Abstract
Treatment of specific immune-mediated neuromuscular disorders involves consideration of many factors including severity of illness, concurrent medical problems, supportive therapies, and immune-modulating therapies. Many immune-modulating therapies are available, including steroids, an increasing number of immunosuppressive drugs, plasmapheresis, and intravenous immunoglobulin (IVIG). Deciding on which immune-modulating therapy involves selecting from those with proven efficacy for a specific disorder and global considerations of which therapies are most appropriate for an individual patient's circumstances. IVIG has become a commonly used therapy as it is well tolerated, easily administered, and is often efficacious with a relatively rapid action. IVIG has become a first-line therapy for several immune-mediated demyelinating polyneuropathies and may play a role in treating exacerbations of myasthenia gravis and selected chronic treatment-refractory cases of Lambert-Eaton myasthenic syndrome, dermatomyositis, and polymyositis.
Original language | English (US) |
---|---|
Pages (from-to) | 340-346 |
Number of pages | 7 |
Journal | Seminars in Neurology |
Volume | 27 |
Issue number | 4 |
DOIs | |
State | Published - Sep 1 2007 |
Keywords
- Chronic inflammatory demyelinative polyneuropathy
- Dermatomyositis
- Guillain-Barré syndrome
- Intravenous immunoglobulin
- Lambert-Eaton myasthenic syndrome
- Multifocal motor neuropathy
- Myasthenia gravis
- Neuromuscular disorders
- Polymyositis
ASJC Scopus subject areas
- Neurology
- Clinical Neurology