2016/2017 Influenza Immunization Orientation PowerPoint ...
Transcript of 2016/2017 Influenza Immunization Orientation PowerPoint ...
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Introduction
This PowerPoint is a tool for health care professionals to use as a self-learning tool in
conjunction with annual influenza immunization orientation.
There is no requirement by the Province-wide Immunization Program, Alberta Health
Services (AHS) to formally submit proof of completion to AHS. However, use may differ
locally and therefore staff should follow instructions given at a local level for formal
submission of the self-test.
For more detailed information it is important for staff to refer to other program resources
such as:
•Vaccine Product Monographs and/or AHS Vaccine Biological pages
•AHS Vaccine Storage and Handling e-learning modules and Standard
•Guidelines for the reporting of adverse events following immunization
•Reporting requirements and data collection guidelines
•Alberta Influenza Immunization Program Policies.
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Section One – Influenza Disease Learning Objectives
Learning Objectives:
The influenza immunizer will be able to:
• recognize the symptoms of influenza
• describe self-care and prevention strategies for
influenza.
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What is influenza?
Influenza, commonly known as “the flu”, is a highly contagious
infection of the airways caused by influenza viruses. It is often referred
to as “seasonal” influenza because these viruses circulate annually in
the winter season in the northern hemisphere.
The timing and duration of influenza season varies - outbreaks can
happen as early as October but most often activity peaks in January or
later. Late season outbreaks occurring in April and even May have
also been reported.
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A, B and C influenza viruses
• Influenza A and B viruses cause seasonal epidemics, while type C
viruses cause mild respiratory illness
• Influenza A viruses are classified into different strains or subtypes
based on two proteins or antigens on the virus surface:
hemagglutinin (H) and neuraminidase (N)
– e.g., H1N1 and H3N2
• Influenza B viruses can be classified into two antigenically distinct
lineages, Yamagata and Victoria like viruses
• Influenza A and B strains are included in
each year's influenza vaccine
• The vaccine does not protect against
influenza C viruses
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Influenza Types – A and B
Type A
(Seasonal, Avian, Swine influenza)
Type B
(Seasonal influenza)
Can cause significant diseaseGenerally causes milder disease
but may also cause severe disease
Infects humans and other species (e.g.
birds; H5N1)Limited to humans
Can cause epidemics and pandemics
(worldwide epidemics)Generally causes milder epidemics
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How strains change each year
• Small changes in influenza viruses occur continually
– New virus strains may not be recognized by the body's immune system
• A person infected with a specific influenza virus strain develops antibodies against that specific strain
• In most years, some or all of the virus strains in the influenza vaccine are updated to align with the changes in the circulating influenza viruses
• Annual influenza immunization is recommended to protect against infection from these changing influenza viruses
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Signs and symptoms of influenza
• Sudden onset
• Typically starts with a headache, chills and cough, followed rapidly
by fever, loss of appetite, muscle aches and fatigue, runny nose,
sneezing, watery eyes and throat irritation
• Nausea, vomiting and diarrhea may also occur,
especially in children
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Influenza, the Common Cold and Gastrointestinal
InfectionType of infection Respiratory infection Gastrointestinal infection
Description / symptoms Influenza Common cold Stomach upset*
Virus involved Influenza A or B Many different kinds of viruses such as
rhinovirus, coronavirus, adenovirus, etc.
Norovirus (Norwalk-like viruses) is the
most common.
Fever Usually high, beginning suddenly and
lasting 3–4 days.
Sometimes Rarely
Headache Usually, can be severe. Rarely Sometimes
Chills, aches, pain Usually, and often severe. Rarely Common
Loss of appetite Sometimes. Sometimes Frequently – usually nausea, vomiting
and diarrhea occur as well.
Cough Usually Sometimes Rarely
Sore throat Sometimes Sometimes Rarely
Sniffles or sneezes Sometimes Usually Rarely
Extreme tiredness Usually – tiredness may last 2–3 weeks
or more.
Rarely Sometimes
Involves whole body Usually Never Stomach and bowel only.
Symptoms appear quickly Yes More gradual Yes
Possible Complications
(Health problems)
Pneumonia, kidney failure, swelling of the
brain and death.
Sinus infection or ear infection. Dehydration (losing more fluid than you
take in).
Vaccine Yearly vaccine provides protection
against two influenza A strains and one
influenza B strain in the TIV and two B
strains in the QIV.
No vaccine available. No vaccine available.
Alberta Health http://www.health.alberta.ca/health-info/influenza-compare-symptoms.html
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The myth of the “stomach flu”
• Many people use the term "stomach flu" to describe illnesses with
nausea, vomiting, or diarrhea. These symptoms can be caused by
many different viruses, bacteria, or even parasites
• While vomiting, diarrhea, and nausea can sometimes occur when
people have influenza (particularly children), these problems are
not the main symptoms of influenza
• Influenza is a respiratory disease - not a stomach or intestinal
disease
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How serious is influenza?
• While the majority of those who become ill will recover, it is estimated that influenza causes about 12,200 hospitalizations and 3,500 deaths in Canada each year
• Some individuals are at higher risk of developing complications from influenza, including:
– Seniors
– Infants and young children
– Adults and children with existing chronic health conditions
– Healthy pregnant women
– Indigenous peoples
– Obese persons
Complications can include pneumonia (bacterial and viral), ear and sinus
infections, dehydration, and worsening of chronic medical conditions, such as
congestive heart failure, asthma, or diabetes.
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How serious is influenza?
The Centers for Disease Control and Prevention (US) conducted a
study to assess the effectiveness of influenza vaccine in decreasing
influenza related deaths in children (6 months to 17 years of age)
• Between July 2010 and June 2014, 358 children died from infection
with influenza; researchers were able to confirm the vaccine status
of 291 of these children:
– Of the 291 children 74% were unimmunized
– The study concluded that influenza vaccination was associated
with reduced risk of laboratory-confirmed influenza-associated
pediatric death
– Increasing influenza vaccination could prevent influenza-
associated deaths among children and adolescentsFlannery B, Reynolds SB, Blanton L, et. al. Influenza Vaccine Effectiveness Against Pediatric Deaths. Pediatrics. 2017. DOI:
10.1542/peds.2016-4244).
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How is influenza spread?
• The virus is spread mainly from person to person when those with
influenza cough or sneeze (droplet spread)
– The droplets are propelled about 3 feet through the air
• People may also become infected by touching an object or a
surface that has the influenza virus on it and then touching their
mouth, eyes or nose
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Influenza incubation
• Individuals with influenza are infectious 1 day before symptoms
develop and up to 5 days after becoming ill
– The period when an infected person is contagious depends on
the age and health of the person
– Young children and people with weakened immune systems
may be contagious for longer than a week
• The time period from exposure to development of symptoms is
about 1 to 4 days, with an average of about 2 days
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Influenza infectivity
• People infected with influenza can spread the disease to others
before they know they are ill, and while they are ill
• Some people can be infected but have no symptoms
– These individuals can still spread the virus to others
• This is important information for those caring for others, such as
parents and all health care workers
• In one published study, 59% of health care workers tested had
evidence of recent influenza infection but could not recall having
symptoms
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Health Care Workers
• Health care workers (HCWs) who have direct patient contact
should consider it their responsibility to provide the highest
standard of care, which includes annual influenza immunization
• In the absence of contraindications, refusal of HCWs who have
direct patient contact to be immunized against influenza implies
failure in their duty of care to patients
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Treatment of influenza
Treatment recommendations for
non-complicated cases include:
• rest
• analgesics
• fluids
• time
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Self care during influenza season
• Get the influenza vaccine every fall.
• Cover your cough with a tissue, or cough or sneeze
into your upper sleeve, not your hands. Then, clean
your hands, and do so every time you cough or sneeze.
• Wash your hands well, and often.
