Notifiable diseases and immunisation Flashcards

1
Q

Passive immunity

A

Protection provided from the transfer of antibodies from immune individuals.

Most commonly cross-placental transfer of antibodies from mother to child (e.g. measles, pertussis).

Or, via transfusion of blood or blood products including immunoglobulin (e.g. Hep B)
Protection is temporary – usually only a few weeks or months.

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2
Q

Passive immunity provided by injection:

A

Human immunoglobulin containing antibodies to the target infection.

Temporarily increases person’s antibody level to that specific infection. Protection gained within a few days but lasts only a few weeks.

Human normal immunoglobulin (HNIG) derived from the pooled plasma of donors and contains antibodies to infectious agents that are currently prevalent in the general population.

Used to protect immunocompromised children exposed to measles and of individuals after exposure to hepatitis A.

Specific immunoglobulins available for tetanus, hepatitis B, rabies and varicella zoster.

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3
Q

Active immunisation

A

Vaccination stimulates immune response and memory to a specific antigen/infection.

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4
Q

Vaccines are made from:

A
  • Inactivated (killed) (e.g. pertussis, inactivated polio)
  • Attenuated live organisms (e.g. yellow fever, MMR, polio, BCG)
  • Secreted products (e.g. tetanus, diphtheria toxoids)
  • The constituents of cell walls/subunits (e.g. Hep B)
  • Recombinant components (experimental)
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5
Q

Herd (population) immunity

A

Herd immunity occurs when a large portion of a community (the herd) becomes immune to a disease. The spread of disease from person to person becomes unlikely when herd immunity is achieved. As a result, the whole community becomes protected — not just those who are immune.

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6
Q

What does vaccine failure mean, and what are the types of vaccine failure?

A

No vaccine offers 100% protection.

Small proportion of individuals get infected despite vaccination.

Primary vaccine failure – person doesn’t develop immunity from vaccine.

Secondary vaccine failure – initially responds but protection wanes over time.

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7
Q

What are the different immunisation groups?

A

Routine immunisation schedule: protecting vulnerable and high-risk groups.

Additional vaccines for individuals with underlying medical conditions.

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8
Q

Dipththeria

A

Corynebacterium diphtheriae.

Bull neck or cutaneous diphtheria.

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9
Q

Tetanus

A

Clostridium tetani.

Once tetany sets in it cannot be reversed.

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10
Q

Pertussis

A

Bordetella pertussis.

Whooping cough - distinct sound they make.

Costophrenic recess is very prominent and so are the ribs because they are breathing so hard.

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11
Q

Polio

A

Poliovirus.

Causes death of neurones = poliomyelitis.

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12
Q

Heamophilus influenzae type B

A

It is a bacterial infection.

Causes:
- Acute epiglottitis
- Periorbital cellulitis

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13
Q

Meningococcal disease

A

Caused by Neisseria meningitidis.

Disease:
- Meningococcal sepsis
- Menigitis

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14
Q

Notification of diseases are important because…

A

Need to prevent further cases.

  • Notification
  • Contact tracing
  • ABx chemoprohylaxis
  • Vaccination
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15
Q

Contact tracing

A

Contact for meningitis is taken to be any person having close contact with a case in the past 7 days.

Close contact includes kissing, sleeping with, spending the night together or spending in excess of eight hours in the same room.

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16
Q

What are the notifiable diseases?

A

Diseases, infections and conditions specifically listed as notifiable under the Public Health (Control of Disease) Act 1984and theHealth Protection (Notification) Regulations 2010.

17
Q

Notifiable diseases - examples:

A
  • Acute encephalitis
  • Acute infectious hepatitis
  • Acute meningitis
  • Acute poliomyelitis
  • Anthrax
  • Botulism
  • Brucellosis
  • Cholera
  • COVID-19
  • Diphtheria
  • Enteric fever (typhoid or paratyphoid fever)
  • Food poisoning
  • Haemolytic uraemic syndrome (HUS)
  • Infectious bloody diarrhoea
  • Invasive group A streptococcal disease
  • Legionnaires’ disease
  • Leprosy
  • Malaria
  • Measles
  • Meningococcal septicaemia
  • Monkeypox
  • Mumps
  • Plague
  • Rabies
  • Rubella
  • Severe Acute Respiratory Syndrome (SARS)
  • Smallpox
  • Tetanus
  • Tuberculosis
  • Typhus
  • Viral haemorrhagic fever (VHF)
  • Whooping cough
  • Yellow fever
18
Q

The Role of surveillance?

A

Detection of any changes in a disease:
Outbreak detection
Early warning
Forecasting

Track changes in disease:
Extent and severity of disease
Risk factors

Allows development of interventions targeted at vulnerable groups.

19
Q

How is the community protected?

A

Investigate: contact tracing, partner notification, lookback exercises, etc…

Identify and protect vulnerable persons: e.g. chemoprophylaxis, immunisation, isolation.

Exclude high risk persons or from high risk settings.

Educate, inform, raise awareness, health promotion.

Coordinate multi-agency responses.

20
Q

What are the key components of disease transmission?

A

Source
Pathways
Receptor

21
Q

Group A Streptococcus (GAS)

A

Gram positive cocci.

Scarlet fever:
- sandpaper rash
- strawberry tongue

Think of:
- risk settings i.e. schools
- co-infectoions i.e. chickenpox.

22
Q

Typhoid fever

A

Salmonella typhi bacteria.

Think:
- Risk factors e.g. travel
- Risk groups e.g. food handlers, health & care staff, young children, doubtful hygiene

23
Q

Hepatitis B

A

Hepatitis B virus

Think:
- Risk factors e.g. travel, medical procedures, infected mother-to-child, blood products

  • Risk groups e.g. MSMs, sex workers, IV drug users, health workers, prisoners
24
Q

Legionnaires disease

A

Legionella pneumophila bacteria.

Hunting for the source!

Think:
- travel
- water-related exposure (jacuzzi, showers, baths, AC systems).