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Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help
Patient-reported outcome measurement (PROM) plays an increasingly important role in palliative care. A variety of measures exists and is used in clinical care, audit and research. However, little is known about professionals' views using these measures. The aim of this study is to describe the...
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Published in: | Health and quality of life outcomes 2011-04, Vol.9 (1), p.27-27 |
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description | Patient-reported outcome measurement (PROM) plays an increasingly important role in palliative care. A variety of measures exists and is used in clinical care, audit and research. However, little is known about professionals' views using these measures. The aim of this study is to describe the use and experiences of palliative care professionals with outcome measures.
A web-based online survey was conducted in Europe and Africa. Professionals working in clinical care, audit and research in palliative care were invited to the survey via national palliative care associations and various databases. Invitation e-mails were sent with a link to the questionnaire.
Overall participation rate 42% (663/1592), overall completion rate 59% (392/663). The majority of respondents were female (63.4%), mean age 46 years (SD 9). 68.1% respondents from Europe and 73.3% from Africa had experiences with outcome measures in palliative care. Non-users reported time constraints, burden, lack of training and guidance as main reasons. In clinical care/audit, assessment of patients' situation, monitoring changes and evaluation of services were main reasons for use. Choice of OMs for research was influenced by validity of the instrument in palliative care and comparability with international literature. Main problems were related to patient characteristics, staff, and outcome measures. Participants expressed the need for more guidance and training in the use of PROMs.
Professionals need more support for the use and implementation of PROMs in clinical practice and research through training and guidance in order to improve patient care. |
doi_str_mv | 10.1186/1477-7525-9-27 |
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A web-based online survey was conducted in Europe and Africa. Professionals working in clinical care, audit and research in palliative care were invited to the survey via national palliative care associations and various databases. Invitation e-mails were sent with a link to the questionnaire.
Overall participation rate 42% (663/1592), overall completion rate 59% (392/663). The majority of respondents were female (63.4%), mean age 46 years (SD 9). 68.1% respondents from Europe and 73.3% from Africa had experiences with outcome measures in palliative care. Non-users reported time constraints, burden, lack of training and guidance as main reasons. In clinical care/audit, assessment of patients' situation, monitoring changes and evaluation of services were main reasons for use. Choice of OMs for research was influenced by validity of the instrument in palliative care and comparability with international literature. Main problems were related to patient characteristics, staff, and outcome measures. Participants expressed the need for more guidance and training in the use of PROMs.
Professionals need more support for the use and implementation of PROMs in clinical practice and research through training and guidance in order to improve patient care.</description><identifier>ISSN: 1477-7525</identifier><identifier>EISSN: 1477-7525</identifier><identifier>DOI: 10.1186/1477-7525-9-27</identifier><identifier>PMID: 21507232</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Africa ; Aged ; Attitude of Health Personnel ; Europe ; Female ; Humans ; Internet ; Male ; Medical care ; Medical personnel ; Middle Aged ; Outcome Assessment (Health Care) - methods ; Palliative Care - standards ; Palliative treatment ; Patient Participation ; Patient Satisfaction ; Practice Patterns, Physicians ; Quality management ; Quality of Life ; Surveys ; Surveys and Questionnaires</subject><ispartof>Health and quality of life outcomes, 2011-04, Vol.9 (1), p.27-27</ispartof><rights>COPYRIGHT 2011 BioMed Central Ltd.</rights><rights>Copyright ©2011 Bausewein et al; licensee BioMed Central Ltd. 2011 Bausewein et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b580t-2f5b368245e5913a0056a4be29de81f562bc21306141667b9ec3fce95324188e3</citedby><cites>FETCH-LOGICAL-b580t-2f5b368245e5913a0056a4be29de81f562bc21306141667b9ec3fce95324188e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112059/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112059/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,37000,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21507232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bausewein, Claudia</creatorcontrib><creatorcontrib>Simon, Steffen T</creatorcontrib><creatorcontrib>Benalia, Hamid</creatorcontrib><creatorcontrib>Downing, Julia</creatorcontrib><creatorcontrib>Mwangi-Powell, Faith N</creatorcontrib><creatorcontrib>Daveson, Barbara A</creatorcontrib><creatorcontrib>Harding, Richard</creatorcontrib><creatorcontrib>Higginson, Irene J</creatorcontrib><creatorcontrib>PRISMA</creatorcontrib><creatorcontrib>PRISMA</creatorcontrib><title>Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help</title><title>Health and quality of life outcomes</title><addtitle>Health Qual Life Outcomes</addtitle><description>Patient-reported outcome measurement (PROM) plays an increasingly important role in palliative care. A variety of measures exists and is used in clinical care, audit and research. However, little is known about professionals' views using these measures. The aim of this study is to describe the use and experiences of palliative care professionals with outcome measures.
