The impact of patient-reported outcome measures in clinical practice for pain: a systematic review
Purpose Patient-reported outcome measures (PROMs) have increasingly been incorporated into clinical practice. Research suggests that PROMs could be viewed as active components of complex interventions and may affect the process and outcome of care. This systematic review examines PROMs in the contex...
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Veröffentlicht in: | Quality of life research 2017-02, Vol.26 (2), p.245-257 |
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description | Purpose Patient-reported outcome measures (PROMs) have increasingly been incorporated into clinical practice. Research suggests that PROMs could be viewed as active components of complex interventions and may affect the process and outcome of care. This systematic review examines PROMs in the context of treatment for non-malignant pain. Methods An electronic search on: MEDLINE, EMBASE, PsycINFO, PsycARTICLES, Cochrane Library and Web of Science identified relevant papers (February 2015). The inclusion criteria were: focused on implementing PROMs into clinical practice, adults, and primary data studies. Critical interpretive synthesis was used to synthesise qualitative and quantitative findings into a theoretical argument. Results Thirteen eligible studies were identified. Synthesis suggested that PROMs may be included in the initial consultation to assess patients and for shared decisionmaking regarding patient care. During the course of treatment, PROMs can be used to track progress, evaluate treatment, and change the course of care; using PROMs may also influence the therapeutic relationship. Posttreatment, using PROMs might directly influence other outcomes such as pain and patient satisfaction. However, although studies have investigated these areas, evidence is weak and inconclusive. Conclusion Due to the poor quality, lack of generalisability and heterogeneity of these studies, it is not possible to provide a comprehensive understanding of how PROMs may impact clinical treatment of non-malignant pain. The literature suggests that PROMs enable pain assessment, decision-making, the therapeutic relationship, evaluation of treatment and may influence outcomes. Further research is needed to provide better evidence as to whether PROMs do indeed have any effects on these domains. |
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Research suggests that PROMs could be viewed as active components of complex interventions and may affect the process and outcome of care. This systematic review examines PROMs in the context of treatment for non-malignant pain. Methods An electronic search on: MEDLINE, EMBASE, PsycINFO, PsycARTICLES, Cochrane Library and Web of Science identified relevant papers (February 2015). The inclusion criteria were: focused on implementing PROMs into clinical practice, adults, and primary data studies. Critical interpretive synthesis was used to synthesise qualitative and quantitative findings into a theoretical argument. Results Thirteen eligible studies were identified. Synthesis suggested that PROMs may be included in the initial consultation to assess patients and for shared decisionmaking regarding patient care. During the course of treatment, PROMs can be used to track progress, evaluate treatment, and change the course of care; using PROMs may also influence the therapeutic relationship. Posttreatment, using PROMs might directly influence other outcomes such as pain and patient satisfaction. However, although studies have investigated these areas, evidence is weak and inconclusive. Conclusion Due to the poor quality, lack of generalisability and heterogeneity of these studies, it is not possible to provide a comprehensive understanding of how PROMs may impact clinical treatment of non-malignant pain. The literature suggests that PROMs enable pain assessment, decision-making, the therapeutic relationship, evaluation of treatment and may influence outcomes. Further research is needed to provide better evidence as to whether PROMs do indeed have any effects on these domains.