Infectious Disease Flashcards

1
Q

What is the purpose of vaccination?

A

A weakened or inactive version of the pathogen is given to stimulate an immune response, reducing the risk and severity of infection with that pathogen.

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2
Q

What are the live vaccines?

A

MI BOOTY:

MMR
Influenza (nasal)

BCG
Oral polio
Oral rotavirus
Typhoid fever
Yellow fever

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3
Q

What is included in the 6-in-1 vaccine?

A
  • diphtheria
  • tetanus
  • pertussis
  • polio
  • haemophilus influenzae type B
  • hepatitis B
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4
Q

When is the 6-in-1 vaccine given?

A

8 weeks

12 weeks

16 weeks

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5
Q

What vaccines are given at 8 weeks old?

A
  • 6-in-1 vaccine
  • meningococcal B
  • rotavirus (oral)
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6
Q

What vaccines are given at 12 weeks old?

A
  • 6-in-1 vaccine (again)
  • pneumococcal
  • rotvirus (oral) (again)
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7
Q

What vaccines are given at 16 weeks old?

A
  • 6-in-1 vaccine (again)
  • meningococcal B (again)
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8
Q

What vaccines are given at 1 year old?

A
  • haemophilus influenza B
  • meningococcal C
  • meningococcal B (again)
  • pneumococcal (again)
  • MMR
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9
Q

What vaccines are given yearly at 2-8 years old?

A

Influenza vaccine (nasal)

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10
Q

What vaccines are given at 3 years 4 months old?

A
  • diphtheria
  • tetanus
  • pertussis
  • polio
  • MMR (again)
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11
Q

What vaccines are given at 12-13 years old?

A

HPV vaccine (2 doses 6 months apart)

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12
Q

What vaccines are given at 14 years old?

A
  • tetanus
  • diphtheria
  • polio
  • meningococcal A, C, W and Y
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13
Q

When should the HPV vaccine be given?

A

To boys and girls aged 13 to 14 years, with two doses spaced 6 to 12 months apart.

It should be given before they become sexually active.

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14
Q

What strains of HPV does Gardasil (current NHS vaccine) protect against?

A

Strains 6 and 11 (genital warts).

Strains 16 and 18 (cervical and anal cancer).

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15
Q

Who is the BCG vaccine offered to?

A

Offered from birth to babies who are at higher risk of tuberculosis:
- relatives from countries of high TB prevalence
- urban areas with high rates of TB
- close contact with people that have TB

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16
Q

Counselling on the link between the MMR vaccine and autism.

A

Andrew Wakefield published a paper in 1998 in the Lancet, where he performed a series of tests on 12 children with autism and chronic enterocolitis. He reported it appeared they started having features of autism after the MMR vaccine. This was very anecdotal evidence based on parents perceptions about when the issues started. This caused a very big media response that generated a lot of fear amongst parents and uncertainty amongst doctors.

Since then the MMR vaccine, as well as other vaccines, have been extensively investigated with much more rigorous scientific research and statistical power, such as a meta-analysis with over one million patients. All subsequent scientific literature has disproved any link between the MMR and autism.

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17
Q

What is the pathophysiology of sepsis?

A

An overwhelming inflammatory response caused by the release of cytokines by macrophages, lymphocytes and mast cells (ie. cytokine storm).

Cytokines stimulates inflammation and the release of nitrous oxide, which causes vasodilation. This causes a distributive shock.

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18
Q

Pathophysiology of disseminated intravascular coagulopathy (DIC).

A

Activation of the coagulation system in sepsis leads to the deposition of fibrin throughout the circulation.

It also leads to consumption of platelets and clotting factors.

This leads to thrombocytopenia, haemorrhages and an inability to form clots and stop bleeding.

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19
Q

Why does blood lactate rise in sepsis?

A

Hypo-perfused tissues attempt to produce energy via anaerobic respiration.

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20
Q

What is septic shock?

A

The body responses to distributive shock by raising heart rate.

When the heart can no longer compensate, blood pressure falls and results in tissue hypo-perfusion. This leads to a rise in blood lactate as the organs begin anaerobic respiration.

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21
Q

Signs of sepsis in children.

A
  • fever or hypothermia
  • poor feeding
  • high pitched or weak cry
  • floppy baby
  • skin colour changes
  • deranged physical observations
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22
Q

Working diagnosis for infants under 3 months with fever.

A

Sepsis until proven otherwise.

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23
Q

Immediate sepsis management.

A
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24
Q

Addition investigations for sepsis.

A
  • CXR (?pneumonia)
  • abdominal / pelvic ultrasound (?intra-abdominal infection)
  • lumbar puncture (?meningitis)
  • meningococcal PCR
  • serum cortisol (?adrenal crisis)
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25
Q

When can antibiotics be stopped in sepsis?

