Bilateral deep brain stimulation of the globus pallidus internus in tardive dystonia
Identifieur interne : 001756 ( Istex/Corpus ); précédent : 001755; suivant : 001757Bilateral deep brain stimulation of the globus pallidus internus in tardive dystonia
Auteurs : Wataru Sako ; Satoshi Goto ; Hideki Shimazu ; Nagako Murase ; Kazuhito Matsuzaki ; Tetsuya Tamura ; Hideo Mure ; Yusuke Tomogane ; Norio Arita ; Hiroo Yoshikawa ; Shinji Nagahiro ; Ryuji KajiSource :
- Movement Disorders [ 0885-3185 ] ; 2008-10-15.
English descriptors
Abstract
Tardive dystonia is a disabling movement disorder as a consequence of exposure to neuroleptic drugs. We followed 6 patients with medically refractory tardive dystonia treated by bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) for 21 ± 18 months. At last follow‐up, the Burke‐Fahn‐Marsden Dystonia Rating Scale (BFMDRS) motor score improved by 86% ± 14%, and the BFMDRS disability score improved by 80% ± 12%. Bilateral GPi‐DBS is a beneficial therapeutic option for the long‐term relief of tardive dystonia. © 2008 Movement Disorder Society
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DOI: 10.1002/mds.22100
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Bilateral GPi‐DBS is a beneficial therapeutic option for the long‐term relief of tardive dystonia. © 2008 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Wataru Sako MD</name><affiliations><json:string>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Satoshi Goto MD, PhD</name><affiliations><json:string>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Hideki Shimazu MD, PhD</name><affiliations><json:string>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Nagako Murase MD, PhD</name><affiliations><json:string>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Kazuhito Matsuzaki MD, PhD</name><affiliations><json:string>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Tetsuya Tamura MD</name><affiliations><json:string>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Hideo Mure MD</name><affiliations><json:string>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Yusuke Tomogane MD, PhD</name><affiliations><json:string>Department of Neurosurgery, Hyogo Medical College, Hyogo, Japan</json:string></affiliations></json:item><json:item><name>Norio Arita MD, PhD</name><affiliations><json:string>Department of Neurosurgery, Hyogo Medical College, Hyogo, Japan</json:string></affiliations></json:item><json:item><name>Hiroo Yoshikawa MD, PhD</name><affiliations><json:string>Department of Neurology, Hyogo Medical College, Hyogo, Japan</json:string></affiliations></json:item><json:item><name>Shinji Nagahiro MD, PhD</name><affiliations><json:string>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item><json:item><name>Ryuji Kaji MD, PhD</name><affiliations><json:string>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>tardive dystonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>deep brain stimulation</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>globus pallidus internus</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Tardive dystonia is a disabling movement disorder as a consequence of exposure to neuroleptic drugs. We followed 6 patients with medically refractory tardive dystonia treated by bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) for 21 ± 18 months. At last follow‐up, the Burke‐Fahn‐Marsden Dystonia Rating Scale (BFMDRS) motor score improved by 86% ± 14%, and the BFMDRS disability score improved by 80% ± 12%. 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normalForm="sgoto@clin.med.tokushima-u.ac.jp">sgoto@clin.med.tokushima‐u.ac.jp</email></contactDetails></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Hideki</givenNames><familyName>Shimazu</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Nagako</givenNames><familyName>Murase</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Kazuhito</givenNames><familyName>Matsuzaki</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Tetsuya</givenNames><familyName>Tamura</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au7" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Hideo</givenNames><familyName>Mure</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au8" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Yusuke</givenNames><familyName>Tomogane</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au9" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Norio</givenNames><familyName>Arita</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au10" creatorRole="author" affiliationRef="#af4"><personName><givenNames>Hiroo</givenNames><familyName>Yoshikawa</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au11" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Shinji</givenNames><familyName>Nagahiro</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au12" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Ryuji</givenNames><familyName>Kaji</familyName><degrees>MD, PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="JP" type="organization"><unparsedAffiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurosurgery, Hyogo Medical College, Hyogo, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurology, Hyogo Medical College, Hyogo, Japan</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">tardive dystonia</keyword><keyword xml:id="kwd2">deep brain stimulation</keyword><keyword xml:id="kwd3">globus pallidus internus</keyword></keywordGroup><fundingInfo><fundingAgency>21st century COE (Center Of Excellence)</fundingAgency><fundingNumber>16101J‐1</fundingNumber></fundingInfo><fundingInfo><fundingAgency>Japan Ministry of Education, Science, Culture, and Sports</fundingAgency></fundingInfo><supportingInformation><p> Additional Supporting Information may be found in the online version of this article. </p><supportingInfoItem><mediaResource alt="supporting information" href="urn-x:wiley:08853185:media:mds22100:MDS22100"></mediaResource><caption>Segment 1. Preoperative state, the patient manifested severe posterior truncal bending and retrocollis. Segment 2. Four years after electrode implantation, continuous bilateral pallidal stimulation remained to produce a marked alleviation of her dystonic symptoms.</caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Tardive dystonia is a disabling movement disorder as a consequence of exposure to neuroleptic drugs. We followed 6 patients with medically refractory tardive dystonia treated by bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) for 21 ± 18 months. At last follow‐up, the Burke‐Fahn‐Marsden Dystonia Rating Scale (BFMDRS) motor score improved by 86% ± 14%, and the BFMDRS disability score improved by 80% ± 12%. Bilateral GPi‐DBS is a beneficial therapeutic option for the long‐term relief of tardive dystonia. © 2008 Movement Disorder Society</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p>Potential conflict of interest: None reported.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Bilateral deep brain stimulation of the globus pallidus internus in tardive dystonia</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>GPi‐DBS in Tardive Dystonia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Bilateral deep brain stimulation of the globus pallidus internus in tardive dystonia</title></titleInfo><name type="personal"><namePart type="given">Wataru</namePart><namePart type="family">Sako</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Satoshi</namePart><namePart type="family">Goto</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><description>Correspondence: Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, 2‐50‐1 Kuramoto, Tokushima 770‐8503, Japan</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hideki</namePart><namePart type="family">Shimazu</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nagako</namePart><namePart type="family">Murase</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kazuhito</namePart><namePart type="family">Matsuzaki</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Tetsuya</namePart><namePart type="family">Tamura</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hideo</namePart><namePart type="family">Mure</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Yusuke</namePart><namePart type="family">Tomogane</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurosurgery, Hyogo Medical College, Hyogo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Norio</namePart><namePart type="family">Arita</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurosurgery, Hyogo Medical College, Hyogo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hiroo</namePart><namePart type="family">Yoshikawa</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurology, Hyogo Medical College, Hyogo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Shinji</namePart><namePart type="family">Nagahiro</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurosurgery, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ryuji</namePart><namePart type="family">Kaji</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Clinical Neuroscience, Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima, Tokushima, Japan</affiliation><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">2008-10-15</dateIssued><dateCaptured encoding="w3cdtf">2007-10-10</dateCaptured><dateValid encoding="w3cdtf">2008-03-31</dateValid><copyrightDate encoding="w3cdtf">2008</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">19</extent><extent unit="words">2061</extent></physicalDescription><abstract lang="en">Tardive dystonia is a disabling movement disorder as a consequence of exposure to neuroleptic drugs. We followed 6 patients with medically refractory tardive dystonia treated by bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) for 21 ± 18 months. At last follow‐up, the Burke‐Fahn‐Marsden Dystonia Rating Scale (BFMDRS) motor score improved by 86% ± 14%, and the BFMDRS disability score improved by 80% ± 12%. Bilateral GPi‐DBS is a beneficial therapeutic option for the long‐term relief of tardive dystonia. © 2008 Movement Disorder Society</abstract><note type="content">*Potential conflict of interest: None reported.</note><note type="funding">21st century COE (Center Of Excellence) - No. 16101J‐1; </note><note type="funding">Japan Ministry of Education, Science, Culture, and Sports</note><subject lang="en"><genre>Keywords</genre><topic>tardive dystonia</topic><topic>deep brain stimulation</topic><topic>globus pallidus internus</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><note type="content"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Segment 1. Preoperative state, the patient manifested severe posterior truncal bending and retrocollis. Segment 2. Four years after electrode implantation, continuous bilateral pallidal stimulation remained to produce a marked alleviation of her dystonic symptoms. - </note><subject><genre>article category</genre><topic>Brief Report</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>13</number></detail><extent unit="pages"><start>1929</start><end>1931</end><total>4</total></extent></part></relatedItem><identifier type="istex">06BF5DF36228081B96041475AC6DE3648727A9B5</identifier><identifier type="DOI">10.1002/mds.22100</identifier><identifier type="ArticleID">MDS22100</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2008 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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