TY - JOUR T1 - Milk versus medicine for the treatment of iron deficiency anaemia in hospitalised infants JF - Archives of Disease in Childhood JO - Arch Dis Child SP - 1033 LP - 1038 DO - 10.1136/adc.2004.067876 VL - 90 IS - 10 AU - C R Wall AU - C C Grant AU - N Taua AU - C Wilson AU - J M D Thompson Y1 - 2005/10/01 UR - http://adc.bmj.com/content/90/10/1033.abstract N2 - Aims: To compare iron fortified follow-on milk (iron follow-on), iron fortified partially modified cows’ milk (iron milk), and iron medicine for the treatment of iron deficiency anaemia (IDA) in hospitalised infants. Methods: In a randomised controlled trial, infants aged 9–23 months with IDA and who were hospitalised with an acute illness received iron follow-on (12 mg/l ferrous iron), iron milk (12.9 mg/l ferrous iron), or iron medicine (ferrous gluconate at 3 mg/kg of elemental iron once daily). All interventions were given for three months. Changes in measures of iron status three months after hospital discharge were determined. Results: A total of 234 infants were randomised. Iron status was measured at follow up in 59 (70%) iron medicine, 49 (66%) iron follow-on, and 54 (70%) iron milk treated infants. There was a significant (mean, 95% CI) increase in haemoglobin (15 g/l, 13 to 16) and iron saturation (9%, 8 to 10) and decrease in ferritin (−53 μg/l, −74 to −31) in all three groups. Mean cell volume increased in iron follow-on (2 fl, 1 to 3) and iron milk (1 fl, 0.1 to 3) treated infants, but not in the iron medicine group (1 fl, −1 to 2). The proportion with IDA decreased in all three groups: iron medicine 93% to 7%, iron follow-on 83% to 8%, and iron milk 96% to 30%. Adverse effects, primarily gastrointestinal, occurred in 23% of the iron medicine, 14% of the iron follow-on, and 13% of the iron milk group. Conclusions: Iron fortified follow-on milk, iron fortified partially modified cows’ milk, and iron medicine all effectively treat IDA in infancy. ER -