A

Low suspicion of bacterial infection;

OR

Patient is clinically well AND two CRP results are negative at 48 hours.

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26
Q

What is meningitis?

A

Inflammation of the meninges, usually due to bacterial or viral infection.

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27
Q

What is meningococcal septicaemia?

A

Meningococcus bacterial infection in the blood stream, which causes a non-blanching rash.

This rash indicates the infection has caused disseminated intravascular coagulopathy (DIC) and subcutaneous haemorrhages.

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28
Q

What is the most common cause of bacterial meningitis in children?

A

Neisseria meningitidis

Streptococcus pneumoniae

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29
Q

What is the most common cause of meningitis in neonates?

A

Group B streptococcus (GBS)

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30
Q

Presentation of meningitis.

A
  • fever
  • neck stiffness
  • vomiting
  • headache
  • photophobia
  • altered consciousness
  • seizure
  • non-blanching rash

Presentation may be non-specific in babies:
- hypotonia
- poor feeding
- lethargy
- hypothermia
- bulging fontanelle

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31
Q

NICE recommend a LP in which circumstances?

A
  • under 1 month with fever
  • 1 to 3 months with fever and clinically unwell
  • under 1 year with unexplained fever and other features of severe illness
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32
Q

What are the two examination tests you can perform to look for meningeal irritation?

A
  • Kernig’s
  • Brudzinski’s test
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33
Q

What is Kernig’s test?

A

Flex the hip and knee to 90°, then extend the knee. If there is resistance or pain, the patient is Kernig sign positive.

34
Q

What is Brudzinski’s test?

A

Lie supine and lift the head, bringing the chin to the chest. If this causes flexion of the hips, the patient is Brudzinski sign positive.

35
Q

What is nuchal rigidity?

A

The inability to flex the neck forward due to the rigidity of the neck muscles.

Indicates meningeal irritation.

36
Q

Community management of bacterial meningitis.

A

Urgent stat injection of benzylpenicillin and transfer to hospital.

37
Q

Diagnostic workup of meningitis.

A
  • blood culture
  • LP + CSF culture
  • CT head
  • FBC
  • CRP
  • U&Es
  • LFTs

Send blood tests for meningococcal PCR.

38
Q

Inpatient management of meningitis under 3 months old.

A
  • Cefotaxime
  • Amoxicillin (cover listeria contracted during pregnancy)

Bacterial meningitis is a notifiable disease, so public health must be informed within 3 days.

39
Q

Inpatient management of meningitis above 3 months old.

A
  • Ceftriaxone

Bacterial meningitis is a notifiable disease, so public health must be informed within 3 days.

40
Q

What is the purpose of steroid prescription in bacterial meningitis?

A

Prescibe dexamethasone to reduce the frequency and severity of hearing loss and neurological damage.

41
Q

PEP for meningitis.

A

Public health will guide PEP.

Close contacts within the last 7 days will be given a single dose of ciprofloxacin.

42
Q

What is the most common cause of viral meningitis?

A
  • herpes simplex virus (HSV)
  • enterovirus
  • varicella zoster virus (VZV)
43
Q

Bacterial vs viral CSF culture.

A
44
Q

Complications of meningitis.

A
  • hearing loss
  • seizures and epilepsy
  • cognitive impairment
  • learning disability
  • memory loss
  • cerebral palsy
45
Q

Contraindications to LP.

A
  • raised intracranial pressure
  • shock
  • convulsions
  • coagulation abnormality
  • local superficial infection at LP site
  • respiratory insufficiency

Perform delayed LP in children with suspected bacterial meningitis when contraindications no longer present

46
Q

What is encephalitis?

A

Inflammation of the brain as a result of infective or non-infective causes.

47
Q

Causes of encephalitis.

A
  • autoimmune
  • herpes simplex virus (HSV)
  • VZV
  • CMV
  • EBV
48
Q

Presentation of encephalitis.

A
  • altered consciousness
  • altered cognition
  • unusual behaviour
  • acute onset of focal neurological symptoms
  • acute onset of focal seizures
  • fever
49
Q

Diagnostic workup of encephalitis.

A
  • LP + CSF culture / PCR
  • CT scan
  • MRI scan
  • EEG recording
  • throat swabs
  • HIV testing
50
Q

Management of encephalitis.

A

IV antiviral medications:
- aciclovir
- ganciclovir

51
Q

Complications of encephalitis.

A
  • lasting fatigue
  • personality / mood changes
  • memory / cognition changes
  • learning disability
  • headaches
  • sensory disturbance
  • seizures
52
Q

What is the cause of infectious mononucelosis?

A

Ebstein Barr Virus (EBV) - secreted in the saliva of infected individuals, and can be infectious several weeks before the illness begins.

53
Q

Features of infectious mononucleosis.

A
  • fever
  • sore throat
  • fatigue
  • lymphadenopathy
  • tonsillar enlargement
  • splenomegaly
54
Q

What are heterophile antibodies?

