Effect of Iron-fortified TPN on Preterm Infants Anemia
Preterm Infants
About this trial
This is an interventional prevention trial for Preterm Infants focused on measuring preterm infant, anemia, iron fortified TPN
Eligibility Criteria
Inclusion Criteria:
- Preterm infants with birth weight less than 2kg Have parenteral nutrition indication With written informed consent of parents or guardian
Exclusion Criteria:
- have already used TPN before randomization Kidney and liver function abnormal have hemolytic disease have hemorrhagic disease have Serious congenital malformation have septicemia have plethora newborn use TPN less than ten days
Sites / Locations
- Xinhua HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Experimental
Experimental
control group
treatment group1
treatment group2
preterm infants of this group with iron-free TPN for more than ten days, compare serum iron, iron protein, total iron binding force, MDA, 8-iso-PGF2α on baseline and after intervention.
preterm infants of this group with iron supplementation of 200μg/kg/d for more than ten days, compare serum iron, iron protein, total iron binding force, MDA, 8-iso-PGF2α on baseline and after intervention.
preterm infants of this group with iron supplementation of 400μg/kg/d for more than ten days, compare serum iron, iron protein, total iron binding force, MDA, 8-iso-PGF2α on baseline and after intervention.