Paeds SAQs · preventive-and-community-paediatrics
Lead exposure and poisoning prevention — formative SAQs
Formative SAQs on childhood lead screening, source control and chelation limits.
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Target exams
SAQ 1 (10 marks)
Parents of a 2-year-old live in a 1950s house. They have been sanding paint. A capillary blood lead is 8 micrograms/dL. The child is asymptomatic. [1]
- What is the next laboratory step and why? (2) [1]
- List five exposure sources you must cover in the history. (3) [1] [2]
- Outline your management plan for the next month, including what you will not promise. (5) [2] [4] [6]
Model answer
Confirm with venous whole blood lead. Capillary samples can be contaminated by surface lead and should not alone drive major decisions. [1]
Sources: deteriorated paint/dust (including renovation), water plumbing, soil, take-home occupational dust, traditional cosmetics/remedies, and pica for non-food items. [1] [2]
Management: stop unsafe sanding; arrange environmental assessment/remediation pathways; educate on wet cleaning and hand washing; assess iron status and diet (iron/calcium support); developmental surveillance; public-health notification as required; retest venous BLL on schedule; test other young household members. Do not promise that any level is fully safe, and do not offer chelation as an IQ-restoring treatment — prevention and source control are the core. [2] [4] [6]
SAQ 2 (10 marks)
A 3-year-old has venous blood lead 52 micrograms/dL after paint-chip pica. The child is irritable with abdominal pain but no seizures. [1]
- Why is this level managed differently from a BLL of 6 micrograms/dL? (2) [1]
- What immediate environmental and clinical steps are required before or with any drug therapy? (4) [1] [2]
- What did the TLC trial teach about succimer and cognition? (4) [6] [8]
Model answer
BLL ≥45 micrograms/dL enters the range where specialist consideration of chelation is standard in CDC-aligned guidance, and symptoms raise urgency. Lower elevations still need source control but usually not chelation. [1]
Remove the child from ongoing exposure; consider abdominal imaging for retained radiopaque material and decontamination if indicated; full clinical assessment; public-health/environmental response; iron assessment; hospital or specialist toxicology involvement for chelation decisions; never chelate while the child returns to the same uncontrolled hazard. [1] [2]
TLC randomised young children with BLL 20–44 micrograms/dL to succimer versus placebo: blood lead fell with succimer, but neuropsychological outcomes were not lastingly improved. Chelation is not a cognitive rescue; primary prevention remains essential. [6] [8]
References
- [1]Mayans L Lead Poisoning in Children. American Family Physician, 2019.PMID 31259498
- [2]COUNCIL ON ENVIRONMENTAL HEALTH Prevention of Childhood Lead Toxicity. Pediatrics, 2016.PMID 27325637
- [4]Canfield RL Intellectual impairment in children with blood lead concentrations below 10 microg per deciliter. The New England journal of medicine, 2003.PMID 12700371
- [6]Rogan WJ The effect of chelation therapy with succimer on neuropsychological development in children exposed to lead. The New England journal of medicine, 2001.PMID 11346806
- [8]Kosnett MJ Chelation for heavy metals (arsenic, lead, and mercury): protective or perilous? Clinical pharmacology and therapeutics, 2010.PMID 20664538