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Usage and impact of patient‐reported outcomes in epilepsy
Background The use of patient‐reported outcomes (PRO) in clinical practice is gaining increasing attention. This study aimed to provide a critical assessment of the current state‐of‐the‐art and beliefs about the use of PRO in the management of people with epilepsy across some European countries. Met...
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Published in: | Brain and behavior 2023-12, Vol.13 (12), p.e3342-n/a |
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creator | Vonck, Kristl Biraben, Arnaud Bosak, Magdalena Jennum, Poul Jørgen Kimiskidis, Vasilios K Marusic, Petr Mitchell, James W. Ferreira, Lara N. Ondrušová, Martina Pana, Adrian Persson, Ulf Oertzen, Tim J. Lattanzi, Simona |
description | Background
The use of patient‐reported outcomes (PRO) in clinical practice is gaining increasing attention. This study aimed to provide a critical assessment of the current state‐of‐the‐art and beliefs about the use of PRO in the management of people with epilepsy across some European countries.
Methods
Structured interviews were conducted with European experts to collect insights about (I) the personal experience with PRO; (II) the value and impact of PRO in the decision‐making process at the national level; and (III) the interest for and use of PRO by national health authorities.
Results
Nine neurologists (Austria, Belgium, Czechia, Denmark, France, Greece, Italy, Poland, and United Kingdom), three health economists (Portugal, Romania, and Sweden), and one epidemiologist (Slovakia) participated. They all stated that PRO are collected at their own countries in the context of clinical trials and/or specific projects. During everyday clinical practice, PRO are collected routinely/almost routinely in Austria and Sweden and only at the discretion of the treating physicians in Czechia, Denmark, France, Greece, and Portugal. There was complete consensus about the favorable impact that the PRO can have in terms of clinical outcomes, healthcare resources utilization, and general patient satisfaction. Only participants from Portugal and Sweden answered that the PRO are perceived as very important by the National Health Authorities of their respective countries.
Conclusions
Differences exist in attitudes and perspectives about PRO in epilepsy across Europe. An active plan is warranted to harmonize the measurement of PRO and ensure they can be relevant to people with epilepsy and health services. |
doi_str_mv | 10.1002/brb3.3342 |
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The use of patient‐reported outcomes (PRO) in clinical practice is gaining increasing attention. This study aimed to provide a critical assessment of the current state‐of‐the‐art and beliefs about the use of PRO in the management of people with epilepsy across some European countries.
Methods
Structured interviews were conducted with European experts to collect insights about (I) the personal experience with PRO; (II) the value and impact of PRO in the decision‐making process at the national level; and (III) the interest for and use of PRO by national health authorities.
Results
Nine neurologists (Austria, Belgium, Czechia, Denmark, France, Greece, Italy, Poland, and United Kingdom), three health economists (Portugal, Romania, and Sweden), and one epidemiologist (Slovakia) participated. They all stated that PRO are collected at their own countries in the context of clinical trials and/or specific projects. During everyday clinical practice, PRO are collected routinely/almost routinely in Austria and Sweden and only at the discretion of the treating physicians in Czechia, Denmark, France, Greece, and Portugal. There was complete consensus about the favorable impact that the PRO can have in terms of clinical outcomes, healthcare resources utilization, and general patient satisfaction. Only participants from Portugal and Sweden answered that the PRO are perceived as very important by the National Health Authorities of their respective countries.
Conclusions
Differences exist in attitudes and perspectives about PRO in epilepsy across Europe. An active plan is warranted to harmonize the measurement of PRO and ensure they can be relevant to people with epilepsy and health services.</description><identifier>ISSN: 2162-3279</identifier><identifier>EISSN: 2162-3279</identifier><identifier>DOI: 10.1002/brb3.3342</identifier><identifier>PMID: 37997564</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Clinical outcomes ; Clinical trials ; Convulsions & seizures ; Decision making ; economics ; Epilepsy ; Health care ; Interviews ; Mental health ; Original ; Patient satisfaction ; patient‐reported outcomes ; Physicians ; Quality of life ; Questionnaires ; seizure</subject><ispartof>Brain and behavior, 2023-12, Vol.13 (12), p.e3342-n/a</ispartof><rights>2023 The Authors. published by Wiley Periodicals LLC.</rights><rights>2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5102-da6b65c0157d467938fd2fbf05351a31a0b0093884aaf9ab2ae453fd829f92c13</citedby><cites>FETCH-LOGICAL-c5102-da6b65c0157d467938fd2fbf05351a31a0b0093884aaf9ab2ae453fd829f92c13</cites><orcidid>0000-0002-3335-3019 ; 0000-0003-2378-7750</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2902885928/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2902885928?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,25752,27923,27924,37011,37012,44589,46051,46475,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37997564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vonck, Kristl</creatorcontrib><creatorcontrib>Biraben, Arnaud</creatorcontrib><creatorcontrib>Bosak, Magdalena</creatorcontrib><creatorcontrib>Jennum, Poul Jørgen</creatorcontrib><creatorcontrib>Kimiskidis, Vasilios K</creatorcontrib><creatorcontrib>Marusic, Petr</creatorcontrib><creatorcontrib>Mitchell, James W.</creatorcontrib><creatorcontrib>Ferreira, Lara N.</creatorcontrib><creatorcontrib>Ondrušová, Martina</creatorcontrib><creatorcontrib>Pana, Adrian</creatorcontrib><creatorcontrib>Persson, Ulf</creatorcontrib><creatorcontrib>Oertzen, Tim J.</creatorcontrib><creatorcontrib>Lattanzi, Simona</creatorcontrib><title>Usage and impact of patient‐reported outcomes in epilepsy</title><title>Brain and behavior</title><addtitle>Brain Behav</addtitle><description>Background
The use of patient‐reported outcomes (PRO) in clinical practice is gaining increasing attention. This study aimed to provide a critical assessment of the current state‐of‐the‐art and beliefs about the use of PRO in the management of people with epilepsy across some European countries.
