Movement Disorders (revue)

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Meta‐analysis of heart valve abnormalities in Parkinson's disease patients treated with dopamine agonists

Identifieur interne : 001E99 ( Istex/Corpus ); précédent : 001E98; suivant : 001F00

Meta‐analysis of heart valve abnormalities in Parkinson's disease patients treated with dopamine agonists

Auteurs : Gregor Simonis ; Joerg T. Fuhrmann ; Ruth H. Strasser

Source :

RBID : ISTEX:22013580F8E1860DF038E7D18AC6F7212F4106FE

English descriptors

Abstract

Valvular heart disease in patients being treated with ergot‐derivative dopamine agonists (Ergot‐DA) for Parkinson's disease has been reported to occur as a consequence of serotonine receptor stimulation. Goal of this analysis was to estimate the incidence of those changes from recently published studies and to determine its clinical relevance. Medline searches were performed to identify cross‐sectional, echocardiographic studies comparing patients treated with dopamine agonists or controls, in terms of valvular changes. Observational studies of valve changes in Parkinsonian patients were used to estimate the incidence of severe valvulopathy. The results from 7 cross‐sectional studies including 477 patients treated with Ergot‐DA, 127 patients with non‐Ergot‐DA, and 364 control patients were analyzed. Moderate‐to‐severe valvular changes were detected in 26% of patients treated with Ergot‐DA, 10% of patients treated with non‐Ergot DA, and 10% of control patients. Severe valvulopathy was less than 1% both in cross‐sectional and observational studies. The high rate of moderate valvular changes in patients treated with Ergot‐DA suggests that close surveillance of the patients is required. Severe valvulopathy was less than 1% in the studies analyzed. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21639

Links to Exploration step

ISTEX:22013580F8E1860DF038E7D18AC6F7212F4106FE

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<abstract lang="en">Valvular heart disease in patients being treated with ergot‐derivative dopamine agonists (Ergot‐DA) for Parkinson's disease has been reported to occur as a consequence of serotonine receptor stimulation. Goal of this analysis was to estimate the incidence of those changes from recently published studies and to determine its clinical relevance. Medline searches were performed to identify cross‐sectional, echocardiographic studies comparing patients treated with dopamine agonists or controls, in terms of valvular changes. Observational studies of valve changes in Parkinsonian patients were used to estimate the incidence of severe valvulopathy. The results from 7 cross‐sectional studies including 477 patients treated with Ergot‐DA, 127 patients with non‐Ergot‐DA, and 364 control patients were analyzed. Moderate‐to‐severe valvular changes were detected in 26% of patients treated with Ergot‐DA, 10% of patients treated with non‐Ergot DA, and 10% of control patients. Severe valvulopathy was less than 1% both in cross‐sectional and observational studies. The high rate of moderate valvular changes in patients treated with Ergot‐DA suggests that close surveillance of the patients is required. Severe valvulopathy was less than 1% in the studies analyzed. © 2007 Movement Disorder Society</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>heart valve abnormalities</topic>
<topic>Cabergoline</topic>
<topic>Pergolide</topic>
<topic>Parkinson's disease</topic>
<topic>meta analysis</topic>
</subject>
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<title>Movement Disorders</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
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<subject>
<genre>article category</genre>
<topic>Research Article</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2007</date>
<detail type="volume">
<caption>vol.</caption>
<number>22</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>13</number>
</detail>
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<start>1936</start>
<end>1942</end>
<total>7</total>
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<identifier type="istex">22013580F8E1860DF038E7D18AC6F7212F4106FE</identifier>
<identifier type="DOI">10.1002/mds.21639</identifier>
<identifier type="ArticleID">MDS21639</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2007 Movement Disorder Society</accessCondition>
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