Lab Values as Indications for Plasmapheresis
Specific lab values that indicate the need for plasmapheresis include rapidly increasing serum creatinine, presence of anti-GBM antibodies with renal dysfunction, high GM-CSF autoantibody titers in refractory pulmonary alveolar proteinosis, and elevated IgM levels (≥5,000 mg/dL) causing hyperviscosity. 1
Renal Indications
ANCA-Associated Vasculitis
- Rapidly increasing serum creatinine - Plasmapheresis is recommended for patients with:
Anti-GBM Disease (Goodpasture's Syndrome)
- Positive anti-GBM antibodies with concurrent renal dysfunction 1
- Plasmapheresis is indicated as part of initial treatment along with immunosuppression
Overlap Syndromes
- Concurrent ANCA and anti-GBM antibodies - Plasmapheresis is suggested for patients with this overlap syndrome 1
Pulmonary Indications
Diffuse Pulmonary Hemorrhage
- Hemoptysis with declining oxygen saturation and pulmonary infiltrates on imaging 1
- Recommended regimen: 60 mL/kg volume replacement, daily until bleeding stops, then every other day for a total of 7-10 treatments 1
Pulmonary Alveolar Proteinosis (PAP)
- High GM-CSF autoantibody titers in autoimmune PAP 1
- Indicated for patients who:
- Remain significantly symptomatic
- Require high-flow supplemental oxygen (≥4 L/min)
- Need two or more whole lung lavages over a one-year period
- Have failed GM-CSF and rituximab therapies 1
Hematologic Indications
Hyperviscosity in Waldenström's Macroglobulinemia
- IgM levels ≥5,000 mg/dL (even if asymptomatic) 1
- Symptomatic hyperviscosity regardless of specific IgM level 1
- Should be performed before rituximab administration to prevent IgM flare 1
Thrombotic Thrombocytopenic Purpura (TTP)
- Severe thrombocytopenia with microangiopathic hemolytic anemia 2
- Elevated LDH and schistocytes on peripheral blood smear
- Low ADAMTS13 activity (<10%)
Neurologic Indications
Autoimmune Encephalitis
- Positive neural autoantibodies (e.g., NMDAR, LGI1) with encephalopathy 1
- Consider when other therapies have failed or rapid improvement is needed
Important Clinical Considerations
Timing is critical - In conditions like pulmonary hemorrhage or rapidly progressive glomerulonephritis, early initiation improves outcomes
Monitoring during treatment:
- For hyperviscosity: Monitor IgM levels
- For ANCA vasculitis: Monitor serum creatinine and clinical symptoms
- For pulmonary hemorrhage: Monitor oxygen saturation and hemoptysis
Potential complications:
- Hemodynamic shifts
- Infection risk
- Thrombosis
- Removal of therapeutic medications (e.g., rituximab)
Common pitfalls:
- Delaying plasmapheresis in life-threatening conditions
- Not collecting appropriate samples before initiating plasmapheresis (may alter antibody test results)
- Failure to provide appropriate replacement fluids
Practical tip: When using plasmapheresis with rituximab, administer rituximab after completing plasmapheresis sessions to prevent removal of the therapeutic antibody 1
Remember that plasmapheresis should be considered as part of a comprehensive treatment approach that typically includes appropriate immunosuppressive therapy for the underlying condition.