Methods
Structured interviews were conducted with European experts to collect insights about (I) the personal experience with PRO; (II) the value and impact of PRO in the decision‐making process at the national level; and (III) the interest for and use of PRO by national health authorities.
Results
Nine neurologists (Austria, Belgium, Czechia, Denmark, France, Greece, Italy, Poland, and United Kingdom), three health economists (Portugal, Romania, and Sweden), and one epidemiologist (Slovakia) participated. They all stated that PRO are collected at their own countries in the context of clinical trials and/or specific projects. During everyday clinical practice, PRO are collected routinely/almost routinely in Austria and Sweden and only at the discretion of the treating physicians in Czechia, Denmark, France, Greece, and Portugal. There was complete consensus about the favorable impact that the PRO can have in terms of clinical outcomes, healthcare resources utilization, and general patient satisfaction. Only participants from Portugal and Sweden answered that the PRO are perceived as very important by the National Health Authorities of their respective countries.
Conclusions
Differences exist in attitudes and perspectives about PRO in epilepsy across Europe. An active plan is warranted to harmonize the measurement of PRO and ensure they can be relevant to people with epilepsy and health services.</description><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Convulsions & seizures</subject><subject>Decision making</subject><subject>economics</subject><subject>Epilepsy</subject><subject>Health care</subject><subject>Interviews</subject><subject>Mental health</subject><subject>Original</subject><subject>Patient satisfaction</subject><subject>patient‐reported outcomes</subject><subject>Physicians</subject><subject>Quality of life</subject><subject>Questionnaires</subject><subject>seizure</subject><issn>2162-3279</issn><issn>2162-3279</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kc1qFTEUx4MottQufAEZcKOL2-ZzJsGFtMWPQkEQuw5nkpPrXGYmYzKj3J2P4DP6JOb21tIKZpNw8uPHOedPyHNGTxil_LRNrTgRQvJH5JCzmq8Eb8zje-8DcpzzhpajmOSSPiUHojGmUbU8JG-uM6yxgtFX3TCBm6sYqgnmDsf5989fCaeYZvRVXGYXB8xVN1Y4dT1OefuMPAnQZzy-vY_I9ft3Xy4-rq4-fbi8OLtaOcUoX3mo21o5ylTjZd0YoYPnoQ1UCcVAMKAtpaWqJUAw0HJAqUTwmptguGPiiFzuvT7Cxk6pGyBtbYTO3hRiWltIc-d6tAy14S0KYNpLVNLUzCO4pmHSA7q6uN7uXdPSDuhdGTNB_0D68Gfsvtp1_G4ZbXita14Mr24NKX5bMM926LLDvocR45It12UWITXdNf7yH3QTlzSWXVluKNdaGa4L9XpPuRRzThjuumHU7iK2u4jtLuLCvrjf_h35N9ACnO6BHyWj7f9N9vzzubhR_gF0Za_0</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Vonck, Kristl</creator><creator>Biraben, Arnaud</creator><creator>Bosak, Magdalena</creator><creator>Jennum, Poul Jørgen</creator><creator>Kimiskidis, Vasilios K</creator><creator>Marusic, Petr</creator><creator>Mitchell, James W.</creator><creator>Ferreira, Lara N.</creator><creator>Ondrušová, Martina</creator><creator>Pana, Adrian</creator><creator>Persson, Ulf</creator><creator>Oertzen, Tim J.</creator><creator>Lattanzi, Simona</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3335-3019</orcidid><orcidid>https://orcid.org/0000-0003-2378-7750</orcidid></search><sort><creationdate>202312</creationdate><title>Usage and impact of patient‐reported outcomes in epilepsy</title><author>Vonck, Kristl ; Biraben, Arnaud ; Bosak, Magdalena ; Jennum, Poul Jørgen ; Kimiskidis, Vasilios K ; Marusic, Petr ; Mitchell, James W. ; Ferreira, Lara N. ; Ondrušová, Martina ; Pana, Adrian ; Persson, Ulf ; Oertzen, Tim J. ; Lattanzi, Simona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5102-da6b65c0157d467938fd2fbf05351a31a0b0093884aaf9ab2ae453fd829f92c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Clinical outcomes</topic><topic>Clinical trials</topic><topic>Convulsions & seizures</topic><topic>Decision making</topic><topic>economics</topic><topic>Epilepsy</topic><topic>Health care</topic><topic>Interviews</topic><topic>Mental health</topic><topic>Original</topic><topic>Patient satisfaction</topic><topic>patient‐reported outcomes</topic><topic>Physicians</topic><topic>Quality of life</topic><topic>Questionnaires</topic><topic>seizure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vonck, Kristl</creatorcontrib><creatorcontrib>Biraben, Arnaud</creatorcontrib><creatorcontrib>Bosak, Magdalena</creatorcontrib><creatorcontrib>Jennum, Poul Jørgen</creatorcontrib><creatorcontrib>Kimiskidis, Vasilios K</creatorcontrib><creatorcontrib>Marusic, Petr</creatorcontrib><creatorcontrib>Mitchell, James W.