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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
Main Authors: 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
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container_title Brain and behavior
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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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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 &amp; Sons, Inc</publisher><subject>Clinical outcomes ; Clinical trials ; Convulsions &amp; 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. 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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 &amp; 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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source Wiley_OA刊; ProQuest - Publicly Available Content Database; PubMed Central
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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