Disparities in the recording of Parkinson's disease on death certificates
Identifieur interne : 001175 ( Istex/Corpus ); précédent : 001174; suivant : 001176Disparities in the recording of Parkinson's disease on death certificates
Auteurs : Joyce C. Pressley ; Ming-Xin Tang ; Karen Marder ; Lucien J. Cote ; Richard MayeuxSource :
- Movement Disorders [ 0885-3185 ] ; 2005-03.
English descriptors
Abstract
Although little is known regarding potential socioeconomic or racial bias in the recording of Parkinson's disease (PD) on death certificates, studies of incidence, prevalence, and the etiology of PD frequently rely on this type of data. A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. This bias is large enough to confound death certificate–based investigations of incidence, prevalence, and risk factors that differ across socioeconomic strata. © 2004 Movement Disorder Society
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DOI: 10.1002/mds.20339
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ISTEX:A8BB4018FA44A9C6C87BE5432C517CFF9E12E324Le document en format XML
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A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. This bias is large enough to confound death certificate–based investigations of incidence, prevalence, and risk factors that differ across socioeconomic strata. © 2004 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Joyce C. Pressley PhD, MPH</name><affiliations><json:string>Department of Epidemiology, The Mailman School of Public Health, New York, New York, USA</json:string><json:string>Department of Health Policy and Management, The Mailman School of Public Health, New York, New York, USA</json:string></affiliations></json:item><json:item><name>Ming‐Xin Tang PhD</name><affiliations><json:string>Department of Biostatistics, The Mailman School of Public Health, New York, New York, USA</json:string><json:string>The Gertrude H. Sergievsky Center, New York, New York, USA</json:string></affiliations></json:item><json:item><name>Karen Marder MD, MPH</name><affiliations><json:string>The Gertrude H. 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Sergievsky Center, New York, New York, USA</json:string><json:string>Department of Neurology, College of Physicians and Surgeons, New York, New York, USA</json:string><json:string>Department of Psychiatry, College of Physicians and Surgeons, New York, New York, USA</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>parkinsonism</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Parkinson's disease</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>epidemiologic methods</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>death certificates</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Although little is known regarding potential socioeconomic or racial bias in the recording of Parkinson's disease (PD) on death certificates, studies of incidence, prevalence, and the etiology of PD frequently rely on this type of data. A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. 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A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. 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Sergievsky Center, New York, New York, USA</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="US" type="organization"><unparsedAffiliation>Department of Neurology, College of Physicians and Surgeons, New York, New York, USA</unparsedAffiliation></affiliation><affiliation xml:id="af6" countryCode="US" type="organization"><unparsedAffiliation>Department of Psychiatry, College of Physicians and Surgeons, New York, New York, USA</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">parkinsonism</keyword><keyword xml:id="kwd2">Parkinson's disease</keyword><keyword xml:id="kwd3">epidemiologic methods</keyword><keyword xml:id="kwd4">death certificates</keyword></keywordGroup><fundingInfo><fundingAgency>National Institutes of Health</fundingAgency><fundingNumber>P50 NS38370</fundingNumber><fundingNumber>1P60MD000206</fundingNumber></fundingInfo><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Although little is known regarding potential socioeconomic or racial bias in the recording of Parkinson's disease (PD) on death certificates, studies of incidence, prevalence, and the etiology of PD frequently rely on this type of data. A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. This bias is large enough to confound death certificate–based investigations of incidence, prevalence, and risk factors that differ across socioeconomic strata. © 2004 Movement Disorder Society</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Disparities in the recording of Parkinson's disease on death certificates</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Parkinson's Disease and Death Certificates</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Disparities in the recording of Parkinson's disease on death certificates</title></titleInfo><name type="personal"><namePart type="given">Joyce C.</namePart><namePart type="family">Pressley</namePart><namePart type="termsOfAddress">PhD, MPH</namePart><affiliation>Department of Epidemiology, The Mailman School of Public Health, New York, New York, USA</affiliation><affiliation>Department of Health Policy and Management, The Mailman School of Public Health, New York, New York, USA</affiliation><description>Correspondence: Columbia University, College of Physicians and Surgeons, 722 West 168th Street, Room 1712, New York, NY 10032</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ming‐Xin</namePart><namePart type="family">Tang</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Department of Biostatistics, The Mailman School of Public Health, New York, New York, USA</affiliation><affiliation>The Gertrude H. Sergievsky Center, New York, New York, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Karen</namePart><namePart type="family">Marder</namePart><namePart type="termsOfAddress">MD, MPH</namePart><affiliation>The Gertrude H. Sergievsky Center, New York, New York, USA</affiliation><affiliation>Department of Neurology, College of Physicians and Surgeons, New York, New York, USA</affiliation><affiliation>Department of Psychiatry, College of Physicians and Surgeons, New York, New York, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Lucien J.</namePart><namePart type="family">Cote</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>The Gertrude H. Sergievsky Center, New York, New York, USA</affiliation><affiliation>Department of Neurology, College of Physicians and Surgeons, New York, New York, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Richard</namePart><namePart type="family">Mayeux</namePart><namePart type="termsOfAddress">MD, MSc</namePart><affiliation>Department of Epidemiology, The Mailman School of Public Health, New York, New York, USA</affiliation><affiliation>The Gertrude H. Sergievsky Center, New York, New York, USA</affiliation><affiliation>Department of Neurology, College of Physicians and Surgeons, New York, New York, USA</affiliation><affiliation>Department of Psychiatry, College of Physicians and Surgeons, New York, New York, USA</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">2005-03</dateIssued><dateCaptured encoding="w3cdtf">2004-01-20</dateCaptured><dateValid encoding="w3cdtf">2004-07-20</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">3</extent><extent unit="references">30</extent><extent unit="words">4787</extent></physicalDescription><abstract lang="en">Although little is known regarding potential socioeconomic or racial bias in the recording of Parkinson's disease (PD) on death certificates, studies of incidence, prevalence, and the etiology of PD frequently rely on this type of data. A national population‐based survey was linked to death certificate data to investigate the concordance of PD reported on death certificates for persons reporting PD during life. Logistic regression was used to identify independent factors associated with differential reporting of PD at death. Among decedents with PD reported during life, 54.8% had PD recorded on the death certificate. Nearly 70% of persons in higher income categories had PD recorded at death compared to 35.4% for those earning $10,000 or less. Age and gender adjusted odds of having PD recorded at death was 2.3 (1.1–3.9), for those with an annual income of $35,000 or more. Income differences remain significant in multivariable models after controlling for age, gender, race, census region, family size, rural residence, and number of chronic medical conditions. In conclusion, this study found socioeconomic bias in the reporting of PD at death. This bias is large enough to confound death certificate–based investigations of incidence, prevalence, and risk factors that differ across socioeconomic strata. © 2004 Movement Disorder Society</abstract><note type="funding">National Institutes of Health - No. P50 NS38370; No. 1P60MD000206; </note><subject lang="en"><genre>Keywords</genre><topic>parkinsonism</topic><topic>Parkinson's disease</topic><topic>epidemiologic methods</topic><topic>death certificates</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>2005</date><detail type="volume"><caption>vol.</caption><number>20</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>315</start><end>321</end><total>7</total></extent></part></relatedItem><identifier type="istex">A8BB4018FA44A9C6C87BE5432C517CFF9E12E324</identifier><identifier type="DOI">10.1002/mds.20339</identifier><identifier type="ArticleID">MDS20339</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 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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