Preschool Screening for Iron Deficiency Anemia
For preschool children (ages 2-5 years), screen annually only if they belong to high-risk populations (low-income families, WIC-eligible, migrants, refugees) or have specific risk factors including low-iron diet, excessive milk intake (>24 oz daily), poverty/food insecurity, or special healthcare needs. 1
Screening Strategy by Risk Level
High-Risk Populations (Universal Screening)
- Screen all children annually from ages 2 to 5 years if they are from low-income families, WIC-eligible, migrant populations, or recently arrived refugees 1
- Initial screening should have occurred at 9-12 months, with repeat at 15-18 months, before entering the annual preschool screening phase 1
Low-Risk Populations (Selective Screening)
- Screen only children with documented risk factors rather than universal screening 1
- Annual risk assessment at ages 2-5 years should identify children with:
Specific Risk Factors Requiring Screening
Dietary red flags that mandate screening include:
- Milk consumption exceeding 24 oz daily, which remains a major contributor to severe IDA in toddlers 1, 2
- History of delayed introduction of iron-fortified foods 1
- Predominantly milk-based diet with inadequate iron-rich foods 1
Medical history concerns requiring screening:
- Previous diagnosis of iron deficiency or anemia 1
- Preterm birth or low birthweight 1
- Chronic conditions affecting iron absorption or utilization 1
Diagnostic Approach When Screening is Positive
Initial Confirmation
- Repeat hemoglobin (Hb) or hematocrit (Hct) to confirm positive screening before initiating treatment 1, 3
- If both tests agree and the child is not acutely ill, make a presumptive diagnosis of IDA and begin treatment 1
Treatment Protocol
- Prescribe 3 mg/kg per day of elemental iron administered between meals 1, 3, 4
- Provide dietary counseling addressing the underlying low iron intake 1, 3
- Limit milk to maximum 24 oz daily to prevent displacement of iron-rich foods 1, 4
Response Assessment at 4 Weeks
- Repeat Hb/Hct after 4 weeks of treatment 1, 3
- An increase of ≥1 g/dL in Hb or ≥3% in Hct confirms IDA diagnosis 1, 3, 4
- If confirmed, continue iron for 2 additional months, then recheck 1, 3
- Reassess approximately 6 months after successful treatment completion 1, 3
Non-Response Management
- If no response after 4 weeks despite compliance and absence of acute illness, obtain additional laboratory tests including MCV, RDW, and serum ferritin 1, 5
- Serum ferritin ≤15 μg/L confirms iron deficiency; >15 μg/L suggests alternative diagnosis 1, 3, 5
- Consider thalassemia carrier status in endemic populations, as this can confound IDA diagnosis 6
Critical Pitfalls to Avoid
Screening errors:
- Using hemoglobin alone misses all cases of iron deficiency without anemia, which may still cause developmental effects 7, 8
- In populations with high thalassemia prevalence, MCV and Mentzer index (MCV/RBC <13) should be incorporated to distinguish thalassemia carriers from IDA 6
- Macrocytosis (present in 32% of children with Down syndrome) can mask IDA; use RDW combined with ferritin for optimal detection in this population 7
Treatment failures:
- Inadequate treatment duration (must continue 2 months after Hb normalization to replenish stores) 3, 4
- Not addressing excessive milk consumption, which strongly correlates with severe IDA in toddlers 2
- Assuming compliance without verification—low follow-up rates (37-42% never return within 6 months) are common in high-risk populations 9
- Spontaneous resolution occurs in 68% of untreated cases, making therapeutic trials unreliable for diagnosis without proper follow-up 9
Dietary counseling must emphasize: