What is the proper administration protocol for Intravenous Immunoglobulin (IVIG)?

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Last updated: September 18, 2025View editorial policy

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Intravenous Immunoglobulin (IVIG) Administration Protocol

IVIG should be administered at a dosage of 1-2 g/kg of ideal body weight, usually given over 2 consecutive days (1 g/kg each day), and may be repeated monthly for 1-6 months depending on the clinical indication. 1

Pre-administration Assessment

  • Check serum IgA levels before administering IVIG, as IgA deficiency may lead to fever, infusion reactions, or severe anaphylaxis 1
  • If IgA deficiency is detected, use an IVIG preparation with reduced IgA levels 1
  • Review patient's medical history for risk factors:
    • Renal insufficiency (requires products without sucrose)
    • History of thrombosis
    • Cardiovascular disease
    • Diabetes (monitor blood glucose during infusion)

Dosing Guidelines by Indication

Immune Thrombocytopenia (ITP)

  • Initial dose: 1 g/kg as a one-time dose 1
  • May be repeated if necessary 1
  • Use in conjunction with corticosteroids when rapid increase in platelet count is required 1

Inflammatory Myopathies (Dermatomyositis/Polymyositis)

  • Dosage: 1-2 g/kg of ideal body weight 1
  • Administration: Usually over 2 consecutive days (1 g/kg each day) 1
  • Frequency: Monthly for 1-6 months 1

Kawasaki Disease

  • Standard dosage: 2 g/kg as a single infusion 1

Administration Protocol

  1. Preparation:

    • Calculate dose based on ideal body weight rather than actual body weight for obese patients 2
    • If dose exceeds 80 g, consider administering over 3-5 days at 0.4 g/kg/day 1
  2. Initial Infusion Rate:

    • Start at 0.5 mg/kg/min 3
    • Gradually increase to 4-8 mg/kg/min as tolerated 3
    • Ensure adequate hydration before infusion 3
  3. Monitoring During Infusion:

    • Monitor vital signs every 15-30 minutes 3
    • Watch for signs of adverse reactions:
      • Headache, flushing, fever
      • Hypertension or hypotension
      • Anaphylactic reactions
  4. Management of Adverse Reactions:

    • Mild reactions: Reduce infusion rate, administer antihistamines 3
    • Moderate to severe reactions: Temporarily stop infusion, administer corticosteroids, restart at slower rate if symptoms resolve 3
    • Anaphylactic reactions: Stop infusion immediately, administer epinephrine, antihistamines, corticosteroids, and provide vital support 3

Special Considerations

  • For patients requiring plasmapheresis, schedule IVIG administration after completion of plasmapheresis sessions to prevent removal of IVIG 3
  • If using rituximab with IVIG, hold plasmapheresis for 48-72 hours after rituximab infusion 3
  • Combined therapy with plasmapheresis and immunosuppression increases infection risk 3

Common Pitfalls to Avoid

  1. Incorrect weight-based dosing: Using actual body weight instead of ideal body weight in obese patients can lead to overdosing and increased adverse effects 2

  2. Failure to check IgA levels: Not checking IgA levels before administration can lead to severe anaphylactic reactions in IgA-deficient patients 1

  3. Infusion rate too rapid: Administering IVIG too quickly is associated with increased adverse reactions 3

  4. Inadequate monitoring: Failing to monitor vital signs during infusion may result in missed early signs of adverse reactions

  5. Poor timing with other therapies: Administering IVIG before plasmapheresis will result in removal of the therapeutic agent and reduced efficacy 3

By following this protocol, you can optimize the safety and efficacy of IVIG administration while minimizing the risk of adverse events.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Immunosuppressive Therapies

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 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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