</description><identifier>ISSN: 0962-9343</identifier><identifier>EISSN: 1573-2649</identifier><identifier>DOI: 10.1007/s11136-016-1449-5</identifier><identifier>PMID: 27815820</identifier><language>eng</language><publisher>Cham: Springer</publisher><subject>Adult ; Clinical medicine ; Clinical outcomes ; Decision making ; Health care ; Humans ; Medicine ; Medicine & Public Health ; Pain ; Pain - psychology ; Patient Reported Outcome Measures ; Patient satisfaction ; Public Health ; Qualitative research ; Quality of life ; Quality of Life Research ; Quantitative analysis ; REVIEW ; Sickness Impact Profile ; Sociodemographics ; Sociology ; Studies ; Systematic review</subject><ispartof>Quality of life research, 2017-02, Vol.26 (2), p.245-257</ispartof><rights>Springer International Publishing 2017</rights><rights>The Author(s) 2016</rights><rights>Quality of Life Research is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-769accbd10b2518c9901218b21ec49b5fe57e53e225343f3396b6743dcc397e3</citedby><cites>FETCH-LOGICAL-c492t-769accbd10b2518c9901218b21ec49b5fe57e53e225343f3396b6743dcc397e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/44853324$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/44853324$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,780,784,803,885,27924,27925,41488,42557,51319,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27815820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holmes, Michelle M.</creatorcontrib><creatorcontrib>Lewith, George</creatorcontrib><creatorcontrib>Newell, David</creatorcontrib><creatorcontrib>Field, Jonathan</creatorcontrib><creatorcontrib>Bishop, Felicity L.</creatorcontrib><title>The impact of patient-reported outcome measures in clinical practice for pain: a systematic review</title><title>Quality of life research</title><addtitle>Qual Life Res</addtitle><addtitle>Qual Life Res</addtitle><description>Purpose Patient-reported outcome measures (PROMs) have increasingly been incorporated into clinical practice. Research suggests that PROMs could be viewed as active components of complex interventions and may affect the process and outcome of care. This systematic review examines PROMs in the context of treatment for non-malignant pain. Methods An electronic search on: MEDLINE, EMBASE, PsycINFO, PsycARTICLES, Cochrane Library and Web of Science identified relevant papers (February 2015). The inclusion criteria were: focused on implementing PROMs into clinical practice, adults, and primary data studies. Critical interpretive synthesis was used to synthesise qualitative and quantitative findings into a theoretical argument. Results Thirteen eligible studies were identified. Synthesis suggested that PROMs may be included in the initial consultation to assess patients and for shared decisionmaking regarding patient care. During the course of treatment, PROMs can be used to track progress, evaluate treatment, and change the course of care; using PROMs may also influence the therapeutic relationship. Posttreatment, using PROMs might directly influence other outcomes such as pain and patient satisfaction. However, although studies have investigated these areas, evidence is weak and inconclusive. Conclusion Due to the poor quality, lack of generalisability and heterogeneity of these studies, it is not possible to provide a comprehensive understanding of how PROMs may impact clinical treatment of non-malignant pain. The literature suggests that PROMs enable pain assessment, decision-making, the therapeutic relationship, evaluation of treatment and may influence outcomes. Further research is needed to provide better evidence as to whether PROMs do indeed have any effects on these domains.</description><subject>Adult</subject><subject>Clinical medicine</subject><subject>Clinical outcomes</subject><subject>Decision making</subject><subject>Health care</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pain</subject><subject>Pain - psychology</subject><subject>Patient Reported Outcome Measures</subject><subject>Patient satisfaction</subject><subject>Public Health</subject><subject>Qualitative research</subject><subject>Quality of life</subject><subject>Quality of Life Research</subject><subject>Quantitative analysis</subject><subject>REVIEW</subject><subject>Sickness Impact Profile</subject><subject>Sociodemographics</subject><subject>Sociology</subject><subject>Studies</subject><subject>Systematic review</subject><issn>0962-9343</issn><issn>1573-2649</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1u1DAUhS0EotOBB2ABssSmGxf_J2aBhKoWKlViM3vL8dy0HiVxsJ2ivj2uUkaFBRt7cb9zfI8PQu8YPWeUNp8yY0xoQpkmTEpD1Au0YaoRhGtpXqINNZoTI6Q4Qac5HyilraH8NTrhTctUy-kGdbs7wGGcnS849nh2JcBUSII5pgJ7HJfi4wh4BJeXBBmHCfshTMG7Ac-pyoIH3MdUpWH6jB3OD7nAWH08TnAf4Ncb9Kp3Q4a3T_cW7a4udxffyc2Pb9cXX2-Il4YX0mjjvO_2jHZcsdYbQxlnbccZVKBTPagGlADOVU3UC2F0pxsp9t4L04DYoi-r7bx0I-x9jZHcYOcURpcebHTB_j2Zwp29jfdW8baV9SO36OzJIMWfC-Rix5A9DIObIC7ZslboRmhVjy36-A96iEuaarpKacW1YpJWiq2UTzHnBP1xGUbtY4F2LdDWAu1jgVZVzYfnKY6KP41VgK9ArqPpFtKzp__j-n4VHXKJ6WgqZauE4FL8Br5VsIs</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Holmes, Michelle M.</creator><creator>Lewith, George</creator><creator>Newell, David</creator><creator>Field, Jonathan</creator><creator>Bishop, Felicity L.</creator><general>Springer</general><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7RV</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>KB0</scope><scope>L.