Pre‐operative evaluations for DBS in dystonia
Identifieur interne : 000989 ( Istex/Corpus ); précédent : 000988; suivant : 000990Pre‐operative evaluations for DBS in dystonia
Auteurs : Stéphane Thobois ; Takaomi Taira ; Cynthia Comella ; Elena Moro ; Susan Bressman ; And Alberto AlbaneseSource :
- Movement Disorders [ 0885-3185 ] ; 2011-06.
English descriptors
Abstract
Background: The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). Methods: The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. Results: Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. Discussion: In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society
Url:
DOI: 10.1002/mds.23481
Links to Exploration step
ISTEX:CDF29A220451B2E392764969D342D83B9A30F5C4Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Pre‐operative evaluations for DBS in dystonia</title><author><name sortKey="Thobois, Stephane" sort="Thobois, Stephane" uniqKey="Thobois S" first="Stéphane" last="Thobois">Stéphane Thobois</name><affiliation><mods:affiliation>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</mods:affiliation></affiliation></author><author><name sortKey="Taira, Takaomi" sort="Taira, Takaomi" uniqKey="Taira T" first="Takaomi" last="Taira">Takaomi Taira</name><affiliation><mods:affiliation>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Comella, Cynthia" sort="Comella, Cynthia" uniqKey="Comella C" first="Cynthia" last="Comella">Cynthia Comella</name><affiliation><mods:affiliation>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</mods:affiliation></affiliation></author><author><name sortKey="Moro, Elena" sort="Moro, Elena" uniqKey="Moro E" first="Elena" last="Moro">Elena Moro</name><affiliation><mods:affiliation>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</mods:affiliation></affiliation></author><author><name sortKey="Bressman, Susan" sort="Bressman, Susan" uniqKey="Bressman S" first="Susan" last="Bressman">Susan Bressman</name><affiliation><mods:affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</mods:affiliation></affiliation></author><author><name sortKey="Albanese, And Alberto" sort="Albanese, And Alberto" uniqKey="Albanese A" first="And Alberto" last="Albanese">And Alberto Albanese</name><affiliation><mods:affiliation>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:CDF29A220451B2E392764969D342D83B9A30F5C4</idno><date when="2011" year="2011">2011</date><idno type="doi">10.1002/mds.23481</idno><idno type="url">https://api.istex.fr/document/CDF29A220451B2E392764969D342D83B9A30F5C4/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000989</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Pre‐operative evaluations for DBS in dystonia</title><author><name sortKey="Thobois, Stephane" sort="Thobois, Stephane" uniqKey="Thobois S" first="Stéphane" last="Thobois">Stéphane Thobois</name><affiliation><mods:affiliation>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</mods:affiliation></affiliation></author><author><name sortKey="Taira, Takaomi" sort="Taira, Takaomi" uniqKey="Taira T" first="Takaomi" last="Taira">Takaomi Taira</name><affiliation><mods:affiliation>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Comella, Cynthia" sort="Comella, Cynthia" uniqKey="Comella C" first="Cynthia" last="Comella">Cynthia Comella</name><affiliation><mods:affiliation>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</mods:affiliation></affiliation></author><author><name sortKey="Moro, Elena" sort="Moro, Elena" uniqKey="Moro E" first="Elena" last="Moro">Elena Moro</name><affiliation><mods:affiliation>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</mods:affiliation></affiliation></author><author><name sortKey="Bressman, Susan" sort="Bressman, Susan" uniqKey="Bressman S" first="Susan" last="Bressman">Susan Bressman</name><affiliation><mods:affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</mods:affiliation></affiliation></author><author><name sortKey="Albanese, And Alberto" sort="Albanese, And Alberto" uniqKey="Albanese A" first="And Alberto" last="Albanese">And Alberto Albanese</name><affiliation><mods:affiliation>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2011-06">2011-06</date><biblScope unit="vol">26</biblScope><biblScope unit="issue">S1</biblScope><biblScope unit="supplement">S1</biblScope><biblScope unit="page" from="S17">S17</biblScope><biblScope unit="page" to="S22">S22</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">CDF29A220451B2E392764969D342D83B9A30F5C4</idno><idno type="DOI">10.1002/mds.23481</idno><idno type="ArticleID">MDS23481</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>DBS</term><term>dystonia</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background: The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). Methods: The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. Results: Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. Discussion: In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Stéphane Thobois MD, PhD</name><affiliations><json:string>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</json:string></affiliations></json:item><json:item><name>Takaomi Taira MD</name><affiliations><json:string>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Cynthia Comella MD</name><affiliations><json:string>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</json:string></affiliations></json:item><json:item><name>Elena Moro MD, PhD</name><affiliations><json:string>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</json:string></affiliations></json:item><json:item><name>Susan Bressman MD, PhD</name><affiliations><json:string>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</json:string></affiliations></json:item><json:item><name>and Alberto Albanese MD, PhD</name><affiliations><json:string>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>DBS</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>dystonia</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Background: The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). Methods: The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. Results: Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. Discussion: In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society</abstract><qualityIndicators><score>7.076</score><pdfVersion>1.3</pdfVersion><pdfPageSize>612 x 810 