• Avoid touching your eyes, nose, or mouth. Germs are
often spread when a person touches something that is
contaminated with germs and then touches their eyes,
nose, or mouth.
• Exercise. Drink plenty of water. Eat well and do not
smoke.
• Avoid crowds when influenza season hits your area.
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Influenza prevention hand washing
√ Use regular soap – antibacterial soap is not necessary.
√ Rub hands vigorously for at least 15 seconds covering all surfaces (Sing Happy Birthday !!).
√ Rinse your hands under running water.
√ Dry hands with clean or disposable towel.
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Self care at work
• Frequently wipe down your keyboard, mouse and phone (for
example with low level disinfectants not with antibacterial wipes).
• If you are ill, stay home from work so you do not spread illness to
others. Children who are ill should stay home from school and
daycare.
• Use hand hygiene frequently, especially after using copy
machines, fax machines, someone else’s computer or phone, or
after sneezing or other contact with your own secretions.
• Wash your hands before eating or drinking during
breaks.
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Review Questions Section 1
1. During which time period are individuals who have been infected
with influenza contagious?
2. Which individuals are at highest risk of developing complications
from influenza?
Note: Answers can be found at the end of the PowerPoint.
Section One - Influenza Disease Knowledge Check
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Section Two – Influenza Vaccine Learning Objectives
Learning Objectives:
The influenza immunizer will be able to:
• describe the influenza immunization program within Alberta
• identify the target client population for this program
• administer influenza vaccine in accordance with local protocols.
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Influenza vaccine development
• Each February, the World Health Organization (WHO) provides a
recommendation on the strains to be included in the influenza
vaccine for the northern hemisphere
• Two influenza "A" viruses and one (trivalent vaccine) or two
(quadrivalent vaccine) influenza "B" virus are selected based on the
characteristics of the current circulating influenza virus strains
• A new vaccine is reformulated each year to protect against new
influenza infections
• Each vaccine lot is tested on healthy individuals to ensure the
vaccine is safe and effective
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Influenza vaccine development (cont’d)
• There are currently seven trivalent inactivated influenza vaccines
(TIV) licensed for use in Canada; one of these is adjuvanted
• There are currently three quadrivalent influenza vaccines licensed
for use in Canada
– Two are quadrivalent inactivated influenza vaccine (QIV)
– One is a live attenuated influenza vaccine (QLAIV)
• For the 2017-2018 influenza immunization program, Alberta will be
using one QIV product and one TIV product. The TIV product will
be used for administration to adults 65 years of age and older living
in Long Term Care or Supportive Living sites only.
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How does inactivated influenza vaccine work?
• Both humoral and cell-mediated responses play a role in immunity
• Administration of inactivated influenza vaccine results in the
production of circulating IgG antibodies to the viral haemagglutinin
as well as a cytotoxic T lymphocyte response
• Humoral antibody levels, which correlate with vaccine protection,
are generally achieved 2 weeks after immunization and immunity
usually lasts less than 1 year
– Initial antibody response may be lower in the elderly with non-
adjuvanted TIV and the immune-compromised
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Effectiveness of influenza vaccine
• Vaccine effectiveness depends on the similarity between vaccine strains and
the strains in circulation during influenza season, as well as individual
factors.
– Influenza immunization prevents disease in 45-85% of healthy individuals
– In the elderly vaccine effectiveness is about half of that of healthy adults;
however influenza immunization decreases the incidence of pneumonia,
hospital admission and death in the elderly, and reduces exacerbations
in persons with chronic obstructive pulmonary disease
• Vaccine efficacy of 50% or lower in healthy adults has been identified during
select seasons of vaccine mismatch. A vaccine that is not perfectly matched
can still offer protection against related viruses making illness milder and
preventing complications.
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Vaccine strains for 2017-2018
The strains that will be included in the 2017-2018 influenza vaccine
for the Northern hemisphere are:
• A/Michigan/45/2015(H1N1)pdm09-like virus
• A/Hong Kong/4801/2014 (H3N2)-like virus
• B/Brisbane/60/2008-like virus
• B/Phuket/3073/2013-like virus (QIV only)
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Facts about inactivated influenza vaccine (TIV/QIV)
• Is an inactivated (killed) vaccine – cannot cause influenza disease in
the vaccine recipient
• The virus is grown in hens’ eggs, inactivated, broken apart and
highly purified
• In addition to the antigen, the vaccine may contain:
- Thimerosal (preservative in multi-dose vials)
- Trace residual amounts of egg proteins, formaldehyde, kanamycin,
neomycin, gentamicin, cetyltrimethylammonium bromide (CTAB),
polysorbate 80, sodium deoxycholate and sucrose
• Check the product monograph as ingredients vary with specific
inactivated influenza vaccines
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Section Two – Influenza Vaccine Knowledge Check
Review Questions Section 2: Part A
1. Which strains of influenza virus are included in the 2017-2018
influenza vaccine for the northern hemisphere?
a) Why are these strains chosen?
2. Why is it necessary to get an influenza immunization each year to
be protected?
3. Can you get influenza disease from the influenza vaccine? Explain.
Note: Answers can be found at the end of the PowerPoint.
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Universal Influenza Immunization Program
Alberta Health (AH) funds a Universal
Influenza Immunization Program.
• All people 6 months of age and older
who live, work or go to school in Alberta
are eligible for vaccine at no charge
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Influenza Immunization Program in Alberta
Alberta Health Services (AHS) coordinates the delivery and administration of
the Universal Influenza Immunization Program. The program will begin with a
public launch October 23, 2017.
• Vaccine may be offered earlier for certain high risk populations (e.g., continuing
care residents, lodge residents, homebound clients, homeless individuals, HCWs,
children 6-59 months in routine immunization clinic) once vaccine is available
• As in previous years, immunization partners (e.g. physicians, pharmacists, private
health agencies, occupational health services) will play an essential role in
achieving the AH immunization targets:
- Seniors aged 65 years and older – 80%
- Children aged 6 months to 23 months – 80%
- Residents of long-term care facilities – 95%
- Staff of long-term care facilities – 95%
- Health Practitioner (HCW) – 80%
- Immunizers – 100%
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Provincially funded influenza vaccines for 2017/2018
Fluzone® (QIV)
(Sanofi Pasteur)Fluad® (TIV – MF59 adjuvanted)
(Seqirus)
Dosage/Route 0.5 mL 0.5 mL IM
Packaging Single Dose: Pre-filled, single dose
syringe (luer lock needles not included)
Multi-dose: 5 mL vial
Pre-filled, single dose syringe
(luer lock needles not included)
Eligibility Individuals who live, work or go to school
in AlbertaIndividuals who live in congregate living facilities,
provided in AHS outreach program and to LTC facilities
Indication 6 months1 and older; pregnant women 65 years of age and older
Ingredients2 Thimerosal-free (single dose formulation
only), formaldehyde, sodium phosphate
buffered isotonic sodium chloride
solution, Triton® X-100
Thimerosal-free, trace amounts of egg proteins,
formaldehyde, kanamycin, neomycin,
cetyltrimethylammonium bromide (CTAB), MF59
adjuvant (squalene, polysorbate 80, sorbitan trioleate,
sodium citrate, citric acid)
Schedule 1 or 2 doses3 1 dose
1Children must be 6 calendar months of age; do not compress this age by using 28 day months2Refer to vaccine product monograph for a complete listing of the ingredients
3Children less than 9 years of age require 2 doses given at a minimum of 4 weeks apart if they have never received seasonal influenza vaccine. This recommendation
applies whether or not the child received monovalent pH1N1 vaccine in 2009-2010.
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Influenza vaccine dosing for specific ages
6 months up to & including 8 years of age
• 2 doses* if never previously immunized with seasonal influenza vaccine (spaced 4 weeks apart – minimum interval)
• 1 dose only if previously immunized with seasonal influenza vaccine
9 years of age and older
• 1 dose
* This recommendation applies whether or not the child received monovalent pH1N1 vaccine in 2009-2010.
