Infection Flashcards

1
Q

What is TORCH?

A

Congenital and neonatal infections:

  • Toxoplasmosis
  • Other (syphilis, parvovirus, VZV, HIV, HBV)
  • Rubella
  • CMV
  • HSV
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2
Q

What is the management of toxoplasmosis?

A
  • Pyrimethamine
  • Sulfadiazine
  • Calcium folinate
  • +Consider prednisolone
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3
Q

What is the management of Syphilis?

A

IM benzathine penicillin

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4
Q

What is the management of parvovirus?

A

Intrauterine = blood transfusion if foetal hydrops
Infant = self-limiting

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5
Q

What is the management of VZV?

A

Mild:

  • Supportive care (e.g. hydration, paracetamol, skin emollients, antihistamines)

Moderate:

  • Oral acyclovir
  • +Supportive care

Severe:

  • IV acyclovir
  • +Supportive care
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6
Q

What is the management of HBV?

A
  • Complete course of HBV vaccination (for all infants of mothers who are HBsAg +ve)
  • Blood test at 12m for HBV infection
  • Mother = tenofovir disoproxil OR lamivudine (no risk of transference through breastfeeding)
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7
Q

What is the management of Rubella?

A
  • Refer to foetal medicine unit and notify HPU
  • Rest, adequate fluids, analgesia
  • Infant = cardiac scans, hearing tests
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8
Q

What is the management of CMV?

A

IV ganciclovir or oral valganciclovir

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9
Q

What is the management of HSV?

A

Acyclovir
if neonate exposed on delivery

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10
Q

What is the management of GBS?

A

Baby:

  • Benzylpenicillin or ampicillin PLUS gentamicin
  • Supportive therapy

Mother (during labour):

  • IV benzylpenicillin
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11
Q

What is the cause and consequence of listeria monocytogenes?

A
  • Mother has mild influenza-like illness and passes to child in placenta
  • Can cause spontaneous abortion, PTL, neonatal sepsis
  • Mortality = 30%
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12
Q

What are the S/S of listeria monocytogenes?

A
  • Meconium stained liquor (MSL) in preterm infant
  • Widespread rash

Can cause:

  • Sepsis
  • Pneumonia
  • Meningitis
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13
Q

What is the management of listeria monocytogenes?

A
  • IV ampicillin
  • +Gentamicin (if severe infection)
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14
Q

What is Kawasaki Disease?

A

Systemic vasculitis disease
characteristically affecting young children (<5yrs)

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15
Q

Who does Kawasaki Disease affect?

A
  • Children 6m-4yrs (peak 1yr)
  • Japanese, Black-Caribbean ethnicity
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16
Q

What are the S/S of Kawasaki Disease?

A

(CRASH + Burn)

  • C = conjunctivitis (bilateral)
  • R = rash (polymorphous, begins hands/feet)
  • A = adenopathy (cervical lymphadenopathy)
  • S = strawberry tongue
  • H = hands + feet swollen / red (and desquamate/peel)
  • Burn = fever >5d (not responsive to antipyretics)
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17
Q

What are the investigations for Kawasaki Disease?

A

Clinical diagnosis

  • FBC (inc. platelets), CRP, ESR
  • Echo
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18
Q

What is the management of Kawasaki Disease?

A

>ADMISSION

1st line: (if within 10d / ongoing inflammation)

  • IVIG
  • Plus high-dose aspirin
  • Consider corticosteroids

2nd line:

  • Infliximab, ciclosporin, plasmapheresis

If > 10 days / no ongoing inflammation:

  • Low-dose aspirin
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19
Q

What is the main complication of Kawasaki Disease?

A

Coronary aneurysms

Early dx key to stop coronary artery aneurysms forming > ECHO

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20
Q

What causes malaria?

A

Protozoa Plasmodium, spread by female Anopheles mosquito

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21
Q

What are the types of malaria?

A
  • Falciparum (most fatal)
  • Ovale
  • Malariae
  • Vivax
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22
Q

What are the S/S of malaria?

A
  • Onset 7-10d after inoculation (<1yr)
  • Fever (cyclical / continuous with spikes)
  • D&V
  • Flu-like sx > shaking, chills, night sweats, headache, myalgia
  • Jaundice
  • Anaemia
  • Thrombocytopaenia
  • Particularly susceptible to cerebral malaria, severe anaemia
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23
Q

What are the investigations for malaria?

