Guillain-Barré syndrome
An acute immune-mediated polyradiculoneuropathy causing progressive symmetrical weakness, areflexia and potentially rapid respiratory or autonomic failure.
In a nutshell
GBS is an acute peripheral polyradiculoneuropathy causing progressive symmetrical weakness and areflexia, often after an infection. The emergency is respiratory or bulbar failure: admit, trend vital capacity and clinical respiratory function, involve critical care early, and treat significant or worsening disease with IV immunoglobulin or plasma exchange.
Classic presentation
Progressive symmetrical leg weakness with reduced or absent reflexes, paraesthesia or neuropathic pain and possible facial, bulbar or autonomic involvement after a recent diarrhoeal or respiratory illness.
Key points
- GBS is a peripheral nerve process: weakness is usually symmetrical and progressive with hyporeflexia or areflexia.
- Serial vital capacity or forced vital capacity and clinical bulbar assessment are more useful than oxygen saturation alone for anticipating respiratory failure.
- CSF albuminocytological dissociation supports GBS but can be absent early; nerve-conduction studies support diagnosis and subtype.
- Anti-GQ1b is most useful when Miller Fisher syndrome is suspected; routine antiganglioside testing has limited value in typical GBS.
- IV immunoglobulin and plasma exchange are alternative disease-modifying treatments; corticosteroids are not recommended for GBS and routine sequential IVIG plus plasma exchange is not supported.
- Rehabilitation, thrombosis prevention, pain management, autonomic monitoring and diagnostic reassessment are part of treatment, not optional extras.
First-line investigation
Serial respiratory and bulbar assessment with neurological examination, supported by lumbar puncture and nerve-conduction studies; do not delay escalation while waiting for a later supportive test.
Management
Admit and protect the airway
Confirm the pattern without delaying treatment
Use one evidence-based immunotherapy
Prevent secondary harm
Exam traps
- Normal oxygen saturation does not exclude impending respiratory failure: trend vital capacity and assess cough, speech, swallow and work of breathing.
- Normal CSF protein early in the illness does not exclude GBS.
- A sensory level, marked asymmetry, early sphincter dysfunction or brisk reflexes should prompt reconsideration of spinal cord or another neurological disease.
- Do not use corticosteroids as disease-modifying treatment for GBS.
- Miller Fisher syndrome is the ophthalmoplegia, ataxia and areflexia variant, not simply an eye presentation of classical GBS.
Illustrations
Key sources
- European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of Guillain-Barré syndrome (Current evidence-based international GBS guideline used as a specialist fallback because there is no newer dedicated UK national GBS guideline; published 2023.)Updated 1 Dec 2023
- NHS: Guillain-Barré syndrome (Current NHS information on symptoms, urgent assessment, investigations, hospital treatment, recovery and follow-up.)Updated 12 Aug 2024
- BNF online (Current UK prescribing information for analgesics, anticoagulants, immunoglobulin and medicines requiring renal, respiratory or interaction checks.)
This page is exam revision material, not medical advice, and must not be used for patient care. Always check drug doses against the BNF and current guidance. Full disclaimer.