-</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170201</creationdate><title>The impact of patient-reported outcome measures in clinical practice for pain: a systematic review</title><author>Holmes, Michelle M. ; Lewith, George ; Newell, David ; Field, Jonathan ; Bishop, Felicity L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-769accbd10b2518c9901218b21ec49b5fe57e53e225343f3396b6743dcc397e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Clinical medicine</topic><topic>Clinical outcomes</topic><topic>Decision making</topic><topic>Health care</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Pain</topic><topic>Pain - psychology</topic><topic>Patient Reported Outcome Measures</topic><topic>Patient satisfaction</topic><topic>Public Health</topic><topic>Qualitative research</topic><topic>Quality of life</topic><topic>Quality of Life Research</topic><topic>Quantitative analysis</topic><topic>REVIEW</topic><topic>Sickness Impact Profile</topic><topic>Sociodemographics</topic><topic>Sociology</topic><topic>Studies</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holmes, Michelle M.</creatorcontrib><creatorcontrib>Lewith, George</creatorcontrib><creatorcontrib>Newell, David</creatorcontrib><creatorcontrib>Field, Jonathan</creatorcontrib><creatorcontrib>Bishop, Felicity L.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Access via ABI/INFORM (ProQuest)</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Global (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Business Premium Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ABI/INFORM Global</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Quality of life research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holmes, Michelle M.</au><au>Lewith, George</au><au>Newell, David</au><au>Field, Jonathan</au><au>Bishop, Felicity L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of patient-reported outcome measures in clinical practice for pain: a systematic review</atitle><jtitle>Quality of life research</jtitle><stitle>Qual Life Res</stitle><addtitle>Qual Life Res</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>26</volume><issue>2</issue><spage>245</spage><epage>257</epage><pages>245-257</pages><issn>0962-9343</issn><eissn>1573-2649</eissn><abstract>Purpose Patient-reported outcome measures (PROMs) have increasingly been incorporated into clinical practice. Research suggests that PROMs could be viewed as active components of complex interventions and may affect the process and outcome of care. This systematic review examines PROMs in the context of treatment for non-malignant pain. Methods An electronic search on: MEDLINE, EMBASE, PsycINFO, PsycARTICLES, Cochrane Library and Web of Science identified relevant papers (February 2015). The inclusion criteria were: focused on implementing PROMs into clinical practice, adults, and primary data studies. Critical interpretive synthesis was used to synthesise qualitative and quantitative findings into a theoretical argument. Results Thirteen eligible studies were identified. Synthesis suggested that PROMs may be included in the initial consultation to assess patients and for shared decisionmaking regarding patient care. During the course of treatment, PROMs can be used to track progress, evaluate treatment, and change the course of care; using PROMs may also influence the therapeutic relationship. Posttreatment, using PROMs might directly influence other outcomes such as pain and patient satisfaction. However, although studies have investigated these areas, evidence is weak and inconclusive. Conclusion Due to the poor quality, lack of generalisability and heterogeneity of these studies, it is not possible to provide a comprehensive understanding of how PROMs may impact clinical treatment of non-malignant pain. The literature suggests that PROMs enable pain assessment, decision-making, the therapeutic relationship, evaluation of treatment and may influence outcomes. Further research is needed to provide better evidence as to whether PROMs do indeed have any effects on these domains.</abstract><cop>Cham</cop><pub>Springer</pub><pmid>27815820</pmid><doi>10.1007/s11136-016-1449-5</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Clinical medicine Clinical outcomes Decision making Health care Humans Medicine Medicine & Public Health Pain Pain - psychology Patient Reported Outcome Measures Patient satisfaction Public Health Qualitative research Quality of life Quality of Life Research Quantitative analysis REVIEW Sickness Impact Profile Sociodemographics Sociology Studies Systematic review |
title | The impact of patient-reported outcome measures in clinical practice for pain: a systematic review |
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