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Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations
Psychiatric symptoms in Guillain-Barré syndrome (GBS) can include anxiety and affective lability, which require treatment to improve functional outcomes. Three cases in which modest doses of selective serotonin reuptake inhibitors (SSRIs), alone or in combination with anticonvulsants, reduced sympto...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2413194/ https://www.ncbi.nlm.nih.gov/pubmed/18568059 |
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author | Brousseau, Kristin Arciniegas, David Harris, Susie |
author_facet | Brousseau, Kristin Arciniegas, David Harris, Susie |
author_sort | Brousseau, Kristin |
collection | PubMed |
description | Psychiatric symptoms in Guillain-Barré syndrome (GBS) can include anxiety and affective lability, which require treatment to improve functional outcomes. Three cases in which modest doses of selective serotonin reuptake inhibitors (SSRIs), alone or in combination with anticonvulsants, reduced symptoms of anxiety and affective lability during acute rehabilitation of GBS are presented. These agents were both more effective and better tolerated than benzodiazepines and appeared to facilitate engagement in rehabilitation therapies, including psychotherapy. Further investigation of the pharmacotherapy of neuropsychiatric disturbances in this population using prospective, blinded, placebo-controlled methods is recommended. |
format | Text |
id | pubmed-2413194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24131942008-06-20 Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations Brousseau, Kristin Arciniegas, David Harris, Susie Neuropsychiatr Dis Treat Original Research Psychiatric symptoms in Guillain-Barré syndrome (GBS) can include anxiety and affective lability, which require treatment to improve functional outcomes. Three cases in which modest doses of selective serotonin reuptake inhibitors (SSRIs), alone or in combination with anticonvulsants, reduced symptoms of anxiety and affective lability during acute rehabilitation of GBS are presented. These agents were both more effective and better tolerated than benzodiazepines and appeared to facilitate engagement in rehabilitation therapies, including psychotherapy. Further investigation of the pharmacotherapy of neuropsychiatric disturbances in this population using prospective, blinded, placebo-controlled methods is recommended. Dove Medical Press 2005-06 /pmc/articles/PMC2413194/ /pubmed/18568059 Text en © 2005 Dove Medical Press Limited. All rights reserved |
spellingShingle | Original Research Brousseau, Kristin Arciniegas, David Harris, Susie Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title | Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title_full | Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title_fullStr | Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title_full_unstemmed | Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title_short | Pharmacologic management of anxiety and affective lability during recovery from Guillain-Barré syndrome: some preliminary observations |
title_sort | pharmacologic management of anxiety and affective lability during recovery from guillain-barré syndrome: some preliminary observations |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2413194/ https://www.ncbi.nlm.nih.gov/pubmed/18568059 |
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