A

A specific type of antibody produced only in EBV infection.

They can be tested for using the Monospot test or Paul-Bunnell test.

As there is a delay to make these antibodies, the tests are 100% specific but only 80% sensitive.

55
Q

Management of infectious mononucleosis.

A

Self-limiting.

Avoid alcohol and contact sports.

56
Q

Complications of infectious mononucleosis.

A
  • splenic rupture
  • glomerulonephritis
  • haemolytic anaemia
  • thrombocytopenia
  • chronic fatigue

Associated with Burkitt’s lymphoma.

57
Q

What is mumps?

A

A viral infection spread via respiratory droplets.

MMR vaccine offers 80% protection against mumps; vaccination history is essential when considering a diagnosis of mumps.

58
Q

Presentation of mumps.

A

Prodrome period of flu-like symptoms, then:
- fever
- muscle aches
- lethargy
- reduced appetite
- headache
- dry mouth

PAROTID GLAND SWELLING with associated pain is a key feature.

59
Q

Management of mumps.

A

Notifiable disease - notify public health of any suspected / confirmed cases.

Supportive management with rest, fluids and analgesia.

60
Q

Complications of mumps.

A
  • pancreatitis
  • orchitis
  • meningitis
  • sensorineural hearing loss
61
Q

Pathophysiology of HIV.

A

RNA retrovirus that enters and destroys CD4 T helper cells.

This causes the patient to become immunocompromised and eventually developing AIDS defining illnesses and opportunistic infections.

62
Q

How is HIV transmitted?

A
  • unprotected anal, vaginal or oral sex
  • mother to child at any stage of pregnancy, birth or breastfeeding
  • mucous membrane, blood or open wound exposure
63
Q

How can transmission of HIV be prevented during birth?

A

Caesarean sections can be considered.

Prophylaxis treatment with IV zidovudine can be given depending on viral load.

64
Q

Can mothers with HIV breastfeed?

A

HIV can be transmitted during breastfeeding even if the mother’s viral load is undetectable.

It is therefore never recommended.

65
Q

When to test children for HIV.

A
  • babies to HIV positive parents
  • suspected immunodeficiency
  • sexually active young adults
  • risk factors (e.g. needle stick injuries, sexual abuse, IV drug use)
66
Q

Treatment for paediatric HIV.

A
  • antiretroviral therapy
  • normal childhood vaccines
  • prophylactic co-trimoxazole (PCP)
  • treatment of opportunistic infections
67
Q

How is hepatitis B transmitted?

A

Direct contact with:
- blood
- bodily fluids

Vertical transmission.

68
Q

Prognosis of hepatitis B infection.

A

Most children fully recover from the infection within 2 months; however a proportion go on to become chronic hepatitis B carriers.

69
Q

Complications of chronic hepatitis B.

A
  • liver cirrhosis
  • hepatocellular carcinoma
70
Q

What are the following viral markers for Hepatitis B?

a) HBsAg

b) HBeAg

c) HBcAb

d) HBsAb

e) HBV DNA

A

a) surface antigen - active infection

b) E antigen - marker of infectivity

c) core antibody - implies past / current infection

d) surface antibody - implies vaccination of past / current infection

e) hepatitis B viral DNA - direct count of viral load.

71
Q

When to test children for hepatitis B.

A
  • children of HepB+ve mothers
  • migrants from endemic areas
  • close contacts of patients with hepB
72
Q

To reduce the risk of the baby contracting hepatitis B, how are neonates with HepB+ve mothers managed at birth?

A
  • hepatitis B vaccine
  • hepatitis B immunoglobulin infusion
73
Q

Is it safe for HepB+ve mothers to breastfeed?

A

Babies of these mothers have already been exposed to the virus during pregnancy and birth.

The general advice is that it is safe to breastfeed provided the baby’s are properly vaccinated.

74
Q

Management of hepatitis B.

A

Asymptomatic and usually do not require treatment.

Monitoring for hepatitis and cirrhosis - consider treatment with antiviral medications.

75
Q

What type of virus is

a) Hepatitis B

b) hepatitis C

A

a) DNA virus

b) RNA virus

76
Q

Disease course of hepatitis C in adults.

A

1/4 fight of the virus and make a full recovery.

3/4 develop chronic hepatitis C.

77
Q

Complications of hepatitis C infection.

A
  • liver cirrhosis
  • hepatocellular carcinoma
78
Q

What is the risk of vertical transmission in hepatitis C?

A

10%

79
Q

How is hepatitis C tested for?

A
  • antibody screening test
  • RNA testing
80
Q

Management of hepatitis C in children.

A

Children often clear the virus spontaneously - chronic infection may require specialist followup to monitor the liver function and hepatitis C viral load.

Any medical treatment is usually delayed until adulthood unless the child is significantly affected.