summer
and into the flu season next year

Page 81
24 September
2009
Slide 81
What adverse events should be
reported?

Page 82
24 September
2009
Slide 82
Any adverse event that the immunisation
service provider considers to be serious or
unexpected should be reported. Serious
adverse events are listed in Appendix 6 of the
Australian Immunisation Handbook 9th
Edition
http://www.health.gov.au/internet/immunise/p
ublishing.nsf/Content/handbook-appendix6

Page 83
24 September
2009
Slide 83
Can patients report adverse events?

Page 84
24 September
2009
Slide 84
Yes
Patients wanting to report an adverse event
can do so by submitting a report online
directly to the Therapeutic Goods
Administration at www.tga.gov.au, or by
calling the Pandemic Hotline on 180 2007.

Page 85
24 September
2009
Slide 85
Pandemic (H1N1) 2009 Influenza
Vaccination Packs

Page 86
24 September
2009
Slide 86
This Pandemic (H1N1) 2009 VacPac (VacPac)
contains equipment sufficient for the
administration of 200 doses of pandemic
H1N1 2009 influenza vaccine (vaccine).
A mini VacPac is only available for GP
surgeries and only includes syringes and
needles only
The components of each VacPac are listed
below:

Page 87
24 September
2009
Slide 87
Item
Quantity/Packaging
1mL syringes
1 box x 220 syringes
Drawing up needles 19g x 38mm
1 box x 44 needles
Injection needles 23g x 25mm
1 box x 200 needles
Injection needles 23g x 38mm
1 box x 40 needles
Alcohol Swabs
1 box x 220 swabs
Sharps containers
3 individual sharps containers
Disposable dishes
6 individual dishes
Disposable Gloves
1 box x 110 gloves
Clinical waste bags and closure
devices
2 individual bags and closures
Sticking Plaster
1 box x 110 plasters
Alcohol Hand Rub
2 x 500mL bottles with
dispensers
Cotton Wool Balls
1 bag x 220 cotton wool balls

Page 88
24 September
2009
Slide 88
Item
Quantity/Packaging
1mL syringes
1 box x 220 syringes
Drawing up needles 19g x 38mm
2 boxes x 44 needles
Injection needles 23g x 25mm
1 box x 200 needles
Drawing up needles 23g x 38mm
3 boxes x 40 needles
GP mini VacPac

Page 89
24 September
2009
Slide 89
Some additional quantities of each
component are provided to cover normal
levels of wastage that may occur in a mass
vaccination situation.
The 19g x 38mm needles have been included
for drawing up along with the 23g x 38mm.
23g x 25mm needles can be used for
administering the vaccine to the majority of
the population.
A quantity of 23g x 38mm needles has also
been provided for use with obese adults.

Page 90
AND FINALLY
Consent

Page 91
24 September
2009
Slide 91
Child and Adult consent form
Containing the following:
- Fact sheet on the vaccine and what pandemic
influenza 2009 is
- Effects of the disease, possible side effects of
vaccination, contraindications and what to do to
reduce side effects
- Care after vaccination
- Pre vaccination checklist
- Client record following vaccination

Page 92
24 September
2009
Slide 92
Documenting consent and reporting data
Consent:
All DoHWA health services should use the national
PANDEMIC (H1N1) 2009 INFLUENZA VACCINE
CONSENT FORM developed by DoHA. These will be
supplied or you may photocopy, or download from
website.
GPs, ACCHOs, residential care facilities and other
non-government health services should obtain and
document informed consent for vaccination using
their usual procedure.

Page 93
24 September
2009
Slide 93
Data reporting:
GPs, ACCHOs, residential care
facilities (metropolitan and regional) complete
the Pandemic Influenza Line List Form and fax
at end of each week to 9388 4820.
Metropolitan mass vaccination clinics. A
CDCD staff member will visit your clinic daily
to collect original consent forms.

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2009
Slide 94
Metropolitan hospitals, workplace and other DoHWA
health services. Photocopy completed consent forms
and send the photocopied version with batch header
at end of each week via medical record courier
Panvax data entry, CDCD, 227 Stubbs Tce, Shenton
Park WA 2008 OR registered mail to Panvax data
entry, CDCD, PO Box 8172 Perth Business Centre
WA 6849.
Regional DoHWA providers. Enter Panvax
vaccination date, batch number and reason for
vaccination on to HCARe and ensure that the patient
is registered on HCARe, as patient-identified data will
be downloaded periodically from HCARe and
uploaded into the statewide Panvax database.

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2009
Slide 95
A call centre will be organised which will act as a
help line to check to see if people have been
vaccinated i.e. which doses they have had. This
number is for health staff only!
1800 243 522
180 2007 – is for the general public

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2009
Slide 96
Quick Consent – just a thought!
It may be best to get clients together and do a group
consent prior to vaccination.
I.E. 1 nurse to go through consent
- 1 admin to check to see it is filled and direct
any errors back to consent nurse (optional)
- then clients can see the vaccinator
That way the vaccinator does not have to go through
the consent

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2009
Slide 97
Trivalent vaccine
To be included in the seasonal influenza
vaccine
?? Next year

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2009
Slide 98
You will receive with each vaccine
order:
Your vaccine
Vacpacks
Consent forms
ADRAC (adverse events form)