GUILLAIN-BARRÉ SYNDROME: EVIDENCE-BASED THERAPEUTIC STRATEGIES

Authors

  • Mauro de Deus Passos Author
  • Ryan Rafael Barros de Macedo Author
  • José Micael Delgado Barbosa Author
  • Stela Santos de Sousa Author
  • Luiz Gustavo Cambruzzi Zimmer Author
  • José Ricardo dos Santos Author
  • Fernando Gomes Costa Author
  • Allan Brendell Nobre Teixeira Author
  • Rubia Martinez Santos Author
  • Gênesis Ribeiro Leite Author
  • Amanda Ramos Palacio Author
  • Natiéli Tais Seleprin Author

Keywords:

Guillain-Barré Syndrome, Immunotherapy, Prognosis, Rehabilitation, Biomarkers, Complement System

Abstract

Guillain-Barré syndrome (GBS) is an acute immune-mediated polyradiculoneuropathy and the leading cause of acquired neuromuscular paralysis in adults, with a low incidence but a significant impact on morbidity, mortality, and functional disability. This narrative review, based on recent international guidelines and high-impact studies, discusses in an integrated manner acute therapeutic strategies, prognostic stratification, rehabilitation, and emerging therapies. In acute treatment, intravenous immunoglobulin (IVIg) and plasmapheresis (PLEX) show globally equivalent efficacy in accelerating functional recovery when used within the therapeutic window, while the isolated use of corticosteroids and the routine repetition of a second course of IVIg are not recommended. Risk stratification using validated scores, such as EGRIS/EGBS, EGOS, and mEGOS, allows estimation of the probability of mechanical ventilation and independent ambulation, and should be used in a complementary way to clinical judgment. In the subacute and chronic phases, supervised and multidisciplinary rehabilitation plays a central role, particularly in reducing fatigue, improving strength and quality of life, compared to unsupervised home programs. In the field of molecular therapies, complement inhibitors, especially C1q blockade, and agents targeting FcRn, still under investigation, are emerging. Simultaneously, neurofilament light chain (NfL) is emerging as an important biomarker of axonal damage and functional prognosis. Together, these advances point to a future of more personalized management of GBS, without negating the need for rigorous application of already established evidence.

DOI: https://doi.org/10.56238/edimpacto2025.091-030

Published

2025-12-10