Fever and Rash; Vaccine Preventable Disease Flashcards

1
Q

What types of Vaccines do we use

A
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2
Q

What do you need to ask the parents in terms of a vaccine-preventable disease history?

A
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3
Q

What is this? what are the signs and issues of this disease?

A

Measles! (highly infectious)

  • 2-3days of fever, conjunctivis, coryza, Kopliks spots (in mucosa of cheek, hard to find)
  • Characteristic rash day 3-7, widespread and diffuse, most unwell at time of rash
  • Complications commone; 10% get secondary infection (ear, pneumonia, croup)
    • 1/1000 encephalitis (15% die, 25-35% long term damage
    • Rarely SSPE: 7-10 years later; degenerative fatal NS disease from persistent measles infection
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4
Q

When do we vaccinate for measles

A

At 15 months then a booster at 4 years, as 10% of people don’t seroconvert on the first dose. Therefore we need the second dose to ensure >95% of people are immune

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5
Q

Do we still get measles outbreaks?

A

Yes, although the last epidemic was 1991, we still yes small outbreaks, mainly in people who either

  1. are not vaccinated
  2. or only had one dose!

2013: Lots in Waikato and Auckland, spread quickly accross the country

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6
Q

What is this rash indicative of

A

Purpura rash, that is indicative of Meningitis.

Meningicoccal Spesis

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7
Q
A

Spinal Fluid shouldn’t have WBC in it.

87% polymorphs (neutrophils)

Low Glucose: As glucose is what’s required for bacteria to survive, low glucose indicated infection

Gram negative coccobaccili: Grew Haemophilis influenza
Seizures in the first 48hrs of hospitalisation
Day 3 Head CT: bilateral extra axial collections and meningeal enhancement consistent with meningitis; ‘empiema’

Follow up: long course of IV AB’s

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8
Q

What is Bacterial meningitis and what is it caused by?

A

Meningitis: inflammation of the meninges (membrane) surrounding the brain

Bacterial meningitis caused by:

  1. S. pneumoniae***
  2. N. meningitidis
  3. Haemophilis influenzaae type b now rarely seen due to vaccination
  • Different pathogens occur at different ages: eg newborn babies; Grp B streptococcous, gram negatives*
  • also Viral agents (herpes simplex and enterovirus) and Tuberculosis*
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9
Q

What is the main part that is targetted of the different pathogens from the meningitis vaccines

A

They all have a distinctive sugary capsule coating that is the immunogenic part of them.

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10
Q

Why are polysaccharide vaccines not very good?

A

Polysaccharides have weak immunogenicity so we (especially young children age <2yrs) produce very weak antibody responses to polysaccharide antigens

We have poor immunological memory to polysaccharide antigens

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11
Q

How have polysaccharide vaccines been revolutionised?

A

But the introduction of Conjugate vaccinations

  • Taking the long polysaccharide sugar chains on the capsule of the bacteria, taking them off and conjugating them into something more immune stimulating.
  • Conjugate sugar to a protein and the IS will remember that life-long!!
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12
Q

Describe Conjugate Vaccines!

A
  • Polysaccharide attached to a carrier protein
  • taken up by B cells
  • Carrier protein digested and antigen presented to helper T cells
  • Converts a T-cell-independent carbohydrate antigen into a T-cell-dependent antigen
  • Good immunogenicity in those 2yrs of age
  • Good production of memory cells
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13
Q

How has conjugate vaccination helped Haemophilus influenza and what is HI?

A

A serious disease almost eradicated by immunisation in the developed world

  • Gram-neg rod
  • Typed by capsule
  • Tybe b most important and prior to vaccination caused 95% of H.flu serious disease
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14
Q

Hib Vaccine

A
  • Induces antibody to PRP capsule, protect against invasive disease
  • Initial HiB vaccines were unconjugated and poorly immunogenic
  • Conjugate vaccines now available
    • PRP polysachareide linked to immunogenic protein
    • Effective in young infants
    • Reduces or eliminates nasopharyngeal colonisation
    • If vaccine uptake is >80% invasive disease is virtually eliminated in a population
    • Protective efficacy of vaccine >98%
  • Given at 6 weeks, 3 months, 5 months and 15 months
  • Still a few cases and most of these have been incomplelety or unimmunised
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15
Q

Streptococcus pneumoniae is a causative agent of Meningitis. Describe it as a bacteria

A
  • Colonises the nasopharynx 5-10%of adults, 20-40% children at any one time
  • Gram + coccus with a polysaccharide external capsule
  • has >90 serotypes of capsular sugar which makes it really hard to vaccinate for! Causes escape of phagocytosis
  • Invasive disease common in children <5yrs especially <2yrs and adults >65yrs
    • ​Bacteraemia, sinusitis
    • otitis media, pneumonia
    • worldwide responsibility for million deaths/yr for children <5yrs
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16
Q

