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PBL SEMINAR. FEVER IN A RETURNED TRAVELLER. OUR PATIENT CASE. Our patient is Jenny Randall , a 23 y.o. female student who presents to her local doctor with cough and fever having recently returned from a 3 week holiday. IMPORTANT. What’s common is common The diagnosis is
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PBL SEMINAR FEVER IN A RETURNED TRAVELLER
OUR PATIENT CASE Our patient is Jenny Randall, a 23 y.o. female student who presents to her local doctor with cough and fever having recently returned from a 3 week holiday
IMPORTANT • What’s common is common • The diagnosis is MALARIA MALARIAMALARIA until proven otherwise.
Travel History: CHOCOLATES • Country of birth • Housing • Occupation • Contacts • Other drugs • Leisure time • Animals • Travel • Eating and Drinking • Sexual history
Take Jenny’s History • HOPC • Travel History: CHOCOLATES
Travel History: CHOCOLATES • Country of birth • Housing • Occupation • Contacts • Other drugs • Leisure time • Animals • Travel • Eating and Drinking • Sexual history
Jenny’s History • Ms Jenny Randall, a previously well 23 year old medical student, presents to her local doctor with a cough and fever. • Jenny recently returned from a 3 week trip to Thailand, Cambodia and Vietnam. • In the 3 days leading up to her presentation at the clinic, Jenny experienced the following symptoms: • fevers • rigours • myalgia • mild non-productive cough • malaise • mild headache • No relevant past medical history • Family history of CVD- father died of AMI at 58 • Medications • OCP • Paracetamol for fever • NKDA • Social History • Smokes 10-20 cigarettes/day, • no ETOH, • one regular and one new sexual partner in past 6 months, uses condoms 100 % of the time
TRAVEL SPECIFIC QUESTIONS • Born in Australia • Travelled to Vietnam via Thailand and Cambodia for 3 weeks during the hot/rainy season • Returned for two weeks before becoming unwell • Stayed in budget, sometimes crowded accommodation throughout recent travel • Exposure to water, mosquitoes, flies • Recent contact has a 'cold' • Took prophylactic Doxycycline for one week before discontinuing • Had pre-travel Typhoid and HepA immunisation and previous HepB immunisation • Often prepared own food, no GI symptoms
!~RED FLAG~! • What symptom stands out as a red flag? • RIGORS! • What are rigors? • Episodes of uncontrollable shakes with or without teeth chattering lasting 15 minutes or more. • What causes them? • Bacterial sepsis e.g. From biliary sepsis or pyelonephritis, visceral abscesses, pneumonia • Malaria • Influenza • Why can we not ignore rigors? • Causes can be immediately life threatening and are treatable!! • !~Admit patient with rigors to hospital~!
Pyrexia of Unknown Origin (PUO) Definition: In adults: T>38.3 for>3 weeks with no known origin despite appropriate Ix. • Approach: - identify cause • Detailed history and regular examination • Confirm temperature objectively, ?admission, ?physiological with circadian pattern • Guide investigation based on initial test results • Blind investigation may be necessary • FBE, ESR, U+E, CRP, LFT, ANA, RhFx, TFT • Regular cultures (any fluid – blood, sputum, urine, stool, CSF) • CXR, CTA, echo • CT, IVP, MRI, PET • Treatment – ideally symptomatic prior to Dx • Empirical A/B therapy may mask an infectious Dx • Empirical steroid therapy may mask inflammatory response w/o treating cause • Undiagnosable PUO – Sx usually spontaneously resolve, good prognosis • Excluded from case differential
Special points for an ID Ex • Gen Inspection • Room • Sputum cup • O2 • IV – anything running • Drain tube • Catheter – check urine • Temp chart • Patient • Distress (RR, diaphoretic, conscious state) • Rash – blanching/non- • Track marks IVDU • Any lines – sepsis? • Weight loss – chronic illness • Hands • Janeway • Splinters • Osler’s nodes • Erythema • Track marks • Bruising, petechiae • Phlebitis • Arthropathy, raynauds - CTD • Face • Eyes – Roth spots (fundoscopy), pallor, jaundice (BW fever) • Mouth – hygeine, ginigivitis, abscess • Neck – lymphadenopathy • Chest • Crepitations, consolidation • Praecordium • New murmur • Abdomen • Tenderness? – localised? • Organomegaly • rashes • Genitourinary • Stool sample • Urinalysis • Discharge • orchitis • Legs • Rash • ulcers
On examination: • Chest clear. Full CVS, respiratory and abdominal examinations NAD • No rashes, joints appeared normal. • Vitals • HR 72 • BP 120/60 • RR 16 • T 36.2 With these history and examination findings, Jenny was sent home with a suspected viral URTI. The next day, Jenny re-presents with continuing fevers, having taken her own temperature measuring 36.9 that morning.