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>1255</abstractCharCount><pdfWordCount>7402</pdfWordCount><pdfCharCount>48803</pdfCharCount><pdfPageCount>10</pdfPageCount><abstractWordCount>173</abstractWordCount></qualityIndicators><title>Pre‐operative evaluations for DBS in dystonia</title><genre><json:string>Serial article</json:string></genre><host><volume>26</volume><pages><total>10</total><last>S22</last><first>S17</first></pages><issn><json:string>0885-3185</json:string></issn><issue>S1</issue><subject><json:item><value>Supplement</value></json:item></subject><genre></genre><language><json:string>unknown</json:string></language><title>Movement Disorders</title><doi><json:string>10.1002/(ISSN)1531-8257</json:string></doi></host><publicationDate>2011</publicationDate><copyrightDate>2011</copyrightDate><doi><json:string>10.1002/mds.23481</json:string></doi><id>CDF29A220451B2E392764969D342D83B9A30F5C4</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/CDF29A220451B2E392764969D342D83B9A30F5C4/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/CDF29A220451B2E392764969D342D83B9A30F5C4/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/CDF29A220451B2E392764969D342D83B9A30F5C4/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Pre‐operative evaluations for DBS in dystonia</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><p>Wiley Subscription Services, Inc., A Wiley Company</p></availability><date>2011</date></publicationStmt><notesStmt><note type="content">*Potential conflict of interest: Nothing to report.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Pre‐operative evaluations for DBS in dystonia</title><author><persName><forename type="first">Stéphane</forename><surname>Thobois</surname><roleName type="degree">MD, PhD</roleName></persName><note type="correspondence"><p>Correspondence: Hôpital Neurologique Pierre Wertheimer, Neurologie C, 59 Bd Pinel, 69677 Lyon, France</p></note><affiliation>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</affiliation></author><author><persName><forename type="first">Takaomi</forename><surname>Taira</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</affiliation></author><author><persName><forename type="first">Cynthia</forename><surname>Comella</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</affiliation></author><author><persName><forename type="first">Elena</forename><surname>Moro</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</affiliation></author><author><persName><forename type="first">Susan</forename><surname>Bressman</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</affiliation></author><author><persName><forename type="first">and Alberto</forename><surname>Albanese</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</affiliation></author></analytic><monogr><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="pISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><idno type="DOI">10.1002/(ISSN)1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2011-06"></date><biblScope unit="vol">26</biblScope><biblScope unit="issue">S1</biblScope><biblScope unit="supplement">S1</biblScope><biblScope unit="page" from="S17">S17</biblScope><biblScope unit="page" to="S22">S22</biblScope></imprint></monogr><idno type="istex">CDF29A220451B2E392764969D342D83B9A30F5C4</idno><idno type="DOI">10.1002/mds.23481</idno><idno type="ArticleID">MDS23481</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2011</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Background: The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). Methods: The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. Results: Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. Discussion: In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>DBS</term></item><item><term>dystonia</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Supplement</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2010-04-24">Received</change><change when="2010-09-21">Registration</change><change when="2011-06">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/CDF29A220451B2E392764969D342D83B9A30F5C4/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>Hoboken</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1531-8257</doi><issn type="print">0885-3185</issn><issn type="electronic">1531-8257</issn><idGroup><id type="product" value="MDS"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="MOVEMENT DISORDERS">Movement Disorders</title><title type="short">Mov. Disord.</title></titleGroup></publicationMeta><publicationMeta level="part" position="75"><doi origin="wiley" registered="yes">10.1002/mds.v26.1s</doi><titleGroup><title type="supplementTitle">Deep Brain Stimulation for Dystonia: State of the Art</title></titleGroup><numberingGroup><numbering type="journalVolume" number="26">26</numbering><numbering type="journalIssue">S1</numbering><numbering type="supplement" number="S1">S1</numbering></numberingGroup><coverDate startDate="2011-06">June 2011</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="50" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.23481</doi><idGroup><id type="unit" value="MDS23481"></id></idGroup><countGroup><count type="pageTotal" number="10"></count></countGroup><titleGroup><title type="articleCategory">Supplement</title><title type="tocHeading1">Supplement</title></titleGroup><copyright ownership="thirdParty">Copyright © 2011 Movement Disorder Society</copyright><eventGroup><event type="manuscriptReceived" date="2010-04-24"></event><event type="manuscriptRevised" date="2010-08-21"></event><event type="manuscriptAccepted" date="2010-09-21"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:3.2.2 mode:FullText" date="2013-06-28"></event><event type="publishedOnlineFinalForm" date="2011-06-20"></event><event type="firstOnline" date="2011-06-20"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-02"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-31"></event></eventGroup><numberingGroup><numbering type="pageFirst">S17</numbering><numbering type="pageLast">S22</numbering></numberingGroup><correspondenceTo>Hôpital Neurologique Pierre Wertheimer, Neurologie C, 59 Bd Pinel, 69677 Lyon, France</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS23481.