Experimental models have suggested potential new treatments for human infla
mmatory neuropathy, but current practice is largely based on empirical tria
ls. Evidence from randomized trials supports the use of intravenous immunog
lobulin in Guillain-Barre syndrome, chronic inflammatory demyelinating poly
radiculoneuropathy (CIDP) and multifocal motor neuropathy with conduction b
lock (MMNCB). In Guillain-Barre syndrome and CIDP intravenous immunoglobuli
n is equivalent to but more convenient than plasma exchange. In MMNCB adequ
ate comparative studies of intravenous immunoglobulin and plasma exchange h
ave not been performed. Corticosteroid treatment is beneficial in CIDP, but
not in Guillain-Barre syndrome and may worsen MMNCB. More randomized trial
s and systematic reviews are needed to improve the evidence base for clinic
al practice. Curr Opin Neurol 12:573-579. (C) 1999 Lippincott Williams & Wi
lkins.