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Plasma Aluminum Concentrations in Pediatric Patients Receiving Long-Term Parenteral Nutrition
Glenda Courtney-Martin1, Christina Kosar2, Alison Campbell3
1Research Institute, The Hospital for Sick Children, Toronto, Canada Group for Improvement of Intestinal Function and Treatment (GIFT), The Hospital for Sick Children, Toronto, Canada glenda.courtney-martin@sickkids.ca.
Insights
Long-term parenteral nutrition (PN) in pediatric patients with intestinal failure (IF) in Canada leads to elevated aluminum (Al) levels, increasing toxicity risk. This highlights a critical need for Al content regulation in PN solutions.
Area of Science:
- Clinical Nutrition
- Toxicology
- Pediatric Medicine
Background:
- Long-term parenteral nutrition (PN) bypasses the gastrointestinal tract, increasing aluminum (Al) toxicity risk.
- Al toxicity complications include metabolic bone disease and neurological impairment.
- Canada lacks regulations on Al content in parenteral products, unlike the US.
Purpose of the Study:
- To assess plasma Al concentrations in pediatric patients receiving long-term PN.
- To determine Al intake from PN solutions in this patient cohort.
- To evaluate the risk of Al toxicity in Canadian pediatric patients with intestinal failure (IF).
Main Methods:
- Retrospective chart review of 27 pediatric patients with IF on long-term PN.
- Comparison of plasma Al concentrations with age- and sex-matched controls.
- Measurement of Al concentration in PN samples from 10 randomly selected patients to calculate Al intake.
Main Results:
- Patients on long-term PN had significantly higher plasma Al concentrations than controls (1195 ± 710 vs 142 ± 63 nmol/L).
- Mean Al intake from PN was 15.4 ± 15 µg/kg, three times the FDA recommended level.
- Al intake was significantly correlated with plasma Al concentration (P = .02, r² = 0.52).
Conclusions:
- Pediatric patients receiving long-term PN for IF in Canada face a significant risk of Al toxicity.
- Elevated plasma Al levels indicate substantial Al absorption from PN solutions.
- The findings underscore the need for Al content monitoring and regulation in PN for vulnerable pediatric populations.
Background:
Patients receiving long-term parenteral nutrition (PN) are at increased risk of aluminium (Al) toxicity because of bypass of the gastrointestinal tract during PN infusion. Complications of Al toxicity include metabolic bone disease (MBD), Al-associated encephalopathy in adults, and impaired neurological development in preterm infants. Unlike the United States, there are no regulations regarding Al content of large- and small-volume parenterals in Canada. We, therefore, aimed to present our data on plasma Al concentration and Al intake from our cohort of pediatric patients receiving long-term PN.
Methods:
Plasma Al concentration was retrospectively gathered from the patient charts of all 27 patients with intestinal failure (IF) receiving long-term PN at The Hospital for Sick Children, Toronto, Canada, and compared with age- and sex-matched controls recruited for comparison. In addition, Al concentration was measured in PN samples collected from 10 randomly selected patients with IF and used to determine their Al intake.
Results:
The plasma Al concentration of patients with IF receiving long-term PN was significantly higher than that of control participants (1195 ± 710 vs 142 ± 63 nmol/L; P < .0001). In the subgroup of 10 patients for whom Al intake from their PN solution was determined, mean ± SD Al intake from PN was 15.4 ± 15 µg/kg, 3 times the Food and Drug Administration upper recommended intake level, and Al intake was significantly related to plasma Al concentration (P = .02, r (2) = 0.52).
Conclusion:
Pediatric patients receiving long-term PN for IF in Canada are at risk for Al toxicity.
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