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Paeds SAQsinfectious-diseases

Paeds SAQs · infectious-diseases

Device-associated and healthcare-associated infection — formative SAQs

Two MedVellum formative short-answer questions on device-associated and healthcare-associated infection in children, covering NHSN surveillance definitions, the multimodal prevention bundle, source control by device removal, antimicrobial de-escalation, and an outbreak scenario on a neonatal unit. The marks and timing support transparent self-assessment; they are not an official board format or pass standard.

20 marks30 min6 min readVerification in progress

Target exams

RACP General PaediatricsRACP DWERACP DCERCPCH Progress+MRCPCH TheoryMRCPCH ClinicalABP General PediatricsACGME PediatricsRCPSC Pediatrics
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Target exams

RACP General PaediatricsRACP DWERACP DCERCPCH Progress+MRCPCH TheoryMRCPCH ClinicalABP General PediatricsACGME PediatricsRCPSC Pediatrics
Prompt
SAQ 1 covers NHSN surveillance definitions, the prevention bundle and source control for a school-age child with suspected central-line-associated bloodstream infection. SAQ 2 covers a cluster of CLABSI on a neonatal unit, outbreak investigation, bundle review and stewardship.
Assessment contract

This is a MedVellum formative exercise: 20 marks over a suggested 30 minutes, divided into two 10-mark SAQs with 15 minutes suggested for each. These marks, timings and grids are authored for transparent practice and self-assessment; they are not a published RACP, RCPCH, ABP or RCPSC examination format, allocation, pass mark or standard-setting method. The NHSN protocol and the SHEA-IDSA compendium are linked only to show the evidence context, not to imply official endorsement of this exercise. [3] [12]

SAQ 1 — A school-age child with a suspected central-line infection

Question 1 — 10 formative marks; suggested time 15 minutes [3]

A previously well 8-year-old girl with a short-bowel syndrome is six days into an admission for a line-related course of antibiotics. She has a tunneled central venous catheter for parenteral nutrition. She spikes a fever with rigors during a line flush, looks unwell, and the exit site is clean with no tunnel erythema. Blood pressure and perfusion are normal. [1] [3]

  1. Define the surveillance syndrome she may have and state the time and device criteria that place it in the device-associated category. (2 marks)
  2. Outline your immediate investigations and empiric management, including your decision on the line. (3 marks)
  3. State the prevention bundle that should have been in place, and name the single greatest modifiable risk factor. (3 marks)
  4. Two days later Staphylococcus aureus grows in both the line and peripheral cultures. What changes about your management and why? (2 marks)
[1] [3] [12]

Full-credit answer — SAQ 1

Reveal full-credit answer for SAQ 1ShowHide

1. Surveillance syndrome and criteria

She may have a central-line-associated bloodstream infection (CLABSI): a laboratory-confirmed bloodstream infection in a patient with a central line in place for more than two calendar days, where the infection is not attributed to another site. The healthcare-associated time convention is onset more than 48 hours after admission, and she is well beyond both thresholds. I would count her against the unit's line-days denominator, but I would treat her on clinical grounds immediately rather than wait for surveillance adjudication. [3] [12]

2. Investigations, empiric therapy and the line decision

I would draw paired blood cultures from a peripheral site and from the line before antibiotics, and send a full blood count, C-reactive protein, electrolytes, renal and liver function, and a lactate. Because she is well perfused and not septic, I would start empiric antistaphylococcal cover for coagulase-negative staphylococci and Staphylococcus aureus, broadened per local guidance. Because the site is clean and she is clinically stable, immediate line removal is not mandated on the first positive culture, but I would set a clear threshold: remove the line if she develops sepsis, a tunnel or pocket infection, persisting or relapsing bacteraemia, or a resistant or high-risk organism. [3] [12]

3. Prevention bundle and the key risk factor

The bundle that should have been in place is multimodal: hand hygiene at the five moments, maximal sterile barriers at insertion, chlorhexidine skin preparation, optimal site selection, scrub-the-hub before every access, intact dressing care, and daily documented review of line necessity. The single greatest modifiable risk factor is the device itself, so the most reliable prevention is removing the line as soon as it is no longer essential. [3] [12]

4. Staphylococcus aureus changes the line decision

Staphylococcus aureus bacteraemia from a line is a high-risk organism with a strong tendency to seed distant foci, so the line should be removed, the child imaged for endocarditis and metastatic infection with echocardiography and targeted imaging, and therapy extended and guided by infectious diseases. This is one of the organisms for which line salvage is not appropriate. [3] [12]

Marking grid — SAQ 1

DomainFull-credit requirementsMarks
Surveillance definitionCLABSI with correct time (>48 h) and device (>2 day) criteria2
Investigations and empiric therapyPaired cultures before antibiotics; antistaphylococcal empiric cover; stated line-removal threshold3
Prevention bundle and risk factorHand hygiene, barriers, chlorhexidine, hub care, daily review; device dwell as key risk3
S. aureus managementRemove line; image for distant foci; prolonged guided therapy2
[1] [3] [12]

Common pitfalls — SAQ 1

  • Treating the surveillance definition as the trigger for clinical action, delaying cultures and antibiotics.
  • Salvaging a line in Staphylococcus aureus bacteraemia, or attributing a single positive culture to contamination without the clinical context.
  • Naming only one bundle element rather than the multimodal bundle, or omitting the daily review of necessity. [3] [12]
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References6ShowHide
  1. [1]Hsu HE, Mathew R, Wang R, et al. Health Care-Associated Infections Among Critically Ill Children in the US, 2013-2018. JAMA pediatrics, 2020.PMID 33017011
  2. [2]Weiner-Lastinger LM, Abner S, Benin AL, et al. Antimicrobial-resistant pathogens associated with pediatric healthcare-associated infections: Summary of data reported to the National Healthcare Safety Network, 2015-2017. Infection control and hospital epidemiology, 2020.PMID 31762428
  3. [3]O'Grady NP, Alexander M, Burns LA, et al. Guidelines for the prevention of intravascular catheter-related infections. American journal of infection control, 2011.PMID 21511081
  4. [4]Miller MR, Griswold M, Harris JM 2nd, et al. Decreasing PICU catheter-associated bloodstream infections: NACHRI's quality transformation efforts. Pediatrics, 2010.PMID 20064860
  5. [9]McDonald LC, Gerding DN, Johnson S, et al. Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA). Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018.PMID 29562266
  6. [12]Yokoe DS, Anderson DJ, Berenholtz SM, et al. A compendium of strategies to prevent healthcare-associated infections in acute care hospitals: 2014 updates. Infection control and hospital epidemiology, 2014.PMID 25026611
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