How is selenium replenishment typically managed?

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Last updated: November 11, 2025View editorial policy

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Selenium Replenishment Management

Selenium replenishment should be initiated when plasma selenium falls below 0.4 mmol/L (<32 mg/L), starting with 100 mg/day via enteral or IV route, with the IV route preferred for rapid correction in severe deficiency, requiring up to 400 mg/day for 7-10 days. 1

Assessment and Monitoring

When to Measure Selenium Status

  • Measure plasma selenium and CRP at baseline in all patients likely to receive parenteral nutrition for more than two weeks or commencing home parenteral nutrition 1
  • Repeat measurements every 3-6 months during ongoing parenteral nutrition, or more frequently based on initial results 1
  • Long-term enteral nutrition patients require monitoring as selenium deficiency may develop depending on the feeding product used 1

Interpreting Selenium Levels

Critical consideration: Inflammation significantly affects plasma selenium interpretation. 1

  • CRP 10-40 mg/L: Expect 15-25% reduction in plasma selenium 1
  • CRP 41-80 mg/L: Expect approximately 35% reduction 1
  • CRP >80 mg/L: Expect approximately 50% reduction 1

Always measure CRP simultaneously with plasma selenium to correct for inflammatory redistribution, as selenium may return to normal without supplementation once inflammation resolves 1

Treatment Thresholds

Absolute Indications for Supplementation

  • Plasma selenium <0.4 mmol/L (<32 mg/L): Always triggers supplementation regardless of inflammatory status 1
  • Plasma selenium <0.75 mmol/L in patients without inflammation (CRP <20 mg/L): Initiate supplementation to prevent immune dysfunction and other non-specific consequences of depletion 1

Dosing Strategies

Standard Maintenance Requirements

  • Home parenteral nutrition without inflammation: 60-100 mg/day to normalize plasma selenium 1
  • Route selection: Enteral route preferred when gastrointestinal tract is available due to high absorption; IV route provides more rapid correction 1

Repletion Dosing for Deficiency

  • Recent reduced intake with depletion: Up to 200 mg/day (twice normal daily amount) with monitoring of plasma selenium levels 1
  • Oral administration acceptable if gastrointestinal tract is functional 1
  • Prolonged enteral nutrition deficiency: 100 mg/day for 2 weeks should restore blood levels and reduce symptoms 1

High-Requirement Clinical Scenarios

Burns patients with high selenium losses:

  • 375 mg/day IV provides more rapid healing and fewer infections 1

Major trauma and cardiac surgery patients:

  • 275 mg/day may provide benefit 1

Renal replacement therapy patients:

  • Increased amounts required due to increased losses and oxidative stress 1

Specific documented losses (e.g., continuous renal replacement therapy):

  • Balance studies guide dosing, which may reach an additional 300 mg/day 1

Rapid Correction Protocol

For plasma selenium <0.4 mmol/L (30 mg/L):

  • IV route for rapid correction: Up to 400 mg/day for at least 7-10 days 1
  • Recheck status after initial correction period 1

Critical Pitfalls to Avoid

Do Not Use High-Dose Selenium in ICU

Meta-analysis shows no consistent benefit from massively increased selenium supply (1000-4000 mg/day) in ICU patients, and this practice is now advised against. 1 This represents an important shift from earlier speculation about potential benefits.

Monitor for Toxicity

  • Upper toxicity limits: Plasma selenium 6-12 mmol/L before toxicity symptoms occur 1
  • Chronic overexposure concerns: Positively associated with type 2 diabetes and high-grade prostate cancer 1
  • Oral tolerable upper limit: 400 mcg/day 2

Account for Inflammation

Common error: Treating low selenium levels during acute inflammation without considering redistribution. Plasma selenium may normalize spontaneously as inflammation resolves without supplementation 1. Always interpret selenium levels in context of CRP values.

Pediatric Considerations

  • Infants on parenteral nutrition: 6 mcg/kg/day prevents biochemical deficiency 1
  • Preterm infants at higher risk for aluminum toxicity with prolonged parenteral selenium administration due to immature renal function 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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