</creatorcontrib><creatorcontrib>Ferreira, Lara N.</creatorcontrib><creatorcontrib>Ondrušová, Martina</creatorcontrib><creatorcontrib>Pana, Adrian</creatorcontrib><creatorcontrib>Persson, Ulf</creatorcontrib><creatorcontrib>Oertzen, Tim J.</creatorcontrib><creatorcontrib>Lattanzi, Simona</creatorcontrib><collection>Wiley_OA刊</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest - Publicly Available Content Database</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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Brain and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vonck, Kristl</au><au>Biraben, Arnaud</au><au>Bosak, Magdalena</au><au>Jennum, Poul Jørgen</au><au>Kimiskidis, Vasilios K</au><au>Marusic, Petr</au><au>Mitchell, James W.</au><au>Ferreira, Lara N.</au><au>Ondrušová, Martina</au><au>Pana, Adrian</au><au>Persson, Ulf</au><au>Oertzen, Tim J.</au><au>Lattanzi, Simona</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Usage and impact of patient‐reported outcomes in epilepsy</atitle><jtitle>Brain and behavior</jtitle><addtitle>Brain Behav</addtitle><date>2023-12</date><risdate>2023</risdate><volume>13</volume><issue>12</issue><spage>e3342</spage><epage>n/a</epage><pages>e3342-n/a</pages><issn>2162-3279</issn><eissn>2162-3279</eissn><abstract>Background
The use of patient‐reported outcomes (PRO) in clinical practice is gaining increasing attention. This study aimed to provide a critical assessment of the current state‐of‐the‐art and beliefs about the use of PRO in the management of people with epilepsy across some European countries.
Methods
Structured interviews were conducted with European experts to collect insights about (I) the personal experience with PRO; (II) the value and impact of PRO in the decision‐making process at the national level; and (III) the interest for and use of PRO by national health authorities.
Results
Nine neurologists (Austria, Belgium, Czechia, Denmark, France, Greece, Italy, Poland, and United Kingdom), three health economists (Portugal, Romania, and Sweden), and one epidemiologist (Slovakia) participated. They all stated that PRO are collected at their own countries in the context of clinical trials and/or specific projects. During everyday clinical practice, PRO are collected routinely/almost routinely in Austria and Sweden and only at the discretion of the treating physicians in Czechia, Denmark, France, Greece, and Portugal. There was complete consensus about the favorable impact that the PRO can have in terms of clinical outcomes, healthcare resources utilization, and general patient satisfaction. Only participants from Portugal and Sweden answered that the PRO are perceived as very important by the National Health Authorities of their respective countries.
Conclusions
Differences exist in attitudes and perspectives about PRO in epilepsy across Europe. An active plan is warranted to harmonize the measurement of PRO and ensure they can be relevant to people with epilepsy and health services.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>37997564</pmid><doi>10.1002/brb3.3342</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3335-3019</orcidid><orcidid>https://orcid.org/0000-0003-2378-7750</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Clinical outcomes Clinical trials Convulsions & seizures Decision making economics Epilepsy Health care Interviews Mental health Original Patient satisfaction patient‐reported outcomes Physicians Quality of life Questionnaires seizure |
title | Usage and impact of patient‐reported outcomes in epilepsy |
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