Sources of unintentional manganese delivery in neonatal parenteral nutrition

Jason Sauberan1, Misty Mercier2, Anup Katheria1

  • 1Neonatal Research Institute, Sharp Mary Birch Hospital for Women & Newborns, San Diego, California, USA.

Abstract

Insights

Magnesium sulfate and calcium gluconate are major sources of unintentional manganese (Mn) exposure in neonatal parenteral nutrition (PN). This hidden Mn delivery can approach recommended dosages, suggesting Mn omission may be viable.

Area of Science:

  • Neonatal medicine
  • Trace element analysis
  • Nutritional biochemistry

Background:

  • Manganese (Mn) neurotoxicity is a significant concern for neonates receiving parenteral nutrition (PN).
  • Previous research identified PN ingredients as a source of daily Mn exposure.
  • This study aimed to pinpoint specific neonatal PN ingredients contributing to unintentional Mn delivery.

Purpose of the Study:

  • Identify the primary sources of unintentional manganese (Mn) delivery in neonatal parenteral nutrition (PN).
  • Quantify Mn concentrations in common PN ingredients.
  • Assess the contribution of these ingredients to the overall Mn load in neonatal PN admixtures.

Main Methods:

  • Inductively coupled plasma-mass spectrometry (ICP-MS) was used to measure Mn concentration in individual PN ingredients.
  • PN admixtures were prepared using standard doses of tested ingredients.
  • Mn concentration in the final PN admixtures was measured to determine total Mn content.

Main Results:

  • Magnesium sulfate and calcium gluconate were identified as the major contributors to unintentional Mn exposure.
  • Maximum Mn concentrations detected were 443 mcg/L in magnesium sulfate and 46.8 mcg/L in calcium gluconate.
  • PN admixtures showed 16%-30% higher Mn content than predicted, delivering up to 0.9 mcg/kg/day without added Mn.

Conclusions:

  • Neonatal PN without added Mn provides Mn levels close to the ASPEN-recommended dosage.
  • A Mn-omission approach for trace element provision in neonatal PN shows potential utility.
  • Further research is required to validate the Mn-omission strategy and assess the clinical impact of unintended Mn delivery.

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