Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades

Abstract This study investigated treatment characteristics of Guillain-Barré syndrome (GBS) in a real-world setting between 2000 and 2019. We analyzed clinical improvement between nadir and last follow-up in patients with severe GBS (defined as having a GBS disability scale > 2 at nadir) and aime...

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Autores principales: Jakob Rath, Gudrun Zulehner, Bernadette Schober, Anna Grisold, Martin Krenn, Hakan Cetin, Fritz Zimprich
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3973d21d9d3743acb19dd9273c18c1c1
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spelling oai:doaj.org-article:3973d21d9d3743acb19dd9273c18c1c12021-12-02T19:16:54ZReal-world treatment of adult patients with Guillain-Barré syndrome over the last two decades10.1038/s41598-021-98501-y2045-2322https://doaj.org/article/3973d21d9d3743acb19dd9273c18c1c12021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-98501-yhttps://doaj.org/toc/2045-2322Abstract This study investigated treatment characteristics of Guillain-Barré syndrome (GBS) in a real-world setting between 2000 and 2019. We analyzed clinical improvement between nadir and last follow-up in patients with severe GBS (defined as having a GBS disability scale > 2 at nadir) and aimed to detect clinical factors associated with multiple treatments. We included 121 patients (74 male; median age 48 [IQR 35–60]) with sensorimotor (63%), pure motor (15%), pure sensory (10%) and localized GBS (6%) as well as Miller Fisher syndrome (6%). 44% of patients were severely affected. All but one patient received at least one immunomodulatory treatment with initially either intravenous immunoglobulins (88%), plasma exchange (10%) or corticosteroids (1%), and 25% of patients received more than one treatment. Severe GBS but not age, sex, GBS subtype or date of diagnosis was associated with higher odds to receive more than one treatment (OR 4.22; 95%CI 1.36–13.10; p = 0.01). Receiving multiple treatments had no adjusted effect (OR 1.30, 95%CI 0.31–5.40, p = 0.72) on clinical improvement between nadir and last follow-up in patients with severe GBS. This treatment practice did not change over the last 20 years.Jakob RathGudrun ZulehnerBernadette SchoberAnna GrisoldMartin KrennHakan CetinFritz ZimprichNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jakob Rath
Gudrun Zulehner
Bernadette Schober
Anna Grisold
Martin Krenn
Hakan Cetin
Fritz Zimprich
Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
description Abstract This study investigated treatment characteristics of Guillain-Barré syndrome (GBS) in a real-world setting between 2000 and 2019. We analyzed clinical improvement between nadir and last follow-up in patients with severe GBS (defined as having a GBS disability scale > 2 at nadir) and aimed to detect clinical factors associated with multiple treatments. We included 121 patients (74 male; median age 48 [IQR 35–60]) with sensorimotor (63%), pure motor (15%), pure sensory (10%) and localized GBS (6%) as well as Miller Fisher syndrome (6%). 44% of patients were severely affected. All but one patient received at least one immunomodulatory treatment with initially either intravenous immunoglobulins (88%), plasma exchange (10%) or corticosteroids (1%), and 25% of patients received more than one treatment. Severe GBS but not age, sex, GBS subtype or date of diagnosis was associated with higher odds to receive more than one treatment (OR 4.22; 95%CI 1.36–13.10; p = 0.01). Receiving multiple treatments had no adjusted effect (OR 1.30, 95%CI 0.31–5.40, p = 0.72) on clinical improvement between nadir and last follow-up in patients with severe GBS. This treatment practice did not change over the last 20 years.
format article
author Jakob Rath
Gudrun Zulehner
Bernadette Schober
Anna Grisold
Martin Krenn
Hakan Cetin
Fritz Zimprich
author_facet Jakob Rath
Gudrun Zulehner
Bernadette Schober
Anna Grisold
Martin Krenn
Hakan Cetin
Fritz Zimprich
author_sort Jakob Rath
title Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
title_short Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
title_full Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
title_fullStr Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
title_full_unstemmed Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades
title_sort real-world treatment of adult patients with guillain-barré syndrome over the last two decades
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3973d21d9d3743acb19dd9273c18c1c1
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