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
Preparation:
Initial Infusion Rate:
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
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
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
Failure to check IgA levels: Not checking IgA levels before administration can lead to severe anaphylactic reactions in IgA-deficient patients 1
Infusion rate too rapid: Administering IVIG too quickly is associated with increased adverse reactions 3
Inadequate monitoring: Failing to monitor vital signs during infusion may result in missed early signs of adverse reactions
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.