IVIG Dilution and Dosing Guidelines
IVIG should be administered at a dose of 2 g/kg of ideal body weight, typically given over 2-5 consecutive days, with specific dosing adjusted based on the clinical indication. 1
Dosing Guidelines by Indication
- Immunodeficiency disorders: 300-400 mg/kg IV monthly for replacement therapy 1
- Autoimmune conditions: 1-2 g/kg of ideal body weight, usually given over 2 consecutive days 1
- Kawasaki Disease: 2 g/kg as a single infusion 1
- Multisystem Inflammatory Syndrome in Children (MIS-C): 2 g/kg based on ideal body weight 2
- Immune Thrombocytopenic Purpura (ITP): 1 g/kg as a one-time dose, which may be repeated if necessary 1
- Immune-related adverse events from checkpoint inhibitors: 2 g/kg over 5 days 2
- Guillain-Barré Syndrome: 0.4 g/kg/day for 5 days for a total dose of 2 g/kg 2
- Invasive bacterial infections with hypogammaglobulinemia: 400 mg/kg body weight every 2-4 weeks 2
Pre-Administration Assessment
- IgA deficiency screening: Check serum IgA level before administering IVIG to prevent severe anaphylactic reactions 1
- Risk factor assessment: Review medical history for renal dysfunction, thrombotic risk, or history of previous infusion reactions 1
- Cardiac function evaluation: Assess cardiac function and fluid status before administering IVIG, particularly in patients with cardiac dysfunction 2
Administration Protocols
- Standard dilution: IVIG should be diluted according to manufacturer's guidelines, typically in 5% dextrose or 0.9% sodium chloride 1
- Initial infusion rate: Begin at a slow rate (0.5-1 mg/kg/min) and gradually increase if tolerated 1
- Divided dosing: In patients with cardiac dysfunction, IVIG may be given in divided doses (1 g/kg daily over 2 days) 2
- Weight-based calculations: Using ideal body weight (IBW) or adjusted body weight (adjBW) rather than actual body weight (ABW) for dose calculations provides similar efficacy with cost savings 3
Premedication Recommendations
- Standard premedication: Diphenhydramine and acetaminophen before IVIG infusion 1
- For patients with history of reactions: Consider adding corticosteroids as premedication 1
Monitoring During Administration
- Vital signs: Monitor blood pressure, heart rate, respiratory rate, and temperature during infusion 1
- Renal function: Monitor urine output and serum creatinine during administration 1
- Infusion reactions: Watch for headache, flushing, chills, myalgia, wheezing, tachycardia, lower back pain, nausea, and hypotension 1
Management of Adverse Reactions
- Mild reactions: Slow or temporarily stop the infusion and administer additional antihistamines or antipyretics 1
- Severe reactions: Immediately cease infusion, administer epinephrine, and notify physician for anaphylaxis or severe hypotension 1
Special Considerations
- Patients with cardiac dysfunction: Consider divided dosing (1 g/kg daily over 2 days) to minimize fluid overload 2
- IgA deficiency: Use IVIG preparations with reduced IgA levels 1
- Dermatological autoimmune diseases: IVIG is typically administered at 2 g/kg distributed over 2-5 days every 4 weeks 4
Pitfalls and Caveats
- Volume overload risk: Patients with cardiac or renal dysfunction are at increased risk; consider slower infusion rates and divided dosing 1
- Thrombotic events: IVIG can increase blood viscosity; ensure adequate hydration and consider anticoagulation in high-risk patients 1
- Cost considerations: Using ideal body weight or adjusted body weight for dosing calculations provides similar efficacy with significant cost savings compared to actual body weight 3
- Initial infusions: Proceed with caution in immunodeficient patients who have not been treated during the previous 8 weeks or never treated, as they are at risk for complement-mediated adverse reactions 5