Fever in a Returning Traveller Flashcards

1
Q

State some common causes of a fever in a returning traveller

A
  • Malaria
  • Dengue
  • Rickettsia
  • Typhoid fever
  • Primary HIV infection
  • Chronic bacterial infections
  • TB
  • Parasitic infections
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2
Q

What are the most common tropical infections seen in clinical practice?

A
  • Malaria
  • Dengue fever
  • Typhoid (enteric fever)
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3
Q

What questions must you ask in the history of someone presenting with fever ONCE you have established that they have been travelling?

A
  • Where? (particularly interested in tropic regions)
  • When did they go?
  • How long did they stay for?
  • Find out the time of onset and nature of various signs & symptoms (in other words make a detailed time line)
  • Where did they stay? (was it a modern hotel or a hostel in rural area. Did they stay with family & friends?)
  • What did they do whilst they were there: recreational activities & exposure?
  • What food did they eat?
  • Sexual history inlcuding sexual exposure whilst abroad and at home
  • Did they have any pre-travel immunizations & chemoprophylaxis?
  • PMH and any predisposition to infection e.g. immunosupressed
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4
Q

When asking about pre-travel immunizations and chemoprophylaxis in a returning traveller, what questions do you want to ask?

A
  • Vaccination against specific diseases e.g. hepatitis A, hepatitis B, typhoid, tetanus
  • Childhood vaccinations e.g.MMR and others such as yellow fever & rabies when appropriate
  • If travel was to malarious area ask whether malaria chemoprophylaxis was taken and ask/investigate as to whether it was taken as directed/correctly. Also ask about personal protective measures e.g. insect repellant, bed-net use etc…
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5
Q

Most of the severe, rapidly progressive infections (e.g. falciparum malaria & haemorrhagic fevers) acquired in tropical or developing countries become apparent within how many months?

A

1-2 months

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6
Q

State some diseases with the following incubation times:

  • 0-10 days
  • 10-21 days
  • >21 days
A
  • 0-10 days: dengue, rickettsia, GI infections
  • 10-21 days: malaria, typhoid, primay HIV
  • >21 days: malaria, TB, parasitic infections, chronic bacterial infections e.g. brucella, joint & bone infections, endocarditis
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7
Q

When examining a returning traveller with fever you must do a thorough clinical examination; what specific organ systems/organs must you pay close attention to and why?

A
  • Cardiovascular: pulse rate that is slow for degree of fever- think typhoid fever
  • Skin:
    • ​Maculopapular rash: dengue, leptospirososis, rickettsia, infectious mononucleosis, primary HIV infection
    • Rose spots: typhoid fever
    • Black necrotic ulcer with erythematous margins: rickettsia
    • Petechia, echhymoses or haemorrhagic lesions: dengue, meningococcaemia & viral haemorrhagic fever
  • Eyes: conjunctival suffusion in leptospirosis
  • Splenomegaly: mononucleosis, malaria, typhoid, brucellosis
  • Neurological system: meningo-encephalitis
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8
Q

What investigations would you consider for a returning traveller presenting with a fever?

A
  • FBCs
  • LFTs
  • U&Es
  • Malaria smears +/- antigen detection dipstick x3 over 24-48hrs
  • Blood cultures x2
  • Urinalysis +/- urine culture
  • Stool culture +/- stool for OVA, cysts and pararsites
  • CXR
  • HIV, hep B, hep C and syphilis serology
  • Acute serology tube to be saved in lab
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9
Q

What is malaria?

A

Infectious disease caused by Plasmodium family of protozoan parasites

(protozoa= single celled organisms)

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10
Q

Discuss how malaria is transmitted

A
  • Spread through bites from female Anopheles mosquitos
  • Mosquito feeds on infected blood. Malaria then reproduces in gut of mosquito producing thousands of sporozoites (malaria spores)
  • The now infected mosquito goes and bites another human/animal and injects a number of malarial sporozoites
  • These malarial sporozoites travel via blood to infect hepatocytes. Once in hepatocytes they can lie dormant as hypozoites for several years (as in P.vivax and P.ovale) or undergo reproduction (at this point no symptoms occur i.e. this is incubation period)
  • Sporozoites in liver become schizonts which rupture to release merozoites into bloodstream
  • Merozoites invade erythrocytes, reproduce in RBCS over a period of 48hrs, and cause RBCs to rupture; resulting in massive release of merozoites and a haemolytic anaemia
  • RBC rupture causes cytokine activation by leucocytes producing characteristic malarial symptoms & fever
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11
Q

