Pallidal stimulation reduces treatment‐induced dyskinesias in “minimal‐change” multiple system atrophy
Identifieur interne : 002D80 ( Istex/Corpus ); précédent : 002D79; suivant : 002D81Pallidal stimulation reduces treatment‐induced dyskinesias in “minimal‐change” multiple system atrophy
Auteurs : Yue Huang ; Raymond Garrick ; Raymond Cook ; Dudley O'Sullivan ; John Morris ; Glenda M. HallidaySource :
- Movement Disorders [ 0885-3185 ] ; 2005-08.
English descriptors
Abstract
Deep brain stimulation therapy is increasingly gaining acceptance in the management of levodopa‐induced dyskinesia and fluctuations in idiopathic Parkinson's disease. It is generally not recommended for the other forms of parkinsonism such as progressive supranuclear palsy or multiple system atrophy where the response to levodopa is usually poor and disease progression more rapid, making any benefit short‐lived. Here, we present an autopsy‐confirmed case of “minimal‐change” multiple system atrophy in whom pallidal stimulation surgery was effective in abolishing severe levodopa‐induced dyskinesia. © 2005 Movement Disorder Society
Url:
DOI: 10.1002/mds.20497
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<caption> Segment 1. A 47‐year‐old woman's prominent bradykinesia and rigidity are shown. There is no tremor. Her most rigid facial expression is not particularly "mask‐like," and ocular movements are normal. She has prominent action‐induced twitches of her fingers, suggestive of cortical myoclonus. Segment 2. The patient's dyskinesia is observed after the administration of Sinemet 100/25 totalling 1,500 mg of L‐dopa daily. Segment 3. Two weeks later after pallidal surgery for deep brain stimulation implantation and still takingL ‐dopa medication, her mobility and general well‐being are greatly improved. No other medications were taken during this period. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. </caption>
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<p>Deep brain stimulation therapy is increasingly gaining acceptance in the management of levodopa‐induced dyskinesia and fluctuations in idiopathic Parkinson's disease. It is generally not recommended for the other forms of parkinsonism such as progressive supranuclear palsy or multiple system atrophy where the response to levodopa is usually poor and disease progression more rapid, making any benefit short‐lived. Here, we present an autopsy‐confirmed case of “minimal‐change” multiple system atrophy in whom pallidal stimulation surgery was effective in abolishing severe levodopa‐induced dyskinesia. © 2005 Movement Disorder Society</p>
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<!--Version 0.6 générée le 4-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Pallidal stimulation reduces treatment‐induced dyskinesias in “minimal‐change” multiple system atrophy</title>
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<titleInfo type="abbreviated" lang="en"><title>Pallidal Stimulation in “Minimal‐Change” MSA</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en"><title>Pallidal stimulation reduces treatment‐induced dyskinesias in “minimal‐change” multiple system atrophy</title>
</titleInfo>
<name type="personal"><namePart type="given">Yue</namePart>
<namePart type="family">Huang</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Prince of Wales Medical Research Institute and the University of New South Wales, Randwick, Australia</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Raymond</namePart>
<namePart type="family">Garrick</namePart>
<namePart type="termsOfAddress">FRACP</namePart>
<affiliation>Department of Neurology, St. Vincent's Hospital, Darlinghurst, Australia</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Raymond</namePart>
<namePart type="family">Cook</namePart>
<namePart type="termsOfAddress">FRACS</namePart>
<affiliation>Department of Surgery, Royal North Shore Hospital, St. Leonards, Australia</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Dudley</namePart>
<namePart type="family">O'Sullivan</namePart>
<namePart type="termsOfAddress">FRACP</namePart>
<affiliation>Department of Neurology, St. Vincent's Hospital, Darlinghurst, Australia</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">John</namePart>
<namePart type="family">Morris</namePart>
<namePart type="termsOfAddress">FRACP, DM</namePart>
<affiliation>Department of Neurology, Westmead Hospital and the University of Sydney, Westmead, Australia</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Glenda M.</namePart>
<namePart type="family">Halliday</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Prince of Wales Medical Research Institute and the University of New South Wales, Randwick, Australia</affiliation>
<description>Correspondence: Prince of Wales Medical Research Institute, Barker Street, Randwick 2031, Australia</description>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre authority="originalCategForm">article</genre>
<originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place><placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2005-08</dateIssued>
<dateCaptured encoding="w3cdtf">2004-06-28</dateCaptured>
<dateValid encoding="w3cdtf">2004-12-14</dateValid>
<copyrightDate encoding="w3cdtf">2005</copyrightDate>
</originInfo>
<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription><internetMediaType>text/html</internetMediaType>
<extent unit="figures">1</extent>
<extent unit="tables">1</extent>
<extent unit="references">15</extent>
<extent unit="words">2556</extent>
</physicalDescription>
<abstract lang="en">Deep brain stimulation therapy is increasingly gaining acceptance in the management of levodopa‐induced dyskinesia and fluctuations in idiopathic Parkinson's disease. It is generally not recommended for the other forms of parkinsonism such as progressive supranuclear palsy or multiple system atrophy where the response to levodopa is usually poor and disease progression more rapid, making any benefit short‐lived. Here, we present an autopsy‐confirmed case of “minimal‐change” multiple system atrophy in whom pallidal stimulation surgery was effective in abolishing severe levodopa‐induced dyskinesia. © 2005 Movement Disorder Society</abstract>
<note type="funding">National Health and Medical Research Council of Australia</note>
<note type="funding">Ian Potter and Clive and Vera Ramaciotti Foundations</note>
<subject lang="en"><genre>Keywords</genre>
<topic>multiple system atrophy</topic>
<topic>dyskinesia</topic>
<topic>globus pallidus stimulation</topic>
<topic>parkinsonism</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>
<note type="content"> This article includes Supplementary Video, available online at http://www.interscience.wiley.com/jpages/0885‐3185/suppmatSupporting Info Item: Segment 1. A 47‐year‐old woman's prominent bradykinesia and rigidity are shown. There is no tremor. Her most rigid facial expression is not particularly "mask‐like," and ocular movements are normal. She has prominent action‐induced twitches of her fingers, suggestive of cortical myoclonus. Segment 2. The patient's dyskinesia is observed after the administration of Sinemet 100/25 totalling 1,500 mg of L‐dopa daily. Segment 3. Two weeks later after pallidal surgery for deep brain stimulation implantation and still takingL ‐dopa medication, her mobility and general well‐being are greatly improved. No other medications were taken during this period. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. - </note>
<subject><genre>article category</genre>
<topic>Brief Report with Video</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>2005</date>
<detail type="volume"><caption>vol.</caption>
<number>20</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>8</number>
</detail>
<extent unit="pages"><start>1042</start>
<end>1047</end>
<total>5</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">D56C0EEF15814A21388B1354ED437B2F41703AA9</identifier>
<identifier type="DOI">10.1002/mds.20497</identifier>
<identifier type="ArticleID">MDS20497</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2005 Movement Disorder Society</accessCondition>
<recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
<recordContentSource>WILEY</recordContentSource>
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