A web-based online survey was conducted in Europe and Africa. Professionals working in clinical care, audit and research in palliative care were invited to the survey via national palliative care associations and various databases. Invitation e-mails were sent with a link to the questionnaire.
Overall participation rate 42% (663/1592), overall completion rate 59% (392/663). The majority of respondents were female (63.4%), mean age 46 years (SD 9). 68.1% respondents from Europe and 73.3% from Africa had experiences with outcome measures in palliative care. Non-users reported time constraints, burden, lack of training and guidance as main reasons. In clinical care/audit, assessment of patients' situation, monitoring changes and evaluation of services were main reasons for use. Choice of OMs for research was influenced by validity of the instrument in palliative care and comparability with international literature. Main problems were related to patient characteristics, staff, and outcome measures. Participants expressed the need for more guidance and training in the use of PROMs.
Professionals need more support for the use and implementation of PROMs in clinical practice and research through training and guidance in order to improve patient care.</description><subject>Adult</subject><subject>Africa</subject><subject>Aged</subject><subject>Attitude of Health Personnel</subject><subject>Europe</subject><subject>Female</subject><subject>Humans</subject><subject>Internet</subject><subject>Male</subject><subject>Medical care</subject><subject>Medical personnel</subject><subject>Middle Aged</subject><subject>Outcome Assessment (Health Care) - methods</subject><subject>Palliative Care - standards</subject><subject>Palliative treatment</subject><subject>Patient Participation</subject><subject>Patient Satisfaction</subject><subject>Practice Patterns, Physicians</subject><subject>Quality management</subject><subject>Quality of Life</subject><subject>Surveys</subject><subject>Surveys and Questionnaires</subject><issn>1477-7525</issn><issn>1477-7525</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1kstv1DAQhyMEoqVw5YgscSgcUvzIJPYFaVXxWKmoCMEVy3HGW1dJHOykUv97vGxZdUWRD57Hbz6Nx1MULxk9Y0zW71jVNGUDHEpV8uZRcbwPPL5nHxXPUrqmlAvO4WlxxBnQJjvHxc_1MPU44Dj7cUMmM_tskohTiDN2JCyzDQOSAU1aIiby5uu3yy_pLfFjFve9zwU3SKyJWJZLwphOiY23xIVIrrCfnhdPnOkTvri7T4ofHz98P_9cXlx-Wp-vLsoWJJ1L7qAVteQVICgmDKVQm6pFrjqUzEHNW8uZoDWrWF03rUIrnEUFgldMShQnxXrH7YK51lP0g4m3Ohiv_wRC3GgTZ2971NJS2SnpQBhbSceUyJ6kQLF1nbE2s97vWNPSDtjZPJBo-gPoYWb0V3oTbrRgjFNQGbDaAVof_gM4zOQR6-1f6e1faaV5kxmnd03E8GvBNOvBJ4t9b0YMS9Ky4YwDF5CVr3fKjcmv86MLmWm3ar3iIKGuQG15Zw-o8ulw8DaM6HyOP1RgY0gpotv3z6jert6_Hb-6P7a9_O-uid8aatNq</recordid><startdate>20110420</startdate><enddate>20110420</enddate><creator>Bausewein, Claudia</creator><creator>Simon, Steffen T</creator><creator>Benalia, Hamid</creator><creator>Downing, Julia</creator><creator>Mwangi-Powell, Faith N</creator><creator>Daveson, Barbara A</creator><creator>Harding, Richard</creator><creator>Higginson, Irene J</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110420</creationdate><title>Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help</title><author>Bausewein, Claudia ; Simon, Steffen T ; Benalia, Hamid ; Downing, Julia ; Mwangi-Powell, Faith N ; Daveson, Barbara A ; Harding, Richard ; Higginson, Irene J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b580t-2f5b368245e5913a0056a4be29de81f562bc21306141667b9ec3fce95324188e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Africa</topic><topic>Aged</topic><topic>Attitude of Health Personnel</topic><topic>Europe</topic><topic>Female</topic><topic>Humans</topic><topic>Internet</topic><topic>Male</topic><topic>Medical care</topic><topic>Medical personnel</topic><topic>Middle Aged</topic><topic>Outcome Assessment (Health Care) - methods</topic><topic>Palliative Care - standards</topic><topic>Palliative treatment</topic><topic>Patient Participation</topic><topic>Patient Satisfaction</topic><topic>Practice Patterns, Physicians</topic><topic>Quality management</topic><topic>Quality of Life</topic><topic>Surveys</topic><topic>Surveys and Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bausewein, Claudia</creatorcontrib><creatorcontrib>Simon, Steffen T</creatorcontrib><creatorcontrib>Benalia, Hamid</creatorcontrib><creatorcontrib>Downing, Julia</creatorcontrib><creatorcontrib>Mwangi-Powell, Faith N</creatorcontrib><creatorcontrib>Daveson, Barbara A</creatorcontrib><creatorcontrib>Harding, Richard</creatorcontrib><creatorcontrib>Higginson, Irene J</creatorcontrib><creatorcontrib>PRISMA</creatorcontrib><creatorcontrib>PRISMA</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Health and quality of life outcomes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bausewein, Claudia</au><au>Simon, Steffen T</au><au>Benalia, Hamid</au><au>Downing, Julia</au><au>Mwangi-Powell, Faith N</au><au>Daveson, Barbara A</au><au>Harding, Richard</au><au>Higginson, Irene J</au><aucorp>PRISMA</aucorp><aucorp>PRISMA</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help</atitle><jtitle>Health and quality of life outcomes</jtitle><addtitle>Health Qual Life Outcomes</addtitle><date>2011-04-20</date><risdate>2011</risdate><volume>9</volume><issue>1</issue><spage>27</spage><epage>27</epage><pages>27-27</pages><issn>1477-7525</issn><eissn>1477-7525</eissn><abstract>Patient-reported outcome measurement (PROM) plays an increasingly important role in palliative care. A variety of measures exists and is used in clinical care, audit and research. However, little is known about professionals' views using these measures. The aim of this study is to describe the use and experiences of palliative care professionals with outcome measures.
A web-based online survey was conducted in Europe and Africa. Professionals working in clinical care, audit and research in palliative care were invited to the survey via national palliative care associations and various databases. Invitation e-mails were sent with a link to the questionnaire.
Overall participation rate 42% (663/1592), overall completion rate 59% (392/663). The majority of respondents were female (63.4%), mean age 46 years (SD 9). 68.1% respondents from Europe and 73.3% from Africa had experiences with outcome measures in palliative care. Non-users reported time constraints, burden, lack of training and guidance as main reasons. In clinical care/audit, assessment of patients' situation, monitoring changes and evaluation of services were main reasons for use. Choice of OMs for research was influenced by validity of the instrument in palliative care and comparability with international literature. Main problems were related to patient characteristics, staff, and outcome measures. Participants expressed the need for more guidance and training in the use of PROMs.
Professionals need more support for the use and implementation of PROMs in clinical practice and research through training and guidance in order to improve patient care.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21507232</pmid><doi>10.1186/1477-7525-9-27</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Africa Aged Attitude of Health Personnel Europe Female Humans Internet Male Medical care Medical personnel Middle Aged Outcome Assessment (Health Care) - methods Palliative Care - standards Palliative treatment Patient Participation Patient Satisfaction Practice Patterns, Physicians Quality management Quality of Life Surveys Surveys and Questionnaires |
title | Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help |
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