State the 5 plasmodium species which can cause malaria

A
  • Plasmodium falciparum
  • Plasmodium vivax
  • Plasmodium ovale
  • Plasmodium malariae
  • Plasmodium knowlesi
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12
Q

Which plasmodium species causes the most severe malaria?

A

P.falciparum

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13
Q

Which two plasmodium species form hypnozoites in liver and consequently have a longer incubation period/can lie dormant for several years?

A
  • Plasmodium vivax
  • Plasmodium ovale
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14
Q

What is meant by tertian rhythm, in regards to malaria?

Why do pts get a tertian rhythm?

A
  • Pts with malaria get fever spikes every 48 hours (can also think of as getting fever every other day or every 3rd day if you count first day of fever as day 1)
  • Merozoites which are released from schizonts in liver infect and reproduce in RBCs; their reproduction in RBCs takes 48hrs. They then cause RBC lysis and release lots more merozoites. These merozoites will then infect more RBCs and start the 48 hr reproduction cycle again. The RBC lysis causes cytokine activation by leucocytes producing characteristic symptoms & fever
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15
Q

Discuss how you can narrow down what the likely plasmodium species causing the malaria is based on how often pt experiences fever?

A
  • Fever every day: falciparium
  • Tertian rhythm (fever every 48hr/every 3rd day/every other day): falciparum, vivax, ovale
  • Quartan malaria (fever every 72hrs/every 4th day): malariae

*NOTE: falciparum can have classical tertian rhythm however it can also have daily RBC rupture leading to daily fevers. Plasmodium malaraie clasically has fever every 4th day. Can also use incubation times to help distinguish between falciparum, vivax and ovale.

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16
Q

What animals, and in what region, is Plasmodium knowlesi common?

A
  • Form of parasite found in southeast Asia primates
  • Malaria presenation may vary but severe disease can quickly become fatal due to rapid mulitiplicaiton of organisms
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17
Q

State some risk factors for developing malaria

A
  • Travel to an endemic area/where malaria is common
  • Lack of chemoprophylaxis
  • Lack of personal protective measures e.g. insect repellant, bed-net
  • Babies & young children have higher risk of developing malaria
  • Using contaminated needles
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18
Q

What regions is malaria common in?

A
  • Sub-saharan africa
  • South east asia
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19
Q

Discuss the incubation times of different species of plasmodium causing malaria

A
  • P.falciparum: 7-14 days
  • P.vivax & P.ovale: 12-18 days (but can be longer- months to years- due to hypnozoite stage in liver)
  • P.malariae: 18-40 days

*Therefore, can see that malaria typically presents within a month of infection

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20
Q

State some symptoms of malaria

A
  • Fever, sweats, rigors
  • Malaise
  • Myalgia
  • Headache
  • Nausea & vomitting
  • Vague abdo pain
  • Diarrhoea (in up to 25%)
21
Q

State what you might find on clinical examination of someone with malaria

A
  • Pallor due to anaemia
  • Hepatosplenomegaly
  • Jaundice (pre-hepatic due to RBC lysis)
22
Q

State what investigations you would do if you suspect malaria, include:

  • Bedside
  • Bloods
  • Imaging

… for each justify why you are doing it/what you might find

A

Bedside

  • ABG: check for hypoxia (may be due to anaemia, microvascular obstruction etc…)
  • BMs: P.falciparum can cause hypoglycaemia
  • Urinalysis: may seen proteinuria if P.falciparum has caused AKI with hameoglobulinuria & proteinuria

Bloods

  • Thick & thin blood smear with Giemsa stain- 3 samples over 3 consecutive days
  • Rapid diagnostic antigen tests
  • FBCs: normocytic anaemia, leukopenia
  • U&Es: may show AKI as complication of P.falciparum malaria
  • LFTs: raised unconjugated bilirubin, abnormal liver enzymes
  • Clotting: P.falciparum can cause DIC
  • G6PD levels: must check before giving anti-malarial medication

Imaging

  • ?CXR: check for pulmonary oedema
23
Q

Which blood bottle do you use to obtain blood for blood smear for malaria?

