infectious disease Flashcards

1
Q

What is the definition of paediatric sepsis?

A
  • SIRS + suspected/ proven infection
    □ SIRS = systemic inflammatory response syndrome
    ® Fever or hypothermia
    ® Tachycardia
    ® Tachypnoea
    ® Leucocytosis or leukocytopenia
    □ Infection = bacteraemia (e.g. bacteria multiplying in the bloodstream)
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2
Q

What is the difinition of severe sepsis in a child?

A
- SEPSIS + multi-organ failure
□ ≥ 2 of the following:
® Respiratory failure
® Renal failure
® Neurologic failure
® Haematological Failure
® Liver failure
□ ARDS (acute respiratory distress syndrome)
® Inflammatory response of the lungs
□ Septic shock (e.g. cardiovascular failure)
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3
Q

What are the responsable pathogens of sepsis in neonates?

A
  • Group B strptococci
  • Escherichia coli
  • Listeria monocytogenes
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4
Q

What are the responsable pathogens of sepsis in children?

A

□ Streptococcus pneumoniae
□ Meningococci
□ Group A streptococci
□ Staphylococcus aureus

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5
Q

What are the symptoms of sepsis in children?

A
  • Fever or hypothermia
  • Cold hands/feet, mottled skin
  • Prolonged capillary refill time
  • Chills/rigors
  • Limb pain
  • Vomiting and/or diarrhoea
  • Muscles weakness
  • Muscle/joint aches
  • Skin rash
  • Diminished urine output
    □ Difficult to pick up in children so ask if the dampness of the nappy is reduced or if the urine colour has changed
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6
Q

What is the paediatric sepsis 6?

A
  • If you start treatment within an hour then outcomes are better
  • Temperature
  • Tachycardia
  • Capillary refill
  • Altered mental state
  • Inappropriate tachypnoea
  • Hypotension
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7
Q

How is sepsis treated in a child?

A
- Supportive treatment
□ A- airway
□ B- breathing
□ C- circulation
□ DEFG= don't ever forget glucose
- Causative treatment
□ Antibiotics with broad-spectrum and good CSF penetration
□ 3rd generation cephalosporins (+amoxicillin if neonate)
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8
Q

What investigations should be done if a child has sepsis

A

□ FBC- leucocytosis, thrombocytopaenia
□ CRP- elevated
□ Coagulation factors deranged clotting due to DIC
□ U and Es, LFTs- renal and hepatic dysfunction
□ Blood gas- metabolic acidosis, raised lactate
□ Glucose- hypoglycaemia
□ Culture
□ CSF
® Cell count and culture- increased WCC, antigen testing, PCR
® Protein and glucose- increased protein level, low glucose
□ Urine culture
□ Skin biopsy
□ Imaging- CT/ MRI head

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9
Q

What pathogens are responable for causing meningitis in neonates?

A

□ Group B streptococci
□ Escherichia coli
□ Listeria monocytogenes

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10
Q

What pathogens are responable for causing meningitis in children?

A

□ Streptococcus pneumoniae
□ Meningococci (Neisseria menangitisis)
□ Haemophilus influenza

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11
Q

What are the symptoms of meningitis in children?

A
□ Nuchal rigidity
□ Headaches, Photophobia
□ Diminished consciousness
□ Focal neurological abnormalities
□ Seizures
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12
Q

What are the symptoms of meningitis in neonates?

A

□ Lethargy, Irritability
□ Bulging fontanelle
□ Seizures
□ ‘nappy pain’
® Stretching of the meninge when lifting the baby up to change the nappy
□ High temperature
□ Tachypnoea
□ Shivering
□ Pin prick rash/ marks or purple bruises anywhere on the body
□ Sometime diarrhoea
□ Vomiting/ refusing to feed
□ Blotchy skin getting paler or turning blue
□ A stiff body with jerky movements or floppy and lifeless
□ Cold hands and feet

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13
Q

Describe the mengococcal rash

A
  • Late sign

- Non-blanching rash e.g. purpura and petechiae - tumbler test

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14
Q

How is meningitis diagnosed in children?

