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...
Saved in:
Main Authors: | , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Published: |
American Academy of Neurology
2019
|
Subjects: | |
Online Access: | http://eprints.um.edu.my/23199/ https://doi.org/10.1212/WNL.0000000000007719 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Universiti Malaya |
id |
my.um.eprints.23199 |
---|---|
record_format |
eprints |
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 |
_version_ |
1654960701120184320 |