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Published on: September 12, 2016
Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis
Mark Lipphardt1, Manuel Wallbach1, Michael J Koziolek1
1Department of Nephrology and Rheumatology, University Medical Center Göttingen, Robert-Koch-Str. 40, D-37075 Goettingen, Germany.
For acute, steroid-unresponsive multiple sclerosis (MS) relapses, both plasma exchange (PE) and immunoadsorption (IA) show similar effectiveness. These apheresis techniques offer viable treatment options when high-dose steroids fail.
Area of Science:
- Neurology
- Immunology
- Clinical Therapeutics
Background:
- Multiple sclerosis (MS) is a central nervous system inflammatory disease causing demyelination and axonal loss.
- Acute MS relapses are initially treated with high-dose intravenous methylprednisolone.
- Glucocorticosteroid-unresponsive relapses necessitate alternative immunomodulatory treatments like apheresis.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy of plasma exchange (PE) and immunoadsorption (IA) for acute, glucocorticosteroid-unresponsive MS relapses.
- To compare treatment responses between PE and IA in patients with MS and neuromyelitis optica (NMO).
Main Methods:
- Systematic review and meta-analysis of observational studies and randomized controlled trials.
- Inclusion of studies investigating PE or IA in various MS courses and NMO.
- Evaluation of data from 1,383 patients.
Main Results:
- Therapy response rates were 76.6% for PE and 80.6% for IA in patients with relapsing-remitting MS and clinically isolated syndrome.
- No significant difference in treatment effectiveness was observed between PE and IA.
- Both PE and IA demonstrated therapeutic benefits in acute, steroid-refractory MS relapses.
Conclusions:
- Plasma exchange and immunoadsorption are comparable and effective treatment options for acute, glucocorticosteroid-unresponsive MS relapses.
- These apheresis methods provide valuable therapeutic alternatives when standard steroid treatment is insufficient.
- Further research may clarify optimal use in specific MS subtypes and NMO.
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