IVIG Infusion Protocol for Patients with Renal Impairment and Thrombotic Risk
In patients with impaired renal function and thrombotic risk, IVIG should be infused at a reduced rate of 1-2 mL/kg/hour with mandatory pre-hydration using saline solutions, discontinuation of diuretics, and avoidance of sucrose-containing preparations when possible. 1
Pre-Infusion Risk Assessment and Preparation
Mandatory Screening
- Check IgA levels before first infusion to identify IgA deficiency (<7 mg/dL), which carries risk of anaphylaxis from anti-IgA antibodies 2
- Baseline renal function testing (serum creatinine, BUN) is essential, as patients with creatinine clearance <60 mL/min are at significantly elevated risk for acute tubular necrosis 1
- Assess for additional risk factors: age >65 years, diabetes, concurrent nephrotoxic medications, and hypovolemia 1
Pre-Treatment Interventions for High-Risk Patients
- Discontinue diuretics before infusion 1
- Initiate IV hydration with normal saline starting before IVIG administration 1
- Hold nephrotoxic agents including NSAIDs, contrast media, and aminoglycosides 1
- Monitor for thrombotic events during and after infusion, particularly in patients with cardiovascular risk factors 2
Infusion Protocol
Dosing Guidelines
The standard therapeutic dose varies by indication:
- Immune thrombocytopenia: 1 g/kg as a single dose, may repeat if necessary 2
- Autoimmune conditions requiring rapid response: 2 g/kg divided over 2-5 days 2, 3
- Immunodeficiency replacement: 0.2-0.4 g/kg monthly 4
Critical caveat: The dose of 90 mg total over 2 days mentioned in some contexts represents severe underdosing—standard dosing for a 30-35 kg child would be 30-70 grams total (1-2 g/kg), not 90 mg 3
Infusion Rate for Renal Protection
For patients with renal impairment or thrombotic risk, infuse at 1-2 mL/kg/hour maximum 1. This is substantially slower than standard rates and is the single most important modification for nephroprotection.
- Start initial infusions cautiously, particularly in treatment-naive patients who face higher risk of complement-mediated reactions 4
- The infusion should be administered over at least 2 hours when given through peripheral access 2
- Central line placement solely for IVIG is discouraged; consider subcutaneous immunoglobulin as alternative for difficult venous access 2
Product Selection
While no definitive evidence proves one formulation safer, acute renal failure has been reported predominantly with sucrose-containing preparations, though also with maltose and glucose formulations 1. When available, consider non-sucrose stabilized products for high-risk patients 1.
Monitoring During and After Infusion
Acute Monitoring
- Watch for anaphylaxis throughout infusion, especially in IgA-deficient patients 2
- Monitor for thrombotic events including deep vein thrombosis, pulmonary embolism, and stroke 2
- Observe for infusion reactions: headache, chills, rigors, fever, myalgia 2
Post-Infusion Surveillance
- Renal function monitoring: Check serum creatinine within 10 days post-infusion, as acute tubular necrosis typically manifests within this timeframe with recovery usually occurring within 10 days 1, 5
- Serial monitoring for patients on chronic therapy: Renal function should be assessed before each infusion cycle 2, 5
- The incidence of IVIG-associated renal impairment is approximately 6.7%, with 1.7% experiencing irreversible damage 5
Long-Term Monitoring for Chronic Therapy
- IgG trough levels every 6-12 months (more frequently in growing children) 2
- Complete blood count and comprehensive metabolic panel at regular intervals 2
- Clinical response assessment to determine if dose adjustment is needed 2
Special Populations
Pregnancy
Pregnant patients requiring IVIG should receive either corticosteroids or IVIG, with mode of delivery based on obstetric indications rather than IVIG therapy 2
HIV and HCV Patients
For secondary ITP due to HIV, treat the underlying infection with antivirals first unless clinically significant bleeding is present 2. For HCV-associated ITP, IVIG is preferred initial treatment with close platelet monitoring due to risk of interferon-induced worsening 2
Common Pitfalls to Avoid
- Do not use standard infusion rates in renal patients—this is the primary cause of osmotic nephrosis 1
- Do not skip IgA screening—rare but potentially fatal anaphylaxis can occur 2
- Do not administer without adequate hydration in high-risk patients 1
- Do not assume all adverse reactions are allergic—volume overload is common and distinct from hypersensitivity 2
- Do not fail to monitor renal function post-infusion—nephrotoxicity may be irreversible if not detected early 5