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Published on: November 29, 2013
Essential fatty acid deficiency in children treated with long-term 100% fish-oil lipid injectable emulsion: A
Kathleen M Gura1, Muralidhar H Premkumar2, Kara L Calkins3
1Department of Pharmacy, Division of Gastroenterology, Hepatology, and Nutrition, Boston Children's Hospital, Boston, Massachusetts, USA.
Insights
Children on long-term fish-oil lipid emulsion for parenteral nutrition-associated cholestasis show a low risk of essential fatty acid deficiency. Continued use of this emulsion is safe and effective, even with low linoleic acid content.
Area of Science:
- Pediatric Nutrition
- Clinical Lipidology
- Parenteral Nutrition
Background:
- Parenteral nutrition-associated cholestasis (PNAC) in infants <2 years can lead to essential fatty acid deficiency.
- Long-term use of 100% fish-oil lipid injectable emulsion (FO-LIE) is common in PNAC.
- Assessing the risk of essential fatty acid deficiency (EFAD) with FO-LIE is critical.
Purpose of the Study:
- To evaluate the severity and risk of EFAD in children <2 years with PNAC receiving long-term 100% FO-LIE.
- To monitor biochemical markers of EFAD over an extended period.
Main Methods:
- A longitudinal descriptive cohort study.
- Included 127 infants receiving 1 g/kg/day of 100% FO-LIE.
- Monitored triene:tetraene ratios for up to 4 years to assess EFAD.
Main Results:
- Serum omega-3 fatty acids increased, while omega-6 decreased and stabilized.
- Median triene:tetraene ratios peaked early and remained low (0.015-0.020).
- Only 3 infants showed biochemical EFAD, with no clinical signs; all resolved with continued FO-LIE.
Conclusions:
- Long-term 100% FO-LIE use in children with PNAC is associated with a low risk of clinical or biochemical EFAD.
- The emulsion is safe and effective for managing EFAD risk, despite lower linoleic and alpha-linolenic acid content.
- Findings support the continued use of 100% FO-LIE in this pediatric population.
Background:
To assess severity and risk of an essential fatty acid deficiency in children <2 years with parenteral nutrition-associated cholestasis on long-term 100% fish-oil lipid injectable emulsion.
Methods:
This longitudinal descriptive cohort study included patients receiving fish-oil lipid injectable emulsion (1 g/kg/day). Triene: tetraene ratios were monitored for up to 4 years and classified as mildly elevated (≥0.05 and <0.2) or essential fatty acid deficiency (≥0.2).
Results:
One hundred and twenty-seven patients with a baseline median age of 14 weeks were included. Serum docosahexaenoic acid and eicosapentaenoic acid levels markedly increased, whereas arachidonic acid, linoleic acid, and α-linolenic acid levels decreased before stabilizing. Median triene: tetraene ratios peaked at 0.027 at week 8 and then stabilized within a range of 0.015 and 0.020 from week 16 until the end of the study. Seven patients had mildly elevated triene: tetraene ratio at the end of the study. Three infants had an essential fatty acid deficiency, but none demonstrated clinical signs consistent with this deficiency. One deficiency was attributed to a laboratory error; two were associated with adverse events. All patients resolved with the continuation of fish-oil lipid injectable emulsion.
Conclusion:
Children with parenteral nutrition-associated cholestasis on long-term fish-oil lipid injectable emulsion are at low risk for a clinical or biochemical essential fatty acid deficiency. These findings indicate that despite its low content of linoleic acid and α-linolenic acid, long-term 1 g/kg/day of 100% fish-oil lipid injectable emulsion is not associated with an essential fatty acid deficiency.
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