A
  • 3 thick and thin blood films (detects parasites inside erythrocytes)
  • Malaria rapid diagnostic tests (RDTs) (detection of parasite antigen or enzymes)
  • Bloods: FBC, Clotting profile, U&Es, LFTs, BM, ABG
  • Urinalysis
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24
Q

What is the management of malaria?

A

General:

  • Bite-prevention (repellent and nets)
  • Prophylaxis - mefloquine
  • Arrange immediate admission (medical emergency)
  • Notify PHE

Non-falciparum:

  • 1st line = Chloroquine + primaquine / ACT

Falciparum:

  • Severe / complicated = IV artesunate (doe minimum 24hrs, then switch to ACT)
  • Uncomplicated = Artemisinin-based combination therapies (ACT)
  • +Supportive care (careful fluid management, renal support, airway protection, control of seizures, transfusion of blood products)
  • +/-ICU
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25
Q

What causes Typhoid Fever?

A

Salmonella typhi or paratyphoid

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26
Q

How is typhoid fever transmitted?

A

Faeco-oral transmission

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27
Q

What are the complications of typhoid fever?

A
  • GI perforation
  • Myocarditis
  • Hepatitis
  • Nephritis
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28
Q

Where have people with typhoid fever commonly travelled to?

A

Pakistan, India, Bangladesh

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29
Q

What are the S/S of typhoid fever?

A
  • Persistent high temperature that gradually increases each day
  • Relative bradycardia
  • Abdominal pain and distension
  • Constipation
  • Headache
  • Anorexia (WL+++)
  • Rose-spots on trunk
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30
Q

What are the investigations for typhoid fever?

A
  • Blood culture (diagnostic)
  • FBC, LFTs
  • Stool culture, urine culture
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31
Q

What is the management for typhoid fever?

A
  • 1st line = IV ceftriaxone + supportive care (antipyretics, fluids)
  • 2nd line (if resistant) = PO azithromycin
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32
Q

What causes Dengue fever?

A

Caused by dengue arbovirus transmitted by Aedes Aegyptii mosquito

33
Q

Where is dengue fever usually imported from?

A

SE Asia or South Africa

34
Q

What are the S/S of dengue fever?

A

Primary infection:

  • Headache (retro-orbital)
  • Fine erythematous sunburn-like rash
  • High fever and myalgia

Other:

  • Hepatomegaly, abdominal distension

Severe:

  • Low WCC, low platelets, haemorrhage

Dengue haemorrhagic fever (secondary infection):

  • Previously infected child > subsequent infection (different strain) > severe capillary leak, hypotension, haemorrhagic manifestations > fluid resus usually helps a lot
  • Due to partially effected host immune response augmenting the severity of the infection
35
Q

What are the investigations for dengue fever?

A
  • PCR viral antigen
  • Serology (positive IgM and IgG)
  • FBC, LFTs, serum albumin (low)
36
Q

What is the management of dengue fever?

A
  • Supportive (fluids and monitoring)
  • ITU (if increased deterioration / severe disease)
37
Q

What causes mumps?

A

Mumps orthorubulavirus

38
Q

How is mumps transmitted?

A

Respiratory secretions

39
Q

What is the timeline of mumps?

A
  • Long incubation period (15-24d)
  • Infectious 5d before and 5d after the parotid swelling (should pass totally in 1-2wks)

> Can still get infected if they had vaccine but likely to be reduced sx

40
Q

What are the S/S of mumps?

A
  • Asx (30%)
  • Headache, fever
  • Parotid swelling
  • Other > pancreatitis, neuritis, arthritis, mastitis, nephritis, thyroiditis, pericarditis
41
Q

What are the investigations for mumps?

A
  • Salivary mumps IgM
42
Q

What is the management of mumps?

A

General:

  • Notify HPU
  • Isolate for 5d from time of parotid swelling

Advise and educate:

  • Self-limiting condition
  • Supportive care (rest, analgesia, fluids)

Safety net for complications:

  • Mumps orchitis > infertility (very rare)
  • Viral meningitis > encephalitis (very rare)
  • Deafness (unilateral and transient)
43
Q

What causes measles?

A

Paramyxovirus

44
Q

How is measles transmitted?

A

Respiratory secretions

One of the most highly communicable diseases (>15m in direct contact is enough to transmit)

45
Q

What is the timeline of measles?