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Return visit for children who need a second dose
• Indicate date to return for second dose of vaccine on the NCR form
and provide a copy of the form to the client
• See local protocol for indicating location for second dose of vaccine
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Thimerosal
• Multi-dose vials of vaccine contain a preservative called thimerosal (ethylmercury)
• Ethylmercury is not the same compound as methylmercury
– Methylmercury is a known neurotoxin in high concentrations or with prolonged exposure (e.g., ingesting some types of fish)
• Ethylmercury is eliminated much more quickly and is less likely to reach toxic levels in the blood than methylmercury
• Studies have found there is no association between immunization with thimerosal-containing vaccines and neurodevelopmental outcomes, including autistic-spectrum disorders
• Additional information regarding thimerosal is available at http://www.phac-aspc.gc.ca/publicat/ccdr-rmtc/07vol33/acs-06/index-eng.php
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Pregnancy and breastfeeding
“NACI recommends the inclusion of all pregnant women,
at any stage of pregnancy, among high priority recipients
of influenza vaccine due to:
• the risk of influenza associated morbidity in pregnant
women
• evidence of adverse neonatal outcomes associated
with maternal respiratory hospitalization or influenza
during pregnancy
• evidence that vaccination of pregnant women
protects their newborns from influenza and influenza-
related hospitalization, and
• evidence that infants born during influenza season to
vaccinated women are less likely to be premature, small
for gestational age, and low birth weight.”
NACI Statement 2017
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Pregnancy and breastfeeding (cont’d)
• QIV is safe for pregnant women at all
stages of pregnancy
• QIV is safe for breastfeeding mothers
*Fluad® is not recommended for use in
pregnant or breastfeeding women
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Reactions to inactivated influenza vaccine
Common Reactions
• Injection site redness, swelling, pain
• Fatigue, headache, myalgia
• Arthralgia, fever, chills, malaise
The majority of people do not have a reaction to TIV/QIV; however some reactions that may occur are outlined below. These reactions generally start 6 to 12 hours after immunization and can last for 1 to 2 days.
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Reactions to TIV/QIV
Rare Reactions
• Immediate, allergic-type responses such as hives, angioedema,
allergic asthma, systemic anaphylaxis
• Guillain-Barré Syndrome (GBS)
• Oculorespiratory Syndrome (ORS)
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Guillain-Barré Syndrome (GBS)
• GBS is an illness that affects the nervous system
– It is rare; general risk is about 2 cases per 100,000 person years
– It is characterized by loss of reflexes and symmetric paralysis
usually beginning in the legs
– It results in complete or near complete recovery in most cases
• It is thought that GBS may be triggered by an infection
– The infection that most commonly precedes GBS is caused by
Campylobacter jejuni bacteria
– Other respiratory or intestinal illnesses and other triggers may
also precede an episode of GBS, including Cytomegalovirus,
Epstein-Barr virus and Mycoplasma pneumoniae
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Guillain-Barré Syndrome (GBS) (cont’d)
• In 1976, the “swine flu” vaccine was associated with an increased
risk of GBS – this has not been found with influenza vaccines
administered after the swine influenza vaccine program according
to the US Institute of Medicine
• Absolute risk of GBS after vaccination is about 1 excess case per 1
million vaccinees above background rate of 10 - 20 cases/million
• Risk of GBS associated with influenza infection is much greater
than that associated with immunization
It is recommended that you DO NOT provide influenza
immunization to people who have been diagnosed with GBS
within 6 weeks of previous influenza immunization.
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Oculorespiratory Syndrome (ORS)
In 2000-2001, Health Canada received increased reports of
unusual symptoms following influenza immunization. These
symptoms were subsequently described as Oculorespiratory
Syndrome (ORS).
Case definition of ORS (onset within 24 hours of immunization)
• bilateral red eyes
and
• one or more of the following respiratory symptoms (cough, wheeze, chest tightness, difficulty breathing, difficulty swallowing, hoarseness, sore throat) with or without facial swelling
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Oculorespiratory Syndrome (ORS) (cont’d)
Immunization recommendations following client report of ORS are based on:
• risk/benefit assessment,
and
• severity of symptoms as perceived by the individual who experienced the symptoms
For immunization recommendations following client report of
ORS:
Refer to Decision Making Algorithm: Influenza Vaccine for
Persons with Previous ORS Symptoms
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ORS Decision Flowchart
How severe were the ORS symptoms?
Mild (easily tolerated, present but not problematic)
Moderate (bothersome, interferes with activities of daily living, requires activity change & possible medication)
Severe (prevents activities of daily living, unable to work or sleep)
May receive the influenza vaccine
May receive the influenza vaccine
Lower respiratory symptoms (wheeze, chest tightness, difficulty breathing) and/or difficulty swallowing (within 24 hrs of immunization)
May receive the influenza vaccine Case should be reviewed by
MOH before receiving subsequent influenza vaccine
Non-lower respiratory symptoms (bilateral red eyes, cough, hoarseness, sore throat, facial swelling)
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Reporting of adverse events following immunization (AEFI)
An adverse event following immunization is defined as a serious or unexpected event
temporarily associated with immunization.
The most commonly reported AEFIs in the 2016-2017 influenza immunization season
were allergic reaction (not anaphylaxis), pain/swelling, rash and severe diarrhea and/or
vomiting.
Local reactions are the most commonly reported event following immunization. A local
reaction of pain and/or swelling is ONLY reportable if:
1.the onset of swelling is within 48 hours following immunization;
AND
2.swelling extends past the nearest joint
OR
severe pain that interferes with the normal use of the limb lasting greater than 4 days
OR
reaction requires hospitalization
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AEFI reporting (cont’d)
Any of the following are also reportable adverse events:
• GBS
• ORS
• Anaphylaxis
• Other allergic reactions
• Any reaction outside of what is expected
• Consult with AHS local Public Health as soon as possible for any case
where there is uncertainty as to whether a symptom following
immunization is related to the immunization.
Report AEFIs or unusual incidents that may occur as per local protocols.
Severe reactions should be reported within 24 hours and all other reactions
within one week to your zone contact. “Reportable AEFIs” are reported to
Alberta Health, and in turn to the National Surveillance Program.
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Contraindications to TIV/QIV
TIV/QIV should not be administered to individuals who:
• Are less than 6 calendar months of age
– Fluad® should not be administered to persons under 65 years of age
• Have had an anaphylactic reaction to a previous dose of influenza vaccine
• Have a known hypersensitivity to any component of the vaccine with the exception of egg
• Have been diagnosed with Guillain-Barré Syndrome within 6 weeks of a
previous dose of influenza vaccine
• Have experienced severe Oculorespiratory Syndrome (ORS) within 24 hrs
of receiving influenza immunization – these individuals should be
assessed further prior to immunizing
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Egg-allergic individuals
• Egg allergy is no longer considered a contraindication for influenza
vaccine (TIV/QIV)
• Egg-allergic individuals may be immunized using TIV/QIV without a
prior influenza vaccine skin test and with the full dose of vaccine,
irrespective of a past severe reaction to egg
• Egg-allergic vaccine recipients should be kept under observation
for 30 minutes following the administration of inactivated influenza
vaccine
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Vaccine deferral
Vaccine may be deferred until later in the following situations:
• Those with serious acute febrile illness usually should not be
immunized until symptoms have abated
Vaccine does not require deferral and can safely be given to the
following individuals:
• Those with mild acute illness, with or without fever
• Individuals who are recovering from illness or are taking antibiotics
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Section Two – Influenza Vaccine Knowledge Check
Review Questions Section 2: Part B
1. In Alberta this year, who is eligible for the influenza vaccine at no
charge?
