Guillain‐Barré syndrome: A comprehensive review
Guillain‐Barré syndrome (GBS) is a potentially devastating yet treatable disorder. A classically postinfectious, immune‐mediated, monophasic polyradiculoneuropathy, it is the leading global cause of acquired neuromuscular paralysis. In most cases, the immunopathological process driving nerve injury...
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Format: | Journal article |
Language: | English |
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Wiley Open Access
2024
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author | Bellanti, R Rinaldi, S |
author_facet | Bellanti, R Rinaldi, S |
author_sort | Bellanti, R |
collection | OXFORD |
description | Guillain‐Barré syndrome (GBS) is a potentially devastating yet treatable disorder. A classically postinfectious, immune‐mediated, monophasic polyradiculoneuropathy, it is the leading global cause of acquired neuromuscular paralysis. In most cases, the immunopathological process driving nerve injury is ill‐defined. Diagnosis of GBS relies on clinical features, supported by laboratory findings and electrophysiology. Although previously divided into primary demyelinating or axonal variants, this dichotomy is increasingly challenged, and is not endorsed by the recent European Academy of Neurology (EAN)/Peripheral Nerve Society (PNS) guidelines. Intravenous immunoglobulin and plasma exchange remain the primary modalities of treatment, regardless of the electrophysiological subtype. Most patients recover, but approximately one‐third require mechanical ventilation, and 5% die. Disease activity and treatment response are currently monitored through interval neurological examination and outcome measures, and the potential role of fluid biomarkers is under ongoing scrutiny. Novel potential therapies for GBS are being explored but none have yet modified clinical practice. This review provides a comprehensive update on the pathological and clinical aspects of GBS for clinicians and scientists. |
first_indexed | 2024-09-25T04:07:53Z |
format | Journal article |
id | oxford-uuid:c9baa848-a1f4-4716-9e1e-198a0b00b26f |
institution | University of Oxford |
language | English |
last_indexed | 2024-09-25T04:07:53Z |
publishDate | 2024 |
publisher | Wiley Open Access |
record_format | dspace |
spelling | oxford-uuid:c9baa848-a1f4-4716-9e1e-198a0b00b26f2024-05-30T20:04:59ZGuillain‐Barré syndrome: A comprehensive reviewJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c9baa848-a1f4-4716-9e1e-198a0b00b26fEnglishJisc Publications RouterWiley Open Access2024Bellanti, RRinaldi, SGuillain‐Barré syndrome (GBS) is a potentially devastating yet treatable disorder. A classically postinfectious, immune‐mediated, monophasic polyradiculoneuropathy, it is the leading global cause of acquired neuromuscular paralysis. In most cases, the immunopathological process driving nerve injury is ill‐defined. Diagnosis of GBS relies on clinical features, supported by laboratory findings and electrophysiology. Although previously divided into primary demyelinating or axonal variants, this dichotomy is increasingly challenged, and is not endorsed by the recent European Academy of Neurology (EAN)/Peripheral Nerve Society (PNS) guidelines. Intravenous immunoglobulin and plasma exchange remain the primary modalities of treatment, regardless of the electrophysiological subtype. Most patients recover, but approximately one‐third require mechanical ventilation, and 5% die. Disease activity and treatment response are currently monitored through interval neurological examination and outcome measures, and the potential role of fluid biomarkers is under ongoing scrutiny. Novel potential therapies for GBS are being explored but none have yet modified clinical practice. This review provides a comprehensive update on the pathological and clinical aspects of GBS for clinicians and scientists. |
spellingShingle | Bellanti, R Rinaldi, S Guillain‐Barré syndrome: A comprehensive review |
title | Guillain‐Barré syndrome: A comprehensive review |
title_full | Guillain‐Barré syndrome: A comprehensive review |
title_fullStr | Guillain‐Barré syndrome: A comprehensive review |
title_full_unstemmed | Guillain‐Barré syndrome: A comprehensive review |
title_short | Guillain‐Barré syndrome: A comprehensive review |
title_sort | guillain barre syndrome a comprehensive review |
work_keys_str_mv | AT bellantir guillainbarresyndromeacomprehensivereview AT rinaldis guillainbarresyndromeacomprehensivereview |