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Paeds Vivasinfectious-diseases

Paeds Vivas · infectious-diseases

Post-arrival infection screening — branching viva

Branching structured-oral viva on the comprehensive post-arrival infection screen for internationally adopted, immigrant and refugee children: the must-not-miss five, the re-verification principle, the IGRA-versus-tuberculin-skin-test choice, the Strongyloides serology that is too often missed, the hepatitis C confirmatory RNA test, the HIV PCR algorithm in the infant under eighteen months, the catch-up immunisation built on serology, and the trauma-informed, interpreter-mediated medical-home frame.

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 seeing a newly arrived refugee family. The parents have brought their four-year-old daughter for a post-arrival health check. They have an overseas folder of records in another language. The registrar asks you what screen this child needs and how you will deliver it.

Opening question

Examiner: The registrar asks what screen this child needs. What is your frame, and what governs it? [9]

Candidate: My frame is that this child needs a single comprehensive post-arrival infection screen targeting the silent infections she looks well with — the must-not-miss five of tuberculosis, HIV, hepatitis B, hepatitis C, and parasitic and intestinal disease — plus a vaccination review, a nutritional assessment, and a developmental and mental-health screen. The single principle that governs it is re-verification: the overseas folder is a starting point, never a substitute, and I repeat every serology that matters in my own laboratory before I act on the paper. I deliver it in a trauma-informed frame with a trained interpreter, because this is the entry to the medical home, not a surveillance exercise. [9] [8]

Examiner: Why the must-not-miss five in particular? [7]

Candidate: Because these are the silent, chronic or latent infections that the child looks well with and that will harm her years from now if I do not find them today — and because every one of them is treatable. Latent tuberculosis reactivates years later and is prevented by a short-course regimen. Chronic hepatitis C is cured with direct-acting antivirals. HIV is transformed by antiretrovirals into a chronic controlled condition. Strongyloides can persist for decades and cause fatal hyperinfection at the first immunosuppression, and it is cured with ivermectin. The point of screening is that the well-looking child is the one carrying these conditions. [7] [10]

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References7ShowHide
  1. [1]Hostetter MK; Iverson S; Thomas W; et al Medical evaluation of internationally adopted children. N Engl J Med, 1991.PMID 1649404
  2. [4]Barnett ED Immunizations and infectious disease screening for internationally adopted children. Pediatr Clin North Am, 2005.PMID 16154464
  3. [7]Shetty AK Infectious Diseases among Refugee Children. Children (Basel), 2019.PMID 31783605
  4. [8]Abu-Shamsieh A; Maw S Pediatric Care for Immigrant, Refugee, and Internationally Adopted Children. Pediatr Clin North Am, 2022.PMID 34794672
  5. [9]Chaves NJ; Paxton GA; Biggs BA; et al The Australasian Society for Infectious Diseases and Refugee Health Network of Australia recommendations for health assessment for people from refugee-like backgrounds: an abridged outline. Med J Aust, 2017.PMID 28403765
  6. [10]Cinardo P; Farrant O; Gunn K; et al Screening for neglected tropical diseases and other infections in refugee and asylum-seeker populations in the United Kingdom. Ther Adv Infect Dis, 2022.PMID 35958977
  7. [11]Wang Z; Posey DL; Brostrom RJ; et al US Postarrival Evaluation of Immigrant and Refugee Children with Latent Tuberculosis Infection Diagnosed Overseas, 2007-2019. J Pediatr, 2022.PMID 35120982
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