2. Is thimerosal in vaccines a threat to health? Explain.
3. Who should not be immunized with influenza vaccine?
4. What is the recommendation for people who have been diagnosed
with Guillain-Barré syndrome within 6 weeks of a previous influenza
immunization?
5. What is the recommendation for clients who have experienced a
mild case of ORS in the past?
Note: Answers can be found at the end of the PowerPoint.
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Section 3: Pneumococcal Immunization Learning Objectives
The immunizer will be able to:
• describe the pneumococcal immunization program within Alberta
• administer pneumococcal polysaccharide vaccine in accordance
with local protocols.
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What is pneumococcal polysaccharide vaccine?
• Pneumococcal vaccines are used to prevent serious illnesses caused by the Streptococcus pneumoniae bacteria
– the vaccine protects against 23 serotypes of this bacteria
• The vaccine is sometimes referred to as the “pneumonia shot”
• The immunization program was implemented nationally in 1998
• The vaccine is provided throughout the year by Public Health or community physician partners, but also in conjunction with the Influenza Immunization Program due to ease of access to target population
• Pneumococcal polysaccharide vaccine is available for eligible people age 24 months and older
• Onset of immunity is about 10 to 15 days after immunization
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Why is pneumococcal polysaccharide vaccine important?
• This vaccine can prevent serious infections, such as bacteremia
and meningitis caused by the Streptococcus pneumoniae bacteria
• Certain populations are more at risk of serious illness caused by
this bacteria, so the vaccine is offered to them to provide protection
• This bacteria is becoming resistant to some of the antibiotics used
to treat it
• Vaccine effectiveness is dependent on the age and immune
competency of the vaccine recipient
– The immunity conferred is serotype specific
– The vaccine is 56% - 81% effective in preventing invasive
pneumococcal disease
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Pneumococcal polysaccharide vaccine eligibility
I. Routine Recommended Immunization
Individuals 65 years of age and older
II. Medically at Risk
Individuals 24 months up to and including 64 years of age with the following:
– Alcoholism; includes individuals with any history of alcohol abuse
– Anatomic or functional asplenia, splenic dysfunction
– Chronic heart disease; includes congestive heart failure, myocardial
infarction and individuals taking heart medications or being followed by a
cardiac specialist
– Chronic cerebrospinal fluid (CSF) leak
– Chronic kidney disease; includes nephrotic syndrome and renal dialysis
– Chronic liver disease; includes chronic hepatitis B, hepatitis C and cirrhosis
due to any cause
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Pneumococcal polysaccharide vaccine eligibility (cont’d)
– Chronic lung disease (including asthma requiring medical treatment within
the last 12 months regardless of whether they are on high dose steroids)
– Chronic neurologic conditions that may impair clearing of oral secretions
– Cochlear implant (candidates and recipients)
– Congenital immune deficiencies involving any part of the immune system,
including B-lymphocyte (humoral) immunity; T-lymphocyte (cell) mediated
immunity; complement system (properdin or factor D deficiencies); or
phagocytic functions.
– Diabetes mellitus; includes both insulin and non insulin dependent
(controlled by oral medication or diet)
– HIV infection
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Pneumococcal polysaccharide vaccine eligibility (cont’d)
– Illicit injection drug use
– Immunosuppressive therapy including use of long term corticosteroids,
monoclonal antibodies (e.g., eculizumab [Soliris®]),chemotherapy, radiation
therapy, post-organ transplant therapy and certain anti-rheumatic drugs
– Malignant neoplasms including leukemia, Hodgkin’s and non-Hodgkin’s
lymphomas, multiple myeloma and other malignancies
– Sickle cell disease and other hemoglobinopathies
• Solid Organ Transplant (SOT) candidates and recipients and Hematopoietic
stem cell (HSCT) recipients 24 months of age and older – See Standard for
Immunization of Transplant Candidates and Recipients #08.304
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Pneumococcal polysaccharide vaccine eligibility (cont’d)
III. High Risk Setting
• Individuals 24 months up to and including 64 years of age who are
homeless or living in chronic disadvantaged situations
– Includes those with no fixed address or living in shelters
• Individuals 24 months up to and including 64 years of age who are
residents of Long Term Care or Continuing Care facilities
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Yes NOMyocardial infarction Repeated pneumonia
Chronic liver disease – includes
cirrhosis, Hepatitis B and Hepatitis C
Fibromyalgia
Chronic Fatigue Syndrome
Hypertension
Pneumococcal polysaccharide vaccine eligibility (cont’d)
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Pneumococcal polysaccharide vaccine
• Provincially funded product - Pneumovax®23 (Merck)
• Dosage is 0.5 mL (comes in a single dose vial)
• Intramuscular injection given in the deltoid
– use 3 cc syringe
– needle size dependent on muscle mass
• Eligible person can receive pneumococcal vaccine with influenza vaccine
on the same visit but it must be given in a separate injection, in a different
immunization site (e.g., one vaccine in left deltoid, one in the right)
• The vaccine should be given at least 14 days prior to initiation of
immunosuppressive therapies (e.g., chemotherapy)
• Check your local protocol for clients who are unsure of past pneumococcal
polysaccharide immunization history
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Schedule and reinforcing dose
• One primary dose is sufficient for most individuals
– Two doses are required for HSCT recipients
• A one-time reinforcing dose is recommended ONLY for individuals with:
– Functional or anatomic asplenia, splenic dysfunction or sickle cell disease
– Chronic renal failure or nephrotic syndrome
– Hepatic cirrhosis
– HIV infection
– Immunosuppression related to disease or therapy (e.g., lymphoma,
Hodgkin’s disease, multiple myeloma, high-dose systemic steroids)
– Solid organ transplant
• This one-time reinforcing dose should be given:
– 5 years after the initial dose of pneumococcal polysaccharide vaccine
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Reinforcing dose
Exception:
• Individuals will be eligible for a dose of pneumococcal
polysaccharide vaccine at 65 years of age and older (as long as 5
years have passed since a previous dose of this vaccine),
regardless of the number of doses received prior to 65 years of
age.
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Pneumococcal polysaccharide vaccine side effects
• Common side effects: small amount of swelling and soreness at the
injection site
• Less common side effects: mild fever, feeling tired, headache and/or
muscle pain
• Some individuals have more serious side
effects such as a large amount of swelling and pain
– People who have a reaction that
concerns them or is an unusual reaction
should contact Health Link at 811 for direction
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Contraindications
Pneumococcal polysaccharide vaccine is contraindicated for the
following people:
• People who have experienced anaphylaxis to a previous dose of
pneumococcal polysaccharide vaccine
• People who have a known severe hypersensitivity to any component
of the vaccine
• Children under 24 months of age
Special consideration needs to be given to clients undergoing
splenectomies, transplants or immunosuppressive therapy. Refer these
individuals to Public Health (in some zones to the Communicable
Disease Unit) for assessment.
66
Section Three – Pneumococcal Immunization Knowledge Check
Review Questions Section 3
1. Are people with asthma eligible for the pneumococcal
polysaccharide vaccine?
Note: Answers can be found the end of the PowerPoint.
67
Section 4 – Vaccine Administration
• Client Interview (Fit to Immunize Assessment)
• Informed Consent
• Vaccine Administration Process
68
Section 4 – Vaccine Administration Learning Objectives
The immunizer will be able to:
• explain the best practices in influenza and pneumococcal
polysaccharide vaccine management and administration
• discuss the vaccines, their use and potential adverse events
following immunization
• administer influenza and pneumococcal polysaccharide vaccine in
accordance with national guidelines and local protocols
69
Fit to immunize assessment
The immunizer will:
• Assess the need for immunization
• Confirm the client has not received a dose of influenza vaccine in the
2017-2018 influenza season
• Complete a “fit to immunize” assessment
– health status today
– history of allergies
– previous reactions
– chronic illness/medications
– pregnancy
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Informed consent
• Clients must give informed consent before immunization
• Prior to immunizing the immunizer must:
– Determine that the client is eligible (lives, works or goes to school in Alberta)
– Review the disease(s)* being prevented
– Review antigen(s)*
– Risks and benefits of getting the vaccine(s)* and not getting the vaccine(s)*
– Side effects and after care
– How the vaccine(s) is given
– Provide the opportunity to ask questions
– Affirm verbal consent
* You will review two vaccines if you are administering pneumococcal polysaccharide vaccine.
