Literature DB >> 28250139

Healthcare and Research Priorities of Adolescents and Young Adults with Systemic Lupus Erythematosus: A Mixed-methods Study.

David J Tunnicliffe1,2, Davinder Singh-Grewal3,4, Jonathan C Craig3,4, Martin Howell3,4, Peter Tugwell3,4, Fiona Mackie3,4, Ming-Wei Lin3,4, Sean G O'Neill3,4, Angelique F Ralph3,4, Allison Tong3,4.   

Abstract

OBJECTIVE: Managing juvenile-onset systemic lupus erythematosus (SLE) is particularly challenging. The disease may be severe, adolescent patients have complex medical and psychosocial needs, and patients must navigate the transition to adult services. To inform patient-centered care, we aimed to identify the healthcare and research priorities of young patients with SLE and describe the reasons underpinning their priorities.
METHODS: Face-to-face, semistructured interviews and focus groups were conducted with patients with SLE, aged from 14 to 26 years, from 5 centers in Australia. For each of the 5 allocation exercises, participants allocated 10 votes to (1) research topics; research questions on (2) medical management, (3) prevention and diagnosis, (4) lifestyle and psychosocial; and (5) healthcare specialties, and discussed the reasons for their choices. Descriptive statistics were calculated for votes and qualitative data were analyzed thematically.
RESULTS: The 26 participants prioritized research that alleviated the psychological burden of SLE. They allocated their votes toward medical and mental health specialties in the management of SLE, while fewer votes were given to physiotherapy/occupational therapy and dietetics. The following 7 themes underpinned the participants' priorities: improving service shortfalls, strengthening well-being, ensuring cost efficiency, minimizing family/community burden, severity of comorbidity or complications, reducing lifestyle disruption, and fulfilling future goals.
CONCLUSION: Young patients with SLE value comprehensive care with greater coordination among specialties. They prioritized research focused on alleviating poor psychological outcomes. The healthcare and research agenda for patients with SLE should include everyone involved, to ensure that the agenda aligns with patient priorities, needs, and values.

Entities:  

Keywords:  ADOLESCENT; HEALTH PRIORITIES; PATIENTS; QUALITATIVE RESEARCH; SYSTEMIC LUPUS ERYTHEMATOSUS

Mesh:

Year:  2017        PMID: 28250139     DOI: 10.3899/jrheum.160720

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  9 in total

1.  Self-management and adherence in childhood-onset systemic lupus erythematosus: what are we missing?

Authors:  O Harry; L E Crosby; A W Smith; L Favier; N Aljaberi; T V Ting; J L Huggins; A C Modi
Journal:  Lupus       Date:  2019-03-24       Impact factor: 2.911

2.  The Your Rheum story: involvement of young people in rheumatology research.

Authors:  Ecem Esen; Suruthi Gnanenthiran; Laura Lunt; Janet E McDonagh
Journal:  BMC Rheumatol       Date:  2022-07-05

3.  The Needs of Adolescents and Young Adults with Chronic Illness: Results of a Quality Improvement Survey.

Authors:  Taryn Allen; Stephanie Reda; Staci Martin; Phoebe Long; Alexis Franklin; Sima Zadeh Bedoya; Lori Wiener; Pamela L Wolters
Journal:  Children (Basel)       Date:  2022-04-02

Review 4.  Mental health care for youth with rheumatologic diseases - bridging the gap.

Authors:  Alaina M Davis; Tamar B Rubinstein; Martha Rodriguez; Andrea M Knight
Journal:  Pediatr Rheumatol Online J       Date:  2017-12-28       Impact factor: 3.054

Review 5.  Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: a study protocol.

Authors:  Casper G Schoemaker; Wineke Armbrust; Joost F Swart; Sebastiaan J Vastert; Jorg van Loosdregt; Anouk Verwoerd; Caroline Whiting; Katherine Cowan; Wendy Olsder; Els Versluis; Rens van Vliet; Marlous J Fernhout; Sanne L Bookelman; Jeannette Cappon; J Merlijn van den Berg; Ellen Schatorjé; Petra C E Hissink Muller; Sylvia Kamphuis; Joke de Boer; Otto T H M Lelieveld; Janjaap van der Net; Karin R Jongsma; Annemiek van Rensen; Christine Dedding; Nico M Wulffraat
Journal:  Pediatr Rheumatol Online J       Date:  2018-09-15       Impact factor: 3.054

6.  Going viral in rheumatology: using social media to show that mechanistic research is relevant to patients with lupus and antiphospholipid syndrome.

Authors:  Thomas C R McDonnell; Chris Wincup; Anisur Rahman; Ian Giles
Journal:  Rheumatol Adv Pract       Date:  2018-03-05

Review 7.  Scoping review of priority setting of research topics for musculoskeletal conditions.

Authors:  Allison M Bourne; Renea V Johnston; Sheila Cyril; Andrew M Briggs; Ornella Clavisi; Gustavo Duque; Ian A Harris; Catherine Hill; Claire Hiller; Steven J Kamper; Jane Latimer; Andrew Lawson; Chung-Wei Christine Lin; Christopher Maher; Diana Perriman; Bethan L Richards; Peter Smitham; William John Taylor; Sam Whittle; Rachelle Buchbinder
Journal:  BMJ Open       Date:  2018-12-16       Impact factor: 2.692

8.  Incorporating Unstructured Patient Narratives and Health Insurance Claims Data in Pharmacovigilance: Natural Language Processing Analysis of Patient-Generated Texts About Systemic Lupus Erythematosus.

Authors:  Shinichi Matsuda; Takumi Ohtomo; Shiho Tomizawa; Yuki Miyano; Miwako Mogi; Hiroshi Kuriki; Terumi Nakayama; Shinichi Watanabe
Journal:  JMIR Public Health Surveill       Date:  2021-06-29

9.  What do young people with rheumatic disease believe to be important to research about their condition? A UK-wide study.

Authors:  Suzanne Parsons; Wendy Thomson; Katharine Cresswell; Bella Starling; Janet E McDonagh
Journal:  Pediatr Rheumatol Online J       Date:  2017-07-03       Impact factor: 3.054

  9 in total

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