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="0"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="110"></count><count type="wordTotal" number="9448"></count></countGroup><titleGroup><title type="main" xml:lang="en">Pre‐operative evaluations for DBS in dystonia<link href="#fn1"></link></title><title type="short" xml:lang="en">Preoperative Evaluations</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Stéphane</givenNames><familyName>Thobois</familyName><degrees>MD, PhD</degrees></personName><contactDetails><email normalForm="stephane.thobois@chu-lyon.fr">stephane.thobois@chu‐lyon.fr</email></contactDetails></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Takaomi</givenNames><familyName>Taira</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Cynthia</givenNames><familyName>Comella</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af4"><personName><givenNames>Elena</givenNames><familyName>Moro</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af5"><personName><givenNames>Susan</givenNames><familyName>Bressman</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af6"><personName><givenNames>and Alberto</givenNames><familyName>Albanese</familyName><degrees>MD, PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="FR" type="organization"><unparsedAffiliation>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="US" type="organization"><unparsedAffiliation>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="CA" type="organization"><unparsedAffiliation>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="US" type="organization"><unparsedAffiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</unparsedAffiliation></affiliation><affiliation xml:id="af6" countryCode="IT" type="organization"><unparsedAffiliation>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">DBS</keyword><keyword xml:id="kwd2">dystonia</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p><b>Background:</b> The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). <b>Methods:</b> The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. <b>Results:</b> Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. <b>Discussion:</b> In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p><b>Potential conflict of interest</b>: Nothing to report.</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>Pre‐operative evaluations for DBS in dystonia</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Preoperative Evaluations</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Pre‐operative evaluations for DBS in dystonia</title></titleInfo><name type="personal"><namePart type="given">Stéphane</namePart><namePart type="family">Thobois</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer and CNRS, UMR 5229, Lyon, France</affiliation><description>Correspondence: Hôpital Neurologique Pierre Wertheimer, Neurologie C, 59 Bd Pinel, 69677 Lyon, France</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Takaomi</namePart><namePart type="family">Taira</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Cynthia</namePart><namePart type="family">Comella</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Elena</namePart><namePart type="family">Moro</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Movement Disorders Center, TWH, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Susan</namePart><namePart type="family">Bressman</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">and Alberto</namePart><namePart type="family">Albanese</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Fondazione IRCCS Istituto Neurologico Carlo Besta and Università Cattolica del Sacro Cuore, Milan, Italy</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">2011-06</dateIssued><dateCaptured encoding="w3cdtf">2010-04-24</dateCaptured><dateValid encoding="w3cdtf">2010-09-21</dateValid><copyrightDate encoding="w3cdtf">2011</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="tables">1</extent><extent unit="references">110</extent><extent unit="words">9448</extent></physicalDescription><abstract lang="en">Background: The preoperative evaluation in dystonia aims at characterizing the severity and topography of motor symptoms in patients, who have previously been selected for deep brain stimulation (DBS). Methods: The literature search was performed using PubMed, CINAHL, and the Cochrane Collaborative databases. Results: Commonly used scales for clinical assessment are the Burke‐Fahn‐Marsden dystonia rating scale for generalized dystonia and the Toronto Western Spasmodic Torticollis Scale for cervical dystonia. Motor assessment is completed by quality of life and functional scales, such as the Short‐Form Health Survey (SF‐36) or the Parkinson's Disease Questionnaire 39. Validated rating scales for cranial or upper limb dystonia are lacking. Discussion: In common clinical practice, these outcome measures can be administered in an open‐label fashion because double blind assessment is only required for ascertaining new treatment indications or research purposes. The same measures are to be used postoperatively to revaluate outcome after DBS. Brain MRI is required to confirm diagnosis and assess structural abnormalities. Other imaging techniques, particularly functional imaging, are used for research purposes. © 2011 Movement Disorder Society</abstract><note type="content">*Potential conflict of interest: Nothing to report.</note><subject lang="en"><genre>Keywords</genre><topic>DBS</topic><topic>dystonia</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Supplement</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>2011</date><detail type="volume"><caption>vol.</caption><number>26</number></detail><detail type="issue"><caption>no.</caption><number>S1</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>S1</number></detail><extent unit="pages"><start>S17</start><end>S22</end><total>10</total></extent></part></relatedItem><identifier type="istex">CDF29A220451B2E392764969D342D83B9A30F5C4</identifier><identifier type="DOI">10.1002/mds.23481</identifier><identifier type="ArticleID">MDS23481</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 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)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000989 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 000989 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:CDF29A220451B2E392764969D342D83B9A30F5C4
|texte= Pre‐operative evaluations for DBS in dystonia
}}
| This area was generated with Dilib version V0.6.23. |  |