Iron deficiency screening for children at 18 months: a cost-utility analysis

Sarah Carsley1, Rui Fu2, Cornelia M Borkhoff2

  • 1Health Promotion, Chronic Disease and Injury Prevention (Carsley), Public Health Ontario; Institute of Health Policy, Management and Evaluation (Fu, Borkhoff, Reid, Baginska, Birken, Maguire, Hancock-Howard, Parkin, Coyte), Dalla Lana School of Public Health, University of Toronto; Child Health Evaluative Sciences (Borkhoff, Birken, Parkin), Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children; Division of Pediatric Medicine and the Pediatric Outcomes Research Team (Borkhoff, Birken, Maguire, Parkin), Department of Pediatrics, Faculty of Medicine, University of Toronto, The Hospital for Sick Children; Department of Pediatrics (Maguire), St. Michael's Hospital and Li Ka Shing Knowledge Institute; Department of Nutritional Sciences (Birken, Maguire), University of Toronto, Toronto, Ont. sarah.carsley@oahpp.ca.

CMAJ Open
|December 5, 2019
PubMed

Insights

Universal iron deficiency screening for 18-month-olds is cost-effective. This program offers better value than targeted screening or no screening, improving neurodevelopmental outcomes.

Area of Science:

  • Pediatric Health
  • Public Health Policy
  • Health Economics

Background:

  • Iron deficiency (ID) peaks in children aged 6 months to 3 years, a critical period for neurodevelopment.
  • Current standard of care involves no routine screening for iron deficiency in this age group.

Purpose of the Study:

  • To evaluate the cost-utility of implementing a universal iron deficiency screening program for 18-month-old children.
  • To compare universal screening with targeted screening and no screening strategies.

Main Methods:

  • A decision tree model was utilized to estimate costs (2019 Canadian dollars) and quality-adjusted life years (QALYs).
  • A societal perspective was adopted, assessing lifetime QALY gains.
  • Data were derived from literature and prospective collection, with sensitivity analyses performed.

Main Results:

  • Both universal and targeted screening programs were found to be cost-effective at a willingness-to-pay threshold of $50,000/QALY.
  • Universal screening yielded an incremental cost of $2965.96 per QALY gained compared to targeted screening, remaining cost-effective.
  • Sensitivity analyses confirmed the robustness of these findings.

Conclusions:

  • A universal iron deficiency screening program for 18-month-olds is a cost-effective strategy over the lifespan.
  • The findings support expanding the 18-month well-baby visit to include iron deficiency screening.
  • Policy-makers and clinicians should consider implementing universal screening to improve child health outcomes.
Abstract