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Paeds SAQsinfectious-diseases

Paeds SAQs · infectious-diseases

Infections in immunocompromised children — formative SAQs

Formative SAQs on the approach to infections in immunocompromised children.

20 marks30 min3 min readVerification in progress

Target exams

RACP General PaediatricsMRCPCH Clinical
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Study tools

Target exams

RACP General PaediatricsMRCPCH Clinical
Prompt
Infections in immunocompromised children

SAQ 1 (10)

A 6-year-old on maintenance chemotherapy for acute lymphoblastic leukaemia presents with a single temperature of 38.6 °C at home. On arrival the child is playing and looks well. There is a central venous catheter in situ; the exit site looks clean. The most recent absolute neutrophil count, two days ago, was 0.3 × 10⁹/L. [1]

  1. State why this child is an emergency despite appearing well, and the immediate management steps (no invented doses). (4) [1] [4]
  2. Describe the focused bedside examination that is high-yield in this child. (3) [1]
  3. Outline the principles of empiric therapy, de-escalation, and the safety-net you give the family. (3) [1]

Model answer

Why an emergency and immediate steps. A febrile neutropenic child is an emergency regardless of appearance, because the neutrophil compartment that produces the visible signs of infection is absent — up to a third of bacteraemic neutropenic children look well at presentation, and height of fever correlates poorly with serious bacterial infection. Immediate steps are: confirm the current neutrophil count on a fresh sample, take blood cultures from every central-line lumen and a peripheral site, and deliver empiric anti-pseudomonal therapy within 60 minutes of fever recognition, then admit. The agent, dose and route follow the local oncology protocol and are confirmed against current guidelines before administration. [1] [4]

High-yield bedside examination. The paediatric assessment triangle gates first — any toxic or shocked appearance escalates to the sepsis bundle. The directed examination then covers five high-yield sites: the central-line exit site and tunnel for erythema, swelling, tenderness or discharge; the perianal area for cellulitis or fissure (easy to miss, changes empiric therapy in neutropenia); the oral mucosa for mucositis; the skin for embolic or fungal lesions; and the sinuses and fundi for invasive fungal disease and candida endophthalmitis. Caregiver concern that the child has changed from baseline is taken as data. [1]

Empiric therapy, de-escalation and safety-net. Empiric monotherapy with an anti-pseudomonal beta-lactam is standard; gram-positive cover (for example, vancomycin) is added only for line infection, mucositis, known colonisation or instability. Therapy is narrowed to a targeted agent when a focus and organism are identified, and stopped at the protocol-defined interval if the child defervesces with negative cultures. Persistent fever prompts a re-search for source with imaging and fungal biomarkers. The family is given a specific, rehearsed safety-net: return immediately for any fever, any new pain or rash, any breathing difficulty, or any parental concern that the child is worse. [1]

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References6ShowHide
  1. [1]Lehrnbecher T Guideline for the Management of Fever and Neutropenia in Pediatric Patients With Cancer and Hematopoietic Cell Transplantation Recipients: 2023 Update. Journal of clinical oncology, 2023.PMID 36689694
  2. [2]Schlapbach LJ International Consensus Criteria for Pediatric Sepsis and Septic Shock. JAMA, 2024.PMID 38245889
  3. [3]Weiss SL Surviving Sepsis Campaign International Guidelines for the Management of Sepsis and Septic Shock in Children 2026. Pediatric critical care medicine, 2026.PMID 41869844
  4. [4]De S Lack of Accuracy of Body Temperature for Detecting Serious Bacterial Infection in Febrile Episodes. The Pediatric infectious disease journal, 2015.PMID 26065864
  5. [5]Lee GM Preventing infections in children and adults with asplenia. Hematology. American Society of Hematology. Education Program, 2020.PMID 33275684
  6. [6]Maertens J ECIL guidelines for preventing Pneumocystis jirovecii pneumonia in patients with haematological malignancies and stem cell transplant recipients. The Journal of antimicrobial chemotherapy, 2016.PMID 27550992
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