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

Publication date

2021-04-07

Authors

Verwoerd, Anouk
Armbrust, Wineke
Cowan, Katherine
van den Berg, Lotte
de Boer, JokeISNI 0000000389203367
Bookelman, Sanne
Britstra, Marjan
Cappon, Jeannette
Certan, Maria
Dedding, Christine

Editors

Advisors

Supervisors

Document Type

Article

Collections

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License

cc_by

Abstract

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.

Keywords

James Lind Alliance, Juvenile idiopathic arthritis, Patient involvement, Research priority setting, Pediatrics, Perinatology, and Child Health, Rheumatology, Immunology and Allergy

Citation

Verwoerd, A, Armbrust, W, Cowan, K, van den Berg, L, de Boer, J, Bookelman, S, Britstra, M, Cappon, J, Certan, M, Dedding, C, van den Haspel, K, Muller, P H, Jongsma, K, Lelieveld, O, van Loosdregt, J, Olsder, W, Rocha, J, Schatorjé, E, Schouten, N, Swart, J F, Vastert, S, Walter, M & Schoemaker, C G 2021, 'Dutch patients, caregivers and healthcare professionals generate first nationwide research agenda for juvenile idiopathic arthritis', Pediatric Rheumatology, vol. 19, no. 1, 52, pp. 1-10. https://doi.org/10.1186/s12969-021-00540-2