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Vaccine management
• All multi-dose vials must be dated upon opening*
– Multi-dose Fluzone® must be discarded 28 days after first
puncture
• Check expiry date of all products being administered
• Communicate use of near expiry vials to other staff members, so
the vaccine can be used before it expires
• Vaccine should be withdrawn from the vial by the immunizer
administering the vaccine
• Do not mix vaccine from vials with different lot numbers
• Do not pre-draw vaccine
* Refer to local protocol for dating vials
72
Preparing the vaccine
• Determine the appropriate vaccine and route of administration
• Provide appropriate information to client
• Detach self from conversation
• For TIV/QIV, visually inspect the vaccine. Do not use if:
– it is discolored
– you notice extraneous particulate matter present
– the multi-dose vial/prefilled syringe is defective
73
Preparing the vaccine (cont’d)
For TIV/QIV
• Determine the site of injection
• For multi-dose vials – select appropriate syringe and needle
– it is not necessary to change needles after drawing up vaccine, unless
the needle is damaged or contaminated
• For prefilled syringes – select appropriate needle to attach to syringe
• Select and read the label on the multi-dose vial or prefilled syringe
• Check the vaccine expiry date
– if applicable, check the date the multi-dose vial was opened
• For prefilled syringes, ensure the lot number on the syringe matches the lot
number on the box (syringe is discarded after administering vaccine and
lot number is recorded from the box)
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Preparing the vaccine (cont’d)
• For multi-dose vials
– agitate the vial before drawing up each dose
– swab the top of the vial and allow it to dry
– withdraw the appropriate dose of the vaccine
• For prefilled syringes
– agitate the prefilled syringe before administration
• Recheck the vaccine label
• Check the record to verify you have the correct vaccine for each
client (e.g., Fluzone®, Fluad® or pneumococcal polysaccharide
vaccine)
75
Administering TIV/QIV
• Expose and position the client’s limb for injection
• Swab the site of injection
• Allow the site to dry for 10 - 15 seconds
• Secure the injection site using the appropriate stabilization
technique
• Insert the needle at a 90º angle
• Administer the vaccine with controlled pressure
• Activate the safety engineered device
• Discard the needle and syringe, and empty vaccine vials into an
appropriate sharps container
• Use a cotton ball and apply pressure to the injection site
• Reinforce the 15 min wait period with the client or parent/guardian
76
Intramuscular injections
Children less than 12 months old
– 3 mL syringe
– 25G 1” needle
– insert at 90 degree angle
– vastus lateralis - middle third
of anterior thigh and slightly
lateral to the midline
Note: This site can be used for
children older than 12 months of
age with inadequate deltoid
muscle mass. Check with a
Public Health Nurse if you are
unsure
77
Intramuscular injections
Children 12 months and older
– 3 mL syringe
– 25G - 5/8” to 1” needle depending on muscle mass
– insert at 90 degree angle
– mid portion of deltoid
Adults
– 3 mL syringe
– 25G - 1” to 1½” needle depending on muscle mass and adipose tissue
– insert at 90 degree angle
– mid portion of deltoid
78
Immunizing mastectomy clients
Single Mastectomy
• Influenza Vaccine Only:
– Give IM in arm opposite to mastectomy
• Influenza and Pneumococcal Vaccine:
– Give both vaccines IM in arm opposite to mastectomy (space injections minimum of 1” apart)
Double Mastectomy
• Influenza Vaccine Only:
– Give IM in Vastus Lateralis
• Influenza and Pneumococcal Vaccine:
– Give both vaccines IM in Vastus Lateralis (space injections minimum of 1” apart)
79
Position & stabilization techniques for vastus lateralis
site (infants less than 12 months)
For injection in the vastus lateralis
80
Position & stabilization techniques for deltoid site
Infants 12 months and older Infants 18 months old and older
(“The pretzel hold”)
81
Section 4 – Vaccine Administration Knowledge Check
Review Questions Section 4
1. Is it important to agitate Fluad® and Fluzone® before drawing up
each dose?
2. After opening a multi-dose vial, it is important to date it. What is the
time frame for expiry for multi-dose Fluzone® vaccine?
Note: Answers can be found at the end of the PowerPoint.
82
Section 5 – Anaphylaxis and Syncope
Anaphylaxis
• Anaphylaxis is a potentially life-threatening allergic reaction
• Very rare (about 1 per 1,000,000 doses) but even so, it should be anticipated with every client
• Pre-immunization screening can prevent episodes - questions about possible allergy to the vaccine or any vaccine component
• Every immunizer should be familiar with the symptoms of anaphylaxis and be ready to initiate appropriate interventions
• Most instances begin within 15 minutes after immunization
All clients are encouraged to wait for 15 minutes after immunization.
– For clients with any known anaphylactic allergies, extend this recommended wait period to 30 minutes
– Have clients remain within a short distance and return immediately for assessment if they feel unwell
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Anaphylaxis recognition & treatment
The immunizer must:
• be able to identify allergic reactions
and anaphylaxis, and know how to
respond appropriately
• be able to distinguish between fainting,
breath-holding spells, anxiety, and
anaphylaxis
• always have an up-to-date anaphylaxis
kit when immunizing
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Histamine/mediators – do what??
They cause:
• Capillary permeability and therefore the escape of plasma into the
tissues
• Widespread dilatation of arterioles and capillaries (vasodilation)
• Smooth muscle contraction
• Over secretion by mucous glands
85
… which is why we see these symptoms…
Respiratory:
dyspnea - wheezing - sneezing
choking - drooling
cyanosis – angioedema - tightness
in throat/chest
Dermatologic (skin):
urticaria - erythema - pruritus
flushing - pale/grey - facial swelling
tingling of mouth or face followed by a feeling of warmth
86
... and these symptoms...
Vascular Collapse (cardiovascular)
rapidly falling blood pressure
sweating
rapid, thready pulse
a feeling of uneasiness, restlessness or anxiety
weakness or dizziness
throbbing in the ears or a headache
Gastrointestinal:
nausea, vomiting
diarrhea
abdominal cramps
87
Anaphylactic shock intervention
The Initial Response …
– Call for help
– Lie the client on his/her back with feet elevated, if possible
– Loosen restrictive clothing around the neck
– Establish an adequate airway
– Note the time
89
Prompt administration of epinephrine is essential
Refer to your local Anaphylaxis Management Guideline and
information in your anaphylaxis kit for direction on how to proceed with
administration of epiNEPHrine and diphenhydramine hydrochloride
(e.g., Benadryl®)
Remember:
Failure to administer epiNEPHrine
promptly is more dangerous than
administering it in a situation where
anaphylaxis is not truly present!
