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Paeds Vivasinfectious-diseases

Paeds Vivas · infectious-diseases

Fever in the returned traveller — branching viva

Branching structured-oral viva on the febrile returning child: the travel history, the same-day malaria film and the single-negative-film pitfall, the five must-not-miss causes, the AQUAMAT evidence for IV artesunate, the dengue critical phase, XDR typhoid empiric therapy, and the public-health responsibilities of notification and isolation.

branching clinical structured oral5 min readVerification in progress

Target exams

RACP DCEMRCPCH ClinicalRCPSC Pediatrics
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Study tools

Target exams

RACP DCEMRCPCH ClinicalRCPSC Pediatrics
Prompt
You are the general paediatrician in the emergency department. A six-year-old boy is brought in with three days of high fever, headache and increasing drowsiness, five days after returning from a three-week visit to grandparents in rural Papua New Guinea. He took no malaria prophylaxis. The registrar asks you what the single most important action is and how you will manage him.

Opening question

Examiner: The registrar asks what the single most important action is. What is it, and why? [2]

Candidate: The single most important action is to recognise that this child has possible severe falciparum malaria and to send a same-day thick and thin malaria blood film in the first blood draw. The frame is that a febrile child who has been in a malaria-endemic area has falciparum malaria until a competent film proves otherwise — and this child is drowsy, acidotic and splenomegalic, so he is not just possibly infected, he is possibly severe. The film is part of the resuscitation, not a downstream test. [11]

Examiner: What else will you do in the first hour? [6]

Candidate: A structured ABC assessment with a paediatric early-warning score, high-flow oxygen for the respiratory distress, and intravenous access. In the same first draw I send a full blood count and film, venous gas and lactate, glucose, urea and electrolytes, liver function tests, C-reactive protein, blood cultures and a urinalysis. I give empiric ceftriaxone because bacterial sepsis cannot be excluded and dual pathology occurs, and I hold IV artesunate ready, because if the film confirms malaria and he is severe, he receives it immediately. [11] [6]

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References7ShowHide
  1. [1]Freedman DO; Weld LH; Kozarsky PE; et al Spectrum of disease and relation to place of exposure among ill returned travelers. N Engl J Med, 2006.PMID 16407507
  2. [2]Wilson ME; Weld LH; Boggild A; et al Fever in returned travelers: results from the GeoSentinel Surveillance Network. Clin Infect Dis, 2007.PMID 17516399
  3. [5]Dondorp AM; Fanello CI; Hendriksen IC; et al Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet, 2010.PMID 21062666
  4. [6]Lalloo DG; Shingadia D; Bell DJ; et al UK malaria treatment guidelines 2016. J Infect, 2016.PMID 26880088
  5. [7]Bhatt S; Gething PW; Brady OJ; et al The global distribution and burden of dengue. Nature, 2013.PMID 23563266
  6. [10]Hagmann SHF; Angelo KM; Huits R; et al Epidemiological and Clinical Characteristics of International Travelers with Enteric Fever and Antibiotic Resistance Profiles of Their Isolates: a GeoSentinel Analysis. Antimicrob Agents Chemother, 2020.PMID 32816733
  7. [11]Kiang KM; Bryant PA; Shingadia D; et al The treatment of imported malaria in children: an update. Arch Dis Child Educ Pract Ed, 2013.PMID 23171589
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