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A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative
BACKGROUND: Delirium is a common disorder in the early phase of stroke. Given the presumed cholinergic deficiency in delirium, we tested treatment with the acetylcholinesterase inhibitor rivastigmine. METHODS: This pilot study was performed within an epidemiological study. In 527 consecutive stroke...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556687/ https://www.ncbi.nlm.nih.gov/pubmed/18803862 http://dx.doi.org/10.1186/1471-2377-8-34 |
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author | Oldenbeuving, Annemarie W de Kort, Paul LM Jansen, Ben PW Kappelle, L Jaap Roks, Gerwin |
author_facet | Oldenbeuving, Annemarie W de Kort, Paul LM Jansen, Ben PW Kappelle, L Jaap Roks, Gerwin |
author_sort | Oldenbeuving, Annemarie W |
collection | PubMed |
description | BACKGROUND: Delirium is a common disorder in the early phase of stroke. Given the presumed cholinergic deficiency in delirium, we tested treatment with the acetylcholinesterase inhibitor rivastigmine. METHODS: This pilot study was performed within an epidemiological study. In 527 consecutive stroke patients presence of delirium was assessed during the first week with the confusion assessment method. Severity was scored with the delirium rating scale (DRS). Sixty-two patients developed a delirium in the acute phase of stroke. Only patients with a severe and persistent delirium (defined as a DRS of 12 or more for more than 24 hours) were enrolled in the present study. In total 26 fulfilled these criteria of whom 17 were treated with orally administered rivastigmine with a total dose between 3 and 12 mg a day. Eight patients could not be treated because of dysphagia and one because of early discharge. RESULTS: No major side effects were recorded. In 16 patients there was a considerable decrease in severity of delirium. The mean DRS declined from 14.8 on day one to 8.5 after therapy and 5.6 after tapering. The mean duration of delirium was 6.7 days (range; 2–17). CONCLUSION: Rivastigmine is safe in stroke patients with delirium even after rapid titration. In the majority of patients the delirium improved after treatment. A randomized controlled trial is needed to establish the usefulness of rivastigmine in delirium after stroke. TRIAL REGISTRATION: Nederlands Trial Register NTR1395 |
format | Text |
id | pubmed-2556687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25566872008-10-01 A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative Oldenbeuving, Annemarie W de Kort, Paul LM Jansen, Ben PW Kappelle, L Jaap Roks, Gerwin BMC Neurol Research Article BACKGROUND: Delirium is a common disorder in the early phase of stroke. Given the presumed cholinergic deficiency in delirium, we tested treatment with the acetylcholinesterase inhibitor rivastigmine. METHODS: This pilot study was performed within an epidemiological study. In 527 consecutive stroke patients presence of delirium was assessed during the first week with the confusion assessment method. Severity was scored with the delirium rating scale (DRS). Sixty-two patients developed a delirium in the acute phase of stroke. Only patients with a severe and persistent delirium (defined as a DRS of 12 or more for more than 24 hours) were enrolled in the present study. In total 26 fulfilled these criteria of whom 17 were treated with orally administered rivastigmine with a total dose between 3 and 12 mg a day. Eight patients could not be treated because of dysphagia and one because of early discharge. RESULTS: No major side effects were recorded. In 16 patients there was a considerable decrease in severity of delirium. The mean DRS declined from 14.8 on day one to 8.5 after therapy and 5.6 after tapering. The mean duration of delirium was 6.7 days (range; 2–17). CONCLUSION: Rivastigmine is safe in stroke patients with delirium even after rapid titration. In the majority of patients the delirium improved after treatment. A randomized controlled trial is needed to establish the usefulness of rivastigmine in delirium after stroke. TRIAL REGISTRATION: Nederlands Trial Register NTR1395 BioMed Central 2008-09-20 /pmc/articles/PMC2556687/ /pubmed/18803862 http://dx.doi.org/10.1186/1471-2377-8-34 Text en Copyright © 2008 Oldenbeuving et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Oldenbeuving, Annemarie W de Kort, Paul LM Jansen, Ben PW Kappelle, L Jaap Roks, Gerwin A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title | A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title_full | A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title_fullStr | A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title_full_unstemmed | A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title_short | A pilot study of rivastigmine in the treatment of delirium after stroke: A safe alternative |
title_sort | pilot study of rivastigmine in the treatment of delirium after stroke: a safe alternative |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556687/ https://www.ncbi.nlm.nih.gov/pubmed/18803862 http://dx.doi.org/10.1186/1471-2377-8-34 |
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