Measurement of costs and scales for outcome evaluation in health economic studies of Parkinson's disease
ABSTRACT Health economic studies in Parkinson's disease (PD) have become increasingly common in recent years. Because several methodologies and instruments have been used to assess cost and outcomes in PD, the Movement Disorder Society (MDS) commissioned a Task Force to assess their properties...
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Veröffentlicht in: | Movement disorders 2014-02, Vol.29 (2), p.169-176 |
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creator | Dodel, Richard Jönsson, Bengt Reese, Jens Peter Winter, Yaroslav Martinez-Martin, Pablo Holloway, Robert Sampaio, Cristina Růžička, Evžen Hawthorne, Graeme Oertel, Wolfgang Poewe, Werner Stebbins, Glenn Rascol, Oliver Goetz, Christopher G. Schrag, Anette |
description | ABSTRACT
Health economic studies in Parkinson's disease (PD) have become increasingly common in recent years. Because several methodologies and instruments have been used to assess cost and outcomes in PD, the Movement Disorder Society (MDS) commissioned a Task Force to assess their properties and make recommendations regarding their use. A systematic literature review was conducted to explore the use of those instruments in PD and to determine which should be selected for this review. We assessed approaches to evaluate cost of illness (COI), cost effectiveness, and cost utilities, which include the use of direct (standard gamble, time trade‐off. and visual analogue scales) and indirect instruments to measure health status and utilities. No validated instruments/models were identified for the evaluation of COI or cost‐effectiveness in patients with PD; therefore, no instruments in this group are recommended. Among utility instruments, only a few of these outcome instruments have been used in the PD population, and only limited psychometric data are available for these instruments with respect to PD. Because psychometric data for further utility instruments in conditions other than PD already exist, the standard gamble and time trade‐off methods and the EQ‐5D (a European quality‐of‐life health states instrument) and Health Utility Index instruments met the criteria for scales that are “recommended (with limitations),” but only the EQ‐5D has been assessed in detail in PD patients. The MDS Task Force recommends further study of these instruments in the PD population to establish core psychometric properties. For the assessment of COI, the Task Force considers the development of a COI instrument specifically for PD, like that available for Alzheimer's disease. © 2013 Movement Disorder Society |
doi_str_mv | 10.1002/mds.25571 |
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Health economic studies in Parkinson's disease (PD) have become increasingly common in recent years. Because several methodologies and instruments have been used to assess cost and outcomes in PD, the Movement Disorder Society (MDS) commissioned a Task Force to assess their properties and make recommendations regarding their use. A systematic literature review was conducted to explore the use of those instruments in PD and to determine which should be selected for this review. We assessed approaches to evaluate cost of illness (COI), cost effectiveness, and cost utilities, which include the use of direct (standard gamble, time trade‐off. and visual analogue scales) and indirect instruments to measure health status and utilities. No validated instruments/models were identified for the evaluation of COI or cost‐effectiveness in patients with PD; therefore, no instruments in this group are recommended. Among utility instruments, only a few of these outcome instruments have been used in the PD population, and only limited psychometric data are available for these instruments with respect to PD. Because psychometric data for further utility instruments in conditions other than PD already exist, the standard gamble and time trade‐off methods and the EQ‐5D (a European quality‐of‐life health states instrument) and Health Utility Index instruments met the criteria for scales that are “recommended (with limitations),” but only the EQ‐5D has been assessed in detail in PD patients. The MDS Task Force recommends further study of these instruments in the PD population to establish core psychometric properties. For the assessment of COI, the Task Force considers the development of a COI instrument specifically for PD, like that available for Alzheimer's disease. © 2013 Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.25571</identifier><identifier>PMID: 23861335</identifier><identifier>CODEN: MOVDEA</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>cost ; cost effectiveness ; Cost of Illness ; cost utility ; Cost-Benefit Analysis - economics ; health economics ; Humans ; Movement disorders ; Parkinson Disease - economics ; Parkinson Disease - therapy ; Parkinson's disease ; Psychometrics</subject><ispartof>Movement disorders, 2014-02, Vol.29 (2), p.169-176</ispartof><rights>2013 Movement Disorder Society</rights><rights>2013 Movement Disorder Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4331-4e24cfd6e2793e8cc27ebce8a92ea57d3bc60110f4feed70f20dd8abeff42f73</citedby><cites>FETCH-LOGICAL-c4331-4e24cfd6e2793e8cc27ebce8a92ea57d3bc60110f4feed70f20dd8abeff42f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.25571$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.25571$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23861335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://research.hhs.se/esploro/outputs/journalArticle/Measurement-of-costs-and-scales-for/991001480373206056$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Dodel, Richard</creatorcontrib><creatorcontrib>Jönsson, Bengt</creatorcontrib><creatorcontrib>Reese, Jens Peter</creatorcontrib><creatorcontrib>Winter, Yaroslav</creatorcontrib><creatorcontrib>Martinez-Martin, Pablo</creatorcontrib><creatorcontrib>Holloway, Robert</creatorcontrib><creatorcontrib>Sampaio, Cristina</creatorcontrib><creatorcontrib>Růžička, Evžen</creatorcontrib><creatorcontrib>Hawthorne, Graeme</creatorcontrib><creatorcontrib>Oertel, Wolfgang</creatorcontrib><creatorcontrib>Poewe, Werner</creatorcontrib><creatorcontrib>Stebbins, Glenn</creatorcontrib><creatorcontrib>Rascol, Oliver</creatorcontrib><creatorcontrib>Goetz, Christopher G.</creatorcontrib><creatorcontrib>Schrag, Anette</creatorcontrib><title>Measurement of costs and scales for outcome evaluation in health economic studies of Parkinson's disease</title><title>Movement disorders</title><addtitle>Mov Disord</addtitle><description>ABSTRACT
Health economic studies in Parkinson's disease (PD) have become increasingly common in recent years. Because several methodologies and instruments have been used to assess cost and outcomes in PD, the Movement Disorder Society (MDS) commissioned a Task Force to assess their properties and make recommendations regarding their use. A systematic literature review was conducted to explore the use of those instruments in PD and to determine which should be selected for this review. We assessed approaches to evaluate cost of illness (COI), cost effectiveness, and cost utilities, which include the use of direct (standard gamble, time trade‐off. and visual analogue scales) and indirect instruments to measure health status and utilities. No validated instruments/models were identified for the evaluation of COI or cost‐effectiveness in patients with PD; therefore, no instruments in this group are recommended. Among utility instruments, only a few of these outcome instruments have been used in the PD population, and only limited psychometric data are available for these instruments with respect to PD. Because psychometric data for further utility instruments in conditions other than PD already exist, the standard gamble and time trade‐off methods and the EQ‐5D (a European quality‐of‐life health states instrument) and Health Utility Index instruments met the criteria for scales that are “recommended (with limitations),” but only the EQ‐5D has been assessed in detail in PD patients. The MDS Task Force recommends further study of these instruments in the PD population to establish core psychometric properties. For the assessment of COI, the Task Force considers the development of a COI instrument specifically for PD, like that available for Alzheimer's disease. © 2013 Movement Disorder Society</description><subject>cost</subject><subject>cost effectiveness</subject><subject>Cost of Illness</subject><subject>cost utility</subject><subject>Cost-Benefit Analysis - economics</subject><subject>health economics</subject><subject>Humans</subject><subject>Movement disorders</subject><subject>Parkinson Disease - economics</subject><subject>Parkinson Disease - therapy</subject><subject>Parkinson's disease</subject><subject>Psychometrics</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhi0EokvhwB9AljgAh7T-TLLHfkBBbaGIlThajj1WXJJ4ySSU_ntc0u4BiZMvz_t4Zl5CXnJ2wBkTh73HA6F1xR-RFdeSF7XQ1WOyYnWtC8lrvUeeIV4zxrnm5VOyJ2Rdcin1irSXYHEeoYdhoilQl3BCagdP0dkOkIY00jRPLvVA4ZftZjvFNNA40BZsN7UUXBpSHx3FafYxJ7Llyo4_4oBpeIPUR8xfwHPyJNgO4cX9u082H95vTj4WF1_OPp0cXRROyTy5AqFc8CWIai2hdk5U0Dio7VqA1ZWXjSvzGiyoAOArFgTzvrYNhKBEqOQ-4YsWb2A7N2Y7xt6OtybZaNoWDYLJR9CMSSUYYyXTZc68XTLbMf2cASfTR3TQdXaANKPhmimlxVqpjL7-B71O8zjkhe6oLGNyLTP1bqHcmBBHCLsxODN3jZncmPnbWGZf3Rvnpge_Ix8qysDhAtzEDm7_bzKXp98elMWSiDjB710id2LKSlbafP98Zs6_bo7F8dWpOZd_AJF7ryQ</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Dodel, Richard</creator><creator>Jönsson, Bengt</creator><creator>Reese, Jens Peter</creator><creator>Winter, Yaroslav</creator><creator>Martinez-Martin, Pablo</creator><creator>Holloway, Robert</creator><creator>Sampaio, Cristina</creator><creator>Růžička, Evžen</creator><creator>Hawthorne, Graeme</creator><creator>Oertel, Wolfgang</creator><creator>Poewe, Werner</creator><creator>Stebbins, Glenn</creator><creator>Rascol, Oliver</creator><creator>Goetz, Christopher G.