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Treatment of levodopa‐induced motor complications

Identifieur interne : 000723 ( Main/Corpus ); précédent : 000722; suivant : 000724

Treatment of levodopa‐induced motor complications

Auteurs : Fabrizio Stocchi ; Michele Tagliati ; C. Warren Olanow

Source :

RBID : ISTEX:FB819C4FEC283B3BB9A75DE1B178F8C4EF044955

English descriptors

Abstract

Chronic levodopa treatment for Parkinson's disease patients is frequently associated with the development of motor complications such as end‐of‐dose wearing‐off and dyskinesias. In this review, we provide an overview of the strategies available for dealing with these problems. Medical management includes manipulation of levodopa dosing to establish the optimum treatment schedule, improving levodopa absorption, catechol‐O‐methyl transferase‐inhibition (COMT), Monoamine oxidase‐B (MAO‐B) inhibition, dopaminergic agonists, amantadine, and continuous dopaminergic infusions. Surgical procedures and particularly deep brain stimulation are also reviewed. It should be noted that none of these treatments has been shown to provide anti‐parkinsonian efficacy that is greater than what can be achieved with levodopa. We highlight the importance of initiating therapy with a treatment strategy that reduces the risk that a Parkinson's disease patient will develop motor complications in the first place. Key Words: Advanced PD, dyskinesias, motor fluctuations, levodopa, dopamine agonists, COMT inhibitors, MAO‐B inhibitors. © 2008 Movement Disorder Society

Url:
DOI: 10.1002/mds.22052

Links to Exploration step

ISTEX:FB819C4FEC283B3BB9A75DE1B178F8C4EF044955

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<dateIssued encoding="w3cdtf">2008</dateIssued>
<dateCaptured encoding="w3cdtf">2007-12-31</dateCaptured>
<dateValid encoding="w3cdtf">2008-03-02</dateValid>
<copyrightDate encoding="w3cdtf">2008</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">Chronic levodopa treatment for Parkinson's disease patients is frequently associated with the development of motor complications such as end‐of‐dose wearing‐off and dyskinesias. In this review, we provide an overview of the strategies available for dealing with these problems. Medical management includes manipulation of levodopa dosing to establish the optimum treatment schedule, improving levodopa absorption, catechol‐O‐methyl transferase‐inhibition (COMT), Monoamine oxidase‐B (MAO‐B) inhibition, dopaminergic agonists, amantadine, and continuous dopaminergic infusions. Surgical procedures and particularly deep brain stimulation are also reviewed. It should be noted that none of these treatments has been shown to provide anti‐parkinsonian efficacy that is greater than what can be achieved with levodopa. We highlight the importance of initiating therapy with a treatment strategy that reduces the risk that a Parkinson's disease patient will develop motor complications in the first place. Key Words: Advanced PD, dyskinesias, motor fluctuations, levodopa, dopamine agonists, COMT inhibitors, MAO‐B inhibitors. © 2008 Movement Disorder Society</abstract>
<note type="content">*Potential conflict of interest: Dr. Stocchi has received honoraria for consultation from Novartis, GSK, BI, Valeant, Lundbeck, TEVA, Roche, Chiesi, and Vernalis.</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>advanced Parkinson's disease</topic>
<topic>dyskinesias</topic>
<topic>motor fluctuations</topic>
<topic>levodopa</topic>
<topic>dopamine agonists</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="Journal">journal</genre>
<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>2008</date>
<detail type="volume">
<caption>vol.</caption>
<number>23</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>S3</number>
</detail>
<detail type="supplement">
<caption>Suppl. no.</caption>
<number>S3</number>
</detail>
<extent unit="pages">
<start>S599</start>
<end>S612</end>
<total>14</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">FB819C4FEC283B3BB9A75DE1B178F8C4EF044955</identifier>
<identifier type="DOI">10.1002/mds.22052</identifier>
<identifier type="ArticleID">MDS22052</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2008 Movement Disorder Society</accessCondition>
<recordInfo>
<recordContentSource>WILEY</recordContentSource>
<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
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