Fever in the returning traveller Flashcards

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1
Q

What are key elements of a travel history?

A
  • Where did you go? → Be specific Include stop-overs Rural or urban
  • When did you go? → Exact dates Timing of symptoms
  • Why did you go? → Visiting friends and relatives etc.
  • What did you do? → Activities
  • What pre-travel vaccines/malaria prophylaxis did you take?
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2
Q

What is the epidemiology of tropical diseases in London?

A
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3
Q

What are the differentials for fevers with clinical findings?

A
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4
Q

Most likely diagnosis?

A

Malaria

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5
Q

Rapoid diagnostic test = RDT

How can you tell its falciparum?

What other information would you like?

  • Glucose
  • Lactate
  • LDH
  • Parasitaemia
  • Something else
A

Parasitaemia - helps guide tx

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6
Q
A

IV Artesunate

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7
Q

Describe the epidemiology of malaria?

A
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8
Q

How many cases of Malaria do we see in the UK? What type are they?

A

1500/ year

Usually falciparum but also vivax

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9
Q

What are the different species of plasodium?

A
  • Plasmodium falciparum - Double-dotted rings
    • Invades erythrocytes of all ages
    • Can be life-threatening
    • Can be drug-resistant
  • Plasmodium vivax “Schaffner’s” dots
  • Plasmodium ovale Enlarged red cells, comet forms, “Schaffner’s” dots
  • Plasmodium malariae Daisy-head appearance; square ring-forms
  • Plasmodium knowlesi
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10
Q

Describe the life cycle of malaria?

A

Vivax and oval also have a liver stage

  • Within humans, there is an erythrocytic stage and an exo-erythrocytic stage
  • Malaria breaks down red cells  haemolysis
  • There is also a liver stage (where the parasite lies dormant in the liver)
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11
Q

What is the prevention and pre-travel advice for malaria?

A
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12
Q

How does malaria present?

A
  • Fevers – cyclical or continuous with spikes
  • Malaria paroxysm – chills, high fever, sweats
  • SEVERE malaria → end-organ damage:
    • High parasitaemia (>2%) or schizont
    • Altered consciousness with/without seizures
    • ARDS
    • Circulatory collapse
    • Metabolic acidosis
    • Renal failure, haemoglobinuria (blackwater fever)
    • Hepatic failure
    • Coagulopathy ± DIC
    • Severe anaemia
    • Hypoglycaemia
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13
Q

How do we diagnose malaria?

A
  • 3 thick and thin blood smears:
    • Field’s or Giemsa (better for species identification) stain
    • Thick: screen for parasites (sensitive)
    • Thin: identify species and quantify parasitaemia
      • Quantifying involves looking at the proportion of red cells that are parasitised
      • Parasitaemia:
        • Child, severe = >2%
        • Adult, severe = >10%
  • Malaria antigen detection tests (rapid antigen test):
    • Paracheck-PF (Detect plasmodial HRP-II (Histidine-Rich Protein II))
    • OptiMAL-IT (Detect parasite LDH=
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14
Q

Summarise : How do we treat malaria?

A
  • Chloroquine – 3 days
  • Eradicate hypnozoites → Primaquine – 14 days (if G6PD normal)
    • If G6PDD, primaquine causes cell haemolysis
    • Effective in the hypnozoite/liver stage
    • Complications = splenic rupture  80% fatality
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15
Q

How do we treat mild falciparum?

A
  • Adults  Oral malarone (atovaquone and proguanil), QDS, 3 days
  • Children  Artemisinin Combination Therapy (ACT)
    • Artemisinin; AND
    • Lumefantrine Mild if not vomiting**, parasitaemia <2%/<10% and ambulant
  • Oral quinine, TDS  doxycycline, OD, 7 days
    • Not used frequently
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16
Q

How do we treat severe falciparum?

A
  • ABC approach
  • Correct hypoglycaemia
  • Cautious hydration (avoid overload)
  • Organ support is necessary
  • IV Artesunate > IV quinine
    • Quinine SEs = cinchonism (tinnitus, dizziness, N&V), arrhythmias, hyperinsulinaemia
    • Hyperinsulinaemia → worst hypoglycaemia
  • Daily parasitaemia monitoring
  • Follow on with oral antimalarials
17
Q
  • 53yo male, returned from Thailand (n.b. city travel > rural)
  • PC – 1/52 fever, headache, joint pain, rash
  • HPC:
    • Return from Thailand 5/7 before admission
    • Similar symptoms 1/52 prior to these – unwell for 3 days then got better. Had Amoxicillin.
    • Painful joints
    • No malaria prophylaxis
  • Examination:
    • T 39 BP 130/80 HR 90
    • Conjunctival injection
    • Cardiorespiratory, abdominal examination – unremarkable
  • Further examination:
    • CXR – clear WCC 2.3 (lymphopenia – i.e. virus)
    • Plts 40 Hb 140 Alb 28, ALT 15 CRP 30

Impression: Undifferentiated fever with a rash (‘sun-burn’-like)

A

Dengue

18
Q

How is dengue transmitted?

A

Aedes mosquito

19
Q

What type of virus is dengue? Where can you get it? How serious is it? What is the incubation period? What is try most common symptom?

A
20
Q

How do we prevent dengue?

A
21
Q

What are the clinical features, ix and management of dengue?

A
22
Q

What is the clinical course of dengue?

A
23
Q
  • 33yo, Indian lady, born in the UK
  • PC – fever, sweats, constipation, dry cough
  • HPC:
    • Fortnight in India 2/52 prior
    • Anorexia, 5kg weight loss, diarrhoea before constipation
    • Confused/ vacant
    • PMHx – Ix for nephrotic syndrome at HH
  • Examination:
    • T 39C BP 110/70 P: 55, Sats 98%, RR=30
    • HS = I+II, Gallop rhythmJVP-angle of mandible
    • Chest – fine bibasal inspiratory creps
    • Abdomen – mild suprapubic tenderness
  • Further tests:
    • WCC 5.7 Plts 150 ALT 66, Alb 18
    • CRP 330 Hb 130 Cr 140, Ur 15
    • CXR – clear
    • ECG – peaked p-waves (‘p pulmonale’
  • Impression: a high fever with a relatively (to the fever) normal HR
    • A fever should send the HR much higher
    • If this does not occur → “Faget Sign”
  • Investigations:
    • Malaria negative; HIV negative
    • Blood culture – gram negative rods on day 3
A
  • Diagnosis: Typhoid fever / Enteric Fever (from Salmonella typhi)
24
Q

Why causes typhoid? What is the incubation? What is the vaccine? Where is it more common?

A
  • Caused by Salmonella typhi or paratyphi
  • Gram-negative rod
  • Insidious onset (incubate 7-18 days; up to 60d)
  • Most imported from South Asia (Indian Subcontinent)
  • Vaccine is only partially protective against S. typhi and offers no protection against S. paratyphi
25
Q

What are the clinical features? incubation period? Complications? Ttre ament?

A
26
Q
A