Vaccines and Immunisation Flashcards

1
Q

Phases of adaptive immunity

A
  1. Antigen recognition
  2. Lymphocyte activation
  3. Antigen elimination
  4. Contraction (homeostasis)
  5. Memory
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2
Q

Live vaccines

A

Virus weakened, often by repeatedly passing virus through a tissue culture in which it replicates poorly
+ activates killer T cells
+ 1/2 doses req for lifelong immunity
- may be reactivated,less safe for people with weakened immune system
- storage, must be refrigerated

eg MMR, varicella, rotavirus

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3
Q

Inactivated vaccines

A
Pathogen treated with heat or chemicals to kill it before introduction into the body
\+ low risk of causing infection
\+ easy to store and transport
- req several doses and boosters
- elicit weaker immunological response

eg polio, hepA, rabies

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4
Q

Subunit vaccines

A

One or more parts of the pathogen such as protein is isolated and introduced to evoke immune response
+ low risk of adr
+ can be used in pt with weakened immune system
- difficult to manufacture
- may req boosters

eg. hepB, influenza, pertussis Pneumococcus

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5
Q

Toxoid vaccines

A

Toxins produced by pathogen is deactivated and introduced into the body
+ stable, easy to distribute
+ unable to cause disease or spread
- may req boosters to maintain immunity

eg diphtheria, tetanus

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6
Q

Recombinant vaccines

A

Produced using genetic engineering, may contain no actual virus or may contain modified strain of virus

eg hepB, HPV

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7
Q

Herd immunity

A

Enough of the population (depending on how contagious the disease is) is immunised to contain the spread of the disease and most community members are protected, including the unimmunised indiv

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8
Q

Vaccines for respiratory (airborne or droplet) transmitted infection (9)

A

influenze, pneumococcus, meningococcus, diphtheria, pertussis, hemophilus influenzae (bacteria), mmr, chicken pox, bsg

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9
Q

Vaccines for contact transmitted infection (3)

A

tetanus, rabies, shingles

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10
Q

General considerations in vaccine use

A

Effectiveness, AE, CI and precautions, simultaneous adm

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11
Q

Vaccines for food and water transmitted infection

A

hepA, typhoid, cholera, rotavirus

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12
Q

Vaccines for vector borne transmitted infection

A

yellow fever, japanese encephalitis dengue, malaria

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13
Q

Effective of vaccines consideration

A

Varies by vaccine eg hepB 95% effective, var 90%

Other factors:
Site given (hepA/B in deltoid and not gluteus)
Pt age and immune status (inf less effective in 80 vs 60)
cold chain problems (not kept at recommended temp)

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14
Q

AE of vaccines

A

General:

  • mild and common: pain at injection site, headache, myalgia
  • uncommon: fever, hematoma
  • severe but rare: anaphylaxis, hypersensitivity
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15
Q

CI/precautions of vaccines

A
  • Fever, may not be able to mount immune response
  • pregnancy
  • immunocompromised
  • allergy to vaccines or components
  • bleeding risk (on anti-coagulaiton or low platelet counts) - precaution
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16
Q

Only exception of simultaneous adm?

A

PCV and meningococcal conjugate vaccine in pt with functional or anatomical asplenia (nonfunctional spleen)
- 4 week interval to avoid interference

17
Q

Can live vaccines adm via intramuscular or SC be adm together?

A

No, 28 days apart

18
Q

Hematoma

A

A collection of blood outside of blood vessels

19
Q

CI/precautions of vaccines

A
  • (Moderate/severe illness) Fever, may not be able to mount immune response
  • pregnancy
  • immunocompromised
  • allergy to vaccines or components
  • bleeding risk (on anti-coagulaiton or low platelet counts) - precaution
20
Q

Vaccine preservative eg.

A

Thiomersal

21
Q

Vaccine stabilisers

A

Inorganic Mg salt such as Mg sulfate, Mg chloride, mixtures of lactose, sorbitol and gelatin, monosodium glutamate and glycine

22
Q

Vaccine trace components eg

A

Formaldehyde, used to deactivate viruses and detoxify bacteria

23
Q

Vaccine precaution!

A

Bleeding risk (on anti-coagulation or low platelet count)

24
Q

Vaccine preservative (prevent contamination) eg.

A

Thiomersal