A
  • Blood:
    □ FBC; leucocytosis, thrombocytopaenia
    □ CRP; elevated
    □ coagulation factors; low levels due to DIC
    □ blood gas; metabolic acidosis
    □ glucose; hypoglycaemia
  • CSF: pleocytosis, increased protein level, low glucose
  • Blood and CSF cultures (antigen testing, PCR)
  • Urine culture, skin biopsy culture
  • Imaging: CT-cerebrum
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15
Q

What is the treatment of menengitis in children?

A
- Supportive treatment:
□ A airway
□ B breathing
□ C circulation
□ DEFG = ‘don’t ever forget glucose’
- Causative treatment:
□ Antibiotics with good penetration in CSF & broad-spectrum:
□ 3rd generation cephalosporins (+ amoxicillin if neonate)
- Chemoprophylaxis
□ Close household contacts
□ Meningococcus B and Streptococcus group A
- Steroids
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16
Q

What are the complications if pneumococcal meningitis?

A
  • Brain damage
  • Hearing loss
  • Hydrocephalus
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17
Q

What diseases cam be either staph. or strep?

A
  • Impetigo
  • Toxic shock syndrome
  • Bacteraemia
  • Cellulitis
  • Septic arthritis
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18
Q

What is streptococci?

A
  • Gram positive cocci
  • Penicillin
  • No resistance issues
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19
Q

What is saphlococci?

A
  • Gram positive cocci
  • Flucloxacillin (=synthetic penicillin resistant to beta-lactamases)
  • Resistance big issue
  • MRSA
  • Carriers
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20
Q

What is the history of a child with scarlet fever?

A
  • Contact
  • Intubation for 2-4 days
  • Malaise fever, tonsillitis
  • Start exanthema
  • Strawberry tongue
  • Squamation (hands and feet)- seen a week or 2 after the acute infection (caused by the exotoxins from strep A)
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21
Q

What causes scalet fever?

A

group A beta-haemolytic streptococci

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22
Q

What age do cgildren get scarlet fever?

A

○ Children under the age of 2 are relatively protected

○ Children over the age of 10 have natural protection (80%)

23
Q

What are the virulance factors of scarlet fever?

A
  • M-protein

- Exotoxins

24
Q

What are the complications of scarlet fever?

A
  • Erysipelas, cellulitis, impetigo
  • Streptococcal toxic shock
  • Rheumatic fever (0.3-3%)
  • Glomerulonephritis
25
Q

Hoe is scarlet fever treated?

A

Penaicillin for 10 days

26
Q

What are the features of impetigo?

A
○ Caused by both staph aureus and strep pyogenes
○ Highly contagious
○ Sore and blisters
○ No systemic symptoms 
○ Yellow brown crustae
27
Q

What is staphylococcal scolded skin syndrome? (SSSS)

A
○ Caused by exotoxins of s. aureus 
○ Mostly kids <5 years (particularly in new-borns
○ Fever
○ Widespread redness
○ Fluid filled blisters 
- Rupture easily 
- Especially in the skin folds 
○ Can lose a lot of proteins and fluid
○ If it is severe they can end up in ICU
28
Q

What are the clinical symptoms of kawasaki disease?

A
- Fever for at least 5 days and four of the five
□ Bilateral conjunctival injection 
□ Changes of the mucous membranes
□ Cervical lymphadenopathy 
□ Polymorphous rash
□ Changes to the extremities 
- Peripheral oedema 
- Peripheral erythema
- Periungual desquamation
29
Q

What is the pathophysiology of kawaasaki disease?

A
  • Self-limiting vasculitis of medium sized arteries
  • KD reported in all racial and ethnic groups
  • Highest prevalence in Japan and Hawaii
  • Increased risk of siblings and twins
  • Aetiology unknown but infectious cause suggested
30
Q

What is the treatment of kawasaki disease?

A
  • To prevent complications like vasculitis coronary arteries
    □ Immunoglobulins
    □ Aspirin
    □ Other immunosuppressive agents
31
Q

What is Henoch-Schoenlein purpura?

A

○ Vasculitis
- Skin
- Kidneys
- GI tract (rare)
○ Associated with previous aspecific viral illness
○ Doesn’t have strawberry tongue, lymphadenopathy etc…
○ Won’t really be ill- they will walk into the clinic

32
Q

What causes an erythematous maculopapulous rash?

A
  • Measles
  • Rubella
  • Enterovirus
  • Cytomegalovirus
  • Human herpesvirus 6
  • Human herpesvirus 7
  • Parvovirus B19
  • Epstein-Barr virus
33
Q

What causes a vestibulobullous rash?

