Paeds SAQs · investigations-procedures-and-technology
Radiation protection and imaging stewardship — formative SAQs
Formative SAQs on the three pillars of radiological protection in children, the linear-no-threshold risk model and the cohort risk estimates, the CT and fluoroscopy dose quantities and the diagnostic reference level, the optimisation levers in paediatric CT, the modern discontinuation of gonadal shielding, and the counselling of a parent about radiation risk.
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SAQ 1 (10 marks)
A 6-year-old boy is being followed by the oncology service after treatment for a Wilms tumour. Over three years he has had multiple surveillance CT scans of the chest and abdomen. The registrar queries whether a routine surveillance CT is again due, and the parent has read that repeated CT scans "will give him cancer." You are asked to advise on the radiation-aware approach. [1] [8]
- State the three pillars of radiological protection, and explain the examinable point about which of them does and does not apply to a patient investigation. (3) [8]
- Quantify, in plain language suitable for the parent, the effective dose and the attributable lifetime cancer risk of a single paediatric CT, and name the cohort evidence that underpins the risk estimate. (4) [1] [2] [3]
- Outline the stewardship approach to this child's surveillance imaging, including the dose-optimisation levers and the role of a non-ionising substitute. (3) [8] [10]
Model answer — SAQ 1
(1) The three pillars (3). The three pillars of radiological protection, set by the International Commission on Radiological Protection, are justification (any exposure must do more good than harm), optimisation (the ALARA principle — As Low As Reasonably Achievable), and dose limitation. The examinable point is that dose limits apply to occupationally exposed staff and to the public, and do not apply to the medical exposure of a patient whose investigation is justified — a justified patient investigation may exceed a staff dose limit, because the limit protects those who receive no benefit, whereas the patient receives the diagnostic benefit that justified the exposure. Justification and optimisation apply to every exposure; dose limitation does not apply to the patient. [8]
(2) The dose and the risk in plain language (4). A single paediatric head CT delivers an effective dose of the order of 1 to 2 mSv, comparable to several months of natural background radiation (around 2 to 3 mSv per year); an abdominal or chest CT is higher, of the order of 2 to 5 mSv and size-dependent. The attributable lifetime cancer risk is small and stochastic — probabilistic, with no safe threshold assumed (the linear-no-threshold model) — and is of the order of one excess cancer per several thousand to ten thousand scans. For the parent, I would frame this as a real but very small increase over the background lifetime cancer risk of roughly one in three, and emphasise that the risk of a justified scan is far smaller than the risk of missing a recurrence it is looking for. The evidence base is the New England Journal analysis of Brenner and Hall, the United Kingdom retrospective cohort of Pearce (leukaemia and brain tumours), the Dutch cohort of Meulepas, and the international EPI-CT consortium, all of which show a small but real dose-response and none of which forbid CT. [1] [2] [3]
(3) The stewardship approach (3). The first step is justification: is this surveillance scan needed now, and what will it change — the oncology surveillance protocol is followed, but each request is a deliberate decision, and the cumulative dose accumulated across the previous scans is part of the present decision. The second step is to consider a non-ionising substitute: MRI-based surveillance, where it answers the question, removes the ionising dose for that examination, and the shift towards MRI surveillance is the radiation-aware strategy. The third step, when CT is the justified modality, is dose optimisation: a size-specific paediatric protocol that scales the milliampere-seconds and kilovoltage peak to the child, a lower kilovoltage peak (typically 80 to 100 kVp), automatic tube current modulation, a limited scan length, a single phase rather than multiphase, and iterative reconstruction. The local protocol is benchmarked against the size-stratified paediatric diagnostic reference level (around the 75th percentile of the dose distribution, a benchmark not a limit). I would track the cumulative dose so that the next request is made against the lifetime total, and document the discussion with the parent. [8] [10]
You have read the opening of this SAQ. The complete unit — every section and its primary-source references — is part of the Paediatrics Fellowship fellowship atlas.
References7Show ledgerHide ledger
- [1]Pearce MS, Salotti JA, Little MP, et al Radiation exposure from CT scans in childhood and subsequent risk of leukaemia and brain tumours: a retrospective cohort study Lancet, 2012.PMID 22681860
- [2]Meulepas JM, Ronckers CM, Smets AMJB, et al Radiation Exposure From Pediatric CT Scans and Subsequent Cancer Risk in the Netherlands J Natl Cancer Inst, 2019.PMID 30020493
- [3]Brenner DJ, Hall EJ Computed tomography--an increasing source of radiation exposure N Engl J Med, 2007.PMID 18046031
- [6]Goske MJ, Applegate KE, Boylan J, et al The Image Gently campaign: working together to change practice AJR Am J Roentgenol, 2008.PMID 18212208
- [8]Frush DP, Frush KS The ALARA concept in pediatric imaging: building bridges between radiology and emergency medicine Pediatr Radiol, 2008.PMID 18810422
- [10]Kanal KM, Butler PF, Chatfield MB, et al U.S. Diagnostic Reference Levels and Achievable Doses for 10 Pediatric CT Examinations Radiology, 2022.PMID 34928733
- [12]Thakur Y, Schofield SC, Bjarnason TA, et al Discontinuing Gonadal and Fetal Shielding in X-Ray Can Assoc Radiol J, 2021.PMID 33573394