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Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis

BACKGROUND: Orthostatic hypotension (OH) is multifactorial in Parkinson’s disease (PD). Antiparkinsonian medication can contribute to OH, leading to increased risk of falls, weakness and fatigue. METHODS: We conducted a systematic review and meta-analysis of randomised controlled trials (RCTs) of an...

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Autores principales: Nimmons, Danielle, Bhanu, Cini, Orlu, Mine, Schrag, Anette, Walters, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386765/
https://www.ncbi.nlm.nih.gov/pubmed/34964392
http://dx.doi.org/10.1177/08919887211060017
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author Nimmons, Danielle
Bhanu, Cini
Orlu, Mine
Schrag, Anette
Walters, Kate
author_facet Nimmons, Danielle
Bhanu, Cini
Orlu, Mine
Schrag, Anette
Walters, Kate
author_sort Nimmons, Danielle
collection PubMed
description BACKGROUND: Orthostatic hypotension (OH) is multifactorial in Parkinson’s disease (PD). Antiparkinsonian medication can contribute to OH, leading to increased risk of falls, weakness and fatigue. METHODS: We conducted a systematic review and meta-analysis of randomised controlled trials (RCTs) of antiparkinsonian drugs associated with OH as an adverse effect, compared to placebo. We searched EMBASE, MEDLINE and Web of Science databases until November 2020. Analysis used fixed-effects models and the GRADE tool to rate quality of evidence. Meta-analysis was performed if 3 or more studies of a drug group were available. RESULTS: Twenty-one RCTs including 3783 patients were included comparing 6 PD drug groups to placebo (MAO-B inhibitors, dopamine agonists, levodopa, COMT inhibitors, levodopa and adenosine receptor antagonists). OH was recorded as an adverse event or measurement of vital signs, without further specification on how this was defined or operationalised. Meta-analysis was performed for MAO-B inhibitors and dopamine agonists, as there were 3 or more studies for these drug groups. In this analysis, compared with placebo, neither MAO-B inhibitors or dopamine agonists were associated with increased risk of OH, (OR 2.28 [95% CI:0.81–6.46]), (OR 1.39 [95% CI:0.97–1.98]). CONCLUSIONS: Most studies did not specifically report OH, or reporting of OH was limited, including how and when it was measured. Furthermore, studies specifically reporting OH included participants that were younger than typical PD populations without multimorbidity. Future trials should address this, for example,, by including individuals over the age of 75, to improve estimations of how antiparkinsonian medications affect risk of OH.
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spelling pubmed-93867652022-08-19 Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis Nimmons, Danielle Bhanu, Cini Orlu, Mine Schrag, Anette Walters, Kate J Geriatr Psychiatry Neurol Reviews BACKGROUND: Orthostatic hypotension (OH) is multifactorial in Parkinson’s disease (PD). Antiparkinsonian medication can contribute to OH, leading to increased risk of falls, weakness and fatigue. METHODS: We conducted a systematic review and meta-analysis of randomised controlled trials (RCTs) of antiparkinsonian drugs associated with OH as an adverse effect, compared to placebo. We searched EMBASE, MEDLINE and Web of Science databases until November 2020. Analysis used fixed-effects models and the GRADE tool to rate quality of evidence. Meta-analysis was performed if 3 or more studies of a drug group were available. RESULTS: Twenty-one RCTs including 3783 patients were included comparing 6 PD drug groups to placebo (MAO-B inhibitors, dopamine agonists, levodopa, COMT inhibitors, levodopa and adenosine receptor antagonists). OH was recorded as an adverse event or measurement of vital signs, without further specification on how this was defined or operationalised. Meta-analysis was performed for MAO-B inhibitors and dopamine agonists, as there were 3 or more studies for these drug groups. In this analysis, compared with placebo, neither MAO-B inhibitors or dopamine agonists were associated with increased risk of OH, (OR 2.28 [95% CI:0.81–6.46]), (OR 1.39 [95% CI:0.97–1.98]). CONCLUSIONS: Most studies did not specifically report OH, or reporting of OH was limited, including how and when it was measured. Furthermore, studies specifically reporting OH included participants that were younger than typical PD populations without multimorbidity. Future trials should address this, for example,, by including individuals over the age of 75, to improve estimations of how antiparkinsonian medications affect risk of OH. SAGE Publications 2021-12-29 2022-09 /pmc/articles/PMC9386765/ /pubmed/34964392 http://dx.doi.org/10.1177/08919887211060017 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Reviews
Nimmons, Danielle
Bhanu, Cini
Orlu, Mine
Schrag, Anette
Walters, Kate
Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title_full Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title_fullStr Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title_full_unstemmed Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title_short Orthostatic Hypotension and Antiparkinsonian Drugs: A Systematic Review and Meta-analysis
title_sort orthostatic hypotension and antiparkinsonian drugs: a systematic review and meta-analysis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386765/
https://www.ncbi.nlm.nih.gov/pubmed/34964392
http://dx.doi.org/10.1177/08919887211060017
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