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The recommendation also applies to infants who are not breast fed but who do not drink at least 17 ounces of fortified formula or milk daily and to children and adolescents who do not drink that much fortified milk or are not exposed regularly to sunlight.
Fortified formula milk for immature infants is widely used in most SCNs, whereas, very few units use human milk to feed preterm infants.
EPO treatment began when infants were tolerating 75% of feeds (non-iron fortified formula or human milk) by the enteral route.
CR is initiated at 14 weeks old, restricting 10% of food intake compared to ad libitum controls, progressing to 25% at 15 weeks and 40% at 16 weeks, the level (3 g daily, NIH-31 fortified formula) maintained for life.
Some literature suggests that late preterm infants are at times sent home relatively quickly with perhaps less support for breastfeeding, which may result in an earlier move to fortified formula [ 20, 21]; this may then reduce the promotion of vitamin D for near-term infants.
A study in the 16 January 2007 issue of Circulation looked at newborns fed either fortified formula, regular formula, or breastmilk for the first nine months of their lives.
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The source of lutein for the fortified formulas was FloraGLO® lutein 20% liquid in safflower oil (Kemin Industries, Inc., Des Moines, Iowa).
However, a baby needs to be drinking at least 32 ounces (about 1 liter) of vitamin-D-fortified formula daily in order to receive an adequate amount of vitamin D, according to the Mayo Clinic.
The reason why lutein availability was different between human milk and lutein-fortified formula remains unclear.
Supplemental iron was given orally or as an iron-fortified formula in 14/15 studies.
Iron was most commonly given orally [ 2, 23, 27, 29- 35] or as an iron-fortified formula [ 2, 24- 26, 28].
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