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Published on: May 16, 2019
Chromium and zinc concentrations in pediatric patients receiving long-term parenteral nutrition
J F Mouser1, E B Hak, R A Helms
1Department of Pharmacy Practice, University of Connecticut, Storrs, USA.
Insights
Pediatric patients on long-term parenteral nutrition (PN) had high serum and urine chromium and zinc levels. Increased cysteine in PN solutions tended to raise zinc concentrations in children.
Area of Science:
- Pediatric Nutrition
- Trace Element Metabolism
- Clinical Chemistry
Background:
- Parenteral nutrition (PN) is crucial for pediatric patients unable to absorb nutrients orally.
- Long-term PN can lead to imbalances in essential trace elements like chromium and zinc.
- Monitoring trace element status is vital for optimizing patient outcomes.
Purpose of the Study:
- To investigate serum, urine, and PN chromium and zinc concentrations in pediatric patients on long-term PN.
- To assess the impact of varying cysteine dosages in PN on zinc levels in children.
Main Methods:
- Measured serum, urine, and PN chromium and zinc in infants and children receiving long-term PN.
- Analyzed trace element levels at baseline and after 4-6 months.
- Monitored zinc levels monthly in children with adjusted cysteine hydrochloride dosages in PN.
Main Results:
- Pediatric patients on long-term PN exhibited abnormally high serum and urine chromium and zinc concentrations.
- Prescribed and delivered dosages of chromium and zinc in PN solutions were often higher than recommended.
- Increasing cysteine dosage in PN solutions correlated with elevated serum and urine zinc levels in children.
Conclusions:
- Standard PN formulations may provide excessive chromium and zinc to pediatric patients.
- Cysteine content in PN solutions can influence zinc absorption and retention.
- Further research is needed to establish optimal trace element dosing in pediatric PN.
Abstract:
Serum, urine, and parenteral nutrition (PN) chromium and zinc concentrations in pediatric patients receiving long-term PN were studied. Serum, urine, and PN chromium and zinc concentrations were measured at baseline and four to six months later in four infants (less than 1 year old) and seven children (1-12 years old) receiving long-term PN. In the children, serum, urine, and PN solution zinc concentrations were measured monthly after the amino acid product was changed from a standard to a pediatric product with monthly dosages of 0, 20, 30, and 40 mg of cysteine hydrochloride per gram of amino acids. The mean +/- S.D. baseline serum chromium concentration was 4.9+/-1.9 microg/L (normal value, <0.3 microg/L); the urine chromium concentration ranged from 3.4 to 32.2 microg/L. The mean +/- S.D. prescribed chromium dosage was 0.18+/-0.05 microg/kg/day, and the dosage delivered in PN solutions was 0.41+/-0.23 microg/ kg/day. At baseline, the mean +/- S.D. serum zinc concentration was 1383+/-472 microg/L (normal range, 430 to 940 microg/L), and the prescribed and delivered zinc dosages were 177+/-10 and 238+/-145 microg/kg/ day, respectively. With 20, 30, and 40 mg of cysteine per gram of amino acids, the mean +/- S.D. serum zinc concentration was 1728+/-782, 1664+/-349, and 1685+/-268 microg/L, respectively, and the actual zinc dosages delivered were 209+/-10, 270+/-148, and 322+/-194 microg/kg/day, respectively. Serum and urine chromium concentrations were abnormally high in infants and children receiving PN solutions supplemented with normal doses of these trace elements; an escalating dosage of cysteine in the children tended to increase serum and urine zinc concentrations.
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