A

Incubation = 7-18d
Infective period = 4d before and 4d after rash

46
Q

What are the S/S of measles?

A
  • Prodrome = high fever, irritability, conjunctivitis, coryza, febrile convulsions
  • Maculopapular rash (face/neck > hands/feet)
  • Koplik spots (small white spots surrounded by red ring in mouth)
  • Cough
47
Q

What are the investigations for measles?

A
  • Measles specific IgG and IgM serology (ELISA)
  • 2nd line = PCR of blood or saliva
48
Q

What is the management for measles?

A

General:

  • Notify HPU
  • Advise it’s self-limiting but likely to cause unpleasant symptoms e.g. rash, fever, cough, conjunctivitis
  • Immunise close contacts and encourage vaccination after acute episode
  • Isolate for 4d after development of rash

Supportive tx

  • Fluids, antipyretics, rest
  • Children isolated in hospital
  • Vitamin A supplements if severe

Safety net for complications

  • Seek urgent medical advice if they develop complications such as: SOB, uncontrolled fever, convulsions / altered consciousness
49
Q

What are the complications of measles?

A
  • Otitis media (most common)
  • Encephalitis (after 102wks) > headache, lethargy, irritability, seizures, coma
  • Sub-acute sclerosing panencephalitis (SSPE) (after 7yrs) > measles dormant in CNS, dementia, death
  • Pneumonia
  • Keratoconjunctivitis
50
Q

What causes Rubella?

A

‘German Measles’ caused by Togavirus

51
Q

How is Rubella transmitted?

A

Spread through coughing and sneezing

52
Q

What is the timeline of rubella?

A
  • Incubation period = 6-21d
  • Infective period = 1wk before to 5d after rash onset
  • Illness period = 7-10d
53
Q

What are the S/S of rubella?

A
  • Prodrome = mild fever / asx
  • Pink maculopapular rash (face > whole body), fades in 3-5d
  • 20% > Forchheimer spots (red spots on soft palate)
  • Lymphadenopathy (suboccipital, postauricular)
  • > No Koplik spots or conjunctivitis
54
Q

What are the investigations for rubella?

A
  • Rubella serology (IgG and IgM) from oral fluid test
  • RT-PCR (2nd line)
55
Q

What is the management for rubella?

A
  • Notify HPU
  • Isolate for 4d after development of rash
  • Advise that it is a self-limiting disease
  • Supportive (fluids, analgesia, rest)
  • Safety net the complications (haemorrhagic complications due to thrombocytopenia)
56
Q

What does Parvovirus B19 cause?

A

“Fifth’s disease / erythema infectiosum / Slapped Cheek”

57
Q

How is parvovirus B19 transmitted?

A
  • Respiratory secretions
  • Vertical transmission
58
Q

When is a patient with Parvovirus B19 infectious?

A

10d before to 1d after rash develops

59
Q

What is parvovirus B19 in pregnancy associated with?

A

Hydrops fetalis

60
Q

What are the RFs for parvovirus B19?

A
  • HIV
  • Sickle cell
61
Q

What are the S/S of parvovirus B19?

A

1st:

  • Asx, or
  • Coryzal illness for 2-3d > latent for 7-10d

2nd:

  • Erythema infectiosum (most common)
  • Red ‘slapped cheek’ rash on face (viraemic phase of fever, malaise, headache, myalgia)
  • Progresses 1w later to maculopapular (lace) like rash in trunk and limbs

Aplastic crisis:

  • Occurs in children with chronic haemolytic anaemia (sickle cell) or immunodeficient

Foetal disease:

  • Maternal transmission
  • Leads to foetal hydrops, death due to severe anaemia
62
Q

What are the investigations for parvovirus B19?

A
  • B19 serology (IgM and IgG)
  • RT-PCR (2nd line)
63
Q

What is the management for parvovirus B19?

A
  • Supportive (fluids, analgesia, rest) > will clear in 3wks
  • Secondary arthritis may be treated with ibuprofen
  • No need to stay off school or avoid pregnant women (not infectious once rash develops)
  • Safety net complications (anaemia, lethargy, pregnancy)
64
Q

What causes chickenpox?

A

Varicella zoster virus (HHv-3)

> Reactivation of dormant virus after chickenpox leads to herpes zoster (shingles)

65
Q

What is the timeline of chickenpox?

A
  • Incubation period = 10-21d
  • Infectious period = 48hrs before rash to last crusted over lesion (5-7d after rash appears)
66
Q

What are the S/S of chickenpox?

