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Guillain–Barré syndrome in low-income and middle-income countries: challenges and prospects

  • National Institute of Neurosciences and Hospital

Research output: Contribution to journal › Review article › Academic › peer-review

87 Citations (Scopus)

Abstract

The epidemiology, clinical characteristics, management and outcome of Guillain–Barré syndrome (GBS) differ between low-income and middle-income countries (LMIC) and high-income countries (HIC). At present, limited data are available on GBS in LMIC and the true incidence of GBS in many LMIC remains unknown. Increased understanding of GBS in LMIC is needed because poor hygiene and high exposure to infections render populations in LMIC vulnerable to GBS outbreaks. Furthermore, insufficient diagnostic and health-care facilities in LMIC contribute to delayed diagnosis in patients with severe presentations of GBS. In addition, the lack of national clinical guidelines and absence of affordable, effective treatments contribute to worse outcomes and higher mortality in LMIC than HIC. Systematic population-based surveillance studies, cohort and case–control studies are required to understand the incidence and risk factors for GBS. Novel, targeted and cost-effective treatment strategies need to be developed in the context of health system challenges in LMIC. To ensure integrative rehabilitation services in LMIC, existing prognostic models must be validated, and responsive outcome measures that are cross-culturally applicable must be developed. Therefore, fundamental and applied research to improve the clinical management of GBS in LMIC should become a critical focus of future research programmes.

Original languageEnglish
Pages (from-to)285-296
Number of pages12
JournalNature Reviews Neurology
Volume17
Issue number5
DOIs
Publication statusPublished - May 2021

Bibliographical note

Acknowledgements:
We thank H.U.R. Javid, M.L. Brito, F.A.A. Gondim, M.-E. Dourado, Y. Wang, S. Elaidy, T.C. Yin, D.R. Ohnmar, M.A. Ul Haq, A.P. Ramos, T. Thomas, K. Bateman, A. Keshavaraj, M. Dekker, W. Howlett, Hoa Nguyen, Hieu Nguyen, S. Khan, K. Prasad, U. Thirugnanam, M. Hakim, B. Alam and G. Mondol for providing comments and completing questionnaires on the differential diagnosis of GBS in their region. The research work of S.E.L. and B.C.J. is supported by ZikaPLAN, a global research consortium funded by the European Union under the Horizon 2020 programme (grant number 734584). Z.I. received restricted grant (number 1K43TW011447-01) support from Fogarty International Center, the National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH) and Annexon Biosciences for activities unrelated to the subject matter of this Review. Q.D.M. received consulting honoraria from Annexon Biosciences for activities unrelated to the subject matter of this Review. B.C.J. received unrestricted support for research from Annexon Biosciences, CSL-Behring, EU Horizon 2020, Griffols, Hansa Biopharma and Prinses Beatrix Spierfonds, for activities unrelated to the subject matter of this Review.

Publisher Copyright: © 2021, Springer Nature Limited.

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