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Nutr Clin Pract. 2012 Aug;27(4):440-91. doi: 10.1177/0884533612446706. Epub 2012 Jun 22.

A.S.P.E.N. position paper: recommendations for changes in commercially available parenteral multivitamin and multi-trace element products.

Author information

1
St. Elizabeth Health Center, Youngstown, OH 44501-1790, USA. vince_vanek@hmis.org

Erratum in

  • Nutr Clin Pract. 2014 Oct;29(5):701. Dosage error in article text.

Abstract

The parenteral multivitamin preparations that are commercially available in the United States (U.S.) meet the requirements for most patients who receive parenteral nutrition (PN). However, a separate parenteral vitamin D preparation (cholecalciferol or ergocalciferol) should be made available for treatment of patients with vitamin D deficiency unresponsive to oral vitamin D supplementation. Carnitine is commercially available and should be routinely added to neonatal PN formulations. Choline should also be routinely added to adult and pediatric PN formulations; however, a commercially available parenteral product needs to be developed. The parenteral multi-trace element (TE) preparations that are commercially available in the U.S. require significant modifications. Single-entity trace element products can be used to meet individual patient needs when the multiple-element products are inappropriate (see Summary/A.S.P.E.N. Recommendations section for details of these proposed modifications).

PMID:
22730042
DOI:
10.1177/0884533612446706
[Indexed for MEDLINE]

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