immunity and immunisation
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innate
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non-specific, non adaptive
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polymorphonuclear luecocytes (neutrophils)
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macrophages
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complement
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kill microbes without any prior exposure
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interact with lymphocytes
- induce cascade of events
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acquired
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specific, adaptive
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B lymphocytes
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plasma cells
- serete antibodies
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memory
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long lived
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rapidly proliferate and secrete large amounts of antibody
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T lymphocytes
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T helper
- directors
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cytotoxic T lymphocytes
- killer
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goal of immunisation = prime and prepare immune system
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respond rapidly and specifically
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prevent/attenuate
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disease
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colonisation
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infection
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Active immunity
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generated by host’s specific immune system
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primary immune response
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plasma cell
- IgM -> IgG
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first response = slow and peaks d30
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secondary immune response
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plasma cell
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IgG
- peaks 4-7d
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Passive immunity
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deosn’t depend on recipient’s immune response for protection
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temproary
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weeks - months
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injection of human IG
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TIG
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ZIG
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HBIG
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Rabies IG
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breast milk
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reproduction number - R0
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number of secondary cases generated by a typical infectious indiviual when rest of population susceptible
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must be above 1 to remain to exist
- else can be eradicated
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Herd immunity threshold
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proportion of immune individuals ina population that must be exceeded to prevent disease transmission
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1-1/R0
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target = 95% of children to be fully immunised by age 8mo then 2yr
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vaccination:
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types
- live microbes - attenuated
- MMR/varicella - rotavirus - attenuated vaccine virus multiplies to a limited extenet - induces immune response similar to wild virus infection - usually very effective - vaccines - MMR - varicella - rotavirus - zoster - BCG
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whole microbes killed
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treat whole cell/birus with chemicals
- inactivation
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organisms remain intact
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cannot cause an infection
- cannot reproduce
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fragments
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toxoid
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some bacterial infections = toxins rather than organisms
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alter toxin -> toxoid
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induce antibodies that neutralise exotoxin
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Recombinant
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HepB/HPV
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gene from pathogen
- antigen -> response
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pure vaccine that is efficient to produce
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Polysaccharide and conjugate vaccines
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poorly immunogenic
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low affinity antibodies
- do not ilicit T-cell responses
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should have maximum 3 doses lifetime
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children \<2yo shouldn’t receive polysaccharide
- ineffective
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administration ilicits immune response
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innate
- stimulate adaptive
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immune memory can last for many years - often life
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may wane
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booster = stimulate memory cells producing more antibodies
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Vaccination ingrediants
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adjuvants
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enhance immune response
- aluminum hydroxide
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preservatives
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stabilisers
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sucrose, lactose, albumin
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surfactants/emulsifierspolysorbate 80
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residuals
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include virus inactivating agents
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antibiotics
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egg protein
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gelatin
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Contraindications
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general contraindications:
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anaphylaxis to previous vaccine dose
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Live viral vaccines should not be given to pregnant women nor to immunosuppressed
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precautions
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acute febrile illness
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minor infection without signifiant fever or systemic upset no reason to delay
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should be postponed if fever >38
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reaction to previous dose
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allergy to vaccine components
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egg
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not CI to MMR
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no longer considered CI to influenza
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thrombocytopenia/bleeding disorder
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administer with caution
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23G or smaller
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can give SC - except hepB
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avoid giving 2 different live parenteral virus vaccine within 4 weeks of each other
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antibody response may interfere
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TIG
- 3mo
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ZIG
- 5mo
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RBC - washed
- 0
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RBC packed
- 5mo
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plasma/platelet
- 7mo
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NOT CONTRAINDICATIONS
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temp \<38
