Guillain-Barré is usually triggered by an infection and is particularly associated with Campylobacter jejuni, cytomegalovirus (CMV) and Epstein-Barr virus (EBV).
The characteristic features of Guillain-Barré syndrome are symmetrical ascending weakness, reduced reflexes, and there may be peripheral loss of sensation or neuropathic pain.
Management of Guillain-Barré syndrome involves supportive care, VTE prophylaxis, IV immunoglobulins (IVIG) first-line, and plasmapheresis is an alternative to IVIG.
The diagnosis of Guillain-Barré syndrome is made clinically, using the Brighton criteria, and is supported by investigations such as nerve conduction studies and lumbar puncture for cerebrospinal fluid.
Most patients with Guillain-Barré syndrome eventually make either a full recovery or are left with minor symptoms, while some are left with significant disability.