The Pattern of Fever Typical malarial fever patterns - not necessarily useful diagnostically • Timeline of Jenny’s ‘fever’ • Day 1 – onset of disease – T? • Day 4 – visit doctor – 36.2 • Day 5 – 10am – 36.9 • Day 5 – afternoon – 36.9 • Day 5 – night – 38.5 • *NO FEVER RECORDED until day 5* • Doesn't always follow typical pattern in all patients • Typically – may be afebrile for days • Atypically (common) – may be febrile or afebrile the entire length of the disease • Accurate recording procedure • Hx of fever given by reliable witness should not be ignored even if it is recorded as afebrile.
DDx!! • Malaria (parasite) • Typhoid (bacteria) • Dengue fever (virus) • Hepatitis A • We want to rule these out before progressing to investigate for other conditions common in returned travellers. THE BIG FOUR
Other Infections To Be Considered in Returned Travellers Developing Countries • Bacterial sepsis other than typhoid (such as meningococcal sepsis, sepsis from abdominal organ perforation, pneumonia, urosepsis) • TB • Dysentry • Schistosomiasis • Amoebic liver abscess • Tick typhus • Viral haemorrhagic fevers other than Dengue World Wide • Influenza • Atypical pneumonia • URTI/viral infection • STI including acute HIV infection • UTI • Pyelonephritis
Incubation Periods • Incubation period: time elapsed between exposure to a pathogenic organism and the onset of symptoms • Jenny returned home 2 weeks prior to feeling unwell (14 day incubation) • no actual fever recorded until 5 days later however atypical presentation is common
BASIC PATHOPHYS. STRAINS OF MALARIA
THE MALARIAL CYCLE 1) MOSQUITO VECTOR 2) EXTRA-ERYTHROCYTIC 3) ERYTHROCYTIC PHASE
Malarial Immunology • Immunological evasion by Malaria – • Malaria avoids WBCs by invading the body’s own cells and using these “self” antigens as a mask for infection. The body only has a chance of reacting during a lysis cycle when the parasites are free in the blood, though time is limited. • Splenic removal is the only effective method of removal. Protozoal aggregation in small capillaries counters this – causes complications
Jenny’s Ix Findings • FBE • HB 110, WCC 7.0, Plt 110 • HB 100, WCC 7.3, Plt 90 • HB 90, WCC 7.2, Plt 96 • HB 95, WCC 7.2, Plt 115 • UECs • Na 140, K 4.0, Ur 7.0, Cr 110 • LFTs • Mildly elevated ALT and bilirubin,otherwise normal • Atypical pneumonia - Legionella, Chlamydia species, Mycoplasmapneumoniae, Pneumocystisjiroveci serology - pending • CXR - clear • Malarial Thick and Thin Film • Negative • Positive for plasmodium falciparum, parasite count 0.2% • parasite count 0.1% • parasite count 0% • Hep A serology - Total Ab positive, IgM negative • Hep B serology - Surface Antibody positive, surface negative • Arbovirus (dengue) serology - negative • HIV serology - negative • Pregnancy Test - negative
Malarial Thick and Thin Blood Films • 3 thick and thin smears 12-24hrs apart should be obtained • Highest yield of peripheral parasites occurs during or soon after a fever spike; however smears should not be delayed to await a fever spike. • Thin Films - qualitative (speciation) • Thick Films - quantitative (parasite count)
Determining types of malaria Histological Differences
Slides • Plasmodium falciparum • P vivax • P ovale • P malariae • Normal
Incidence • 3 billion people (1/2 world’s population) living in areas at risk • 1-2 million deaths per year • 5th most common cause of death from infection worldwide • 2nd most common cause of death from infection in Africa
Where malaria occurs Most countries in the tropics 107 countries
Transmission patterns • Social and Economic Toll • Cost to individuals • Cost to government
Risk factors for travellers • Destination • Season • Accommodation • Activities • Failure to carry out protective measures • Taking counterfeit or substandard anti-malarials Who is the most vulnerable? • Young children • Pregnant women • Immunocompromised individuals • Immigrants from endemic areas living in non-endemic areas