90
Syncope post immunization
• Fainting is also known as syncope or vasovagal syncope
• Vasovagal syncope is triggered by a stimulus (anxiety) that causes
an exaggerated response in the part of the nervous system that
regulates involuntary body functions (like heart rate and blood flow)
• When a stimulus triggers an exaggerated response, both heart rate
and blood pressure drop, quickly reducing blood flow to the brain
and leading to loss of consciousness
91
Syncope post immunization
• In about 25% of cases, reduced blood flow can result in jerking
movements that resemble seizures
• These movements are more common when fainting occurs soon
after immunization, and disappear when consciousness is regained
• Clients fainting due to vasovagal syncope recover quickly, usually
within seconds or a few minutes
92
Signs and symptoms of syncope
Musculoskeletal
• muscles relaxed
• weakness
• incontinence (rare)
• clonic jerks of limbs and face
Respiratory
• normal or yawning
Dermatologic
• pallor/grey color - sweating
93
Signs and symptoms of syncope (cont’d)
Gastrointestinal
• vomiting - nausea
Cardiovascular
• hypotension, slow weak pulse
• ringing in ears
Neurological
• light headedness, dizziness
• spots before the eyes
• dazed
• unconsciousness
94
Facts about syncope
• There is a clear incidence peak in age 10 to 19 years, with a
smaller peak at age 4-6 years
– After the age of 20 years, the incidence decreases with age
• 57.5% occur in females
• The incidence of fainting is under-reported
• Most cases occur within 5 minutes of
immunization
• Fainting can result in head trauma if a client falls
– The goal is to prevent falls!
95
Tips to prevent syncope
• Administer vaccine while client is seated
• Maintain a calm and confident demeanor
• Observe anxious client while seated until anxiety has resolved after
immunization
• Have clients with a history of fainting lie down prior to administering
vaccine
• Client with pre-syncopal symptoms (such as dizziness, anxiety,
pallor, perspiration, trembling, or cool, clammy skin) should sit or lie
down until symptoms resolve
96
Assisting clients after syncope
• Assist the client to lay down with feet elevated
• Ensure the client’s airway is open (ABCs)
• Monitor for signs of allergic reaction
• Call for assistance if needed
• Cover the client with a blanket for warmth if available
• Wipe the client’s forehead with a damp cool cloth
• May offer fluids
• Have the client resume a standing position in stages (sit, stand,
walk)
• Observe the client until the symptoms have resolved
97
Anxiety spells
• Signs and Symptoms
– Fearful
– Pale
– Diaphoretic
– Complains of light headedness, dizziness, numbness, and
tingling of face and extremities
– Hyperventilation
• Treatment
– Reassurance
– Instruct to relax and breathe slowly
98
Breath holding
• Occurs in young children when upset
• Signs and symptoms:
– Suddenly become quiet but still very agitated
– Facial flushing & perioral cyanosis
– Often ends with resumption of crying, or a brief period of
unconsciousness during which time breathing resumes
• Treatment
– Reassurance
99
Section 5 - Anaphylaxis and Syncope Knowledge Check
Review Questions Section 5
1. What is the incidence of anaphylaxis after immunization?
2. Should you withhold epiNEPHrine if you are not completely sure
whether the client is experiencing anaphylaxis?
3. What is the percentage of people who experience jerking
movements that resemble seizures after fainting?
Note: Answers can be found at the end of the power point.
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Section 6- Infection Prevention & Control (IPC)
• Hand hygiene is the single most important action that decreases
the spread of infection
• Hand hygiene is done with:
– Alcohol-based hand rub (ABHR)
– Regular liquid soap, water and disposable hand towels
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Hand hygiene
• Alcohol-based hand rub (ABHR)
– Approved AHS product
– Use sufficient ABHR to rub all surfaces of hands (2-3 pumps)
including between fingers and the base of the thumbs for a
minimum of 15 seconds
• Regular liquid soap, water and disposable hand towels
– Wet hands, apply soap, rub all surfaces for minimum 15
seconds
– Rinse with clear, running water
– Recommended if hands are visibly soiled
• Apply AHS approved hand creams to maintain skin integrity
• Glove use is not a substitute for hand hygiene
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Four Moments of Hand Hygiene
• Before each client contact or contact with their environment
• Before aseptic procedures (such as immunization)
• After blood and body fluid exposure risk (such as after
immunization)
• After contact with the client or their environment
• AHS Hand Hygiene Policy and Procedure
http://www.albertahealthservices.ca/info/Page14956.aspxs
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Hand hygiene at large immunization sites
• Examples only, not limited to these occasions:
– Start and end of shift
– Before and after contact with the client
– Before handling immunization supplies (entering vaccine bags),
including the set up of immunizing stations
– After vaccine administered and before handling other equipment,
such as papers and pens
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4
IPC for vaccine administration
• Clean and disinfect clinic table/ work surface with appropriate low-
level disinfectant (e.g., accelerated hydrogen peroxide, quaternary
ammonium compounds)
– This is a two step procedure
– Always start the disinfection stage with a clean cloth
• Cover table/work station with a large clean drape
• Use a small drape in front of immunizing staff as a clean work area
– avoid placing papers/pens on this area
• Place appropriate puncture resistant biohazard container for use at
point of contact to dispose of sharps immediately after use
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5
Preparing for immunization in large public clinic sites
• Maintain small drape as the clean surface for the immunization station
(needles, syringes, swabs, etc)
• When documenting on the NCR, do not put the NCR on the small
drape
– Available space on the large drape can be used or the small drape
folded in half before placing the NCR or other paperwork on top.
This ensures the inner surface remains clean
• When station not in use:
– Drape with a clean drape (e.g., coffee times, meal times)
• Drapes used to cover the immunization stations can be reused for the
day
– Ensure they are folded so the inside portion maintains a clean field
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Preparing for immunization at large public clinic sites
• During the clinic:
– Immunization station and tables are cleaned and disinfected at
the start of the clinic and at the end of the clinic, not at the
beginning and end of staff shifts
• Cleaning and disinfection of the station during the shift needs to
be done only if the area becomes dirty/contaminated/wet
– At that time, the area would be cleaned, disinfected and set up
• At the end of the day, for sites that are only there for the day:
– Clean and disinfect station per IPC Guidelines but not set up for
the next day
• For sites where the campaign is ongoing & stations used next day:
– Area cleaned, disinfected & set up with fresh supplies and
draped in preparation for the next day.
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Cleaning of blood and body fluids
• Appropriate Personal Protective Equipment (PPE) must be worn
– Gloves must be worn and if there is the possibility of splashing,
further PPE (gown, mask and eye protection) may be required
• Clean area by blotting blood/body fluids with disposable towels,
discarding in a regular plastic-lined waste container
– in addition, for non porous surfaces, clean area with soap & water
– once clean-up is completed, tie garbage bag and place in regular
garbage
• After initial cleaning, disinfect with a fresh solution of bleach 1:9 or
use a low level disinfectant
• Thoroughly clean equipment (e.g. mop &handle, pail) before re-use
• Wash hands with soap and running water
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Influenza/pneumococcal vaccine recording
Information required to be recorded on all clients includes:
• Client demographic information
– full name, personal health number, date of birth, gender,
address including postal code
• Reason code for immunization
• Dose number
• Vaccine name & lot number
• Dosage administered
• Site of injection
• Route of administration
• Date of immunization
• Immunizer’s first initial and last name, designation & signature
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Influenza/pneumococcal vaccine recording (cont’d)
• Immunizer’s full name to be recorded on back of white copy (first
page)
• Public Health will utilize the Influenza/Pneumococcal Vaccine
Record for recording purposes
– Vaccine record is in a duplicate format - no carbon record (NCR)
– White copy to be kept by AHS
– Client receives yellow copy as their record of immunization
– Client copy has aftercare information on the back
• Community providers may utilize the Influenza/Pneumococcal
Vaccine Record (NCR) for recording purposes. A PDF fillable form
is available or a record of their own choosing can be used.
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Choosing the reason for immunization code from the Priority List
When completing the documentation, include the immunization
“reason code”. Start at the top of the priority list, and choose the
first code that applies (e.g. If the client is a health care worker, is
pregnant, and has asthma, choose code #03 “Health care worker”
because it is higher on the list).
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Influenza Vaccine Priority List
When determining which code to pick, start at the top of the list and choose the first code that applies
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Pneumococcal Vaccine Priority List
Calgary Zone Public Health will be offering Prevnar® 13 at large public immunization clinics.
