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Published on: November 9, 2017
[Present treatment of Guillain-Barre syndrome]
1Service de Reanimation Médicale, Hôpital Raymond Poincaré, 92380 Garches. jean-claude.raphael@rpc.ap-hop-paris.fr
Insights
Guillain-Barré Syndrome (GBS) management focuses on plasma exchange (PE) and intravenous immunoglobulins (IVIg) as effective treatments. Corticosteroids are not beneficial for GBS patients.
Area of Science:
- Neurology
- Immunology
Context:
- Guillain-Barré Syndrome (GBS) affects 1.5 per 100,000 individuals annually.
- GBS has a 5% mortality rate, with 10% of patients experiencing severe disability.
- Specialist care, intensive therapy, and rehabilitation are crucial for GBS patient outcomes.
Purpose:
- To clarify treatment indications and effectiveness for Guillain-Barré Syndrome.
- To compare plasma exchange (PE) and intravenous immunoglobulins (IVIg) in GBS management.
Summary:
- Plasma exchange (PE) is the primary treatment for Guillain-Barré Syndrome, with varying session recommendations based on disease severity.
- High-dose IVIg (0.4 g/kg daily for 5 days) is as effective as PE for moderate to severe GBS.
- Treatment choice between PE and IVIg depends on contraindications and availability; further trials are ongoing.
Impact:
- Optimized treatment protocols for Guillain-Barré Syndrome can improve patient outcomes.
- Understanding the efficacy of PE and IVIg guides clinical decision-making in GBS management.
- Ongoing research aims to refine GBS treatment strategies for different disease severities.
Abstract:
The annual incidence of Guillain-Barré Syndrome is 1.5 per 100,000. The mortality rate is about 5%, and 10% of patients remain severely disabled one year after neurological onset. Specialist teams, intensive care and rehabilitation are essential for patient management and should be provided in appropriate hospital units. Neither oral nor intravenous corticosteroids are beneficial. Plasma exchange (PE) is the first-line treatment, improving outcome in several randomised, controlled clinical trials. The indications for treatment have been clarified. Two PE sessions are recommended for patients who are able to walk (mild forms), with two additional sessions if they deteriorate. Four sessions are sufficient for patients who are unable to walk unaided (moderate) or who require mechanical ventilation (severe). Further PE sessions are not helpful for patients with more severe disease, or if there is no response. High-dose intravenous immunoglobulins (0.4 g/kg daily for 5 days) and PE are equally effective in patients with intermediate and severe forms. The choice between the two treatments depends on their respective contraindications and local availability. A trial is underway to determine the indications and optimal dose of IVIg and the optimal number of PE sessions in the different disease severities.
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