A

EDTA bottle (small red top bottle which you use for FBC)

24
Q

Why do you need to do 3 blood films on 3 consecutive days to exclude malaria?

A

Due to 48hr cycle of merozoites being released into blood. Sample may be negative on days when parastie not released but positive a day or tow later when merozoites are released from RBCs

25
Q

Discuss the difference between thin and thick blood films including what each is used for

A

Thick

  • Analyses larger volume of RBCs
  • Sample is ‘laked’ to rupture RBCs
  • Used to identify if parasite is present

Thin

  • RBCs not lysed/ruptured
  • Used to idenitfy Plasmodium species and calculate the % of RBCs infected with parasites
26
Q

State some symptoms, signs and laboratory results that may indicate a pt has severe malaria

A

Symptoms & Signs

  • Impaired consciousness
  • Prostration (generalized weakness meaning pt is unable to sit up or walk without assitance)
  • Seizures/convulsions (>2 in 24hr)
  • Deep breathing
  • Circulatory collapse or shock
  • Clinical jaundice and evidence of other vital organ dysfunction
  • Abnormal spontaneous bleeding

Laboratory results

  • Hypoglycaemia
  • Metabolic acidosis
  • Severe normocytic anaemia
  • Hyperparasitaemia (>2%)
  • Hyperlactaemia (>5mmol/L)
  • AKI
  • Pulmonary oedema
27
Q

What enzyme level must you check prior to giving anti-malarial drugs?

A

G6PD

28
Q

Discuss the management of non-severe and/or non-falciparum malaria

A
  1. Chloroquine: effective against most non-falciparum malaria
    • If P.vivax or P.ovale also treat with primaquine as it is used to destroy liver hypnozoites
29
Q

Discuss the management of severe malaria of any species and of falciparum malaria- include management of complicated & uncomplicated

A

All pts with falciparum malaria must be admitted for treatment as they can deteriorate quickly. Although we talk about treatement for non-falciparum malaria, if a pt has severe non-falciparum malaria we will treat them as per complicated falciparum guidelines.

Uncomplicated falciparum- treat with oral:

  1. Artemether with lumefantrine (Riamet)
  2. Proguanil and atovaquone (Malarone)
  3. Quinine sulphate followed by doxycycline

Complicated falciparum- treat with IV:

  1. ​Artesunate & doxycycline
  2. IV quinine dihydrochloride with ECG monitoring

NOTE: 1= first line, 2= second line etc

30
Q

State some potential complications of P.falciparum malaria

A
  • Cerebral malaria
  • Seizures
  • Reduced consciousness
  • AKI
  • Pulmonary oedema
  • DIC
  • Severe haemolytic anaemia
  • Multi-organ failure & death
31
Q

State some general advice you can give to pts travelling to areas with malaria

A
  • Raise awareness of locations that are high risk
  • Advice that no method is 100% effective alone
  • Use mosquito spray in mosquito exposed areas
  • Use mosquito nets and barriers in sleeping areas
  • Seek medical advice if symptoms develop
  • Take antimalarial medication as reccomended
32
Q

Antimalarial medications are around 90% effective at preventing infections. State the 3 options of antimalarials

A
  • Malarone (proguanil & atovaquone)
    • ​​​Take daily 2 days before, during & 1 week after being in endemic area
    • Most expensive but best side effect profile
  • Mefloquine
    • Take once weekly 2 weeks before, during & 4 weeks after being in endemic area
  • Doxycycline
    • Take dialy 2 days before, during & 4 weeks after being in endemic area
33
Q

State some side effects of the following anti-malarial drugs:

  • Malarone
  • Mefloquine
  • Doxycycline
A

Malarone (proguanil & atovaquone)

  • Headaches, nausea

Mefloquine

  • Diarrhoea, neuropsyhchiatric symtpoms e.g. insomnia, dizziness, bad dreams, mental clouding, seizures

Doxycyline

  • Diarrhoea, thrush, photosensitivity
34
Q

What is dengue fever?