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atopy
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treatment with abx or locally acting steroids
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breastfeeding mum/child
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neonatal jaundive
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low wieght in otherwise well
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child being over usual age
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previous hypotonic-hyporesponsive episode
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ghistory of vaccination disease
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prematurity in otherwise well
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stabel neurological conditions
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egg allergy
- no longer CI to MMR
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fhx
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cold chain maagement
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stored at +2 - +8degC at all times
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must use pharmaceutical refridgerator
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monitor with electronic temperature recording device
- records and doenloads data on a monthly basis
Informed consent
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they have achoice
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why being offered
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what is involved
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probable benefits, risks, side-effects, failure rates and alternatives
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risks and benefits of not receiving treament
checklist
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unwell
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fever >38
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ever had a severe reaction before
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severe allergies to vaccine compents
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gelatin
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egg
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neomycin
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appropriate spacing
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prgnant/planning pregnancy
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undiagnosed or evolving neuroloigcal condition
Giving vaccine
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skin prep
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not necessary
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etoh may inactivate live attenuated vaccine
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IM
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MMR = SC
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rotavirus = oral
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Common vaccine responses:
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DTaP
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localised pain
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mild fever
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grizzly unsettled - 24-48hrs
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drowsiness
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extensive limb swelling after 4th dose
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Hep B
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very occ. soreness and redness at injection site
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mildfever
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MMR
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discomfort at injection site
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5-12 days:
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mild fever with faint rash (not infectious)
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head cold/runny nose
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cough and / or puffy eyes
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swelling of salivary glands
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adult Td
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localised discomfrot
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redness and swelling
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influenza
- mild fever
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pneumococcal
- pain
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HPV
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localised discomfort
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heavy arm
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mild fever
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nausea
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dizziness
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headache
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Hypotonic-hyporesponsive episode
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sudden onset of pallor/cyanosis, limpness and reduced responsiveness
- no other cause
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1-48hours after vaccination
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resolves spontaneously
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Adrenaline not recommended
- don’t have respiratory and circulatory problems
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report to CARM
Antivaccination
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take concerns seriously
- respond appropriately with as much infomration as possible
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explore reasons for antivaccination
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personal experience
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philisophical beliefs
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dissatisfaction
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people take on board what makes sense to them
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people are unlikely to vaccinate if they perceive that there is little risk of disease; anad that vaccines are not safe and do not work
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Themes:
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‘cover up’ - information suprressed to keep true facts hidden
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‘excavation of the facts’ - evidence against immunisation cna be found if searched for
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‘unholy alliance for profit’
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‘towards totalitarianism’ - increase state control
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‘us and them’
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‘poisonous cocktails’
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highly regulated
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aluminium
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noramlly all aluminium excreted through urine
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foods = 10-15mg aluminium/day
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mercury
- NO VACCINES ON NZNIS contain THIOMERSAL
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‘cause of idiopathic illnesses’
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MMR: no evidence MMR causes autism
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allergic disease (asthma)
- 2005/2012 cochrane review no evidence MMR
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SUDI
- chance
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overload/overwhelm infant immune system
- multiple microbial challenges in the environment
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‘back to nature’ - natural is better than man-made
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natural immunity may last longer
- both are protective
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immunity for Hib \<2yo, HPV, tetanus = better compared to natural infection
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disease is not serious
healthy children can and do still die from these diseases; and many more would do so if it were not for vaccination
disease is uncommon
disease is common in unimmunised populations and can easily recur and spread if immunisation rates drop
vaccine is ineffective
need to have studies showing effectiveness prior to introduction of vaccine
immunity wanes following natural infection
duration = variety of factors
subunit vaccines require primary courses and boosters
polysaccharide do not generate long-lived memory cells
if interval = short; duration of immunity can be affected - why minimum intervals required
in very young and very old - immune persistance limited
‘most cases are in immunised children’
100 children
90% immunisation with 90%efficacy
81/100 immune
10 susceptible b/c not having vaccine
9 b/c vaccine failure
vaccine is unsafe
need to be tested
homeopathy
no scientific evidence that supports homeopathy for preventing disease