A
  • Pyrexia, headache, abdominal pain, malaise
  • Crops of vesicles appear over 3-5d
  • Head, neck, trunk (less on limbs) > itchy
  • Papule > vesicle > crust > several stages at once
67
Q

What is the management of chickenpox?

A

Supportive:

  • Fluids, analgesia (no ibuprofen), rest
  • Advice > nail short, loose clothing, adequate fluid,
  • Isolate from > immunocompromised, pregnant women, neonates, keep off school

Admit if serious complications:

  • Secondary bacterial superinfection > sudden high fever, toxic shock, necrotising fasciitis
  • Encephalitis
  • Purpura fulminans > purpuric skin rash
  • Dehydration (severe)
  • Immunocompetent = oral acyclovir (if <24hrs of rash)
  • Immunocompromised = IV acyclovir > oral acyclovir

Prophylactic prevention:

  • Human VZV IVIG
68
Q

What causes hand, foot, and mouth disease?

A

Most commonly due to Coxsackie A16 virus

Severe = enterovirus 71
Atypical = Coxsackie A6

69
Q

What are the S/S of hand, foot, and mouth disease?

A
  • Painful, itchy, vesicular lesions (hand, foot, mouth, tongue, buttocks)
  • Mild systemic features > fever, sore throat, spots in mouth > develop into ulcers
70
Q

What is the management of hand, foot, and mouth disease?

A
  • Supportive > fluids, analgesia, rest (will clear in 7-10d)
  • Safety net > dehydration, if doesn’t clear up in 2wks, pregnancy
  • Don’t need to be kept off school but HPA recommend they do until better
71
Q

What causes Roseola Infantum?

A

HHV6
(Sixth disease / exanthum subitem)

72
Q

When are children infected with Roseola Infantum?

A
  • Most children infected by 2yrs (6m-2yrs)
  • Highly infectious during whole period of disease
  • > Infected VERY young compared to other infections
73
Q

What are the S/S of roseola infantum?

A

Fever followed later by rash

  • High fever and malaise (3-4d) > generalised macular (small pink spots) rash appears as fever wanes
  • Rash starts on neck/body and spread to arms, lasts 1-2d, non-itchy, blanching
  • Many have febrile illness and never develop a rash, commonly misdiagnosed as measles/rubella
  • Febrile convulsions in 10-15%
  • Sore throat, lymphadenopathy, coryzal sx, D&V
  • Nagayama spots (spots on the uvula and soft palate)
    >Lack of Koplik spots (white spots on buccal mucosa)
74
Q

What are the investigations of roseola infantum?

A
  • HHV6/7 serology (IgG and IgM)
  • Measles & rubella serology (similar presentation)
75
Q

What is the management of roseola infantum?

A
  • Supportive > fluids, rest, analgesia > will clear in ~1w
  • No need to stay off school
  • Safety net the complications > high fever, febrile convulsions
76
Q

What are the investigations for HIV in children?

A
  • > 18m = antibody detection (ELISA)
  • <18m (still have transplacental anti-HIV IgG from mother) = PCR of virus
  • > Measured at birth, on discharge, 6wks, 12wks, 18m
77
Q

What is the management of HIV in children?

A

Reducing Vertical Transmission:

  • C-section will be recommended
  • Cord clamped as soon as possible and baby bathed immediately after birth
  • Zidovudine monotherapy for 2-4wks (low/med risk) or PEP combination (high risk)
  • Women not to breastfeed
  • Give all immunisations including BCG (unless mod-high risk of transmission)

PCR HIV virons at 6 and 12w (at least 2 and 8w after stopping prophylaxis)

  • Baby will have passive IgG from mother up until at least 6m

Decision to start is based on a combination of clinical status, HIV viral load and CD4 count
IMPORTANT: infants should start ART shortly after diagnosis because they are at higher risk of disease progression

  • PCP prophylaxis with co-trimoxazole is given to infants who are HIV-infected, and for older patients with low CD4 counts

Other aspects of management:

  • Immunisation (except BCG)
  • MDT approach
  • Regular follow-up with particular attention to weight and developmental progress
78
Q

What is the management if an immunocompromised patient comes into contact with chicken pox?

A

Immunocompromised patients and newborns with peripartum exposure should receive varicella zoster immunoglobulin (VZIG).

If chickenpox develops then IV aciclovir should be considered