Discuss the difference between dengue fever and dengue haemorrhagic fever

A

Disease caused by dengue viruses-which belong to flavivirus family- which is transmitted by the mosquito Aedes aegypti. Dengue fever can be mild causing fever, rash, myalgia & arthralgia or it can be severe (in which case it is called dengue haemorrhagic fever) causing fever, bleeding, shock and potentially death.

35
Q

In what regions is dengue fever present?

A
  • South America
  • Southeast Asia
  • Africa
36
Q

What is the incubation time for dengue?

A

~8 to 10 days

37
Q

What are the symptoms & signs of dengue fever?

A
  • Skin flushing (with islands of normal skin) which may develop into maculpapular rash
  • Fever
  • Headache
  • Pain behind eyes
  • Myalgia
  • Arthraglia
  • Nausea & vomitting
  • Abdo pain
  • Loss of appetite
    *
38
Q

What investigations would you do if you suspet dengue fever, include:

  • Bedside
  • Bloods
  • Imaging

… for each justify why you are doing it/what results will be

A

Bedside

  • Positive tourniquet test

Bloods

  • FBCs: thrombocytopenia, leukopenia
  • LFTs: elevated AST & ALT (AST:ALT >2 support diagnosis of DHF)
  • Albumin: suggests plasma leakage and support diagnosis of DHF
  • Dengue serology
  • RT-PCR

Imaging

  • ?CXR: if think may be pleural effusion
39
Q

Most cases of dengue haemorrhagic fever occur in children; true or false?

A

True

40
Q

What is meant by a positive tourniquet test in dengue fever?

A
  • Inflate BP cuff to midway between diastolic and systolic BP and leave for 5 mins
  • Count the number of petechiae per square inch (in area where BP cuff was inflated)
  • >20= positive result
41
Q

Discuss the management of dengue fever

A

Pts are classified into 3 groups (A,B,C) based on WHO guidance; this aims to identify severity of infection. Pts who are in group A can be managed at home. Group B & C pts require hospital treatment (with group C requiring emergency treatment).

Treatment is with fluids, antipyretics and transfusion of blood proudcts as needed.

42
Q

What is typhoid fever?

A

Infection caused by Salmonella typhi or Salmonella paratyphi. Transmission route is via faecal-oral (e.g. drink water that has been contaminated with infected persons stools).

*NOTE: typhoid infection is disease caused by Salmonella typhi. Enteric fever is disease caused by Salmonella paratyphi. The terms typhoid infection and enteric fever are used to describe both diseases; hence, why it can be caused by either.

43
Q

What regions is typhoid fever common in?

A
  • Asia
  • Africa
  • Middle east
  • Southern & central America

*In places with poor sanitisation

44
Q

State some signs & symptoms of typhoid fever

A

Symptoms

  • Sustained fever
  • Anorexia
  • Malaise
  • Vague abdo discomfort
  • Constipation or diarrhoea
  • Dry cough

Signs

  • Pulse-temperature dissociation (low pulse rate for temperature)
  • Hepatosplenomegaly
  • Rose spots on chest & abdomen (30-50%- but may disappear before presentation)
45
Q

What laboratory findings might you find in a pt with typhoid fever?

A

Laboratory findings are non-specific:

  • Leucopenia
  • Lymphopenia
  • Raised CRP
46
Q

How do you diagnose typhoid fever?

A

Isolation of organisms in blood cultures (detects 80-100% of cases if you take 2 cultures). Can also take stool, urine and bone marrow cultures.

47
Q

Discuss the management of typhoid fever

A
  1. Empiral antibiotics: IV ceftriazone 2g OC
  2. Once sensitivities known switch to:
    • PO ciprofloxacin 500mg BD
    • or PO azithromycin 500mg OD
48
Q

Are there any vaccines against typhoid fever and if so how effective are they?

A

Vaccines ~70% effective

49
Q

If a pt is travelling to an area where typhoid is prevalent, alongside vaccination what else can you offer?

A

Advice such as:

  • Only drinking bottled or boiled water
  • Avoiding foods that could be potentially contaminated