Current treatment practice of Guillain-Barré syndrome

ObjectiveTo define the current treatment practice of Guillain-Barré syndrome (GBS).MethodsThe study was based on prospective observational data from the first 1,300 patients included in the International GBS Outcome Study. We described the treatment practice of GBS in general, and for (1) severe for...

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Main Authors: Verboon, Christine, Doets, Alex Y., Galassi, Giuliana, Davidson, Amy, Waheed, Waqar, Péréon, Yann, Shahrizaila, Nortina, Kusunoki, Susumu, Lehmann, Helmar C., Harbo, Thomas, Monges, Soledad, Van den Bergh, Peter, Willison, Hugh J., Cornblath, David R., Jacobs, Bart C.
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Published: American Academy of Neurology 2019
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Online Access:http://eprints.um.edu.my/23199/
https://doi.org/10.1212/WNL.0000000000007719
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spelling my.um.eprints.231992019-12-03T08:29:05Z http://eprints.um.edu.my/23199/ Current treatment practice of Guillain-Barré syndrome Verboon, Christine Doets, Alex Y. Galassi, Giuliana Davidson, Amy Waheed, Waqar Péréon, Yann Shahrizaila, Nortina Kusunoki, Susumu Lehmann, Helmar C. Harbo, Thomas Monges, Soledad Van den Bergh, Peter Willison, Hugh J. Cornblath, David R. Jacobs, Bart C. R Medicine ObjectiveTo define the current treatment practice of Guillain-Barré syndrome (GBS).MethodsThe study was based on prospective observational data from the first 1,300 patients included in the International GBS Outcome Study. We described the treatment practice of GBS in general, and for (1) severe forms (unable to walk independently), (2) no recovery after initial treatment, (3) treatment-related fluctuations, (4) mild forms (able to walk independently), and (5) variant forms including Miller Fisher syndrome, taking patient characteristics and hospital type into account.ResultsWe excluded 88 (7%) patients because of missing data, protocol violation, or alternative diagnosis. Patients from Bangladesh (n = 189, 15%) were described separately because 83% were not treated. IV immunoglobulin (IVIg), plasma exchange (PE), or other immunotherapy was provided in 941 (92%) of the remaining 1,023 patients, including patients with severe GBS (724/743, 97%), mild GBS (126/168, 75%), Miller Fisher syndrome (53/70, 76%), and other variants (33/40, 83%). Of 235 (32%) patients who did not improve after their initial treatment, 82 (35%) received a second immune modulatory treatment. A treatment-related fluctuation was observed in 53 (5%) of 1,023 patients, of whom 36 (68%) were re-treated with IVIg or PE.ConclusionsIn current practice, patients with mild and variant forms of GBS, or with treatment-related fluctuations and treatment failures, are frequently treated, even in absence of trial data to support this choice. The variability in treatment practice can be explained in part by the lack of evidence and guidelines for effective treatment in these situations. © American Academy of Neurology. American Academy of Neurology 2019 Article PeerReviewed Verboon, Christine and Doets, Alex Y. and Galassi, Giuliana and Davidson, Amy and Waheed, Waqar and Péréon, Yann and Shahrizaila, Nortina and Kusunoki, Susumu and Lehmann, Helmar C. and Harbo, Thomas and Monges, Soledad and Van den Bergh, Peter and Willison, Hugh J. and Cornblath, David R. and Jacobs, Bart C. (2019) Current treatment practice of Guillain-Barré syndrome. Neurology, 93 (1). e59-e76. ISSN 0028-3878 https://doi.org/10.1212/WNL.0000000000007719 doi:10.1212/WNL.0000000000007719
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
spellingShingle R Medicine
Verboon, Christine
Doets, Alex Y.
Galassi, Giuliana
Davidson, Amy
Waheed, Waqar
Péréon, Yann
Shahrizaila, Nortina
Kusunoki, Susumu
Lehmann, Helmar C.
Harbo, Thomas
Monges, Soledad
Van den Bergh, Peter
Willison, Hugh J.
Cornblath, David R.
Jacobs, Bart C.
Current treatment practice of Guillain-Barré syndrome
description ObjectiveTo define the current treatment practice of Guillain-Barré syndrome (GBS).MethodsThe study was based on prospective observational data from the first 1,300 patients included in the International GBS Outcome Study. We described the treatment practice of GBS in general, and for (1) severe forms (unable to walk independently), (2) no recovery after initial treatment, (3) treatment-related fluctuations, (4) mild forms (able to walk independently), and (5) variant forms including Miller Fisher syndrome, taking patient characteristics and hospital type into account.ResultsWe excluded 88 (7%) patients because of missing data, protocol violation, or alternative diagnosis. Patients from Bangladesh (n = 189, 15%) were described separately because 83% were not treated. IV immunoglobulin (IVIg), plasma exchange (PE), or other immunotherapy was provided in 941 (92%) of the remaining 1,023 patients, including patients with severe GBS (724/743, 97%), mild GBS (126/168, 75%), Miller Fisher syndrome (53/70, 76%), and other variants (33/40, 83%). Of 235 (32%) patients who did not improve after their initial treatment, 82 (35%) received a second immune modulatory treatment. A treatment-related fluctuation was observed in 53 (5%) of 1,023 patients, of whom 36 (68%) were re-treated with IVIg or PE.ConclusionsIn current practice, patients with mild and variant forms of GBS, or with treatment-related fluctuations and treatment failures, are frequently treated, even in absence of trial data to support this choice. The variability in treatment practice can be explained in part by the lack of evidence and guidelines for effective treatment in these situations. © American Academy of Neurology.
format Article
author Verboon, Christine
Doets, Alex Y.
Galassi, Giuliana
Davidson, Amy
Waheed, Waqar
Péréon, Yann
Shahrizaila, Nortina
Kusunoki, Susumu
Lehmann, Helmar C.
Harbo, Thomas
Monges, Soledad
Van den Bergh, Peter
Willison, Hugh J.
Cornblath, David R.
Jacobs, Bart C.
author_facet Verboon, Christine
Doets, Alex Y.
Galassi, Giuliana
Davidson, Amy
Waheed, Waqar
Péréon, Yann
Shahrizaila, Nortina
Kusunoki, Susumu
Lehmann, Helmar C.
Harbo, Thomas
Monges, Soledad
Van den Bergh, Peter
Willison, Hugh J.
Cornblath, David R.
Jacobs, Bart C.
author_sort Verboon, Christine
title Current treatment practice of Guillain-Barré syndrome
title_short Current treatment practice of Guillain-Barré syndrome
title_full Current treatment practice of Guillain-Barré syndrome
title_fullStr Current treatment practice of Guillain-Barré syndrome
title_full_unstemmed Current treatment practice of Guillain-Barré syndrome
title_sort current treatment practice of guillain-barré syndrome
publisher American Academy of Neurology
publishDate 2019
url http://eprints.um.edu.my/23199/
https://doi.org/10.1212/WNL.0000000000007719
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