What is Invasive Pneumoccal disease (IPD)

A
  • When pneumococci are isolated from usually sterile sites; cerebrospinal fluid (meningitis), blood (bactereamia) or pleural space/lung tissue (pneumonia)
  • In children
    • major cause of mortality and morbity <2yrs
    • most common bacterial cause of otitis media
  • For all age age groups
    • commonest cause of bacterial pneumonia
    • meningococci and pneumococcimost common causes
17
Q

For many years, we used the polysaccharide vaccine ($20), what is this and why is it shit?

A
  • Contains capsular polysaccharide from each of the 23 most common infecting serotypes
    • used in splenectomy, immunosuppresed, chronic illness
    • poorly immunogenic, doesn’t cause a big response, BUT for people with a poor immune system
    • elderly (>65yrs recommended not funded)
    • NOT useful in those younger then 2yrs; because you don’t have the ability to respond!

so the conjugate vaccine is finding immunogenic protein carrier (toxoids) and conjugating them to polysaccharides; these became part of the vaccine scheme in 2008

18
Q

Since introduction into NZ and other countries The S.pn conjugate vaccine has had….

A
  • 97% efficacy against invasive (meningits and bactereamia) pneumococcal disease aused by the vaccine serotypes
  • 10% reduction in clinical pneumonia needing hospital
  • 30% reduction in xray confirmed pneumonia
    • some reduction in otitis media
    • less AB resistant serotypes
  • Significant protection of those not recieving the vaccine (older children >5yrs and adults = herd immunity)
19
Q

What is Neisseria meningitidis

A
  • Like Hib and pneumococci; the polysaccharide capsule is an important virulence
  • N. meningitidis is an exclusive human pathogen transmitted by droplets from colonised upper respiratory mucosal membranes
  • 12 serotypes based on capsular polysaccharode
  • 90%meningitis cases are caused by strains belonging to serotypes A, B, C: these can cause epidemics
    • serotype B happened early 2000’s stopped by vaccine, but there are still cases today!
20
Q

What’s the prominent age group of meningitis patients?

A

Adolescent disease; mainly all <1yr, a smaller peak at 1-4yr

21
Q

Why is the N. meningitidis so hard to make a proper vaccine against?

A
  • Antibodies play a major role in protection
  • Polysaccharide capsule poorly immunogenic compared with proteins of cell wall and outer membrane
  • polysaccharide capsule of serogroup B composed of same sugars as those found on the surface of human immature neural cells
    • so lymphocytes that could produce antibodie to capsule are deleted in fetal development (we may be immunotolerant to that particular poly sach.
    • makes it really hard to make a vaccine against Type B!!!
22
Q

What is the NZ MenzB vaccine

How effective is it as a vaccine!

(for meningitis type B)

A
  • Outer membrane inside the capsule
  • two outer membrane proteins (Por A and Por B) are the main components
  • Antibodies to these proteins can cause
    1. Complement activation
    2. Phagocytosis

Didn’t produce lasting antibodies but helped lesser epidemic short term (so now no longer in use)

23
Q

What meningicoccal vaccines are available?

Since type B is no longer in use

A
  • Two purifed capsular polysaccharide and conjugate protein vaccines for serotypes
    • A
    • C
    • W135
    • Y
    • Same principal as for HiB and pneumococcal conjugates
  • Men. C conjugate vaccine on schedule fro aussie and UK
  • New MenB (BexSero) vaccine on schedule in UK; uses 4 target proteins of serogroup B strain including the NZ MenzB porin targets
24
Q

The majority of people are covered by vaccines, around 90-95% immunised, and have less of disparities in terms of ethnicity and socioeconomic status, so what are the issues still remaining and waht are some reasons for refusing immunisations?

A
  • Timeliness:young infants not getting their vaccinations on time; which increases risk
  • areas of challenge: maori and deprivation
  • Challenges in maintaining:
    • systems
    • complex social media and anti-immunisation
    • shifting priorites
  • Theirs no link between MMR and autism, and has been disproven
25
Q

MYTH: I heard excess vaccines give mercury poisoning

A

Thiomersal: a preservative in vaccines converted to ethylmercury in the body

  • no vaccine now given on national immunisation schedue contain thiomersal; used in very small amounts as an adjuvant in adult DT and some flu vaccines (not the current one)
26
Q

MYTH: Giving too many vaccines might weaken the immune system

A

THe number of antigens now used is less then the original small pox vacc.

27
Q

What are the main anti-vaccine arguments?

A