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Determination of pain and response to methylprednisolone in Guillain-Barré syndrome
Pain can be a serious problem in patients with Guillain-Barré syndrome (GBS). Different pain symptoms and the effect of methylprednisolone on pain are evaluated. METHODS: GBS patients were recruited from a randomized placebo-controlled study comparing intravenous immunoglobulin (IVIg) + methylpredni...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Steinkopff-Verlag
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778673/ https://www.ncbi.nlm.nih.gov/pubmed/17426908 http://dx.doi.org/10.1007/s00415-006-0515-2 |
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author | Ruts, Liselotte van Koningsveld, Rinske Jacobs, Bart C. van Doorn, Pieter A. |
author_facet | Ruts, Liselotte van Koningsveld, Rinske Jacobs, Bart C. van Doorn, Pieter A. |
author_sort | Ruts, Liselotte |
collection | PubMed |
description | Pain can be a serious problem in patients with Guillain-Barré syndrome (GBS). Different pain symptoms and the effect of methylprednisolone on pain are evaluated. METHODS: GBS patients were recruited from a randomized placebo-controlled study comparing intravenous immunoglobulin (IVIg) + methylprednisolone (500 mg for 5 days) versus IVIg + placebo. Presence and severity of pain were prospectively scored at randomization and after 4 weeks. Efficacy of methylprednisolone was evaluated using endpoints: percentage of patients with pain and percentage of patients improving in pain-severity level. Medical records of the subgroup of patients treated in the Erasmus MC were screened retrospectively for different pain symptoms and course. Pain was scored at different time intervals: within 4 weeks before randomization and 0–2, 2–4, 4–24, 24–52 weeks after randomization. RESULTS: 123 (55%) of 223 patients had pain at randomization. In 70%, pain already started before onset of weakness. Methylprednisolone did not show a positive effect on the presence and reduction of pain. In the subgroup of 39 patients, backache (33%), interscapular (28%), muscle (24%), radicular pain (18%) and painful par-/dysaesthesiae (18%) were most frequently present within the period of 4 weeks before randomization. Twenty-six percent had extreme pain 0–2 weeks after randomization. Most symptoms of pain decreased after this period, but painful par-/dysaesthesiae and muscle pain often remained present during at least 6 months. CONCLUSIONS: Pain frequently occurs, often starts before onset of weakness and may cause severe complaints. Especially painful par-/dysaesthesiae and muscle pain may persist for months. Methylprednisolone seems to have no significant effect on the presence and intensity of pain. |
format | Text |
id | pubmed-2778673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Steinkopff-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27786732009-11-20 Determination of pain and response to methylprednisolone in Guillain-Barré syndrome Ruts, Liselotte van Koningsveld, Rinske Jacobs, Bart C. van Doorn, Pieter A. J Neurol Original Communication Pain can be a serious problem in patients with Guillain-Barré syndrome (GBS). Different pain symptoms and the effect of methylprednisolone on pain are evaluated. METHODS: GBS patients were recruited from a randomized placebo-controlled study comparing intravenous immunoglobulin (IVIg) + methylprednisolone (500 mg for 5 days) versus IVIg + placebo. Presence and severity of pain were prospectively scored at randomization and after 4 weeks. Efficacy of methylprednisolone was evaluated using endpoints: percentage of patients with pain and percentage of patients improving in pain-severity level. Medical records of the subgroup of patients treated in the Erasmus MC were screened retrospectively for different pain symptoms and course. Pain was scored at different time intervals: within 4 weeks before randomization and 0–2, 2–4, 4–24, 24–52 weeks after randomization. RESULTS: 123 (55%) of 223 patients had pain at randomization. In 70%, pain already started before onset of weakness. Methylprednisolone did not show a positive effect on the presence and reduction of pain. In the subgroup of 39 patients, backache (33%), interscapular (28%), muscle (24%), radicular pain (18%) and painful par-/dysaesthesiae (18%) were most frequently present within the period of 4 weeks before randomization. Twenty-six percent had extreme pain 0–2 weeks after randomization. Most symptoms of pain decreased after this period, but painful par-/dysaesthesiae and muscle pain often remained present during at least 6 months. CONCLUSIONS: Pain frequently occurs, often starts before onset of weakness and may cause severe complaints. Especially painful par-/dysaesthesiae and muscle pain may persist for months. Methylprednisolone seems to have no significant effect on the presence and intensity of pain. Steinkopff-Verlag 2007-04-11 2007-10 /pmc/articles/PMC2778673/ /pubmed/17426908 http://dx.doi.org/10.1007/s00415-006-0515-2 Text en © Steinkopff-Verlag 2007 |
spellingShingle | Original Communication Ruts, Liselotte van Koningsveld, Rinske Jacobs, Bart C. van Doorn, Pieter A. Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title | Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title_full | Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title_fullStr | Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title_full_unstemmed | Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title_short | Determination of pain and response to methylprednisolone in Guillain-Barré syndrome |
title_sort | determination of pain and response to methylprednisolone in guillain-barré syndrome |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778673/ https://www.ncbi.nlm.nih.gov/pubmed/17426908 http://dx.doi.org/10.1007/s00415-006-0515-2 |
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