Skip to main content
Top
Published in: Pediatric Nephrology 10/2015

01-10-2015 | Original Article

Renal formulas pretreated with medications alters the nutrient profile

Authors: Jacob M. Taylor, Leah Oladitan, Susan Carlson, Jill M. Hamilton-Reeves

Published in: Pediatric Nephrology | Issue 10/2015

Login to get access

Abstract

Background

Pretreating renal formulas with medications to lower the potassium and phosphorus content is common in clinical practice; however, the effect of this treatment on other nutrients is relatively unstudied. We examine whether nutrient composition is affected by pretreating renal formulas with sodium polystyrene sulfonate (SPS) suspension and sevelamer carbonate.

Methods

Fixed medication doses and treatment times were utilized to determine changes in the nutrient composition of Suplena® and Similac® PM 60/40. The effect of simultaneously adding both medications (co-administration) to the formula on the nutrient composition of Suplena® was also evaluated.

Results

Pretreatment of Suplena® with SPS reduced the concentrations of calcium (11–38 %), copper (3–11 %), manganese (3–16 %), phosphorus (0–7 %), potassium (6–34 %), and zinc (5–20 %) and increased those of iron (9–34 %), sodium (89–260 %), and sulfur (19–45 %) and the pH (0.20–0.50 units). Pretreatment of Similac® PM 60/40 with SPS reduced the concentrations of calcium (8–29 %), copper (5–19 %), magnesium (3–26 %), and potassium (33–63 %) and increased those of iron (13–87 %) and sodium (86–247 %) and the pH (0.40–0.81 units). Pretreatment of both formulas with the SPS suspension led to significant increases in the aluminum concentration in both formulas (507–3957 %). No differences in potassium concentration were observed between treatment times. Unexpectedly, the levels of neither phosphorus nor potassium were effectively reduced in Suplena® pretreated with sevelamer carbonate alone or when co-administered with SPS.