A
- Varicella-zoster virus
□ Individual lesions
□ Different stages of development 
- Herpes simplex virus 
□ Vesicles on tongue and around mouth 
□ Group of lesions all in the same stage of development 
- Enterovirus 
□ Hand foot and mouth disease
□ Only supportive treatment
34
Q

What causes a petechial and purpuric rash?

A
  • Rubella (congenital)
  • Enterovirus
  • Cytomegalovirus (congenital)
35
Q

What can varicella zoster virus cause?

A
  • Primary infection (varicella, chickenpox)

- Recurrent infection (zoster)

36
Q

What is the intubation period of VZV?

A

14 days (10-21)

37
Q

What is the clinical presentation of VZV infections?

A
  • Mild malaise and fever (kids are not sick)
  • Exanthema: papules turn into vesicles turn into pustules turn into crustae turns into scarring and new lesions for 5-7 days
  • Itching
38
Q

What are the complications of VZV infections?

A
  • Secondary strep. Staph infections of the skin (10-15%)

- Meningoencephalitis, cerebellitis, arthritis

39
Q

What is the treatment of VZV infections?

A

○ Therapy : (Val)acyclovir (only if they are immunocompromised or a neonate)
○ Prevention: Vaccination (active/ passive)

40
Q

What are the warning signs that a VZV infection is serious?

A
  • High fever
  • New lesions >10 days
  • Inflamed lesions
  • General malaise
41
Q

What are the different herpes simplex viruses?

A

HSV 1 (oral) and HSV 2 (genital)

42
Q

What is the clinical presentation of herpes simplex virus?

A
  • Stomatitis (primary infection)

- Recurrent cold sores

43
Q

What are the complications of herpes simplex virus infections?

A
  • Kerato conjunctivitis
  • Encephalitis
  • Systemic neonatal infections
  • Immunocompromised children
44
Q

What is the therapy of HSV?

A
  • Self limiting

- (Val)acyclovir

45
Q

Discuss HSV and neonates

A
  • Birth canal/ direct contact
  • Day 4-21 of life
  • 70-80% disseminated/ CNS infections
    □ Sepsis
    □ Meningoencephalitis
    □ Hepatitis (jaundice, bleeding)
  • 20-30% skin/ eye/ mouth (SEM) disease
  • High mortality
    □ Without acyclovir >50%
    □ With acyclovir 20-30%
46
Q

What is the cause of hand-foot and mouth disease?

A
  • Enterovirus
    □ Coxasackie A16
    □ Enterovirus 71
47
Q

What is the intubation period of hand-foot and mouth disease?

A

3-6 days

48
Q

What is the clinical presentation of hand-foot and mouth disease?

A

□ Exanthema and enanthema
□ Painful lesions
□ Recovery in 5 to 10 days

49
Q

What is the presenting symptoms of paediatric HIV/AIDS?

A
  • Recurrent common childhood RTIs
  • Persistent oral thrush
  • Erythematous papular rash
  • Generalised lymphadenopathy
  • Recurrent/ disseminated VSV/ HSV infections
  • Failure to thrive
  • Developmental delays
  • Opportunistic infections: CMV pneumonia/ retinitis, PCP (pneumocystic joroveci pneumonia)
50
Q

Discuss chronic granulomatous disease

A

○ 65% x-linked, 35% autosomal recessive
○ Life threatening recurrent severe bacterial and fungal infections
○ Diagnosis: DHR test
○ HSCT as curative treatment option

51
Q

Discuss invasive fungal infections

A

○ Presenting symptom of primary immunodeficiency
○ In children with neutropenia due to leukaemia and/or chemotherapy
○ Invasive candidiasis in premature neonates due to immature (but physiological) immune system
○ In children admitted to PICU and treated with broad spectrum antibiotics and/or abdominal surgery

52
Q

Discuss candida infections

A
○ Endogenous
○ Birth canal, hands of health care worker's
○ Positive blood cultures 
○ Candidemia
○ Budding of yeast-cells
○ Pseudo hyphae in tissues 
○ Metastatic foci
53
Q

Discuss Aspergillus infections

A
○ Exogenous
○ Air, water, environment 
○ Negative blood cultures 
○ No sporulation in vivo
○ Hyphal growth in tissue
○ Angio-invasive