What nutritional supplements are recommended for a patient with Acute Kidney Injury (AKI)?

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Nutritional Supplementation in Acute Kidney Injury

Patients with AKI require supplementation of trace elements (selenium, zinc, copper) and water-soluble vitamins (thiamine, vitamin C, folate), with increased attention to these losses if undergoing kidney replacement therapy, while avoiding high-dose glutamine and using renal-specific rather than standard multivitamins. 1

Trace Element Supplementation

Monitor and supplement trace elements due to increased requirements during critical illness and large losses during kidney replacement therapy (KRT). 1

Priority Trace Elements:

  • Selenium and Zinc: Serum levels decrease significantly during continuous KRT (CKRT) due to increased utilization in critical illness and dialysis losses 1. Standard supplementation of 50 mg/day zinc and 75 mg/day selenium may not correct deficiencies in patients on chronic KRT, suggesting even higher requirements 1

  • Copper: Large effluent losses during CKRT far exceed nutritional intakes 1. When CKRT is required for more than 2 weeks, measure blood copper levels and consider intravenous administration of approximately 3 mg/day to prevent deficiency 1

Water-Soluble Vitamin Supplementation

Water-soluble vitamins should be monitored and supplemented, with special attention to vitamin C, folate, and thiamine. 1

Specific Vitamin Requirements:

  • Thiamine (B1): Daily losses during dialysis are approximately 4 mg/day, with deficiency documented in 24.7% of hemodialysis patients 1, 2. Patients on CKRT may require 100-300 mg/day 2

  • Vitamin C: Daily effluent losses are approximately 68 mg 1. Supplement at least 90 mg/day for men and 75 mg/day for women, but do not greatly exceed these amounts due to oxalate accumulation risk 2

  • Folate: Daily losses during dialysis are approximately 0.3 mg 1

  • Vitamin B6: Deficiency documented in 35.1% of hemodialysis patients 1, 2

Renal-Specific vs. Standard Multivitamins

Use renal-specific multivitamins rather than standard multivitamins in AKI patients, particularly those on dialysis. 2

Critical Differences:

  • Renal vitamins contain lower or absent fat-soluble vitamins (A, E, K) to prevent toxicity, while providing adequate water-soluble vitamins to replace dialysis losses 2

  • Vitamin A accumulates to toxic levels in kidney disease because retinol-binding protein is normally catabolized in renal tubules; standard multivitamins containing vitamin A pose significant toxicity risk and should be avoided 2

  • Renal formulas have lower electrolyte content (sodium, potassium, phosphorus) to prevent hyperkalemia and hyperphosphatemia 2

  • Vitamin K is typically excluded from renal vitamins, which is particularly important for patients on anticoagulants like warfarin 2

Protein and Amino Acid Supplementation

Enteral supplementation of amino acids is recommended to achieve protein goals, with patients on KRT requiring at least 1.5 g/kg/day plus an additional 0.2 g/kg/day to compensate for amino acid losses during dialysis. 1, 3, 4, 5

Important Caveats:

  • Moderately restricted protein regimens may be considered ONLY in metabolically stable AKI patients without catabolic conditions and not undergoing KRT 1. This applies to selected non-catabolic conditions such as drug-induced isolated AKI or contrast-associated AKI 1

  • When catabolic status exists, protein restriction invariably worsens nitrogen balance and is contraindicated 1

Supplements to AVOID

High-Dose Glutamine:

In critically ill patients with AKI, additional high-dose parenteral glutamine shall NOT be administered. 1

  • The REDOX study demonstrated that high doses of intravenous or enteral alanyl-glutamine are harmful in the subgroup of critically ill patients with kidney failure 1

  • This recommendation stands despite documented glutamine losses of approximately 1.2 g/day during CKRT 1

Omega-3 Fatty Acids:

There is insufficient evidence to support routine use of omega-3 PUFA supplements or parenteral nutrition solutions enriched with omega-3 in hospitalized AKI patients. 1

  • No randomized controlled trials currently support their use in hospitalized patients with AKI, despite interesting experimental data 1

Electrolyte Monitoring

Electrolyte abnormalities are common in AKI patients receiving KRT and must be closely monitored. 1

Common Abnormalities with KRT:

  • Hypophosphatemia (prevalence 60-80% in ICU) is associated with respiratory failure, cardiac arrhythmias, and prolonged hospitalization 1

  • Hypokalemia and hypomagnesemia are common with intensive/prolonged KRT 1

  • The initiation of KRT is a major risk factor for development of hypophosphatemia 1

Clinical Algorithm for Supplementation

  1. Assess metabolic status: Determine if patient is catabolic or metabolically stable 1

  2. If on KRT or anticipated KRT >2 weeks:

    • Initiate renal-specific multivitamin 2
    • Monitor and supplement selenium, zinc, copper 1
    • Ensure adequate water-soluble vitamins (thiamine, folate, vitamin C, B6) 1
    • Monitor copper levels if CKRT >2 weeks 1
  3. Protein supplementation: Provide 1.5-1.7 g/kg/day if on KRT 1, 3, 4

  4. Avoid: High-dose glutamine supplementation 1

  5. Monitor electrolytes closely: Particularly phosphate, potassium, magnesium 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Renal Vitamins vs. Multivitamins for Kidney Disease Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Nutritional support in acute kidney injury.

Journal of nephrology, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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