</creator><creator>Schrag, Anette</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>201402</creationdate><title>Measurement of costs and scales for outcome evaluation in health economic studies of Parkinson's disease</title><author>Dodel, Richard ; Jönsson, Bengt ; Reese, Jens Peter ; Winter, Yaroslav ; Martinez-Martin, Pablo ; Holloway, Robert ; Sampaio, Cristina ; Růžička, Evžen ; Hawthorne, Graeme ; Oertel, Wolfgang ; Poewe, Werner ; Stebbins, Glenn ; Rascol, Oliver ; Goetz, Christopher G. ; Schrag, Anette</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4331-4e24cfd6e2793e8cc27ebce8a92ea57d3bc60110f4feed70f20dd8abeff42f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>cost</topic><topic>cost effectiveness</topic><topic>Cost of Illness</topic><topic>cost utility</topic><topic>Cost-Benefit Analysis - economics</topic><topic>health economics</topic><topic>Humans</topic><topic>Movement disorders</topic><topic>Parkinson Disease - economics</topic><topic>Parkinson Disease - therapy</topic><topic>Parkinson's disease</topic><topic>Psychometrics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dodel, Richard</creatorcontrib><creatorcontrib>Jönsson, Bengt</creatorcontrib><creatorcontrib>Reese, Jens Peter</creatorcontrib><creatorcontrib>Winter, Yaroslav</creatorcontrib><creatorcontrib>Martinez-Martin, Pablo</creatorcontrib><creatorcontrib>Holloway, Robert</creatorcontrib><creatorcontrib>Sampaio, Cristina</creatorcontrib><creatorcontrib>Růžička, Evžen</creatorcontrib><creatorcontrib>Hawthorne, Graeme</creatorcontrib><creatorcontrib>Oertel, Wolfgang</creatorcontrib><creatorcontrib>Poewe, Werner</creatorcontrib><creatorcontrib>Stebbins, Glenn</creatorcontrib><creatorcontrib>Rascol, Oliver</creatorcontrib><creatorcontrib>Goetz, Christopher G.</creatorcontrib><creatorcontrib>Schrag, Anette</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dodel, Richard</au><au>Jönsson, Bengt</au><au>Reese, Jens Peter</au><au>Winter, Yaroslav</au><au>Martinez-Martin, Pablo</au><au>Holloway, Robert</au><au>Sampaio, Cristina</au><au>Růžička, Evžen</au><au>Hawthorne, Graeme</au><au>Oertel, Wolfgang</au><au>Poewe, Werner</au><au>Stebbins, Glenn</au><au>Rascol, Oliver</au><au>Goetz, Christopher G.</au><au>Schrag, Anette</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measurement of costs and scales for outcome evaluation in health economic studies of Parkinson's disease</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov Disord</addtitle><date>2014-02</date><risdate>2014</risdate><volume>29</volume><issue>2</issue><spage>169</spage><epage>176</epage><pages>169-176</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><coden>MOVDEA</coden><abstract>ABSTRACT
Health economic studies in Parkinson's disease (PD) have become increasingly common in recent years. Because several methodologies and instruments have been used to assess cost and outcomes in PD, the Movement Disorder Society (MDS) commissioned a Task Force to assess their properties and make recommendations regarding their use. A systematic literature review was conducted to explore the use of those instruments in PD and to determine which should be selected for this review. We assessed approaches to evaluate cost of illness (COI), cost effectiveness, and cost utilities, which include the use of direct (standard gamble, time trade‐off. and visual analogue scales) and indirect instruments to measure health status and utilities. No validated instruments/models were identified for the evaluation of COI or cost‐effectiveness in patients with PD; therefore, no instruments in this group are recommended. Among utility instruments, only a few of these outcome instruments have been used in the PD population, and only limited psychometric data are available for these instruments with respect to PD. Because psychometric data for further utility instruments in conditions other than PD already exist, the standard gamble and time trade‐off methods and the EQ‐5D (a European quality‐of‐life health states instrument) and Health Utility Index instruments met the criteria for scales that are “recommended (with limitations),” but only the EQ‐5D has been assessed in detail in PD patients. The MDS Task Force recommends further study of these instruments in the PD population to establish core psychometric properties. For the assessment of COI, the Task Force considers the development of a COI instrument specifically for PD, like that available for Alzheimer's disease. © 2013 Movement Disorder Society</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23861335</pmid><doi>10.1002/mds.25571</doi><tpages>8</tpages></addata></record> |
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subjects | cost cost effectiveness Cost of Illness cost utility Cost-Benefit Analysis - economics health economics Humans Movement disorders Parkinson Disease - economics Parkinson Disease - therapy Parkinson's disease Psychometrics |
title | Measurement of costs and scales for outcome evaluation in health economic studies of Parkinson's disease |
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