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Employee Data Collection
AHS Workplace Health and Safety (WHS) and Covenant Health
Occupational Health and Safety (OHS) require notification of
employee immunization for the following reasons:
• In the event of an outbreak, influenza immunization status of
employees is required to manage the outbreak
• AHS WHS/Covenant Health OHS are required to provide overall
organizational rates of influenza immunization each year – doses
provided by Public Health are included in the rates.
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Employee Data Collection (cont’d)
When an AHS or Covenant Health employee presents at a
Public Health Clinic for influenza immunization you will need to:
1. Determine if the employee works for AHS or Covenant
Health
2. Have the employee complete the bottom section of the
NCR form
3. The NCR will be sent to AHS WHS or Covenant Health
OHS for data entry; follow Zone processes.
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Employee Data Collection (cont’d)
Please remember the following:
• Identify the employee:
03 Health care worker □ AHS/Covenant Employee
• Have the employee complete the bottom portion of the NCR form
– Ensure all fields have been completed including their employee number
– Ensure staff are aware that not completing the section may lead to work
restrictions or reassignment during an influenza outbreak until confirmation of
influenza immunization is provided
• White copy to be kept by Public Health
• Yellow copy to be given to the AHS or Covenant Health employee
• Employee copy has aftercare information on back
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Data collection (cont’d)
• All immunization providers are required to account for vaccine
doses administered, vaccine doses wasted and vaccine doses on
hand. The rationale for requiring data collection is as follows:
– To determine influenza immunization rates
– To be accountable for doses administered and meet
requirements of government auditing processes
– To monitor vaccine safety
– For planning and operational decisions for subsequent seasonal
programs
• Refer to local protocols for data collection instructions
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Influenza/Pneumococcal Self Learning Test
1. Influenza vaccine can be a live or inactivated vaccine. True or False
2. The influenza virus is spread only through droplets in the air. True or False
3. Influenza is contagious only after symptoms appear. True or False
4. In general, higher rates of influenza occur during which time of the year in North
America?
a. Year round
b. September through December
c. December through March
d. April through September
5. Influenza vaccines are most effective at preventing influenza infection in
persons 65 years of age and older. True or False
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Influenza/Pneumococcal Self Learning Test
6. How effective is influenza vaccine in preventing the disease when it is given to
healthy individuals when strains in the vaccine are similar to the strains
circulating during that influenza season?
a. 40-50%
b. 60-70%
c. 45-85%
d. 70-90%
7. Influenza vaccine should not be offered until after influenza disease is common
in the community. True or False
8. The correct dose of TIV/QIV for an 18-month-old child is:
a. 0.25 mL
b. 0.5 mL
c. 0.75 mL
d. 1 mL
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Influenza/Pneumococcal Self Learning Test
9. For an 8-year-old boy who has never received influenza vaccine, how many
doses will he need to receive this season?
a. One
b. Two
10. The most common side effects after inactivated influenza immunization are:
a. Flu like symptoms
b. Redness, soreness and swelling at the injection site
c. Guillain-Barré syndrome
d. Systemic symptoms of headache, fever, runny nose
11. Which vaccines would you offer to a 65-year-old man who has chronic lung
disease?
a. Influenza
b. Pneumococcal Polysaccharide 23
c. Both Influenza and Pneumococcal Polysaccharide 23
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Influenza/Pneumococcal Self Learning Test
12. A 4-year-old-girl has a severe kidney infection with high fever. She should
receive the influenza vaccine today.
True or False
13. While screening a 60-year-old man you find out that he has a history of
difficulty breathing after eating eggs. He required a visit to the emergency room
to resolve the situation. He should receive influenza vaccine today.
True or False
14. A 72-year-old woman is taking antibiotics for a minor wound infection. She
should receive influenza vaccine today.
True or False
15. A 28-year-old man is HIV positive. He should receive influenza vaccine today
and be assessed for history of pneumococcal vaccine.
True or False
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Influenza/Pneumococcal Self Learning Test
16. Signs of an anaphylactic reaction include:
a. Swelling of the mouth and throat
b. Hives
c. Difficulty breathing
d. Hypotension
e. All of the above
17. The ventral gluteal site is an appropriate site for inactivated influenza vaccine
administration, with the exception of a client who has had a double
mastectomy with lymph node removal.
True or False
18. A client states she had red eyes “a few years ago” following immunization with
influenza vaccine. She did not have any other symptoms. She should be
immunized today.
True or False
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Influenza/Pneumococcal Self Learning Test
19. The immune system can easily be overloaded by more than one immunization.
True or False
20. It is important to change the needle after drawing up each dose of vaccine.
True or False
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Can too many vaccines weaken the immune system?
• Vaccines do not weaken the immune system. Rather, they harness
and train it to defend, rapidly, against vaccine-preventable diseases
before illness can occur. Getting an annual influenza vaccine is a
good way to keep both yourself and your immune system healthy.
• Our immune systems are bombarded with constant challenges –
from bacteria in food to the dust we breathe. Compared to what the
immune system typically encounters and manages each day,
vaccines are literally a drop in the ocean. At present, infants
receiving recommended vaccines starting at two months of age
come into contact with only 34 antigens – just 34 antigens among
the millions handled every day by our immune systems.
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Should I get the influenza vaccine if I am healthy?
• You may not be in a group that is at
high risk for influenza related complications,
but your patients/residents/clients may be,
and members of your family may be as well.
• If you get influenza, you put people
around you at high risk for serious
illness. You can help ensure that
they stay healthy this winter by protecting
yourself.
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If residents/patients get immunized, why should I?
• Can you be sure that all those you care for were immunized? What if they weren’t?
• Health care providers who have direct patient contact should consider it their responsibility to provide the highest standard of care which includes annual influenza immunization.
• Getting immunized will add an extra level of certainty that you will not get influenza, and will not pass it on to others.
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Can the influenza vaccine give me influenza?
• Immunization with inactivated vaccine cannot cause influenza disease because the vaccine does not contain live viruses.
• The vaccine takes about two weeks to become completely effective, so you could still get influenza during these two weeks. If you get influenza after this period, you may experience milder symptoms than if you had not had the immunization.
• Many people confuse influenza with a cold or other respiratory infections, which the vaccine will not protect you against.
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Should I get an influenza vaccine every year?
YES…
• Strains of the influenza virus change every year, and new vaccines are produced to counter them as soon as they are identified
• The immunization you had last year will likely not be effective against this year’s virus
• Even if you have avoided getting influenza so far, it does not mean that you will not get sick this year
• By not getting the influenza immunization, you are increasing your chances of becoming ill
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References
1. Alberta Health: Government of Alberta. (2017, July). Alberta’s Influenza Immunization Program Policy
2. Alberta Health, Health System Accountability and Performance Division, Alberta Vaccine Cold Chain policy (2017, April).
3. Do Bugs Need Drugs (September 2011). Healthy Hands at Work: Being sick at work is everyone’s business, Employer Handbook. http://www.dobugsneeddrugs.org/wp-content/uploads/employer-handbook.pdf
4. Do Bugs Need Drugs (August 2014). Healthy Hands at Work: Being sick at work is everyone’s business, Worker Handbook. http://www.dobugsneeddrugs.org/wp-content/uploads/worker-handbook.pdf
5. Centers for Disease Control and Prevention. Epidemiology and Prevention of Vaccine-Preventable Diseases. Hamborsky J, Kroger A, Wolfe S, eds. 13th ed. Washington D.C. Public Health Foundation 2015.