Conclusions

Pretreating formula with medications alters nutrients other than the intended target(s). Future studies should be aimed at predicting the loss of these nutrients or identifying alternative methods for managing serum potassium and phosphorus levels in formula-fed infants. The safety of pretreating formula with SPS suspension should also be examined.
Appendix
Available only for authorised users
Literature
1.
go back to reference National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases (2014) U.S. Renal Data System. USRDS 2014 Annual Data Report: Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases (2014) U.S. Renal Data System. USRDS 2014 Annual Data Report: Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda
2.
go back to reference Wong H, Mylrea K, Feber J, Drukker A, Filler G (2006) Prevalence of complications in children with chronic kidney disease according to KDOQI. Kidney Int 70:585–590PubMed Wong H, Mylrea K, Feber J, Drukker A, Filler G (2006) Prevalence of complications in children with chronic kidney disease according to KDOQI. Kidney Int 70:585–590PubMed
3.
go back to reference Rivard AL, Raup SM, Beilman GJ (2004) Sodium polystyrene sulfonate used to reduce the potassium content of a high-protein enteral formula: a quantitative analysis. J Parenter Enteral Nutr 28:76–78CrossRef Rivard AL, Raup SM, Beilman GJ (2004) Sodium polystyrene sulfonate used to reduce the potassium content of a high-protein enteral formula: a quantitative analysis. J Parenter Enteral Nutr 28:76–78CrossRef
4.
go back to reference Bunchman TE, Wood EG, Schenck MH, Weaver KA, Klein BL, Lynch RE (1991) Pretreatment of formula with sodium polystyrene sulfonate to reduce dietary potassium intake. Pediatr Nephrol 5:29–32CrossRefPubMed Bunchman TE, Wood EG, Schenck MH, Weaver KA, Klein BL, Lynch RE (1991) Pretreatment of formula with sodium polystyrene sulfonate to reduce dietary potassium intake. Pediatr Nephrol 5:29–32CrossRefPubMed
5.
go back to reference Starbuck WC (1972) Reduction of potassium and calcium in milk by sodium sulfonated polystyrene resins. Kidney Int 2:175–177CrossRefPubMed Starbuck WC (1972) Reduction of potassium and calcium in milk by sodium sulfonated polystyrene resins. Kidney Int 2:175–177CrossRefPubMed
6.
go back to reference Raaijmakers R, Houkes LM, Schröder CH, Willems JL, Monnens LA (2013) Pre-treatment of dairy and breast milk with sevelamer hydrochloride and sevelamer carbonate to reduce phosphate. Perit Dial Int 33:565–572PubMedCentralCrossRefPubMed Raaijmakers R, Houkes LM, Schröder CH, Willems JL, Monnens LA (2013) Pre-treatment of dairy and breast milk with sevelamer hydrochloride and sevelamer carbonate to reduce phosphate. Perit Dial Int 33:565–572PubMedCentralCrossRefPubMed
7.
go back to reference Warady BA, Neu AM, Schaefer F (2014) Optimal care of the infant, child, and adolescent on dialysis: 2014 update. Am J Kidney Dis 64:128–142CrossRefPubMed Warady BA, Neu AM, Schaefer F (2014) Optimal care of the infant, child, and adolescent on dialysis: 2014 update. Am J Kidney Dis 64:128–142CrossRefPubMed
8.
go back to reference Thompson K, Flynn J, Okamura D, Zhou L (2013) Pretreatment of formula or expressed breast milk with sodium polystyrene sulfonate (kayexalate) as a treatment for hyperkalemia in infants with acute or chronic renal insufficiency. J Ren Nutr 23:333–339CrossRefPubMed Thompson K, Flynn J, Okamura D, Zhou L (2013) Pretreatment of formula or expressed breast milk with sodium polystyrene sulfonate (kayexalate) as a treatment for hyperkalemia in infants with acute or chronic renal insufficiency. J Ren Nutr 23:333–339CrossRefPubMed
9.
go back to reference Cameron JC, Kennedy D, Feber J, Wong E, Geier P, Vaillancourt R (2013) Pretreatment of infant formula with sodium polystyrene sulfonate : focus on optimal amount and contact time. Paediatr Drugs 15:43–48CrossRefPubMed Cameron JC, Kennedy D, Feber J, Wong E, Geier P, Vaillancourt R (2013) Pretreatment of infant formula with sodium polystyrene sulfonate : focus on optimal amount and contact time. Paediatr Drugs 15:43–48CrossRefPubMed
10.
go back to reference Fassinger N, Dabbagh S, Mukhopadhyay S, Lee DY (1998) Mineral content of infant formula after treatment with sodium polystyrene sulfonate or calcium polystyrene sulfonate. Adv Perit Dial 14:274–277PubMed Fassinger N, Dabbagh S, Mukhopadhyay S, Lee DY (1998) Mineral content of infant formula after treatment with sodium polystyrene sulfonate or calcium polystyrene sulfonate. Adv Perit Dial 14:274–277PubMed
11.
go back to reference Bonnet L, Goudable J, Accominotti M, Fontaine D, Cochat P (1997) Effect of ion exchange resins on the composition of milk. Nephrologie 18:287–289PubMed Bonnet L, Goudable J, Accominotti M, Fontaine D, Cochat P (1997) Effect of ion exchange resins on the composition of milk. Nephrologie 18:287–289PubMed
12.
