Movement Disorders (revue)

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Patient and caregiver quality of life in Huntington's disease

Identifieur interne : 002064 ( Istex/Corpus ); précédent : 002063; suivant : 002065

Patient and caregiver quality of life in Huntington's disease

Auteurs : Rebecca E. Ready ; Melissa Mathews ; Anne Leserman ; Jane S. Paulsen

Source :

RBID : ISTEX:6E37707EAD71DABBB39B3D98A97DDBFA87CBCF45

English descriptors

Abstract

Little is known about subjective perceptions of quality of life (QOL) in Huntington's disease (HD). The current study determined correlates of patient and caregiver QOL and assessed change over time. Participants were 22 patient‐caregiver dyads, who rated QOL at baseline and 6 months later. Overall, patients' functional and cognitive impairment were significantly correlated with patient and caregiver QOL. Neuropsychiatric symptoms had differential impact on patient and caregiver QOL. Furthermore, when patients recalled their QOL about a previous time, their recall may have been negatively biased. Clinical implications of results are discussed. Future work is needed because subjective QOL is an important outcome measure in therapeutic trials. © 2008 Movement Disorder Society

Url:
DOI: 10.1002/mds.21920

Links to Exploration step

ISTEX:6E37707EAD71DABBB39B3D98A97DDBFA87CBCF45

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<affiliation>Department of Psychiatry, University of Iowa Hospital and Clinics, Iowa City, Iowa</affiliation>
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<name type="personal">
<namePart type="given">Jane S.</namePart>
<namePart type="family">Paulsen</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Department of Psychiatry, University of Iowa Hospital and Clinics, Iowa City, Iowa</affiliation>
<affiliation>Department of Psychology, University of Iowa, Iowa City, Iowa</affiliation>
<affiliation>Department of Neurology, University of Iowa Hospital and Clinics, Iowa City, Iowa</affiliation>
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<dateIssued encoding="w3cdtf">2008-04-15</dateIssued>
<dateCaptured encoding="w3cdtf">2007-08-08</dateCaptured>
<dateValid encoding="w3cdtf">2007-11-28</dateValid>
<copyrightDate encoding="w3cdtf">2008</copyrightDate>
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<abstract lang="en">Little is known about subjective perceptions of quality of life (QOL) in Huntington's disease (HD). The current study determined correlates of patient and caregiver QOL and assessed change over time. Participants were 22 patient‐caregiver dyads, who rated QOL at baseline and 6 months later. Overall, patients' functional and cognitive impairment were significantly correlated with patient and caregiver QOL. Neuropsychiatric symptoms had differential impact on patient and caregiver QOL. Furthermore, when patients recalled their QOL about a previous time, their recall may have been negatively biased. Clinical implications of results are discussed. Future work is needed because subjective QOL is an important outcome measure in therapeutic trials. © 2008 Movement Disorder Society</abstract>
<note type="funding">High Q Foundation to JSP</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>Huntington's disease</topic>
<topic>quality of life</topic>
<topic>caregiver</topic>
<topic>neuropsychiatric symptoms</topic>
<topic>self‐report</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>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>5</number>
</detail>
<extent unit="pages">
<start>721</start>
<end>726</end>
<total>6</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">6E37707EAD71DABBB39B3D98A97DDBFA87CBCF45</identifier>
<identifier type="DOI">10.1002/mds.21920</identifier>
<identifier type="ArticleID">MDS21920</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2007 Movement Disorder Society</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
</recordInfo>
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<serie></serie>
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