6. Immunize Canada. Influenza. Retrieved August 21, 2014 from http://www.immunize.cpha.ca/en/diseases-vaccines/influenza.aspx
7. Health Canada. Health Products and Food Branch Inspectorate. (April 28, 2011) Guidelines for Temperature Control of Drug Products during Storage and Transportation (GUI-0069). http://www.hc-sc.gc.ca/dhp-mps/compli-conform/gmp-bpf/docs/gui-0069-eng.php
8. Merck Canada Inc. (July 27, 2016). PNEUMOVAX®23 (pneumococcal vaccine, polyvalent, MSD Std.). Product monograph.
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References
9. Merck Canada Inc. (July 25, 2014). ZOSTAVAX® (zoster vaccine live, attenuated [Oka/Merck]). Product monograph.
10. National Advisory Committee on Immunization. Canadian immunization guide (Evergreen Edition). Ottawa, ON: Public Health Agency of Canada. http://www.phac-aspc.gc.ca/publicat/cig-gci/index-eng.php
11. National Advisory Committee on Immunization (2017). Canadian Immunization Guide Chapter on Influenza and Statement on Seasonal Influenza Vaccine for 2017-2018. Ottawa, ON: Public Health Agency of Canada.
12. Seqirus UK Limited. (2017). FLUAD® (Influenza Vaccine, Surface Antigen, Inactivated, Adjuvanted with MF59C.1). Product Monograph.
13. Public Health Agency of Canada (PHAC). National vaccine storage and handling guidelines for immunization providers 2015. Retrieved August 15, 2017 from https://www.canada.ca/en/public-health/services/publications/healthy-living/national-vaccine-storage-handling-guidelines-immunization-providers-2015.html
14. Public Health Agency of Canada (PHAC). Influenza. Retrieved August 15, 2017 from http://www.phac-aspc.gc.ca/influenza/index-eng.php
15. Sanofi Pasteur Inc. (April 2017). FLUZONE® Quadrivalent (Influenza Virus Vaccine Quadrivalent Types A and B (Spit Virion). Product Monograph.
16. Alberta Health, Health System Accountability and Performance Division, Alberta Immunization Policy (2017, June 15). Influenza Vaccine: FLUAD®
17. Alberta Health, Health System Accountability and Performance Division, Alberta Immunization Policy (2017, June 15). Influenza Vaccine: Fluzone®
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Answer Keys
Section One- Influenza Disease Knowledge Check Answers
1. During which time period are individuals who have been infected with
influenza contagious?
• Individuals with influenza are infectious 1 day before symptoms develop and
up to 5 days after becoming ill. The period when an infected person is
contagious depends on the age and health of the person. Young children and
people with weakened immune systems may be contagious for longer than a
week.
2. Which individuals are at highest risk of developing complications from
influenza?
• Children 6 to 59 months of age, pregnant women, those 65 years of age and
over, individuals with chronic health conditions, aboriginal people and those
who are morbidly obese are at higher risk of developing complications from
influenza illness. Complications can include pneumonia (bacterial and viral),
ear and sinus infections, dehydration, and worsening of chronic medical
conditions, such as congestive heart failure, asthma or diabetes.
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Answer Keys
Section Two Part A - Influenza Vaccine Knowledge Check Answers
1. Which strains of influenza virus are included in the 2017-2018 influenza
vaccine for the northern hemisphere?
• Strains included in the 2017-2018 vaccine include:
• A/Michigan/45/2015 (H1N1)pdm09–like virus
• A/Hong Kong/4801/2014 (H3N2)-like virus
• B/Brisbane/60/2008-like virus
• B/Phuket/3073/2013-like virus (QIV only)
2. Why are these strains chosen?
• Each February, the World Health Organization (WHO) makes a
recommendation on the strains to be included in the influenza vaccine for the
northern hemisphere. Two influenza “A” viruses and one (for trivalent
vaccines) or two (for quadrivalent vaccines) influenza “B” virus are selected
based on the characteristics of the current circulating and new influenza virus
strains).
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Answer Key
3. Why is it necessary to get an influenza immunization each year to be
protected?
• A new vaccine is reformulated each year to protect against new infections.
Each vaccine lot is tested on healthy individuals to ensure the vaccine is safe
and effective.
4. Can you get influenza disease from the influenza vaccine? Explain.
• No. TIV/QIV is an inactivated (killed) vaccine and therefore you cannot get
influenza disease from the vaccine. QLAIV is a live vaccine which does not
cause influenza disease in the vaccine recipient because the vaccine virus is
attenuated or weakened.
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Answer Key
Section Two Part B- Influenza Vaccine Knowledge Check Answers
1. In Alberta this year, who is eligible for the influenza vaccine at no charge?
• Alberta Health (AH) funds a Universal Influenza Immunization Program,
where all people 6 months of age and older who live, work or go to school in
Alberta are eligible for vaccine at no charge.
2. Is Thimerosal in vaccines a threat to health? Explain.
• No. Thimerosal (ethylmercury) is a preservative used in multi-dose vials of
vaccine – it is not the same compound as methylmercury, which is a known
neurotoxin in high concentrations, or with prolonged exposure (e.g., ingesting
some types of fish). Ethylmercury is excreted from the body much faster and
is less likely to reach toxic levels in the blood than methylmercury. Multi-dose
vials of vaccine contain very small amounts of thimerosal. Studies have
demonstrated that there is no association between immunization with
thimerosal-containing vaccines and neurodevelopmental outcomes, including
autistic-spectrum disorders.
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Answer Key
3. Who should not be immunized with influenza vaccine?
• TIV/QIV should not be administered to:
– children less than 6 calendar months of age
• Fluad® should not be administered to persons under 65 years of age or
women who are pregnant or breastfeeding
– people with a known hypersensitivity to any component of the vaccine
– those with a previous anaphylactic reaction to influenza vaccine
– people who have been diagnosed with Guillain-Barré syndrome within 6 weeks
of a previous influenza immunization
– people who have had severe Oculorespiratory Syndrome (ORS) after influenza
immunization - these individuals should be assessed further prior to
immunizing.
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Answer Key
4. What is the recommendation for people who have been diagnosed with
Guillain-Barré syndrome within 6 weeks of a previous influenza
immunization?
• It is recommended that you do not provide influenza immunization to people
who have been diagnosed with GBS within 6 weeks of previous influenza
immunization.
5. What is the recommendation for clients who have experienced a mild case
of ORS in the past?
• They may receive the vaccine. Utilize the ORS Decision Flowchart to guide
immunization decision.
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Answer Key
Section Three- Pneumococcal Immunization Knowledge Check Answers
1. Are people with asthma eligible for the pneumococcal polysaccharide
vaccine?
• Yes if they have required medical attention in the last 12 months.
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Section Four- Vaccine Administration Knowledge Check Answers
1. Is it important to agitate Fluad® and Fluzone® before drawing up or
administering each dose?
• Yes. Agitate the vial or prefilled syringe before drawing up each dose.
2. After opening a multi-dose vial, it is important to date it. What is the time
frame for expiry for multi-dose Fluzone® vaccine?
• Yes. Open vials of multi-dose Fluzone® must be discarded 28 days after the
first puncture.
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Section Five- Anaphylaxis & Syncope Knowledge Check Answers
1. What is the incidence of anaphylaxis after immunization?
• Although anaphylaxis is very rare with an incidence of about 1 per 1,000,000
doses, it should be anticipated with every client.
2. Should you withhold epinephrine if you are not completely sure whether the
client is experiencing anaphylaxis, but you are pretty certain?
• No. Prompt administration of epinephrine is essential.
• Refer to your local Anaphylaxis Guideline and information in your anaphylaxis kit
for direction on how to proceed with administration of epinephrine and
diphenhydramine hydrochloride (e.g., Benadryl®).
• Failure to administer epinephrine promptly is more dangerous than administering it
in a situation where anaphylaxis is not truly present!
3. What is the percentage of people who experience jerking movements that
resemble seizures after fainting?
• In about 25% of cases, reduced blood flow can result in jerking movements that
resemble seizures. These movements are more common when fainting occurs
soon after immunization and disappear when consciousness is regained.
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Self Test Answer Key
1. True
2. False
3. False
4. December through March
5. False
6. 45-85%
7. False
8. 0.5 mL
9. Two
10.Redness, soreness and swelling at the injection site