go back to reference Ferrara E, Lemire J, Reznik VM, Grimm PC (2004) Dietary phosphorus reduction by pretreatment of human breast milk with sevelamer. Pediatr Nephrol 19:775–779CrossRefPubMed Ferrara E, Lemire J, Reznik VM, Grimm PC (2004) Dietary phosphorus reduction by pretreatment of human breast milk with sevelamer. Pediatr Nephrol 19:775–779CrossRefPubMed
14.
go back to reference Bartosh SM, Leverson G, Robillard D, Sollinger HW (2003) Long-term outcomes in pediatric renal transplant recipients who survive into adulthood. Transplantation 76:1195–1200CrossRefPubMed Bartosh SM, Leverson G, Robillard D, Sollinger HW (2003) Long-term outcomes in pediatric renal transplant recipients who survive into adulthood. Transplantation 76:1195–1200CrossRefPubMed
15.
go back to reference Reina de la Torre ML, Navarro-Alarcon M, del Moral LM, Lopez GSH, Palomares-Bayo M, Oliveras Lopez MJ, Blanca Herrera RM, Agil A (2014) Serum Zn levels and Cu/Zn ratios worsen in hemodialysis patients, implying increased cardiovascular risk: a 2-year longitudinal study. Biol Trace Elem Res 158:129–135CrossRefPubMed Reina de la Torre ML, Navarro-Alarcon M, del Moral LM, Lopez GSH, Palomares-Bayo M, Oliveras Lopez MJ, Blanca Herrera RM, Agil A (2014) Serum Zn levels and Cu/Zn ratios worsen in hemodialysis patients, implying increased cardiovascular risk: a 2-year longitudinal study. Biol Trace Elem Res 158:129–135CrossRefPubMed
16.
go back to reference Roozbeh J, Sharifian M, Sagheb MM, Shabani S, Hamidian Jahromi A, Afshariani R, Pakfetrat M, Salehi O (2011) Comment on: does zinc supplementation affect inflammatory markers in hemodialysis patients? Ren Fail 33:466–467CrossRefPubMed Roozbeh J, Sharifian M, Sagheb MM, Shabani S, Hamidian Jahromi A, Afshariani R, Pakfetrat M, Salehi O (2011) Comment on: does zinc supplementation affect inflammatory markers in hemodialysis patients? Ren Fail 33:466–467CrossRefPubMed
18.
go back to reference Bock DE, Prabhakaran V, Filler G (2009) Picture of the month: severe zinc deficiency in infancy (acrodermatitis enteropathica-like picture). Arch Pediatr Adolesc Med 163:765–766CrossRefPubMed Bock DE, Prabhakaran V, Filler G (2009) Picture of the month: severe zinc deficiency in infancy (acrodermatitis enteropathica-like picture). Arch Pediatr Adolesc Med 163:765–766CrossRefPubMed
19.
go back to reference American Academy of Pediatrics. Committee on Nutrition, Kleinman RE (2004) Pediatric nutrition handbook. American Academy of Pediatrics, Elk Grove Village American Academy of Pediatrics. Committee on Nutrition, Kleinman RE (2004) Pediatric nutrition handbook. American Academy of Pediatrics, Elk Grove Village
21.
go back to reference Priest ND (2004) The biological behaviour and bioavailability of aluminium in man, with special reference to studies employing aluminium-26 as a tracer: review and study update. J Environ Monit 6:375–403CrossRefPubMed Priest ND (2004) The biological behaviour and bioavailability of aluminium in man, with special reference to studies employing aluminium-26 as a tracer: review and study update. J Environ Monit 6:375–403CrossRefPubMed
22.
go back to reference Bishop NJ, Morley R, Day JP, Lucas A (1997) Aluminum neurotoxicity in preterm infants receiving intravenous-feeding solutions. N Engl J Med 336:1557–1561CrossRefPubMed Bishop NJ, Morley R, Day JP, Lucas A (1997) Aluminum neurotoxicity in preterm infants receiving intravenous-feeding solutions. N Engl J Med 336:1557–1561CrossRefPubMed
23.
go back to reference Cannata-Andia JB (2001) Reconsidering the importance of long-term low-level aluminum exposure in renal failure patients. Semin Dial 14:5–7CrossRefPubMed Cannata-Andia JB (2001) Reconsidering the importance of long-term low-level aluminum exposure in renal failure patients. Semin Dial 14:5–7CrossRefPubMed
24.
go back to reference Hutchison AJ, Smith CP, Brenchley PE (2011) Pharmacology, efficacy and safety of oral phosphate binders. Nat Rev Nephrol 7:578–589CrossRefPubMed Hutchison AJ, Smith CP, Brenchley PE (2011) Pharmacology, efficacy and safety of oral phosphate binders. Nat Rev Nephrol 7:578–589CrossRefPubMed
25.
go back to reference Van Goidsenhoven GM, Gray OV, Price AV, Sanderson PH (1954) The effect of prolonged administration of large doses of sodium bicarbonate in man. Clin Sci (Lond) 13:383–401 Van Goidsenhoven GM, Gray OV, Price AV, Sanderson PH (1954) The effect of prolonged administration of large doses of sodium bicarbonate in man. Clin Sci (Lond) 13:383–401
Metadata
Title
Renal formulas pretreated with medications alters the nutrient profile
Authors
Jacob M. Taylor
Leah Oladitan
Susan Carlson
Jill M. Hamilton-Reeves
Publication date
01-10-2015
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Nephrology / Issue 10/2015
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-015-3115-5

Other articles of this Issue 10/2015

Pediatric Nephrology 10/2015 Go to the issue