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Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis

BACKGROUND: Involving the end-users of scientific research (patients, carers and clinicians) in setting research priorities is important to formulate research questions that truly make a difference and are in tune with the needs of patients. We therefore aimed to generate a national research agenda...

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Autores principales: Verwoerd, Anouk, Armbrust, Wineke, Cowan, Katherine, van den Berg, Lotte, de Boer, Joke, Bookelman, Sanne, Britstra, Marjan, Cappon, Jeannette, Certan, Maria, Dedding, Christine, van den Haspel, Karin, Muller, Petra Hissink, Jongsma, Karin, Lelieveld, Otto, van Loosdregt, Jorg, Olsder, Wendy, Rocha, Johanna, Schatorjé, Ellen, Schouten, Natasja, Swart, Joost F., Vastert, Sebastiaan, Walter, Margot, Schoemaker, Casper G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028801/
https://www.ncbi.nlm.nih.gov/pubmed/33827608
http://dx.doi.org/10.1186/s12969-021-00540-2
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author Verwoerd, Anouk
Armbrust, Wineke
Cowan, Katherine
van den Berg, Lotte
de Boer, Joke
Bookelman, Sanne
Britstra, Marjan
Cappon, Jeannette
Certan, Maria
Dedding, Christine
van den Haspel, Karin
Muller, Petra Hissink
Jongsma, Karin
Lelieveld, Otto
van Loosdregt, Jorg
Olsder, Wendy
Rocha, Johanna
Schatorjé, Ellen
Schouten, Natasja
Swart, Joost F.
Vastert, Sebastiaan
Walter, Margot
Schoemaker, Casper G.
author_facet Verwoerd, Anouk
Armbrust, Wineke
Cowan, Katherine
van den Berg, Lotte
de Boer, Joke
Bookelman, Sanne
Britstra, Marjan
Cappon, Jeannette
Certan, Maria
Dedding, Christine
van den Haspel, Karin
Muller, Petra Hissink
Jongsma, Karin
Lelieveld, Otto
van Loosdregt, Jorg
Olsder, Wendy
Rocha, Johanna
Schatorjé, Ellen
Schouten, Natasja
Swart, Joost F.
Vastert, Sebastiaan
Walter, Margot
Schoemaker, Casper G.
author_sort Verwoerd, Anouk
collection PubMed
description BACKGROUND: Involving the end-users of scientific research (patients, carers and clinicians) in setting research priorities is important to formulate research questions that truly make a difference and are in tune with the needs of patients. We therefore aimed to generate a national research agenda for Juvenile Idiopathic Arthritis (JIA) together with patients, their caregivers and healthcare professionals through conducting a nationwide survey among these stakeholders. METHODS: The James Lind Alliance method was used, tailored with additional focus groups held to involve younger patients. First, research questions were gathered through an online and hardcopy survey. The received questions that were in scope were summarised and a literature search was performed to verify that questions were unanswered. Questions were ranked in the interim survey, and the final top 10 was chosen during a prioritisation workshop. RESULTS: Two hundred and seventy-eight respondents submitted 604 questions, of which 519 were in scope. Of these 604 questions, 81 were generated in the focus groups with younger children. The questions were summarised into 53 summary questions. An evidence checking process verified that all questions were unanswered. A total of 303 respondents prioritised the questions in the interim survey. Focus groups with children generated a top 5 of their most important questions. Combining this top 5 with the top 10s of patients, carers, and clinicians led to a top 21. Out of these, the top 10 research priorities were chosen during a final workshop. Research into pain and fatigue, personalised treatment strategies and aetiology were ranked high in the Top 10. CONCLUSIONS: Through this study, the top 10 research priorities for JIA of patients, their caregivers and clinicians were identified to inform researchers and research funders of the research topics that matter most to them. The top priority involves the treatment and mechanisms behind persisting pain and fatigue when the disease is in remission.
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spelling pubmed-80288012021-04-09 Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis Verwoerd, Anouk Armbrust, Wineke Cowan, Katherine van den Berg, Lotte de Boer, Joke Bookelman, Sanne Britstra, Marjan Cappon, Jeannette Certan, Maria Dedding, Christine van den Haspel, Karin Muller, Petra Hissink Jongsma, Karin Lelieveld, Otto van Loosdregt, Jorg Olsder, Wendy Rocha, Johanna Schatorjé, Ellen Schouten, Natasja Swart, Joost F. Vastert, Sebastiaan Walter, Margot Schoemaker, Casper G. Pediatr Rheumatol Online J Research Article BACKGROUND: Involving the end-users of scientific research (patients, carers and clinicians) in setting research priorities is important to formulate research questions that truly make a difference and are in tune with the needs of patients. We therefore aimed to generate a national research agenda for Juvenile Idiopathic Arthritis (JIA) together with patients, their caregivers and healthcare professionals through conducting a nationwide survey among these stakeholders. METHODS: The James Lind Alliance method was used, tailored with additional focus groups held to involve younger patients. First, research questions were gathered through an online and hardcopy survey. The received questions that were in scope were summarised and a literature search was performed to verify that questions were unanswered. Questions were ranked in the interim survey, and the final top 10 was chosen during a prioritisation workshop. RESULTS: Two hundred and seventy-eight respondents submitted 604 questions, of which 519 were in scope. Of these 604 questions, 81 were generated in the focus groups with younger children. The questions were summarised into 53 summary questions. An evidence checking process verified that all questions were unanswered. A total of 303 respondents prioritised the questions in the interim survey. Focus groups with children generated a top 5 of their most important questions. Combining this top 5 with the top 10s of patients, carers, and clinicians led to a top 21. Out of these, the top 10 research priorities were chosen during a final workshop. Research into pain and fatigue, personalised treatment strategies and aetiology were ranked high in the Top 10. CONCLUSIONS: Through this study, the top 10 research priorities for JIA of patients, their caregivers and clinicians were identified to inform researchers and research funders of the research topics that matter most to them. The top priority involves the treatment and mechanisms behind persisting pain and fatigue when the disease is in remission. BioMed Central 2021-04-07 /pmc/articles/PMC8028801/ /pubmed/33827608 http://dx.doi.org/10.1186/s12969-021-00540-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Verwoerd, Anouk
Armbrust, Wineke
Cowan, Katherine
van den Berg, Lotte
de Boer, Joke
Bookelman, Sanne
Britstra, Marjan
Cappon, Jeannette
Certan, Maria
Dedding, Christine
van den Haspel, Karin
Muller, Petra Hissink
Jongsma, Karin
Lelieveld, Otto
van Loosdregt, Jorg
Olsder, Wendy
Rocha, Johanna
Schatorjé, Ellen
Schouten, Natasja
Swart, Joost F.
Vastert, Sebastiaan
Walter, Margot
Schoemaker, Casper G.
Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title_full Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title_fullStr Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title_full_unstemmed Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title_short Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
title_sort dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028801/
https://www.ncbi.nlm.nih.gov/pubmed/33827608
http://dx.doi.org/10.1186/s12969-021-00540-2
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